CRISPR/CAS-RELATED METHODS AND COMPOSITIONS FOR TREATING SICKLE CELL DISEASE

- EDITAS MEDICINE, INC.

CRISPR/CAS-related compositions and methods for treatment of Sickle Cell Disease (SCD) are disclosed.

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Description
REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. application Ser. No. 15/129,367, filed Sep. 26, 2016, which is a national phase of International Application No. PCT/US2015/022856, filed Mar. 26, 2015, which claims the benefit of U.S. Provisional Application No. 61/970,588, filed Mar. 26, 2014, and U.S. Provisional Application No. 62/084,487, filed Nov. 25, 2014, the contents of each of which are hereby incorporated by reference in their entirety.

FIELD OF THE INVENTION

The invention relates to CRISPR/CAS-related methods and components for editing of a target nucleic acid sequence, or modulating expression of a target nucleic acid sequence, and applications thereof in connection with Sickle Cell Disease (SCD).

SEQUENCE LISTING

This application contains a Sequence Listing, which was submitted in ASCII format via EFS-Web, and is hereby incorporated by reference in its entirety. The ASCII copy, created on Jan. 19, 2022, is named SequenceListing.txt and is 3,905 KB in size.

BACKGROUND

Sickle Cell Disease (SCD), also known as Sickle Cell Anemia (SCA), is a common inherited hematologic disease. It affects 80,000-90,000 people in the United States. It is common in people of African descent and in Hispanic-Americans with the prevalence of SCD being 1 in 500 and 1 in 1,000, respectively.

SCD is caused by a mutation in the beta-globin (HBB) gene. HBB is located on chromosome 11 within the HBB gene cluster, which includes genes encoding the delta globin chain, A gamma chain, G gamma chain. The alpha-globin gene is located on chromosome 16. A point mutation (e.g., GAG→GTG) results in the substitution of valine for glutamic acid at amino acid position 6 in exon 1 of the HBB gene. Beta hemoglobin chains with this mutation are expressed as HbS. The disease is inherited in an autosomal recessive manner, so that only patients with two HbS alleles have SCD. Subjects who have sickle cell trait (are heterozygous for HbS) only display a phenotype if they are severely dehydrated or oxygen deprived.

Normal adult hemoglobin (Hb) is composed of a tetramer made from two alpha-globin chains and two beta-globin chains. In SCD, the valine at position 6 of the beta-chain is hydrophobic and causes a change in conformation of the beta-globin protein when it is not bound to oxygen. HbS is more likely to polymerize and leads to the characteristic sickle shaped red blood cells (RBCs) found in SCD.

Sickle shape RBCs cause multiple manifestations of disease, which include, e.g., anemia, sickle cell crises, vaso-occlusive crises, aplastic crises and acute chest syndrome. The disease has varous manifestations, e.g., vaso-occlusive crisis, splenic sequestration crisis and anemia. Subjects may also suffer from acute chest crisis and infarcts of extremities, end organs and central nervous system. Treatment includes, e.g., hydration, transfusion and analgesics. Treatment of SCD also includes, e.g., the use of hydroxyurea, supplementation with folic acid, and penicillin prophylaxis during childhood. Bone marrow transplants have been demonstrated to cure SCD.

Thus, there remains a need for additional methods and compositions that can be used to treat SCD.

SUMMARY OF THE INVENTION

Methods and compositions discussed herein, provide for the treatment and prevention of Sickle Cell Disease (SCD), also known as Sickle Cell Anemia (SCA). SCD is an inherited hematologic disease.

In healthy individuals, two beta-globin molecules pair with two alpha-globin molecules to form normal hemoglobin (Hb). In SCD, mutations in the beta-globin (HBB) gene, e.g., a point mutation (GAG→GTG) that results in the substitution of valine for glutamic acid at amino acid position 6 of the beta-globin molecule, cause production of sickle hemoglobin (HbS). HbS is more likely to polymerize and leads to the characteristic sickle shaped red blood cells (RBCs). Sickle shaped RBCs give rise to multiple manifestations of disease, such as, anemia, sickle cell crises, vaso-occlusive crises, aplastic crises and acute chest syndrome. Alpha-globin can also pair with fetal hemoglobin (HbF), which significantly moderates the severe anemia and other symptoms of SCD. However, the expression of HbF is negatively regulated by the BCL11A gene product.

Methods and compositions disclosed herein provide a number of approaches for treating SCD. As is discussed in more detail below, methods described herein provide for treating SCD by correcting a target position in the HBB gene to provide corrected, or functional, e.g., wild type, beta-globin. Methods and compositions discussed herein can be used to treat or prevent SCD by altering the BCL11A gene (also known as B-cell CLL/lymphoma 11A, BCL11A-L, BCL11A-S, BCL11A-XL, CTIP1, HBFQTL5 and ZNF). BCL11A encodes a zinc-finger protein that is involved in the regulation of globin gene expression. By altering the BCL11A gene (e.g., one or both alleles of the BCL11A gene), the levels of gamma globin can be increased. Gamma globin can replace beta globin in the hemoglobin complex and effectively carry oxygen to tissues, thereby ameliorating SCD disease phenotypes.

In one aspect, methods and compositions discussed herein, provide for the correction of the underlying genetic cause of SCD, e.g., the correction of a mutation at a target position in the HBB gene, e.g., correction of a mutation at amino acid position 6, e.g., an E6V substitution in the HBB gene.

Mutations in the HBB gene (also known as beta-globin and CD113t-C) have been shown to cause SCD. Mutations leading to SCD can be described based on their target positions in the HBB gene. In an embodiment, the target position is E6, e.g., E6V, in the HBB gene.

“SCD target point position”, as used herein, refers to a target position in the HBB gene, typically a single nucleotide, which, if mutated, can result in a protein having a mutant amino acid and give rise to SCD. In an embodiment, the SCD target position is the target position at which a change can give rise to an E6 mutant protein, e.g., a protein having an E6V substitution.

While much of the disclosure herein is presented in the context of the mutation in the HBB gene that gives rise to an E6 mutant protein (e.g., E6V mutant protein), the methods and compositions herein are broadly applicable to any mutation, e.g., a point mutation or a deletion, in the HBB gene that gives rise to SCD.

While not wishing to be bound by theory, it is believed that, in an embodiment, a mutation at an SCD target point position in the HBB gene is corrected, e.g., by homology directed repair (HDR), as described herein.

In one aspect, methods and compositions discussed herein may be used to alter the BCL11A gene to treat or prevent SCD, by targeting the BCL11A gene, e.g., coding or non-coding regions of the BCL11A gene. Altering the BCL11A gene herein refers to reducing or eliminating (1) BCL11A gene expression, (2) BCL11A protein function, or (3) the level of BCL11A protein.

In an embodiment, the coding region (e.g., an early coding region) of the BCL11A gene is targeted for alteration. In an embodiment, a non-coding sequence (e.g., an enhancer region, a promoter region, an intron, 5′UTR, 3′UTR, or polyadenylation signal) is targeted for alteration.

In an embodiment, the method provides an alteration that comprises disrupting the BCL11A gene by the insertion or deletion of one or more nucleotides mediated by Cas9 (e.g., enzymatically active Cas9 (eaCas9), e.g., Cas9 nuclease or Cas9 nickase) as described below. This type of alteration is also referred to as “knocking out” the BCL11A gene.

In another embodiment, the method provides an alteration that does not comprise nucleotide insertion or deletion in the BCL11A gene and is mediated by enzymatically inactive Cas9 (eiCas9) or an eiCas9-fusion protein, as described below. This type of alteration is also referred to as “knocking down” the BCL11A gene.

In an embodiment, the methods and compositions discussed herein may be used to alter the BCL11A gene to treat or prevent SCD by knocking out one or both alleles of the BCL11A gene. In an embodiment, the coding region (e.g., an early coding region) of the BCL11A gene, is targeted to alter the gene. In an embodiment, a non-coding region of the BCL11A gene (e.g., an enhancer region, a promoter region, an intron, 5′ UTR, 3′UTR, polyadenylation signal) is targeted to alter the gene. In an embodiment, an enhancer (e.g., a tissue-specific enhancer, e.g., a myeloid enhancer, e.g., an erythroid enhancer) is targeted to alter the gene. BCL11A erythroid enhancer comprises an approximate 12.4 kb fragment of BCL11A intron2, located between approximate+52.0 to +64.4 kilobases (kb) from the Transcription Start Site (TSS+52 kb to TSS+64.4 kb, see FIG. 10). It's also referred to herein as chromosome 2 location 60,716,189-60,728,612 (according to UCSC Genome Browser hg 19 human genome assembly). Three deoxyribonuclese I hypersensitive sites (DHSs), TSS+62 kb, TSS+58 kb and TSS+55 kb are located in this region. Deoxyribonuclease I sensitivity is a marker for gene regulatory elements. While not wishing to be bound by theory, it's believed that deleting the ehancer region (e.g., TSS+52 kb to TSS+64.4 kb) may reduce or eliminate BCL11A expression in erythroid precursors which leads to gamma globin derepression while sparing BCL11A expression in nonerythoroid lineages. In an embodiment, the method provides an alteration that comprises a deletion of the enhancer region (e.g., a tissue-specific enhancer, e.g., a myleloid enhancer, e.g., an erythroid enhancer) or a protion of the region resulting in disruption of one or more DNase 1-hypersensitivie sites (DHS). In an embodiment, the method provides an alteration that comprises an insertion or deletion of one or more nucleotides. As described herein, in an embodiment, a targeted knockout approach is mediated by non-homologous end joining (NHEJ) using a CRISPR/Cas system comprising an enzymatically active Cas9 (eaCas9). In an embodiment, a targeted knockout approach alters the BCL11A gene. In an embodiment, a targeted knockout approach reduces or eliminates expression of functional BCL11A gene product. In an embodiment, targeting affects one or both alleles of the BCL11A gene. In an embodiment, an enhancer disruption approach reduces or eliminates expression of functional BCL11A gene product in the erythroid lineage.

“SCD target knockout position”, as used herein, refers to a position in the BCL11A gene, which if altered, e.g., disrupted by insertion or deletion of one or more nucleotides, e.g., by NHEJ-mediated alteration, results in reduction or elimination of expression of functional BCL11A gene product. In an embodiment, the position is in the BCL11A coding region, e.g., an early coding region. In an embodiment, the position is in the BCL11A non-coding region, e.g., an enhancer region.

In an embodiment, methods and compositions discussed herein, provide for altering (e.g., knocking out) the BCL11A gene. In an embodiment, knocking out the BCL11A gene herein refers to (1) insertion or deletion (e.g., NHEJ-mediated insertion or deletion) of one or more nucleotides in close proximity to or within the early coding region of the BCL11A gene, or (2) deletion (e.g., NHEJ-mediated deletion) of a genomic sequence including the erythroid enhancer of the BCL11A gene,

In an embodiment, the SCD target knockout position is altered by genome editing using the CRISPR/Cas9 system. The SCD target knockout position may be targeted by cleaving with either a single nuclease or dual nickases, e.g., to induce insertion or deletion (e.g., NHEJ-mediated insertion or deletion) of one or more nucleotides in close proximity to or within the early coding region of the SCD target knockout position or to delete (e.g., mediated by NHEJ) a genomic sequence including the erythroid enhancer of the BCL11A gene.

In an embodiment, the methods and compositions described herein introduce one or more breaks in close proximity to or within the early coding region in at least one allele of the BCL11A gene. In an embodiment, a single strand break is introduced in close proximity to or within the early coding region in at least one allele of the BCL11A gene. In an embodiment, the single strand break will be accompanied by an additional single strand break, positioned by a second gRNA molecule.

In an embodiment, a double strand break is introduced in close proximity to or within the early coding region in at least one allele of the BCL11A gene. In an embodiment, a double strand break will be accompanied by an additional single strand break positioned by a second gRNA molecule. In an embodiment, a double strand break will be accompanied by two additional single strand breaks positioned by a second gRNA molecule and a third gRNA molecule.

In an embodiment, a pair of single strand breaks is introduced in close proximity to or within the early coding region in at least one allele of the BCL11A gene. In an embodiment, the pair of single strand breaks will be accompanied by an additional double strand break, positioned by a third gRNA molecule. In an embodiment, the pair of single strand breaks will be accompanied by an additional pair of single strand breaks positioned by a third gRNA molecule and a fourth gRNA molecule.

In an embodiment, two double strand breaks are introduced to flank the erythroid enhancer at the in the BCL11A gene (one 5′ and the other one 3′ to the erythroid enhancer) to remove (e.g., delete) the genomic sequence including the erythroid enhancer. It is contemplated herein that in an embodiment the deletion of the genomic sequence including the erythroid enhancer is mediated by NHEJ. In an embodiment, the breaks (i.e., the two double strand breaks) are positioned to avoid unwanted deletion of certain elements, such as endogenous splice sites. The breaks, i.e., two double strand breaks, can be positioned upstream and downstream of the erythroid enhancer, as discussed herein.

In an embodiment, two sets of breaks (e.g., one double strand break and a pair of single strand breaks) are introduced to flank the erythroid enhancer in the BCL11A gene (one set 5′ and the other set 3′ to the erythroid enhancer) to remove (e.g., delete) the genomic sequence including the erythroid enhancer. It is contemplated herein that in an embodiment the deletion of the genomic sequence including the erythroid enhancer is mediated by NHEJ. In an embodiment, the breaks (i.e., the double strand break and the pair of single strand breaks) are positioned to avoid unwanted deletion of certain chromosome elements, such as endogenous splice sites. The breaks, e.g., the double strand break and the pair of single strand breaks, can be positioned upstream and downstream of the erythroid enhancer, as discussed herein.

In an embodiment, two sets of breaks (e.g., two pairs of single strand breaks) are introduced to flank the erythroid enhancer at the SCD target position in the BCL11A gene (one set 5′ and the other set 3′ to the erythroid enhancer) to remove (e.g., delete) the genomic sequence including the erythroid enhancer. It is contemplated herein that in an embodiment the deletion of the genomic sequence including the erythroid enhancer is mediated by NHEJ. In an embodiment, the breaks (i.e., the two pairs of single strand breaks) are positioned to avoid unwanted deletion of certain chromosome elements, such as endogenous splice sites. The breaks, e.g., the two pairs of single strand breaks, can be positioned upstream and downstream of the erythroid enhancer, as discussed herein.

In an embodiment, the methods and compositions discussed herein may be used to alter the BCL11A gene to treat or prevent SCD by knocking down one or both alleles of the BCL11A gene. In one embodiment, the coding region of the BCL11A gene, is targeted to alter the gene. In another embodiment, a non-coding region (e.g., an enhancer region, a promoter region, an intron, 5′ UTR, 3′UTR, polyadenylation signal) of the BCL11A gene is targeted to alter the gene. In an embodiment, the promoter region of the BCL11A gene is targeted to knock down the expression of the BCL11A gene. A targeted knockdown approach alters, e.g., reduces or eliminates the expression of the BCL11A gene. As described herein, in an embodiment, a targeted knockdown is mediated by targeting an enzymatically inactive Cas9 (eiCas9) or an eiCas9 fused to a transcription repressor domain or chromatin modifying protein to alter transcription, e.g., to block, reduce, or decrease transcription, of the BCL11A gene.

“SCD target knockdown position”, as used herein, refers to a position, e.g., in the BCL11A gene, which if targeted by an eiCas9 or an eiCas9 fusion described herein, results in reduction or elimination of expression of functional BCL11A gene product. In an embodiment, transcription is reduced or eliminated. In an embodiment, the position is in the BCL11A promoter sequence. In an embodiment, a position in the promoter sequence of the BCL11A gene is targeted by an enzymatically inactive Cas9 (eiCas9) or an eiCas9-fusion protein, as described herein.

In an embodiment, one or more gRNA molecule comprising a targeting domain configured to target an enzymatically inactive Cas9 (eiCas9) or an eiCas9 fusion protein (e.g., an eiCas9 fused to a transcription repressor domain), sufficiently close to a SCD target knockdown position to reduce, decrease or repress expression of the BCL11A gene.

“SCD target position”, as used herein, refers to any of an SCD target point position, SCD target knockout position, or SCD target knockdown position, as described herein.

In one aspect, disclosed herein is a gRNA molecule, e.g., an isolated or non-naturally occurring gRNA molecule, comprising a targeting domain which is complementary with a target domain from the HBB gene or BCL11A gene.

When two or more gRNAs are used to position two or more cleavage events, e.g., double strand or single strand breaks, in a target nucleic acid, it is contemplated that the two or more cleavage events may be made by the same or different Cas9 proteins. For example, when two gRNAs are used to position two double strand breaks, a single Cas9 nuclease may be used to create both double strand breaks. When two or more gRNAs are used to position two or more single stranded breaks (single strand breaks), a single Cas9 nickase may be used to create the two or more single strand breaks. When two or more gRNAs are used to position at least one double strand break and at least one single strand break, two Cas9 proteins may be used, e.g., one Cas9 nuclease and one Cas9 nickase. It is contemplated that when two or more Cas9 proteins are used that the two or more Cas9 proteins may be delivered sequentially to control specificity of a double strand versus a single strand break at the desired position in the target nucleic acid.

In an embodiment, the targeting domain of the first gRNA molecule and the targeting domain of the second gRNA molecule hybridize to the target domain through complementary base pairing to opposite strands of the target nucleic acid molecule. In an embodiment, the gRNA molecule and the second gRNA molecule are configured such that the PAMs are oriented outward.

In an embodiment, the targeting domain of a gRNA molecule is configured to avoid unwanted target chromosome elements, such as repeat elements, e.g., an Alu repeat, or the endogenous splice sites, in the target domain. The gRNA molecule may be a first, second, third and/or fourth gRNA molecule.

In an embodiment, the targeting domain of a gRNA molecule is configured to position a cleavage event sufficiently far from a preselected nucleotide, e.g., the nucleotide of a coding region, such that the nucleotide is not altered. In an embodiment, the targeting domain of a gRNA molecule is configured to position an intronic cleavage event sufficiently far from an intron/exon border, or naturally occurring splice signal, to avoid alteration of the exonic sequence or unwanted splicing events. The gRNA molecule may be a first, second, third and/or fourth gRNA molecule, as described herein.

In an embodiment, a point mutation in the HBB gene, e.g., at E6, e.g., E6V, is targeted, e.g., for correction. In an embodiment, the targeting domain of a gRNA molecule comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 1A-1D. In an embodiment, the targeting domain is selected from those in Tables 1A-1D. For example, in an embodiment, the targeting domain is:

(SEQ ID NO: 387) AAGGUGAACGUGGAUGAAGU; (SEQ ID NO: 388) GUAACGGCAGACUUCUCCUC; (SEQ ID NO: 389) GUGAACGUGGAUGAAGU; or (SEQ ID NO: 390) ACGGCAGACUUCUCCUC.

In an embodiment, when the SCD target point position is E6, e.g., E6V, and two gRNAs are used to position two breaks, e.g., two single stranded breaks, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Tables 1A-1D.

In an embodiment, a point mutation in the HBB gene, e.g., at E6, e.g., E6V, is targeted, e.g., for correction. In an embodiment, the targeting domain of a gRNA molecule comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 13A-13D. In an embodiment, the targeting domain is selected from those in Tables 13A-13D. For example, in an embodiment, the targeting domain is:

(SEQ ID NO: 6803) GGUGCACCUGACUCCUG; or (SEQ ID NO: 6804) GUAACGGCAGACUUCUCCAC.

In an embodiment, when the SCD target point position is E6, e.g., E6V, and two gRNAs are used to position two breaks, e.g., two single stranded breaks, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Tables 13A-13D.

In an embodiment, a point mutation in the HBB gene, e.g., at E6, e.g., E6V, is targeted, e.g., for correction. In an embodiment, the targeting domain of a gRNA molecule comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 14A-14C. In an embodiment, the targeting domain is selected from those in Tables 14A-14C.

In an embodiment, when the SCD target point position is E6, e.g., E6V, and two gRNAs are used to position two breaks, e.g., two single stranded breaks, in the target nucleic acid sequence, each guide RNA is selected from one of Tables 14A-14C.

In an embodiment, a point mutation in the HBB gene, e.g., at E6, e.g., E6V, is targeted, e.g., for correction. In an embodiment, the targeting domain of a gRNA molecule comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 24A-24D. In an embodiment, the targeting domain is selected from those in Tables 24A-24D.

In an embodiment, when the SCD target point position is E6, e.g., E6V, and two gRNAs are used to position two breaks, e.g., two single stranded breaks, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Tables 24A-24D.

In an embodiment, a point mutation in the HBB gene, e.g., at E6, e.g., E6V, is targeted, e.g., for correction. In an embodiment, the targeting domain of a gRNA molecule comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 25A-25B. In an embodiment, the targeting domain is selected from those in Tables 25A-25B.

In an embodiment, when the SCD target point position is E6, e.g., E6V, and two gRNAs are used to position two breaks, e.g., two single stranded breaks, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Tables 25A-25B.

In an embodiment, a point mutation in the HBB gene, e.g., at E6, e.g., E6V, is targeted, e.g., for correction. In an embodiment, the targeting domain of a gRNA molecule comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from Table 26. In an embodiment, the targeting domain is selected from those in Table 26.

In an embodiment, when the SCD target point position is E6, e.g., E6V, and two gRNAs are used to position two breaks, e.g., two single stranded breaks, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from Table 26. In another embodiment, a position in the coding region, e.g., the early coding region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 2A-2F. In an embodiment, the targeting domain is selected from those in Tables 2A-2F. In another embodiment, the targeting domain is:

(SEQ ID NO: 486) UGGCAUCCAGGUCACGCCAG; (SEQ ID NO: 487) GAUGCUUUUUUCAUCUCGAU; (SEQ ID NO: 488) GCAUCCAAUCCCGUGGAGGU; (SEQ ID NO: 489) UUUUCAUCUCGAUUGGUGAA; (SEQ ID NO: 490) CCAGAUGAACUUCCCAUUGG; (SEQ ID NO: 491) AGGAGGUCAUGAUCCCCUUC; (SEQ ID NO: 492) CAUCCAGGUCACGCCAG; (SEQ ID NO: 493) GCUUUUUUCAUCUCGAU; (SEQ ID NO: 494) UCCAAUCCCGUGGAGGU; (SEQ ID NO: 495) UCAUCUCGAUUGGUGAA; (SEQ ID NO: 496) GAUGAACUUCCCAUUGG; or (SEQ ID NO: 497) AGGUCAUGAUCCCCUUC.

In an embodiment, when the SCD target knockout position is the BCL11A coding region, e.g., early coding region, and more than one gRNA is used to position breaks, e.g., two single stranded breaks or two double stranded breaks, or a combination of single strand and double strand breaks, e.g., to create one or more indels, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Tables 2A-2F.

In another embodiment, a position in the coding region, e.g., the early coding region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Table 4A-4E. In an embodiment, the targeting domain is selected from those in Table 4A-4E. In another embodiment, the targeting domain is:

(SEQ ID NO: 3073) GAGCUCCAUGUGCAGAACGA; (SEQ ID NO: 3074) GAGCUCCCAACGGGCCG; (SEQ ID NO: 3075) GAGUGCAGAAUAUGCCCCGC; (SEQ ID NO: 3076) GAUAAACAAUCGUCAUCCUC; (SEQ ID NO: 3077) GAUGCCAACCUCCACGGGAU; (SEQ ID NO: 3078) GCAGAAUAUGCCCCGCA; (SEQ ID NO: 3079) GCAUCCAAUCCCGUGGAGGU; (SEQ ID NO: 3080) GCCAACCUCCACGGGAU; (SEQ ID NO: 3081) GCUCCCAACGGGCCGUGGUC; or (SEQ ID NO: 3082) GGAGCUCUAAUCCCCACGCC.

In an embodiment, when the SCD target knockout position is the BCL11A coding region, e.g., early coding region, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create one or more indels, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 4A-4E.

In another embodiment, a position in the coding region, e.g., the early coding region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Table 5A-5E. In an embodiment, the targeting domain is selected from those in Table 5A-5E.

In an embodiment, when the SCD target knockout position is the BCL11A coding region, e.g., early coding region, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create one or more indels, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 5A-5E.

In another embodiment, a position in the coding region, e.g., the early coding region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Table 6A-6B. In an embodiment, the targeting domain is selected from those in Table 6A-6B.

In an embodiment, when the SCD target knockout position is the BCL11A coding region, e.g., early coding region, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create one or more indels, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 6A-6B.

In another embodiment, a position in the coding region, e.g., the early coding region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Table 15A-15D. In an embodiment, the targeting domain is selected from those in Table 15A-15D.

In an embodiment, when the SCD target knockout position is the BCL11A coding region, e.g., early coding region, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create one or more indels, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 15A-15D.

In another embodiment, a position in the coding region, e.g., the early coding region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Table 16A-16E. In an embodiment, the targeting domain is selected from those in Table 16A-16E.

In an embodiment, when the SCD target knockout position is the BCL11A coding region, e.g., early coding region, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create one or more indels, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 16A-16E.

In another embodiment, a position in the coding region, e.g., the early coding region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Table 17A-17B. In an embodiment, the targeting domain is selected from those in Table 17A-17B.

In an embodiment, when the SCD target knockout position is the BCL11A coding region, e.g., early coding region, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create one or more indels, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 17A-17B.

In another embodiment, a position in the non-coding region, e.g., the enhancer region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 7A-7D. In an embodiment, the targeting domain is selected from those in Tables 7A-7D. In another embodiment, the targeting domain is:

(SEQ ID NO: 4835) GAAAAUACUUACUGUACUGC; (SEQ ID NO: 4836) GAAAGCAGUGUAAGGCU; (SEQ ID NO: 4837) GGCUGUUUUGGAAUGUAGAG; or (SEQ ID NO: 4838) GUGCUACUUAUACAAUUCAC.

In an embodiment, when the SCD target knockout position is the non-coding region, e.g., the enhancer region, of the BCL11A gene, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create a deletion, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 7A-7D.

In another embodiment, a position in the non-coding region, e.g., the enhancer region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 8A-8D. In an embodiment, the targeting domain is selected from those in Tables 8A-8D.

In an embodiment, when the SCD target knockout position is the non-coding region, e.g., the enhancer region, of the BCL11A gene, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create a deletion, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 8A-8D.

In another embodiment, a position in the non-coding region, e.g., the enhancer region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from Table 9. In an embodiment, the targeting domain is selected from those in Table 9.

In an embodiment, when the SCD target knockout position is the non-coding region, e.g., the enhancer region, of the BCL11A gene, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create a deletion, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 9.

In another embodiment, a position in the non-coding region, e.g., the enhancer region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 21A-21E. In an embodiment, the targeting domain is selected from those in Tables 21A-21E. In an embodiment, when the SCD target knockout position is the non-coding region, e.g., the enhancer region, of the BCL11A gene, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create a deletion, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 21A-21E.

In another embodiment, a position in the non-coding region, e.g., the enhancer region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 22A-22E. In an embodiment, the targeting domain is selected from those in Tables 22A-22E. In an embodiment, when the SCD target knockout position is the non-coding region, e.g., the enhancer region, of the BCL11A gene, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create a deletion, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 22A-22E.

In another embodiment, a position in the non-coding region, e.g., the enhancer region, of the BCL11A gene is targeted, e.g., for knockout. In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 23A-23C. In an embodiment, the targeting domain is selected from those in Tables 23A-23C.

In an embodiment, when the SCD target knockout position is the non-coding region, e.g., the enhancer region, of the BCL11A gene, and more than one gRNA is used to position breaks, e.g., two single strand breaks or two double strand breaks, or a combination of single strand and double strand breaks, e.g., to create a deletion, in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Table 23A-23C.

In an embodiment, the targeting domain of the gRNA molecule is configured to target an enzymatically inactive Cas9 (eiCas9) or an eiCas9 fusion protein (e.g., an eiCas9 fused to a transcription repressor domain), sufficiently close to an SCD knockdown target position to reduce, decrease or repress expression of the BCL11A gene. In an embodiment, the targeting domain is configured to target the promoter region of the BCL11A gene to block transcription initiation, binding of one or more transcription enhancers or activators, and/or RNA polymerase. One or more gRNA may be used to target an eiCas9 to the promoter region of the BCL11A gene.

In an embodiment, when the BCL11A promoter region is targeted, e.g., for knockdown, the targeting domain can comprise a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 3A-3C. In an embodiment, the targeting domain is selected from those in Tables 3A-3C.

In an embodiment, when the SCD target knockdown position is the BCL11A promoter region and more than one gRNA is used to position an eiCas9 or an eiCas9-fusion protein (e.g., an eiCas9-transcription repressor domain fusion protein), in the target nucleic acid sequence, the targeting domain of each guide RNA is selected from one of Tables 3A-3C.

In an embodiment, when the BCL11A promoter region is targeted, e.g., for knockdown, the targeting domain can comprise a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 10A-10D. In an embodiment, the targeting domain is selected from those in Tables 10A-10D. In another embodiment, the targeting domain is:

(SEQ ID NO: 4981) GACGACGGCUCGGUUCACAU; (SEQ ID NO: 4982) GACGCCAGACGCGGCCCCCG; (SEQ ID NO: 4983) GCCUUGCUUGCGGCGAGACA; (SEQ ID NO: 4984) GGCUCCGCGGACGCCAGACG; (SEQ ID NO: 4985) GACGGCUCGGUUCACAU; (SEQ ID NO: 4986) GCCGCGUCUGGCGUCCG; or (SEQ ID NO: 4987) GCGGGCGGACGACGGCU.

In an embodiment, when the SCD target knockdown position is the BCL11A promoter region and more than one gRNA is used to position an eiCas9 or an eiCas9-fusion protein (e.g., an eiCas9-transcription repressor domain fusion protein), in the target nucleic acid sequence, each guide RNA is selected from one of Tables 10A-10D.

In an embodiment, when the BCL11A promoter region is targeted, e.g., for knockdown, the targeting domain can comprise a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 11A-11D. In an embodiment, the targeting domain is selected from those in Tables 11A-11D.

In an embodiment, when the SCD target knockdown position is the BCL11A promoter region and more than one gRNA is used to position an eiCas9 or an eiCas9-fusion protein (e.g., an eiCas9-transcription repressor domain fusion protein), in the target nucleic acid sequence, each guide RNA is selected from one of Tables 11A-11D.

In an embodiment, when the BCL11A promoter region is targeted, e.g., for knockdown, the targeting domain can comprise a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from Table 12. In an embodiment, the targeting domain is selected from those in Table 12.

In an embodiment, when the SCD target knockdown position is the BCL11A promoter region and more than one gRNA is used to position an eiCas9 or an eiCas9-fusion protein (e.g., an eiCas9-transcription repressor domain fusion protein), in the target nucleic acid sequence, each guide RNA is selected from Table 12.

In an embodiment, when the BCL11A promoter region is targeted, e.g., for knockdown, the targeting domain can comprise a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 18A-18C. In an embodiment, the targeting domain is selected from those in Tables 18A-18C.

In an embodiment, when the SCD target knockdown position is the BCL11A promoter region and more than one gRNA is used to position an eiCas9 or an eiCas9-fusion protein (e.g., an eiCas9-transcription repressor domain fusion protein), in the target nucleic acid sequence, each guide RNA is selected from one of Tables 18A-18C.

In an embodiment, when the BCL11A promoter region is targeted, e.g., for knockdown, the targeting domain can comprise a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 19A-19E. In an embodiment, the targeting domain is selected from those in Tables 19A-19E.

In an embodiment, when the SCD target knockdown position is the BCL11A promoter region and more than one gRNA is used to position an eiCas9 or an eiCas9-fusion protein (e.g., an eiCas9-transcription repressor domain fusion protein), in the target nucleic acid sequence, each guide RNA is selected from one of Tables 19A-19E.

In an embodiment, when the BCL11A promoter region is targeted, e.g., for knockdown, the targeting domain can comprise a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 20A-20C. In an embodiment, the targeting domain is selected from those in Tables 20A-20C.

In an embodiment, when the SCD target knockdown position is the BCL11A promoter region and more than one gRNA is used to position an eiCas9 or an eiCas9-fusion protein (e.g., an eiCas9-transcription repressor domain fusion protein), in the target nucleic acid sequence, each guide RNA is selected from one of Tables 20A-20C.

In an embodiment, the targeting domain comprises a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence selected from any one of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. In an embodiment, the targeting domain is selected from those in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31.

In an embodiment, the targeting domain which is complementary with the BCL11A gene is 16 nucleotides or more in length. In an embodiment, the targeting domain is 16 nucleotides in length. In an embodiment, the targeting domain is 17 nucleotides in length. In another embodiment, the targeting domain is 18 nucleotides in length. In still another embodiment, the targeting domain is 19 nucleotides in length. In still another embodiment, the targeting domain is 20 nucleotides in length. In still another embodiment, the targeting domain is 21 nucleotides in length. In still another embodiment, the targeting domain is 22 nucleotides in length. In still another embodiment, the targeting domain is 23 nucleotides in length. In still another embodiment, the targeting domain is 24 nucleotides in length. In still another embodiment, the targeting domain is 25 nucleotides in length. In still another embodiment, the targeting domain is 26 nucleotides in length.

In an embodiment, the targeting domain comprises 16 nucleotides.

In an embodiment, the targeting domain comprises 17 nucleotides.

In an embodiment, the targeting domain comprises 18 nucleotides.

In an embodiment, the targeting domain comprises 19 nucleotides.

In an embodiment, the targeting domain comprises 20 nucleotides.

In an embodiment, the targeting domain comprises 21 nucleotides.

In an embodiment, the targeting domain comprises 22 nucleotides.

In an embodiment, the targeting domain comprises 23 nucleotides.

In an embodiment, the targeting domain comprises 24 nucleotides.

In an embodiment, the targeting domain comprises 25 nucleotides.

In an embodiment, the targeting domain comprises 26 nucleotides.

In an embodiment, the gRNA, e.g., a gRNA comprising a targeting domain, which is complementary with the HBB gene or BCL11A gene, is a modular gRNA. In another embodiment, the gRNA is a unimolecular or chimeric gRNA.

HBB gRNA as described herein may comprise from 5′ to 3′: a targeting domain (comprising a “core domain”, and optionally a “secondary domain”); a first complementarity domain; a linking domain; a second complementarity domain; a proximal domain; and a tail domain. In an embodiment, the proximal domain and tail domain are taken together as a single domain.

In an embodiment, a gRNA comprises a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 20 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In another embodiment, a gRNA comprises a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 25 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In another embodiment, a gRNA comprises a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 30 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In another embodiment, a gRNA comprises a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 40 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

A cleavage event, e.g., a double strand or single strand break, is generated by a Cas9 molecule. The Cas9 molecule may be an enzymatically active Cas9 (eaCas9) molecule, e.g., an eaCas9 molecule that forms a double strand break in a target nucleic acid or an eaCas9 molecule forms a single strand break in a target nucleic acid (e.g., a nickase molecule). Alternatively, in an embodiment, the Cas9 molecule may be an enzymatically inactive Cas9 (eiCas9) molecule or a modified eiCas9 molecule, e.g., the eiCas9 molecule is fused to Krüppel-associated box (KRAB) to generate an eiCas9-KRAB fusion protein molecule.

In an embodiment, the eaCas9 molecule catalyzes a double strand break.

In an embodiment, the eaCas9 molecule comprises HNH-like domain cleavage activity but has no, or no significant, N-terminal RuvC-like domain cleavage activity. In this case, the eaCas9 molecule is an HNH-like domain nickase, e.g., the eaCas9 molecule comprises a mutation at D10, e.g., D10A. In another embodiment, the eaCas9 molecule comprises N-terminal RuvC-like domain cleavage activity but has no, or no significant, HNH-like domain cleavage activity. In an embodiment, the eaCas9 molecule is an N-terminal RuvC-like domain nickase, e.g., the eaCas9 molecule comprises a mutation at H840, e.g., H840A. In an embodiment, the eaCas9 molecule is an N-terminal RuvC-like domain nickase, e.g., the eaCas9 molecule comprises a mutation at N863, e.g., N863A.

In an embodiment, a single strand break is formed in the strand of the target nucleic acid to which the targeting domain of said gRNA is complementary. In another embodiment, a single strand break is formed in the strand of the target nucleic acid other than the strand to which the targeting domain of said gRNA is complementary.

In another aspect, disclosed herein is a nucleic acid, e.g., an isolated or non-naturally occurring nucleic acid, e.g., DNA, that comprises (a) a sequence that encodes a gRNA molecule comprising a targeting domain that is complementary with a target domain, e.g., with an SCD target position, in the HBB gene or BCL11A gene as disclosed herein.

In an embodiment, the nucleic acid encodes a gRNA molecule, e.g., a first gRNA molecule, comprising a targeting domain configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to an SCD target position in the HBB gene or BCL11A gene to allow alteration, e.g., alteration associated with HDR or NHEJ, of the an SCD target position in the HBB gene or BCL11A gene.

In an embodiment, the nucleic acid encodes a gRNA molecule, e.g., a first gRNA molecule, comprising a targeting domain configured to target an enzymatically inactive Cas9 (eiCas9) or an eiCas9 fusion protein (e.g., an eiCas9 fused to a transcription repressor domain), sufficiently close to an SCD knockdown target position to reduce, decrease or repress expression of the BCL11A gene.

In an embodiment, the nucleic acid encodes a gRNA molecule, e.g., the first gRNA molecule, comprising a targeting domain comprising a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any one of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. In an embodiment, the nucleic acid encodes a gRNA molecule comprising a targeting domain is selected from those in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31.

In an embodiment, the nucleic acid encodes a modular gRNA, e.g., one or more nucleic acids encode a modular gRNA. In another embodiment, the nucleic acid encodes a chimeric gRNA. The nucleic acid may encode a gRNA, e.g., the first gRNA molecule, comprising a targeting domain comprising 16 nucleotides or more in length. In one embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 16 nucleotides in length. In another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 17 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 18 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 19 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 20 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 21 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 22 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 23 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 24 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 25 nucleotides in length. In still another embodiment, the nucleic acid encodes a gRNA, e.g., the first gRNA molecule, comprising a targeting domain that is 26 nucleotides in length.

In an embodiment, the targeting domain comprises 16 nucleotides.

In an embodiment, the targeting domain comprises 17 nucleotides.

In an embodiment, the targeting domain comprises 18 nucleotides.

In an embodiment, the targeting domain comprises 19 nucleotides.

In an embodiment, the targeting domain comprises 20 nucleotides.

In an embodiment, the targeting domain comprises 21 nucleotides.

In an embodiment, the targeting domain comprises 22 nucleotides.

In an embodiment, the targeting domain comprises 23 nucleotides.

In an embodiment, the targeting domain comprises 24 nucleotides.

In an embodiment, the targeting domain comprises 25 nucleotides.

In an embodiment, the targeting domain comprises 26 nucleotides.

In an embodiment, a nucleic acid encodes a gRNA comprising from 5′ to 3′: a targeting domain (comprising a “core domain”, and optionally a “secondary domain”); a first complementarity domain; a linking domain; a second complementarity domain; a proximal domain; and a tail domain. In an embodiment, the proximal domain and tail domain are taken together as a single domain.

In an embodiment, a nucleic acid encodes a gRNA e.g., the first gRNA molecule, comprising a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 20 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, a nucleic acid encodes a gRNA e.g., the first gRNA molecule, comprising a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 30 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, a nucleic acid encodes a gRNA e.g., the first gRNA molecule, comprising a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 30 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, a nucleic acid encodes a gRNA comprising e.g., the first gRNA molecule, a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 40 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, a nucleic acid comprises (a) a sequence that encodes a gRNA molecule e.g., the first gRNA molecule, comprising a targeting domain that is complementary with a target domain in the HBB gene or BCL11A gene as disclosed herein, and further comprising (b) a sequence that encodes a Cas9 molecule.

The Cas9 molecule may be an enzymatically active Cas9 (eaCas9) molecule, e.g., an eaCas9 molecule that forms a double strand break in a target nucleic acid or an eaCas9 molecule forms a single strand break in a target nucleic acid (e.g., a nickase molecule). Alternatively, in an embodiment, the Cas9 molecule may be an enzymatically inactive Cas9 (eiCas9) molecule or a modified eiCas9 molecule, e.g., the eiCas9 molecule is fused to Krüppel-associated box (KRAB) to generate an eiCas9-KRAB fusion protein molecule.

A nucleic acid disclosed herein may comprise (a) a sequence that encodes a gRNA molecule comprising a targeting domain that is complementary with a target domain in the HBB gene or BCL11A gene as disclosed herein; (b) a sequence that encodes a Cas9 molecule; and further comprises (c)(i) a sequence that encodes a second gRNA molecule described herein having a targeting domain that is complementary to a second target domain of the HBB gene or BCL11A gene, and optionally, (c)(ii) a sequence that encodes a third gRNA molecule described herein having a targeting domain that is complementary to a third target domain of the HBB gene or BCL11A gene; and optionally, (c)(iii) a sequence that encodes a fourth gRNA molecule described herein having a targeting domain that is complementary to a fourth target domain of the HBB gene or BCL11A gene.

In an embodiment, a nucleic acid encodes a second gRNA molecule comprising a targeting domain configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to an SCD target position in the HBB gene or BCL11A gene, to allow alteration, e.g., alteration associated with HDR or NHEJ, of an SCD target position in the HBB gene or BCL11A gene, either alone or in combination with the break positioned by said first gRNA molecule.

In an embodiment, the nucleic acid encodes a second gRNA molecule comprising a targeting domain configured to target an enzymatically inactive Cas9 (eiCas9) or an eiCas9 fusion protein (e.g., an eiCas9 fused to a transcription repressor domain), sufficiently close to an SCD knockdown target position to reduce, decrease or repress expression of the BCL11A gene.

In an embodiment, a nucleic acid encodes a third gRNA molecule comprising a targeting domain configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to an SCD target position in the HBB gene or BCL11A gene to allow alteration, e.g., alteration associated with HDR or NHEJ, of an SCD target position in the HBB gene or BCL11A gene, either alone or in combination with the break positioned by the first and/or second gRNA molecule.

In an embodiment, the nucleic acid encodes a third gRNA molecule comprising a targeting domain configured to target an enzymatically inactive Cas9 (eiCas9) or an eiCas9 fusion protein (e.g., an eiCas9 fused to a transcription repressor domain), sufficiently close to an SCD knockdown target position to reduce, decrease or repress expression of the BCL11A gene.

In an embodiment, a nucleic acid encodes a fourth gRNA molecule comprising a targeting domain configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to an SCD target position in the HBB gene or BCL11A gene to allow alteration, e.g., alteration associated with HDR or NHEJ, of an SCD target position in the HBB gene or BCL11A gene, either alone or in combination with the break positioned by the first gRNA molecule, the second gRNA molecule and/or the third gRNA molecule.

In an embodiment, the nucleic acid encodes a fourth gRNA molecule comprising a targeting domain configured to target an enzymatically inactive Cas9 (eiCas9) or an eiCas9 fusion protein (e.g., an eiCas9 fused to a transcription repressor domain), sufficiently close to an SCD knockdown target position to reduce, decrease or repress expression of the BCL11A gene.

In an embodiment, the nucleic acid encodes a second gRNA molecule. The second gRNA is selected to target the same SCD target position as the first gRNA molecule. Optionally, the nucleic acid may encode a third gRNA, and further optionally, the nucleic acid may encode a fourth gRNA molecule. The third gRNA molecule and the fourth gRNA molecule are selected to target the same SCD target position as the first and/or second gRNA molecules.

In an embodiment, the nucleic acid encodes a second gRNA molecule comprising a targeting domain comprising a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from one of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. In an embodiment, the nucleic acid encodes a second gRNA molecule comprising a targeting domain selected from those in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. In an embodiment, when a third or fourth gRNA molecule are present, the third and fourth gRNA molecules may independently comprise a targeting domain comprising a sequence that is the same as, or differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from one of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. In a further embodiment, when a third or fourth gRNA molecule are present, the third and fourth gRNA molecules may independently comprise a targeting domain selected from those in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31.

In an embodiment, the nucleic acid encodes a second gRNA which is a modular gRNA, e.g., wherein one or more nucleic acid molecules encode a modular gRNA. In another embodiment, the nucleic acid encoding a second gRNA is a chimeric gRNA. In another embodiment, when a nucleic acid encodes a third or fourth gRNA, the third and/or fourth gRNA may be a modular gRNA or a chimeric gRNA. When multiple gRNAs are used, any combination of modular or chimeric gRNAs may be used.

A nucleic acid may encode a second, a third, and/or a fourth gRNA comprising a targeting domain comprising 16 nucleotides or more in length. In an embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 16 nucleotides in length. In another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 17 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 18 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 19 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 20 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 21 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 22 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 23 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 24 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 25 nucleotides in length. In still another embodiment, the nucleic acid encodes a second gRNA comprising a targeting domain that is 26 nucleotides in length.

In an embodiment, the targeting domain comprises 16 nucleotides.

In an embodiment, the targeting domain comprises 17 nucleotides.

In an embodiment, the targeting domain comprises 18 nucleotides.

In an embodiment, the targeting domain comprises 19 nucleotides.

In an embodiment, the targeting domain comprises 20 nucleotides.

In an embodiment, the targeting domain comprises 21 nucleotides.

In an embodiment, the targeting domain comprises 22 nucleotides.

In an embodiment, the targeting domain comprises 23 nucleotides.

In an embodiment, the targeting domain comprises 24 nucleotides.

In an embodiment, the targeting domain comprises 25 nucleotides.

In an embodiment, the targeting domain comprises 26 nucleotides.

In an embodiment, a nucleic acid encodes a second, a third, and/or a fourth gRNA comprising from 5′ to 3′: a targeting domain (comprising a “core domain”, and optionally a “secondary domain”); a first complementarity domain; a linking domain; a second complementarity domain; a proximal domain; and a tail domain. In an embodiment, the proximal domain and tail domain are taken together as a single domain.

In an embodiment, a nucleic acid encodes a second, a third, and/or a fourth gRNA comprising a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 20 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, a nucleic acid encodes a second, a third, and/or a fourth gRNA comprising a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 30 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, a nucleic acid encodes a second, a third, and/or a fourth gRNA comprising a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 35 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, a nucleic acid encodes a second, a third, and/or a fourth gRNA comprising a linking domain of no more than 25 nucleotides in length; a proximal and tail domain, that taken together, are at least 40 nucleotides in length; and a targeting domain equal to or greater than 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, when the HBB gene is corrected, e.g., by HDR, the nucleic acid encodes (a) a sequence that encodes a gRNA molecule comprising a targeting domain that is complementary with a target domain in the HBB gene as disclosed herein; (b) a sequence that encodes a Cas9 molecule; optionally, (c)(i) a sequence that encodes a second gRNA molecule described herein having a targeting domain that is complementary to a second target domain of the HBB gene, and further optionally, (c)(ii) a sequence that encodes a third gRNA molecule described herein having a targeting domain that is complementary to a third target domain of the HBB gene; and still further optionally, (c)(iii) a sequence that encodes a fourth gRNA molecule described herein having a targeting domain that is complementary to a fourth target domain of the HBB gene; and further may comprise (d) a template nucleic acid (in an embodiment where an exogenous template is used).

In an embodiment, a mutation in the HBB gene is corrected, e.g., by HDR, using an exogenously provided template nucleic acid.

In an embodiment, the template nucleic acid is a single stranded nucleic acid. In another embodiment, the template nucleic acid is a double stranded nucleic acid. In an embodiment, the template nucleic acid comprises a nucleotide sequence, e.g., of one or more nucleotides, that will be added to or will template a change in the target nucleic acid. In another embodiment, the template nucleic acid comprises a nucleotide sequence that may be used to modify the target position. In another embodiment, the template nucleic acid comprises a nucleotide sequence, e.g., of one or more nucleotides, that corresponds to wild type sequence of the target nucleic acid, e.g., of the target position.

The template nucleic acid may comprise a replacement sequence, e.g., a replacement sequence from the Table 27. In an embodiment, the template nucleic acid comprises a 5′ homology arm, e.g., a 5′ homology arm from Table 27. In another embodiment, the template nucleic acid comprises a 3′ homology arm, e.g., a 3′ homology arm from Table 27.

In another embodiment, a mutation in the HBB gene is corrected, e.g., by HDR, without using an exogenously provided template nucleic acid. While not wishing to be bound by theory, it is believed that an endogenous region of homology can mediate HDR-based correction. In an embodiment, alteration of the target sequence occurs by HDR with an endogenous genomic donor sequence. In an embodiment, the endogenous genomic donor sequence is located on the same chromosome as the target sequence. In another embodiment, the endogenous genomic donor sequence is located on a different chromosome from the target sequence. In an embodiment, the endogenous genomic donor sequence comprises one or more nucleotides derived from the HBD gene. Mutations in the HBB gene that can be corrected (e.g., altered) by HDR with an endogenous genomic donor sequence include, e.g., a point mutation at E6, e.g., E6V.

As described above, a nucleic acid may comprise (a) a sequence encoding a gRNA molecule comprising a targeting domain that is complementary with a target domain in the HBB gene or BCL11A gene, and (b) a sequence encoding a Cas9 molecule.

In an embodiment, (a) and (b) are present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., the same adeno-associated virus (AAV) vector. In an embodiment, the nucleic acid molecule is an AAV vector. Exemplary AAV vectors that may be used in any of the described compositions and methods include an AAV2 vector, a modified AAV2 vector, an AAV3 vector, a modified AAV3 vector, an AAV6 vector, a modified AAV6 vector, an AAV8 vector and an AAV9 vector.

In another embodiment, (a) is present on a first nucleic acid molecule, e.g. a first vector, e.g., a first viral vector, e.g., a first AAV vector; and (b) is present on a second nucleic acid molecule, e.g., a second vector, e.g., a second vector, e.g., a second AAV vector. The first and second nucleic acid molecules may be AAV vectors.

In another embodiment, the nucleic acid may further comprise (c) a sequence that encodes a second, third and/or fourth gRNA molecule as described herein. In an embodiment, the nucleic acid comprises (a), (b) and (c). Each of (a) and (c) may be present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., the same adeno-associated virus (AAV) vector. In an embodiment, the nucleic acid molecule is an AAV vector.

In another embodiment, (a) and (c) are on different vectors. For example, (a) may be present on a first nucleic acid molecule, e.g. a first vector, e.g., a first viral vector, e.g., a first AAV vector; and (c) may be present on a second nucleic acid molecule, e.g., a second vector, e.g., a second vector, e.g., a second AAV vector. In an embodiment, the first and second nucleic acid molecules are AAV vectors.

In another embodiment, each of (a), (b), and (c) are present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., an AAV vector. In an embodiment, the nucleic acid molecule is an AAV vector. In an alternate embodiment, one of (a), (b), and (c) is encoded on a first nucleic acid molecule, e.g., a first vector, e.g., a first viral vector, e.g., a first AAV vector; and a second and third of (a), (b), and (c) is encoded on a second nucleic acid molecule, e.g., a second vector, e.g., a second vector, e.g., a second AAV vector. The first and second nucleic acid molecule may be AAV vectors.

In an embodiment, (a) is present on a first nucleic acid molecule, e.g., a first vector, e.g., a first viral vector, a first AAV vector; and (b) and (c) are present on a second nucleic acid molecule, e.g., a second vector, e.g., a second vector, e.g., a second AAV vector. The first and second nucleic acid molecule may be AAV vectors.

In another embodiment, (b) is present on a first nucleic acid molecule, e.g., a first vector, e.g., a first viral vector, e.g., a first AAV vector; and (a) and (c) are present on a second nucleic acid molecule, e.g., a second vector, e.g., a second vector, e.g., a second AAV vector. The first and second nucleic acid molecule may be AAV vectors.

In another embodiment, (c) is present on a first nucleic acid molecule, e.g., a first vector, e.g., a first viral vector, e.g., a first AAV vector; and (b) and (a) are present on a second nucleic acid molecule, e.g., a second vector, e.g., a second vector, e.g., a second AAV vector. The first and second nucleic acid molecule may be AAV vectors.

In another embodiment, each of (a), (b) and (c) are present on different nucleic acid molecules, e.g., different vectors, e.g., different viral vectors, e.g., different AAV vector. For example, (a) may be on a first nucleic acid molecule, (b) on a second nucleic acid molecule, and (c) on a third nucleic acid molecule. The first, second and third nucleic acid molecule may be AAV vectors.

In another embodiment, when a third and/or fourth gRNA molecule are present, each of (a), (b), (c)(i), (c)(ii) and (c)(iii) may be present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., an AAV vector. In an embodiment, the nucleic acid molecule is an AAV vector. In an alternate embodiment, each of (a), (b), (c)(i), (c)(ii) and (c)(iii) may be present on the different nucleic acid molecules, e.g., different vectors, e.g., the different viral vectors, e.g., different AAV vectors. In further embodiments, each of (a), (b), (c)(i), (c)(ii) and (c)(iii) may be present on more than one nucleic acid molecule, but fewer than five nucleic acid molecules, e.g., AAV vectors.

In another embodiment, when (d) a template nucleic acid is present, each of (a), (b), and (d) may be present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., an AAV vector. In an embodiment, the nucleic acid molecule is an AAV vector. In an alternate embodiment, each of (a), (b), and (d) may be present on the different nucleic acid molecules, e.g., different vectors, e.g., the different viral vectors, e.g., different AAV vectors. In further embodiments, each of (a), (b), and (d) may be present on more than one nucleic acid molecule, but fewer than three nucleic acid molecules, e.g., AAV vectors.

In another embodiment, when (d) a template nucleic acid is present, each of (a), (b), (c)(i) and (d) may be present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., an AAV vector. In an embodiment, the nucleic acid molecule is an AAV vector. In an alternate embodiment, each of (a), (b), (c)(i) and (d) may be present on the different nucleic acid molecules, e.g., different vectors, e.g., the different viral vectors, e.g., different AAV vectors. In further embodiments, each of (a), (b), (c)(i) and (d) may be present on more than one nucleic acid molecule, but fewer than four nucleic acid molecules, e.g., AAV vectors.

In another embodiment, when (d) a template nucleic acid is present, each of (a), (b), (c)(i), (c)(ii) and (d) may be present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., an AAV vector. In an embodiment, the nucleic acid molecule is an AAV vector. In an alternate embodiment, each of (a), (b), (c)(i), (c)(ii) and (d) may be present on the different nucleic acid molecules, e.g., different vectors, e.g., the different viral vectors, e.g., different AAV vectors. In further embodiments, each of (a), (b), (c)(i), (c)(ii) and (d) may be present on more than one nucleic acid molecule, but fewer than five nucleic acid molecules, e.g., AAV vectors.

In another embodiment, when (d) a template nucleic acid is present, each of (a), (b), (c)(i), (c)(ii), (c)(iii) and (d) may be present on the same nucleic acid molecule, e.g., the same vector, e.g., the same viral vector, e.g., an AAV vector. In an embodiment, the nucleic acid molecule is an AAV vector. In an alternate embodiment, each of (a), (b), (c)(i), (c)(ii), (c)(iii) and (d) may be present on the different nucleic acid molecules, e.g., different vectors, e.g., the different viral vectors, e.g., different AAV vectors. In further embodiments, each of (a), (b), (c)(i), (c)(ii), (c)(iii) and (d) may be present on more than one nucleic acid molecule, but fewer than six nucleic acid molecules, e.g., AAV vectors.

The nucleic acids described herein may comprise a promoter operably linked to the sequence that encodes the gRNA molecule of (a), e.g., a promoter described herein. The nucleic acid may further comprise a second promoter operably linked to the sequence that encodes the second, third and/or fourth gRNA molecule of (c), e.g., a promoter described herein. The promoter and second promoter differ from one another. In an embodiment, the promoter and second promoter are the same.

The nucleic acids described herein may further comprise a promoter operably linked to the sequence that encodes the Cas9 molecule of (b), e.g., a promoter described herein.

In another aspect, disclosed herein is a composition comprising (a) a gRNA molecule comprising a targeting domain that is complementary with a target domain in the HBB gene or BCL11A gene, as described herein. The composition of (a) may further comprise (b) a Cas9 molecule, e.g., a Cas9 molecule as described herein. A composition of (a) and (b) may further comprise (c) a second, third and/or fourth gRNA molecule, e.g., a second, third and/or fourth gRNA molecule described herein. A composition of (a), (b) and (c) may further comprise (d) a template nucleic acid (in an embodiment where an exogenous template is used). In an embodiment, the composition is a pharmaceutical composition. The Compositions described herein, e.g., pharmaceutical compositions described herein, can be used in treating SCD in a subject, e.g., in accordance with a method disclosed herein.

In another aspect, disclosed herein is a method of altering a cell, e.g., altering the structure, e.g., altering the sequence, of a target nucleic acid of a cell, comprising contacting said cell with: (a) a gRNA that targets the HBB gene or BCL11A gene, e.g., a gRNA as described herein; (b) a Cas9 molecule, e.g., a Cas9 molecule as described herein; and optionally, (c) a second, third and/or fourth gRNA that targets HBB gene or BCL11A gene, e.g., a gRNA; and optionally, (d) a template nucleic acid, as described herein.

In an embodiment, the method comprises contacting said cell with (a) and (b).

In an embodiment, the method comprises contacting said cell with (a), (b), and (c).

In an embodiment, the method comprises contacting said cell with (a), (b), (c) and (d).

In an embodiment, the gRNA targets the HBB gene and no exogenous template nucleic acid is contacted with the cell.

The gRNA of (a) and optionally (c) may be selected from any of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, or a gRNA that differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31.

In an embodiment, the method comprises contacting a cell from a subject suffering from or likely to develop SCD. The cell may be from a subject having a mutation at an SCD target position in the HBB gene or a subject which would benefit from having a mutation at an SCD target position in the BCL11A gene.

In an embodiment, the cell being contacted in the disclosed method is an erythroid cell. The contacting may be performed ex vivo and the contacted cell may be returned to the subject's body after the contacting step. In another embodiment, the contacting step may be performed in vivo.

In an embodiment, the method of altering a cell as described herein comprises acquiring knowledge of the sequence at an SCD target position in said cell, prior to the contacting step. Acquiring knowledge of the sequence at an SCD target position in the cell may be by sequencing the HBB gene or BCL11A gene, or a portion of the HBB gene or BCL11A gene.

In an embodiment, the contacting step of the method comprises contacting the cell with a nucleic acid, e.g., a vector, e.g., an AAV vector, that expresses at least one of (a), (b), and (c). In an embodiment, the contacting step of the method comprises contacting the cell with a nucleic acid, e.g., a vector, e.g., an AAV vector, that expresses each of (a), (b), and (c). In another embodiment, the contacting step of the method comprises delivering to the cell a Cas9 molecule of (b) and a nucleic acid which encodes a gRNA (a) and optionally, a second gRNA (c)(i) (and further optionally, a third gRNA (c)(iv) and/or fourth gRNA (c)(iii).

In an embodiment, the contacting step of the method comprises contacting the cell with a nucleic acid, e.g., a vector, e.g., an AAV vector, that expresses at least one of (a), (b), (c) and (d). In an embodiment, the contacting step of the method comprises contacting the cell with a nucleic acid, e.g., a vector, e.g., an AAV vector, that expresses each of (a), (b), and (c). In another embodiment, the contacting step of the method comprises delivering to the cell a Cas9 molecule of (b), a nucleic acid which encodes a gRNA of (a) and a template nucleic acid of (d), and optionally, a second gRNA (c)(i) (and further optionally, a third gRNA (c)(iv) and/or fourth gRNA (c)(iii).

In an embodiment, contacting comprises contacting the cell with a nucleic acid, e.g., a vector, e.g., an AAV vector, e.g., an AAV2 vector, a modified AAV2 vector, an AAV3 vector, a modified AAV3 vector, an AAV6 vector, a modified AAV6 vector, an AAV8 vector or an AAV9 vector.

In an embodiment, contacting comprises delivering to the cell a Cas9 molecule of (b), as a protein or an mRNA, and a nucleic acid which encodes (a) and optionally a second, third and/or fourth gRNA of (c).

In an embodiment, contacting comprises delivering to the cell a Cas9 molecule of (b), as a protein or an mRNA, said gRNA of (a), as an RNA, and optionally said second, third and/or fourth gRNA of (c), as an RNA.

In an embodiment, contacting comprises delivering to the cell a gRNA of (a) as an RNA, optionally said second, third and/or fourth gRNA of (c) as an RNA, and a nucleic acid that encodes the Cas9 molecule of (b).

In another aspect, disclosed herein is a method of treating or preventing a subject suffering from or likely to develop SCD, e.g., altering the structure, e.g., sequence, of a target nucleic acid of the subject, comprising contacting the subject (or a cell from the subject) with:

(a) a gRNA that targets the HBB gene or BCL11A gene, e.g., a gRNA disclosed herein;

(b) a Cas9 molecule, e.g., a Cas9 molecule disclosed herein; and

optionally, (c)(i) a second gRNA that targets the HBB gene or BCL11A gene, e.g., a second gRNA disclosed herein, and

further optionally, (c)(ii) a third gRNA, and still further optionally, (c)(iii) a fourth gRNA that target the HBB gene or BCL11A gene, e.g., a third and fourth gRNA disclosed herein.

The method of treating a subject may further comprise contacting the subject (or a cell from the subject) with (d) a template nucleic acid (in an embodiment where an exogenous template is used), e.g., a template nucleic acid disclosed herein.

In an embodiment, a template nucleic acid is used when the method of treating a subject uses HDR to alter the sequence of the target nucleic acid of the subject. In an embodiment, the gRNA targets the HBB gene and no exogenous template nucleic acid is contacted with the subject (or a cell from the subject).

In an embodiment, contacting comprises contacting with (a) and (b).

In an embodiment, contacting comprises contacting with (a), (b), and (c)(i).

In an embodiment, contacting comprises contacting with (a), (b), (c)(i) and (c)(ii).

In an embodiment, contacting comprises contacting with (a), (b), (c)(i), (c)(ii) and (c)(iii).

In an embodiment, contacting comprises contacting with (a), (b), (c)(i) and (d).

In an embodiment, contacting comprises contacting with (a), (b), (c)(i), (c)(ii) and (d).

In an embodiment, contacting comprises contacting with (a), (b), (c)(i), (c)(ii), (c)(iii) and (d).

The gRNA of (a) or (c) (e.g., (c)(i), (c)(ii), or (c)(iii) may be selected from any of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, or a gRNA that differs by no more than 1, 2, 3, 4, or 5 nucleotides from, a targeting domain sequence from any of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31.

In an embodiment, the method comprises acquiring knowledge of the sequence (e.g., a mutation) of an SCD target position in said subject.

In an embodiment, the method comprises acquiring knowledge of the sequence (e.g., a mutation) of an SCD target position in said subject by sequencing the HBB gene or BCL11A gene or a portion of the HBB gene or BCL11A gene.

In an embodiment, the method comprises correcting a mutation at an SCD target position in the HBB gene.

In an embodiment, the method comprises correcting a mutation at an SCD target position in the HBB gene by HDR.

In an embodiment, the method comprises introducing a mutation at an SCD target position in the BCL11A gene.

In an embodiment, the method comprises introducing a mutation at an SCD target position in the BCL11A gene by NHEJ.

When the method comprises correcting the mutation at an SCD target position by HDR, a Cas9 of (b), at least one guide RNA, e.g., a guide RNA of (a) and a template nucleic acid of (d) are included in the contacting step.

In an embodiment, a cell of the subject is contacted ex vivo with (a), (b), (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii). In an embodiment, said cell is returned to the subject's body.

In an embodiment, a cell of the subject is contacted is in vivo with (a), (b) (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, the cell of the subject is contacted in vivo by intravenous delivery of (a), (b), (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, the cell of the subject is contacted in vivo by intramuscular delivery of (a), (b), (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, the cell of the subject is contacted in vivo by subcutaneous delivery of (a), (b), (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, the cell of the subject is contacted in vivo by intra-bone marrow (IBM) delivery of (a), (b), (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, contacting comprises contacting the subject with a nucleic acid, e.g., a vector, e.g., an AAV vector, described herein, e.g., a nucleic acid that encodes at least one of (a), (b), (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, contacting comprises delivering to said subject said Cas9 molecule of (b), as a protein or mRNA, and a nucleic acid which encodes (a), a nucleic acid of (d) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, contacting comprises delivering to the subject the Cas9 molecule of (b), as a protein or mRNA, the gRNA of (a), as an RNA, a nucleic acid of (d) and optionally the second, third and/or fourth gRNA of (c), as an RNA.

In an embodiment, contacting comprises delivering to the subject the gRNA of (a), as an RNA, optionally said second, third and/or fourth gRNA of (c), as an RNA, a nucleic acid that encodes the Cas9 molecule of (b), and a nucleic acid of (d).

When the method comprises (1) introducing a mutation at an SCD target position by NHEJ or (2) knocking down expression of the BCL11A gene by targeting the promoter region, a Cas9 of (b) and at least one guide RNA, e.g., a guide RNA of (a) are included in the contacting step.

In an embodiment, a cell of the subject is contacted ex vivo with (a), (b) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii). In an embodiment, said cell is returned to the subject's body.

In an embodiment, a populations of cells from a subject is contacted ex vivo with (a), (b) and optionally (c) to correct the E6V mutation in the HBB gene and a second population of cells from the subject is contacted ex vivo with (a), (b) and optionally (c) to introduce a mutation in the BCL11A gene to knockout the BCL11A gene. A mixture of the two cell populations may be returned to the subject's body to treat or prevent SCD.

In an embodiment, a cell of the subject is contacted is in vivo with (a), (b) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii). In an embodiment, the cell of the subject is contacted in vivo by intravenous delivery of (a), (b) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii). In an embodiment, the cell of the subject is contacted in vivo by intramuscular delivery of (a), (b) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii). In an embodiment, the cell of the subject is contacted in vivo by subcutaneous delivery of (a), (b) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii). In an embodiment, the cell of the subject is contacted in vivo by intra-bone marrow (IBM) delivery of (a), (b) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, contacting comprises contacting the subject with a nucleic acid, e.g., a vector, e.g., an AAV vector, described herein, e.g., a nucleic acid that encodes at least one of (a), (b), and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, contacting comprises delivering to said subject said Cas9 molecule of (b), as a protein or mRNA, and a nucleic acid which encodes (a) and optionally (c)(i), further optionally (c)(ii), and still further optionally (c)(iii).

In an embodiment, contacting comprises delivering to the subject the Cas9 molecule of (b), as a protein or mRNA, the gRNA of (a), as an RNA, and optionally the second, third and/or fourth gRNA of (c), as an RNA.

In an embodiment, contacting comprises delivering to the subject the gRNA of (a), as an RNA, optionally said second, third and/or fourth gRNA of (c), as an RNA, and a nucleic acid that encodes the Cas9 molecule of (b).

In another aspect, disclosed herein is a reaction mixture comprising a gRNA, a nucleic acid, or a composition described herein, and a cell, e.g., a cell from a subject having, or likely to develop SCD, or a subject having a mutation at an SCD target position in the HBB gene, or a cell from a subject which would benefit from having a mutation at an SCD target position in the BCL11A gene.

In another aspect, disclosed herein is a kit comprising, (a) gRNA molecule described herein, or nucleic acid that encodes the gRNA, and one or more of the following:

(b) a Cas9 molecule, e.g., a Cas9 molecule described herein, or a nucleic acid or mRNA that encodes the Cas9;

(c)(i) a second gRNA molecule, e.g., a second gRNA molecule described herein or a nucleic acid that encodes (c)(i);

(c)(ii) a third gRNA molecule, e.g., a second gRNA molecule described herein or a nucleic acid that encodes (c)(ii);

(c)(iii) a fourth gRNA molecule, e.g., a second gRNA molecule described herein or a nucleic acid that encodes (c)(iii);

(d) a template nucleic acid (in an embodiment where an exogenous template is used), e.g., a template nucleic acid described herein.

In an embodiment, the kit comprises nucleic acid, e.g., an AAV vector, that encodes one or more of (a), (b), (c)(i), (c)(ii), (c)(iii) and (d).

In an aspect, the disclosure features a gRNA molecule, referred to herein as a governing gRNA molecule, comprising a targeting domain which is complementary to a target domain on a nucleic acid that encodes a component of the CRISPR/Cas system introduced into a cell or subject. In an embodiment, the governing gRNA molecule targets a nucleic acid that encodes a Cas9 molecule or a nucleic acid that encodes a target gene gRNA molecule. In an embodiment, the governing gRNA comprises a targeting domain that is complementary to a target domain in a sequence that encodes a Cas9 component, e.g., a Cas9 molecule or target gene gRNA molecule. In an embodiment, the target domain is designed with, or has, minimal homology to other nucleic acid sequences in the cell, e.g., to minimize off-target cleavage. For example, the targeting domain on the governing gRNA can be selected to reduce or minimize off-target effects. In an embodiment, a target domain for a governing gRNA can be disposed in the control or coding region of a Cas9 molecule or disposed between a control region and a transcribed region. In an embodiment, a target domain for a governing gRNA can be disposed in the control or coding region of a target gene gRNA molecule or disposed between a control region and a transcribed region for a target gene gRNA. While not wishing to be bound by theory, it is believed that altering, e.g., inactivating, a nucleic acid that encodes a Cas9 molecule or a nucleic acid that encodes a target gene gRNA molecule can be effected by cleavage of the targeted nucleic acid sequence or by binding of a Cas9 molecule/governing gRNA molecule complex to the targeted nucleic acid sequence.

The compositions, reaction mixtures and kits, as disclosed herein, can also include a governing gRNA molecule, e.g., a governing gRNA molecule disclosed herein.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

Headings, including numeric and alphabetical headings and subheadings, are for organization and presentation and are not intended to be limiting.

Other features and advantages of the invention will be apparent from the detailed description, drawings, and from the claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1I are representations of several exemplary gRNAs.

FIG. 1A depicts a modular gRNA molecule derived in part (or modeled on a sequence in part) from Streptococcus pyogenes (S. pyogenes) as a duplexed structure (SEQ ID NOS: 42 and 43, respectively, in order of appearance);

FIG. 1B depicts a unimolecular (or chimeric) gRNA molecule derived in part from S. pyogenes as a duplexed structure (SEQ ID NO: 44);

FIG. 1C depicts a unimolecular gRNA molecule derived in part from S. pyogenes as a duplexed structure (SEQ ID NO: 45);

FIG. 1D depicts a unimolecular gRNA molecule derived in part from S. pyogenes as a duplexed structure (SEQ ID NO: 46);

FIG. 1E depicts a unimolecular gRNA molecule derived in part from S. pyogenes as a duplexed structure (SEQ ID NO: 47);

FIG. 1F depicts a modular gRNA molecule derived in part from Streptococcus thermophilus (S. thermophilus) as a duplexed structure (SEQ ID NOS: 48 and 49, respectively, in order of appearance);

FIG. 1G depicts an alignment of modular gRNA molecules of S. pyogenes and S. thermophilus (SEQ ID NOS: 50-53, respectively, in order of appearance).

FIGS. 1H-1I depicts additional exemplary structures of unimolecular gRNA molecules.

FIG. 1H shows an exemplary structure of a unimolecular gRNA molecule derived in part from S. pyogenes as a duplexed structure (SEQ ID NO: 45).

FIG. 11 shows an exemplary structure of a unimolecular gRNA molecule derived in part from S. aureus as a duplexed structure (SEQ ID NO: 40).

FIGS. 2A-2G depict an alignment of Cas9 sequences from Chylinski et al. (RNA Biol. 2013; 10(5): 726-737). The N-terminal RuvC-like domain is boxed and indicated with a “Y”. The other two RuvC-like domains are boxed and indicated with a “B”. The HNH-like domain is boxed and indicated by a “G”. Sm: S. mutans (SEQ ID NO: 1); Sp: S. pyogenes (SEQ ID NO: 2); St: S. thermophilus (SEQ ID NO: 3); Li: L. innocua (SEQ ID NO: 4). Motif: this is a motif based on the four sequences: residues conserved in all four sequences are indicated by single letter amino acid abbreviation; “*” indicates any amino acid found in the corresponding position of any of the four sequences; and “-” indicates any amino acid, e.g., any of the 20 naturally occurring amino acids, or absent.

FIGS. 3A-3B show an alignment of the N-terminal RuvC-like domain from the Cas9 molecules disclosed in Chylinski et al (SEQ ID NOS: 54-103, respectively, in order of appearance). The last line of FIG. 3B identifies 4 highly conserved residues.

FIGS. 4A-4B show an alignment of the N-terminal RuvC-like domain from the Cas9 molecules disclosed in Chylinski et al. with sequence outliers removed (SEQ ID NOS: 104-177, respectively, in order of appearance). The last line of FIG. 4B identifies 3 highly conserved residues.

FIGS. 5A-5C show an alignment of the HNH-like domain from the Cas9 molecules disclosed in Chylinski et al (SEQ ID NOS: 178-252, respectively, in order of appearance). The last line of FIG. 5C identifies conserved residues.

FIGS. 6A-6B show an alignment of the HNH-like domain from the Cas9 molecules disclosed in Chylinski et al. with sequence outliers removed (SEQ ID NOS: 253-302, respectively, in order of appearance). The last line of FIG. 6B identifies 3 highly conserved residues.

FIGS. 7A-7B depict an alignment of Cas9 sequences from S. pyogenes and Neisseria meningitidis (N. meningitidis). The N-terminal RuvC-like domain is boxed and indicated with a “Y”. The other two RuvC-like domains are boxed and indicated with a “B”. The HNH-like domain is boxed and indicated with a “G”. Sp: S. pyogenes; Nm: N. meningitidis. Motif: this is a motif based on the two sequences: residues conserved in both sequences are indicated by a single amino acid designation; “*” indicates any amino acid found in the corresponding position of any of the two sequences; “-” indicates any amino acid, e.g., any of the 20 naturally occurring amino acids, and “-” indicates any amino acid, e.g., any of the 20 naturally occurring amino acids, or absent.

FIG. 8 shows a nucleic acid sequence encoding Cas9 of N. meningitidis (SEQ ID NO: 303). Sequence indicated by an “R” is an SV40 NLS; sequence indicated as “G” is an HA tag; and sequence indicated by an “O” is a synthetic NLS sequence; the remaining (unmarked) sequence is the open reading frame (ORF).

FIGS. 9A and 9B are schematic representations of the domain organization of S. pyogenes Cas 9. FIG. 9A shows the organization of the Cas9 domains, including amino acid positions, in reference to the two lobes of Cas9 (recognition (REC) and nuclease (NUC) lobes). FIG. 9B shows the percent homology of each domain across 83 Cas9 orthologs.

FIG. 10 shows chromosome 2 location (according to UCSC Genome Browser hg 19 human genome assembly) that corresponds to BCL11A intron 2. Three erythroid DHSs are labeled as distance in kilobases from BCL11A TSS (+62, +58 and +55). BCL11A transcription is from right to left.

FIG. 11 depicts the efficiency of NHEJ mediated by a Cas9 molecule and exemplary gRNA molecules targeting three different regions of the BCL11A locus.

FIGS. 12A-12B depict detected deletion events resulting from co-transfection of exemplary gRNA molecules, BCL11A-2983W and BCL11A-2981W.

FIG. 12A depicts schematic of DNA sequence recognized by BCL11A-2983W and BCL11A-2981W, which flanks the putative erythroid enhancer elements.

FIG. 12B depicts sequenced deletion events from the TOPO cloning of the PCR using primers that flank the enhancer region. A product is obtained when a deletion event has taken place.

FIGS. 13A-13B depicts detected deletion events resulting from co-transfection of the exemplary gRNA molecules, BCL11A-2995W and BCL11A-2984W.

FIG. 13A depicts Schematic of DNA sequence recognized by BCL11A-2995W and BCL11A-2984W, which flanks the putative erythroid enhancer elements.

FIG. 13B depicts sequenced deletion events from the TOPO cloning of the PCR using primers that flank the enhancer region. A product is obtained when a deletion event has taken place.

FIG. 14 depicts a scheme of the pair 8/15 of gRNAs surrounding the sickle mutation in combination with a Cas9 nickase (D10A or N863A). The nickases are shown as the grey ovals.

FIG. 15 depicts the percentages of total editing event after a wildtype Cas9 or a Cas9 nickase (D10A or N863A). A preprentation of at least three independent experiments for each condition is shown.

FIG. 16A depicts the frequency of deletions a wildtype Cas9 or a Cas9 nickase (D10A or N863A). A representation of at least 3 independent experiments for each condition is shown.

FIG. 16B depicts the frequency distribution of the length of deletions using a wildtype Cas9 and gRNA 8 (similar results have been obtained with gRNA 15).

FIG. 16C depicts the frequency distribution of the length of deletions using a Cas9 nickase (D10A) with gRNAs 8/15 (similar results have been obtained using Cas9 N863A).

FIG. 17A depicts the frequency of gene conversion a wildtype Cas9 or a Cas9 nickase (D10A or N863A).

FIG. 17B shows a scheme representing the region of similarity between the HBB and HBD loci.

FIG. 18 depicts the frequency of different lengths of HBD sequences that were incorporated into the HBB locus.

FIG. 19A depicts the frequency of insertions using a wildtype Cas9 or a Cas9 nickase (D10A or N863A). A representation of at least three independent experiments for each condition is shown.

FIG. 19B depicts examples of common reads observed in U2OS cells electroporated with plasmid encoding Cas9 N863 and gRNA 8/15 pair. The HBB reference is shown on the top.

FIG. 20A is a schematic representation of the donor template.

FIG. 20B depicts the frequency of HDR using a wildtype Cas9 or a Cas9 nickase (D10A or N863A).

FIG. 20C depicts different forms of nonors and there contribution to HDR.

FIG. 21 depicts genome editing of the HBB locus in bone marrow leukemia K562 hematopoietic cells after electroporation of Cas9 protein complexed to HBB gRNAs 8 and 15 (RNP) or Cas9 mRNA co-delivered with HBB gRNAs 8 and 15 (RNA).

DETAILED DESCRIPTION Definitions

“Alt-HDR” or “alternative HDR”, or alternative homology-directed repair, as used herein, refers to the process of repairing DNA damage using a homologous nucleic acid (e.g., an endogenous homologous sequence, e.g., a sister chromatid, or an exogenous nucleic acid, e.g., a template nucleic acid). Alt-HDR is distinct from canonical HDR in that the process utilizes different pathways from canonical HDR, and can be inhibited by the canonical HDR mediators, RAD51 and BRCA2. Also, alt-HDR uses a single-stranded or nicked homologous nucleic acid for repair of the break.

“Canonical HDR”, or canonical homology-directed repair, as used herein, refers to the process of repairing DNA damage using a homologous nucleic acid (e.g., an endogenous homologous sequence, e.g., a sister chromatid, or an exogenous nucleic acid, e.g., a template nucleic acid). Canonical HDR typically acts when there has been significant resection at the double strand break, forming at least one single stranded portion of DNA. In a normal cell, HDR typically involves a series of steps such as recognition of the break, stabilization of the break, resection, stabilization of single stranded DNA, formation of a DNA crossover intermediate, resolution of the crossover intermediate, and ligation. The process requires RAD51 and BRCA2, and the homologous nucleic acid is typically double-stranded.

Unless indicated otherwise, the term “HDR” as used herein encompasses canonical HDR and alt-HDR.

“Domain”, as used herein, is used to describe segments of a protein or nucleic acid. Unless otherwise indicated, a domain is not required to have any specific functional property.

Calculations of homology or sequence identity between two sequences (the terms are used interchangeably herein) are performed as follows. The sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). The optimal alignment is determined as the best score using the GAP program in the GCG software package with a Blossum 62 scoring matrix with a gap penalty of 12, a gap extend penalty of 4, and a frame shift gap penalty of 5. The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position. The percent identity between the two sequences is a function of the number of identical positions shared by the sequences.

“Governing gRNA molecule”, as used herein, refers to a gRNA molecule that comprises a targeting domain that is complementary to a target domain on a nucleic acid that comprises a sequence that encodes a component of the CRISPR/Cas system that is introduced into a cell or subject. A governing gRNA does not target an endogenous cell or subject sequence. In an embodiment, a governing gRNA molecule comprises a targeting domain that is complementary with a target sequence on: (a) a nucleic acid that encodes a Cas9 molecule; (b) a nucleic acid that encodes a gRNA which comprises a targeting domain that targets the HBB or BCL11A gene (a target gene gRNA); or on more than one nucleic acid that encodes a CRISPR/Cas component, e.g., both (a) and (b). In an embodiment, a nucleic acid molecule that encodes a CRISPR/Cas component, e.g., that encodes a Cas9 molecule or a target gene gRNA, comprises more than one target domain that is complementary with a governing gRNA targeting domain. While not wishing to be bound by theory, it is believed that a governing gRNA molecule complexes with a Cas9 molecule and results in Cas9 mediated inactivation of the targeted nucleic acid, e.g., by cleavage or by binding to the nucleic acid, and results in cessation or reduction of the production of a CRISPR/Cas system component. In an embodiment, the Cas9 molecule forms two complexes: a complex comprising a Cas9 molecule with a target gene gRNA, which complex will alter the HBB or BCL11A gene; and a complex comprising a Cas9 molecule with a governing gRNA molecule, which complex will act to prevent further production of a CRISPR/Cas system component, e.g., a Cas9 molecule or a target gene gRNA molecule. In an embodiment, a governing gRNA molecule/Cas9 molecule complex binds to or promotes cleavage of a control region sequence, e.g., a promoter, operably linked to a sequence that encodes a Cas9 molecule, a sequence that encodes a transcribed region, an exon, or an intron, for the Cas9 molecule. In an embodiment, a governing gRNA molecule/Cas9 molecule complex binds to or promotes cleavage of a control region sequence, e.g., a promoter, operably linked to a gRNA molecule, or a sequence that encodes the gRNA molecule. In an embodiment, the governing gRNA, e.g., a Cas9-targeting governing gRNA molecule, or a target gene gRNA-targeting governing gRNA molecule, limits the effect of the Cas9 molecule/target gene gRNA molecule complex-mediated gene targeting. In an embodiment, a governing gRNA places temporal, level of expression, or other limits, on activity of the Cas9 molecule/target gene gRNA molecule complex. In an embodiment, a governing gRNA reduces off-target or other unwanted activity. In an embodiment, a governing gRNA molecule inhibits, e.g., entirely or substantially entirely inhibits, the production of a component of the Cas9 system and thereby limits, or governs, its activity.

“Modulator”, as used herein, refers to an entity, e.g., a drug, that can alter the activity (e.g., enzymatic activity, transcriptional activity, or translational activity), amount, distribution, or structure of a subject molecule or genetic sequence. In an embodiment, modulation comprises cleavage, e.g., breaking of a covalent or non-covalent bond, or the forming of a covalent or non-covalent bond, e.g., the attachment of a moiety, to the subject molecule. In an embodiment, a modulator alters the, three dimensional, secondary, tertiary, or quaternary structure, of a subject molecule. A modulator can increase, decrease, initiate, or eliminate a subject activity.

“Large molecule”, as used herein, refers to a molecule having a molecular weight of at least 2, 3, 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100 kD. Large molecules include proteins, polypeptides, nucleic acids, biologics, and carbohydrates.

A “polypeptide”, as used herein, refers to a polymer of amino acids having less than 100 amino acid residues. In an embodiment, it has less than 50, 20, or 10 amino acid residues.

“Non-homologous end joining” or “NHEJ”, as used herein, refers to ligation mediated repair and/or non-template mediated repair including canonical NHEJ (cNHEJ), alternative NHEJ (altNHEJ), microhomology-mediated end joining (MMEJ), single-strand annealing (SSA), and synthesis-dependent microhomology-mediated end joining (SD-MMEJ).

A “reference molecule”, e.g., a reference Cas9 molecule or reference gRNA, as used herein, refers to a molecule to which a subject molecule, e.g., a subject Cas9 molecule of subject gRNA molecule, e.g., a modified or candidate Cas9 molecule is compared. For example, a Cas9 molecule can be characterized as having no more than 10% of the nuclease activity of a reference Cas9 molecule. Examples of reference Cas9 molecules include naturally occurring unmodified Cas9 molecules, e.g., a naturally occurring Cas9 molecule such as a Cas9 molecule of S. pyogenes, S. aureus or S. thermophilus. In an embodiment, the reference Cas9 molecule is the naturally occurring Cas9 molecule having the closest sequence identity or homology with the Cas9 molecule to which it is being compared. In an embodiment, the reference Cas9 molecule is a sequence, e.g., a naturally occurring or known sequence, which is the parental form on which a change, e.g., a mutation has been made.

“Replacement”, or “replaced”, as used herein with reference to a modification of a molecule does not require a process limitation but merely indicates that the replacement entity is present.

“Small molecule”, as used herein, refers to a compound having a molecular weight less than about 2 kD, e.g., less than about 2 kD, less than about 1.5 kD, less than about 1 kD, or less than about 0.75 kD.

“Subject”, as used herein, may mean either a human or non-human animal. The term includes, but is not limited to, mammals (e.g., humans, other primates, pigs, rodents (e.g., mice and rats or hamsters), rabbits, guinea pigs, cows, horses, cats, dogs, sheep, and goats). In an embodiment, the subject is a human. In another embodiment, the subject is poultry.

“Treat”, “treating” and “treatment”, as used herein, mean the treatment of a disease in a mammal, e.g., in a human, including (a) inhibiting the disease, i.e., arresting or preventing its development; (b) relieving the disease, i.e., causing regression of the disease state; and (c) curing the disease.

“Prevent”, “preventing” and “prevention”, as used herein, means the prevention of a disease in a mammal, e.g., in a human, including (a) avoiding or precluding the disease; (2) affecting the predisposition toward the disease, e.g., preventing at least one symptom of the disease or to delay onset of at least one symptom of the disease.

“X” as used herein in the context of an amino acid sequence, refers to any amino acid (e.g., any of the twenty natural amino acids) unless otherwise specified.

Methods of Repairing Mutation(s) in the HBB Gene

One approach to treat or prevent SCD is to repair (i.e., correct) one or more mutations in the HBB gene, e.g., by HDR. In this approach, mutant HBB allele(s) are corrected and restored to wild type state. While not wishing to be bound by theory, it is believed that correction of the glutamic acid to valine substitution at amino acid 6 in the beta-globin gene restores wild type beta-globin production within erythroid cells. The method described herein can be performed in all cell types. Beta-globin is expressed in cells of erythroid cell lineage. In an embodiment, an erythroid cell is targeted.

In an embodiment, one HBB allele is repaired in the subject. In another embodiment, both HBB alleles are repaired in the subject. In either situation, the subject can be cured of disease. As the disease only displays a phenotype when both alleles are mutated, repair of a single allele is adequate for a cure.

In one aspect, methods and compositions discussed herein, provide for the correction of the underlying genetic cause of SCD, e.g., the correction of a mutation at a target position in the HBB gene, e.g., correction of a mutation at amino acid position 6, e.g., an E6V substitution in the HBB gene.

In an embodiment, the method provides for the correction of a mutation at a target position in the HBB gene, e.g., correction of a mutation at amino acid position 6, e.g., an E6V substitution in the HBB gene. As described herein, in one embodiment, the method comprises the introduction of one or more breaks (e.g., single strand breaks or double strand breaks) sufficiently close to (e.g., either 5′ or 3′ to) the target position in the HBB gene, e.g., E6V.

In an embodiment, the targeting domain of the gRNA molecule is configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to (e.g., either 5′ or 3′ to) the target position in the HBB gene, e.g., E6V to allow correction, e.g., an alteration in the HBB gene, e.g., an alternation associated with HDR. In an embodiment, the targeting domain is configured such that a cleavage event, e.g., a double strand or single strand break, is positioned within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of a the target position in the HBB gene, e.g., E6V. The break, e.g., a double strand or single strand break, can be positioned upstream or downstream of the target position in the HBB gene, e.g., E6V.

In an embodiment, a second, third and/or fourth gRNA molecule is configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to (e.g., either 5′ or 3′ to) the target position in the HBB gene, e.g., E6V to allow correction, e.g., an alteration associated with HDR in the HBB gene. In an embodiment, the targeting domain is configured such that a cleavage event, e.g., a double strand or single strand break, is positioned within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of a the target position in the HBB gene, e.g., E6V. The break, e.g., a double strand or single strand break, can be positioned upstream or downstream of the target position in the HBB gene, e.g., E6V.

In an embodiment, a single strand break is accompanied by an additional single strand break, positioned by a second, third and/or fourth gRNA molecule, as discussed below. For example, The targeting domains bind configured such that a cleavage event, e.g., the two single strand breaks, are positioned within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position in the HBB gene, e.g., E6V. In an embodiment, the first and second gRNA molecules are configured such, that when guiding a Cas9 nickase, a single strand break will be accompanied by an additional single strand break, positioned by a second gRNA, sufficiently close to one another to result in an alteration of the target position in the HBB gene, e.g., E6V. In an embodiment, the first and second gRNA molecules are configured such that a single strand break positioned by said second gRNA is within 10, 20, 30, 40, or 50 nucleotides of the break positioned by said first gRNA molecule, e.g., when the Cas9 is a nickase. In an embodiment, the two gRNA molecules are configured to position cuts at the same position, or within a few nucleotides of one another, on different strands, e.g., essentially mimicking a double strand break.

In an embodiment, a double strand break can be accompanied by an additional double strand break, positioned by a second, third and/or fourth gRNA molecule, as is discussed below. For example, the targeting domain of a first gRNA molecule is configured such that a double strand break is positioned upstream of the target position in the HBB gene, e.g., E6V, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position; and the targeting domain of a second gRNA molecule is configured such that a double strand break is positioned downstream the target position in the HBB gene, e.g., E6V, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position.

In an embodiment, a double strand break can be accompanied by two additional single strand breaks, positioned by a second gRNA molecule and a third gRNA molecule. For example, the targeting domain of a first gRNA molecule is configured such that a double strand break is positioned upstream of the target position in the HBB gene, e.g., E6V, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position; and the targeting domains of a second and third gRNA molecule are configured such that two single strand breaks are positioned downstream of the target position in the HBB gene, e.g., E6V, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position. In an embodiment, the targeting domain of the first, second and third gRNA molecules are configured such that a cleavage event, e.g., a double strand or single strand break, is positioned, independently for each of the gRNA molecules.

In an embodiment, a first and second single strand breaks can be accompanied by two additional single strand breaks positioned by a third gRNA molecule and a fourth gRNA molecule. For example, the targeting domain of a first and second gRNA molecule are configured such that two single strand breaks are positioned upstream of the target position in the HBB gene, e.g., E6V, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position in the HBB gene, e.g., E6V; and the targeting domains of a third and fourth gRNA molecule are configured such that two single strand breaks are positioned downstream of the target position in the HBB gene, e.g., E6V, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position in the HBB gene, e.g., E6V.

In an embodiment, a mutation in the HBB gene, e.g., E6V is corrected using an exogenously provided template nucleic acid, e.g., by HDR. In another embodiment, a mutation in the HBB gene, e.g., E6V is corrected without using an exogenously provided template nucleic acid, e.g., by HDR. In an embodiment, alteration of the target sequence occurs with an endogenous genomic donor sequence, e.g., by HDR. In an embodiment, the endogenous genomic donor sequence comprises one or more nucleotides derived from the HBD gene. In an embodiment, a mutation in the HBB gene, e.g., E6V is corrected by an endogenous genomic donor sequence (e.g, an HBD gene). In an embodiment, an eaCas9 molecule, e.g., an eaCas9 molecule described herein, is used. In an embodiment, the eaCas9 molecule comprises HNH-like domain cleavage activity but has no, or no significant, N-terminal RuvC-like domain cleavage activity. In an embodiment, the eaCas9 molecule is an HNH-like domain nickase. In an embodiment, the eaCas9 molecule comprises a mutation at D10 (e.g., D10A). In an embodiment, the eaCas9 molecule comprises N-terminal RuvC-like domain cleavage activity but has no, or no significant, HNH-like domain cleavage activity. In an embodiment, the eaCas9 molecule is an N-terminal RuvC-like domain nickase. In an embodiment, the eaCas9 molecule comprises a mutation at H840 (e.g., H840A) or N863 (e.g., N863A).

Methods of Altering BCL11A

One approach to increase the expression of HbF involves identification of genes whose products play a role in the regulation of globin gene expression. One such gene is BCL11A. It plays a role in the regulation of γ globin expression. It was first identified because of its role in lymphocyte development. BCL11A encodes a zinc finger protein that is thought to be involved in the stage specific regulation of γ globin expression. The BCL11A gene product is expressed in adult erythroid precursor cells and down-regulation of its expression leads to an increase in 7 globin expression. In addition, it appears that the splicing of the BCL11A mRNA is developmentally regulated. In embryonic cells, it appears that the shorter BCL11A mRNA variants, known as BCL11A-S and BCL11A-XS are primary expressed, while in adult cells, the longer BCL11A-L and BCL11A-XL mRNA variants are predominantly expressed. See, Sankaran et al (2008) Science 322 p. 1839. The BCL11A protein appears to interact with the β globin locus to alter its conformation and thus its expression at different developmental stages. Thus, if BCL11A expression is altered e.g., disrupted (e.g., reduced or eliminated), it results in the elevation of γ globin and HbF production.

Disclosed herein are methods for altering the SCD target position in the BCL11A gene. Altering the SCD target position is achieved, e.g., by:

(1) knocking out the BCL11A gene:

    • (a) insertion or deletion (e.g., NHEJ-mediated insertion or deletion) of one or more nucleotides in close proximity to or within the early coding region of the BCL11A gene, or
    • (b) deletion (e.g., NHEJ-mediated deletion) of a genomic sequence including the erythroid enhancer of the BCL11A gene, or

(2) knocking down the BCL11A gene mediated by enzymatically inactive Cas9 (eiCas9) molecule or an eiCas9-fusion protein by targeting the promoter region of the gene.

All approaches give rise to alteration of the BCL11A gene.

In one embodiment, methods described herein introduce one or more breaks near the early coding region in at least one allele of the BCL11A gene. In another embodiment, methods described herein introduce two or more breaks to flank the erythroid enhancer of SCD target knockout position. The two or more breaks remove (e.g., delete) genomic sequence including the erythorid enhancer. In another embodiment, methods described herein comprises knocking down the BCL11A gene mediated by enzymatically inactive Cas9 (eiCas9) molecule or an eiCas9-fusion protein by targeting the promoter region of SCD target knockdown position. All methods described herein result in alteration of the BCL11A gene.

NHEJ-Mediated Introduction of an Indel in Close Proximity to or within the Early Coding Region of the SCD Knockout Position

In an embodiment, the method comprises introducing a NHEJ-mediated insertion or deletion of one more nucleotides in close proximity to the SCD target knockout position (e.g., the early coding region) of the BCL11A gene. As described herein, in one embodiment, the method comprises the introduction of one or more breaks (e.g., single strand breaks or double strand breaks) sufficiently close to (e.g., either 5′ or 3′ to) the early coding region of the SCD target knockout position, such that the break-induced indel could be reasonably expected to span the SCD target knockout position (e.g., the early coding region). While not wishing to be bound by theory, it is believed that NHEJ-mediated repair of the break(s) allows for the NHEJ-mediated introduction of an indel in close proximity to within the early coding region of the SCD target knockout position.

In an embodiment, the targeting domain of the gRNA molecule is configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to the early coding region in the BCL11A gene to allow alteration, e.g., alteration associated with NHEJ in the BCL11A gene. In an embodiment, the targeting domain is configured such that a cleavage event, e.g., a double strand or single strand break, is positioned within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of a SCD target knockout position. The break, e.g., a double strand or single strand break, can be positioned upstream or downstream of a SCD target knockout position in the BCL11A gene.

In an embodiment, a second gRNA molecule comprising a second targeting domain is configured to provide a cleavage event, e.g., a double strand break or a single strand break, sufficiently close to the early coding region in the BCL11A gene, to allow alteration, e.g., alteration associated with NHEJ in the BCL11A gene, either alone or in combination with the break positioned by said first gRNA molecule. In an embodiment, the targeting domains of the first and second gRNA molecules are configured such that a cleavage event, e.g., a double strand or single strand break, is positioned, independently for each of the gRNA molecules, within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position. In an embodiment, the breaks, e.g., double strand or single strand breaks, are positioned on both sides of a nucleotide of a SCD target knockout position in the BCL11A gene. In an embodiment, the breaks, e.g., double strand or single strand breaks, are positioned on one side, e.g., upstream or downstream, of a nucleotide of a SCD target knockout position in the BCL11A gene.

In an embodiment, a single strand break is accompanied by an additional single strand break, positioned by a second gRNA molecule, as discussed below. For example, The targeting domains bind configured such that a cleavage event, e.g., the two single strand breaks, are positioned within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the early coding region in the BCL11A gene. In an embodiment, the first and second gRNA molecules are configured such, that when guiding a Cas9 nickase, a single strand break will be accompanied by an additional single strand break, positioned by a second gRNA, sufficiently close to one another to result in alteration of the early coding region in the BCL11A gene. In an embodiment, the first and second gRNA molecules are configured such that a single strand break positioned by said second gRNA is within 10, 20, 30, 40, or 50 nucleotides of the break positioned by said first gRNA molecule, e.g., when the Cas9 is a nickase. In an embodiment, the two gRNA molecules are configured to position cuts at the same position, or within a few nucleotides of one another, on different strands, e.g., essentially mimicking a double strand break.

In an embodiment, a double strand break can be accompanied by an additional double strand break, positioned by a second gRNA molecule, as is discussed below. For example, the targeting domain of a first gRNA molecule is configured such that a double strand break is positioned upstream of the early coding region in the BCL11A gene, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position; and the targeting domain of a second gRNA molecule is configured such that a double strand break is positioned downstream of the early coding region in the BCL11A gene, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position.

In an embodiment, a double strand break can be accompanied by two additional single strand breaks, positioned by a second gRNA molecule and a third gRNA molecule. For example, the targeting domain of a first gRNA molecule is configured such that a double strand break is positioned upstream of the early coding region in the BCL11A gene, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position; and the targeting domains of a second and third gRNA molecule are configured such that two single strand breaks are positioned downstream of the early coding region in the BCL11A gene, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the target position. In an embodiment, the targeting domain of the first, second and third gRNA molecules are configured such that a cleavage event, e.g., a double strand or single strand break, is positioned, independently for each of the gRNA molecules.

In an embodiment, a first and second single strand breaks can be accompanied by two additional single strand breaks positioned by a third gRNA molecule and a fourth gRNA molecule. For example, the targeting domain of a first and second gRNA molecule are configured such that two single strand breaks are positioned upstream of the early coding region in the BCL11A gene, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the early coding region in the BCL11A gene; and the targeting domains of a third and fourth gRNA molecule are configured such that two single strand breaks are positioned downstream of a SCD target knockout position in the early coding region in the BCL11A gene, e.g., within 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 450 or 500 nucleotides of the early coding region in the BCL11A gene.

NHEJ-Mediated Deletion of the Erythroid Enhancer at the SCD Target Position

In an embodiment, the method comprises introducing a NHEJ-mediated deletion of a genomic sequence including the erythroid enhancer. As described herein, in one embodiment, the method comprises the introduction of two double strand breaks-one 5′ and the other 3′ to (i.e., flanking) the SCD target position (e.g., the erythroid enhancer). Two gRNAs, e.g., unimolecular (or chimeric) or modular gRNA molecules, are configured to position the two double strand breaks on opposite sides of the SCD target knockdown position (e.g., the erythroid enhancer) in the BCL11A gene. In an embodiment, the first double strand break is positioned upstream of the erythroid enhancer within intron 2 (e.g., between TSS+0.75 kb to TSS+52.0 kb), and the second double strand break is positioned downstream of the erythroid enhancer within intron 2 (e.g., between TSS+64.4 kb to TSS+84.7 kb) (see FIG. 10). In an embodiment, the two double strand breaks are positioned to remove a portion of the erythroid enhancer resulting in disruption of one or more DHSs. In an embodiment, the breaks (i.e., the two double strand breaks) are positioned to avoid unwanted target chromosome elements, such as repeat elements, e.g., an Alu repeat, or the endogenous splice sites.

The first double strand break may be positioned as follows:

    • (1) upstream of the 5′ end of the erythroid enhancer in intron 2 (e.g., between TSS+0.75 kb to TSS+52.0 kb), or
    • (2) within the erythroid enhancer provided that a portion of the erythroid enhancer is removed resulting in disruption of one or more DHSs (e.g., between TSS+52.0 kb to TSS+64.4 kb), and the second double strand break to be paired with the first double strand break may be positioned as follows:
    • (1) downstream the 3′ end of the erythroid enhancer in intron 2 (e.g., between TSS+64.4 kb to TSS+84.7 kb), or
    • (2) within the erythroid enhancer provided that a portion of the erythroid enhancer is removed resulting in disruption of one or more DHSs (e.g., between TSS+52.0 kb to TSS+64.4 kb).

For example, the first double strand break may be positioned in the BCL11A gene:

(1) between TSS+0.75 kb to TSS+10 kb,

(2) between TSS+10 kb to TSS+20 kb,

(3) between TSS+20 kb to TSS+30 kb,

(4) between TSS+30 kb to TSS+40 kb,

(5) between TSS+40 kb to TSS+45 kb,

(6) between TSS+45 kb to TSS+47.5 kb,

(7) between TSS+47.5 kb to TSS+50 kb,

(8) between TSS+50 kb to TSS+51 kb,

(9) between TSS+51 kb to TSS+51.1 kb,

(10) between TSS+51.1 kb to TSS+51.2 kb,

(11) between TSS+51.2 kb to TSS+51.3 kb,

(12) between TSS+51.3 kb to TSS+51.4 kb,

(13) between TSS+51.4 kb to TSS+51.5 kb,

(14) between TSS+51.5 kb to TSS+51.6 kb,

(15) between TSS+51.6 kb to TSS+51.7 kb,

(16) between TSS+51.7 kb to TSS+51.8 kb,

(17) between TSS+51.8 kb to TSS+51.9 kb,

(18) between TSS+51.9 kb to TSS+52 kb,

(19) between TSS+52 kb to TSS+53 kb,

(20) between TSS+53 kb to TSS+54 kb,

(21) between TSS+54 kb to TSS+55 kb,

(22) between TSS+55 kb to TSS+56 kb,

(23) between TSS+56 kb to TSS+57 kb,

(24) between TSS+57 kb to TSS+58 kb,

(25) between TSS+58 kb to TSS+59 kb,

(26) between TSS+59 kb to TSS+60 kb,

(27) between TSS+60 kb to TSS+61 kb,

(28) between TSS+61 kb to TSS+62 kb,

(29) between TSS+62 kb to TSS+63 kb,

(30) between TSS+63 kb to TSS+64 kb, or

(31) between TSS+64 kb to TSS+64.4 kb,

and the second double strand break to be paired with the first double strand break may be positioned in the BCL11A gene:

(1) between TSS+52 kb to TSS+53 kb,

(2) between TSS+53 kb to TSS+54 kb,

(3) between TSS+54 kb to TSS+55 kb,

(4) between TSS+55 kb to TSS+56 kb,

(5) between TSS+56 kb to TSS+57 kb,

(6) between TSS+57 kb to TSS+58 kb,

(7) between TSS+58 kb to TSS+59 kb,

(8) between TSS+59 kb to TSS+60 kb,

(9) between TSS+60 kb to TSS+61 kb,

(10) between TSS+61 kb to TSS+62 kb,

(11) between TSS+62 kb to TSS+63 kb,

(12) between TSS+63 kb to TSS+64 kb,

(13) between TSS+64 kb to TSS+64.4 kb,

(14) between TSS+64.4 kb to TSS+65 kb,

(15) between TSS+65 kb to TSS+65.1 kb,

(16) between TSS+65.1 kb to TSS+65.2 kb,

(17) between TSS+65.2 kb to TSS+65.3 kb,

(18) between TSS+65.3 kb to TSS+65.4 kb,

(19) between TSS+65.4 kb to TSS+65.5 kb,

(20) between TSS+65.5 kb to TSS+65.7 kb,

(21) between TSS+65.7 kb to TSS+65.8 kb,

(22) between TSS+65.8 kb to TSS+65.9 kb,

(23) between TSS+65.9 kb to TSS+66 kb,

(24) between TSS+66 kb to TSS+67 kb,

(25) between TSS+67 kb to TSS+68 kb,

(26) between TSS+68 kb to TSS+69 kb,

(27) between TSS+69 kb to TSS+70 kb,

(28) between TSS+70 kb to TSS+75 kb,

(29) between TSS+75 kb to TSS+80 kb, or

(30) between TSS+80 kb to TSS+84.4 kb.

While not wishing to be bound by theory, it is believed that the two double strand breaks allow for NHEJ-mediated deletion of erythroid enhancer in the BCL11A gene.

In an embodiment, the method comprises introducing a NHEJ-mediated deletion of a genomic sequence including the erythroid enhancer. As described herein, in one embodiment, the method comprises the introduction of two sets of breaks (e.g., one double strand break and a pair of single strand breaks)—one 5′ and the other 3′ to (i.e., flanking) the SCD target position (e.g., the erythroid enhancer). Two gRNAs, e.g., unimolecular (or chimeric) or modular gRNA molecules, are configured to position the two sets of breaks (either the double strand break or the pair of single strand breaks) on opposite sides of the SCD target knockdown position (e.g., the erythroid enhancer) in the BCL11A gene. In an embodiment, the first set of breaks (either the double strand break or the pair of single strand breaks) is positioned upstream of the erythroid enhancer within intron 2 (e.g., between TSS+0.75 kb to TSS+52.0 kb), and the second set of breaks (either the double strand break or the pair of single strand breaks) is positioned downstream of the erythroid enhancer within intron 2 (e.g., between TSS+64.4 kb to TSS+84.7 kb) (see FIG. 10). In an embodiment, the two sets of breaks (either the double strand break or the pair of single strand breaks) are positioned to remove a portion of the erythroid enhancer resulting in disruption of one or more DHSs. In an embodiment, the breaks (i.e., the two sets of breaks (either the double strand break or the pair of single strand breaks)) are positioned to avoid unwanted target chromosome elements, such as repeat elements, e.g., an Alu repeat, or the endogenous splice sites.

The first set of breaks (either the double strand break or the pair of single strand breaks) may be positioned as follows:

    • (1) upstream of the 5′ end of the erythroid enhancer in intron 2 (e.g., between TSS+0.75 kb to TSS+52.0 kb), or
    • (2) within the erythroid enhancer provided that a portion of the erythroid enhancer is removed resulting in disruption of one or more DHSs (e.g., between TSS+52.0 kb to TSS+64.4 kb),
      and the second set of breaks (either the double strand break or the pair of single strand breaks) to be paired with the first set of breaks (either the double strand break or the pair of single strand breaks) may be positioned as follows:
    • (1) downstream the 3′ end of the erythroid enhancer in intron 2 (e.g., between TSS+64.4 kb to TSS+84.7 kb), or
    • (2) within the erythroid enhancer provided that a portion of the erythroid enhancer is removed resulting in disruption of one or more DHSs (e.g., between TSS+52.0 kb to TSS+64.4 kb).

For example, the first set of breaks (either the double strand break or the pair of single strand breaks) may be positioned in the BCL11A gene:

(1) between TSS+0.75 kb to TSS+10 kb,

(2) between TSS+10 kb to TSS+20 kb,

(3) between TSS+20 kb to TSS+30 kb,

(4) between TSS+30 kb to TSS+40 kb,

(5) between TSS+40 kb to TSS+45 kb,

(6) between TSS+45 kb to TSS+47.5 kb,

(7) between TSS+47.5 kb to TSS+50 kb,

(8) between TSS+50 kb to TSS+51 kb,

(9) between TSS+51 kb to TSS+51.1 kb,

(10) between TSS+51.1 kb to TSS+51.2 kb,

(11) between TSS+51.2 kb to TSS+51.3 kb,

(12) between TSS+51.3 kb to TSS+51.4 kb,

(13) between TSS+51.4 kb to TSS+51.5 kb,

(14) between TSS+51.5 kb to TSS+51.6 kb,

(15) between TSS+51.6 kb to TSS+51.7 kb,

(16) between TSS+51.7 kb to TSS+51.8 kb,

(17) between TSS+51.8 kb to TSS+51.9 kb,

(18) between TSS+51.9 kb to TSS+52 kb,

(19) between TSS+52 kb to TSS+53 kb,

(20) between TSS+53 kb to TSS+54 kb,

(21) between TSS+54 kb to TSS+55 kb,

(22) between TSS+55 kb to TSS+56 kb,

(23) between TSS+56 kb to TSS+57 kb,

(24) between TSS+57 kb to TSS+58 kb,

(25) between TSS+58 kb to TSS+59 kb,

(26) between TSS+59 kb to TSS+60 kb,

(27) between TSS+60 kb to TSS+61 kb,

(28) between TSS+61 kb to TSS+62 kb,

(29) between TSS+62 kb to TSS+63 kb,

(30) between TSS+63 kb to TSS+64 kb, or

(31) between TSS+64 kb to TSS+64.4 kb,

and the second set of breaks (either the double strand break or the pair of single strand breaks) to be paired with the first set of breaks (either the double strand break or the pair of single strand breaks) may be positioned in the BCL11A gene:

(1) between TSS+52 kb to TSS+53 kb,

(2) between TSS+53 kb to TSS+54 kb,

(3) between TSS+54 kb to TSS+55 kb,

(4) between TSS+55 kb to TSS+56 kb,

(5) between TSS+56 kb to TSS+57 kb,

(6) between TSS+57 kb to TSS+58 kb,

(7) between TSS+58 kb to TSS+59 kb,

(8) between TSS+59 kb to TSS+60 kb,

(9) between TSS+60 kb to TSS+61 kb,

(10) between TSS+61 kb to TSS+62 kb,

(11) between TSS+62 kb to TSS+63 kb,

(12) between TSS+63 kb to TSS+64 kb,

(13) between TSS+64 kb to TSS+64.4 kb,

(14) between TSS+64.4 kb to TSS+65 kb,

(15) between TSS+65 kb to TSS+65.1 kb,

(16) between TSS+65.1 kb to TSS+65.2 kb,

(17) between TSS+65.2 kb to TSS+65.3 kb,

(18) between TSS+65.3 kb to TSS+65.4 kb,

(19) between TSS+65.4 kb to TSS+65.5 kb,

(20) between TSS+65.5 kb to TSS+65.7 kb,

(21) between TSS+65.7 kb to TSS+65.8 kb,

(22) between TSS+65.8 kb to TSS+65.9 kb,

(23) between TSS+65.9 kb to TSS+66 kb,

(24) between TSS+66 kb to TSS+67 kb,

(25) between TSS+67 kb to TSS+68 kb,

(26) between TSS+68 kb to TSS+69 kb,

(27) between TSS+69 kb to TSS+70 kb,

(28) between TSS+70 kb to TSS+75 kb,

(29) between TSS+75 kb to TSS+80 kb, or

(30) between TSS+80 kb to TSS+84.4 kb.

While not wishing to be bound by theory, it is believed that the two sets of breaks (either the double strand break or the pair of single strand breaks) allow for NHEJ-mediated deletion of erythroid enhancer in the BCL11A gene.

In an embodiment, the method comprises introducing a NHEJ-mediated deletion of a genomic sequence including the erythroid enhancer. As described herein, in one embodiment, the method comprises the introduction of two sets of breaks (e.g., two pairs of single strand breaks)-one 5′ and the other 3′ to (i.e., flanking) the SCD target position (e.g., the erythroid enhancer). Two gRNAs, e.g., unimolecular (or chimeric) or modular gRNA molecules, are configured to position the two sets of breaks on opposite sides of the SCD target knockdown position (e.g., the erythroid enhancer) in the BCL11A gene. In an embodiment, the first set of breaks (i.e., the first pair of single strand breaks) is positioned upstream of the erythroid enhancer within intron 2 (e.g., between TSS+0.75 kb to TSS+52.0 kb), and the second set of breaks (i.e., the second pair of single strand breaks) is positioned downstream of the erythroid enhancer within intron 2 (e.g., between TSS+64.4 kb to TSS+84.7 kb) (see FIG. 10). In an embodiment, the two sets of breaks (e.g., two pairs of single strand breaks)) are positioned to remove a portion of the erythroid enhancer resulting in disruption of one or more DHSs. In an embodiment, the breaks (i.e., the two pairs of single strand breaks) are positioned to avoid unwanted target chromosome elements, such as repeat elements, e.g., an Alu repeat, or the endogenous splice sites.

The first pair of single strand breaks may be positioned as follows:

    • (1) upstream of the 5′ end of the erythroid enhancer in intron 2 (e.g., between TSS+0.75 kb to TSS+52.0 kb), or
    • (2) within the erythroid enhancer provided that a portion of the erythroid enhancer is removed resulting in disruption of one or more DHSs (e.g., between TSS+52.0 kb to TSS+64.4 kb),
      and the second pair of single strand breaks to be paired with the first pair of single strand breaks may be positioned as follows:
    • (1) downstream the 3′ end of the erythroid enhancer in intron 2 (e.g., between TSS+64.4 kb to TSS+84.7 kb), or
    • (2) within the erythroid enhancer provided that a portion of the erythroid enhancer is removed resulting in disruption of one or more DHSs (e.g., between TSS+52.0 kb to TSS+64.4 kb).

For example, the pair of single strand breaks may be positioned in the BCL11A gene:

(1) between TSS+0.75 kb to TSS+10 kb,

(2) between TSS+10 kb to TSS+20 kb,

(3) between TSS+20 kb to TSS+30 kb,

(4) between TSS+30 kb to TSS+40 kb,

(5) between TSS+40 kb to TSS+45 kb,

(6) between TSS+45 kb to TSS+47.5 kb,

(7) between TSS+47.5 kb to TSS+50 kb,

(8) between TSS+50 kb to TSS+51 kb,

(9) between TSS+51 kb to TSS+51.1 kb,

(10) between TSS+51.1 kb to TSS+51.2 kb,

(11) between TSS+51.2 kb to TSS+51.3 kb,

(12) between TSS+51.3 kb to TSS+51.4 kb,

(13) between TSS+51.4 kb to TSS+51.5 kb,

(14) between TSS+51.5 kb to TSS+51.6 kb,

(15) between TSS+51.6 kb to TSS+51.7 kb,

(16) between TSS+51.7 kb to TSS+51.8 kb,

(17) between TSS+51.8 kb to TSS+51.9 kb,

(18) between TSS+51.9 kb to TSS+52 kb,

(19) between TSS+52 kb to TSS+53 kb,

(20) between TSS+53 kb to TSS+54 kb,

(21) between TSS+54 kb to TSS+55 kb,

(22) between TSS+55 kb to TSS+56 kb,

(23) between TSS+56 kb to TSS+57 kb,

(24) between TSS+57 kb to TSS+58 kb,

(25) between TSS+58 kb to TSS+59 kb,

(26) between TSS+59 kb to TSS+60 kb,

(27) between TSS+60 kb to TSS+61 kb,

(28) between TSS+61 kb to TSS+62 kb,

(29) between TSS+62 kb to TSS+63 kb,

(30) between TSS+63 kb to TSS+64 kb, or

(31) between TSS+64 kb to TSS+64.4 kb,

and the second pair of single strand breaks to be paired with the first pair of single strand breaks may be positioned in the BCL11A gene:

(1) between TSS+52 kb to TSS+53 kb,

(2) between TSS+53 kb to TSS+54 kb,

(3) between TSS+54 kb to TSS+55 kb,

(4) between TSS+55 kb to TSS+56 kb,

(5) between TSS+56 kb to TSS+57 kb,

(6) between TSS+57 kb to TSS+58 kb,

(7) between TSS+58 kb to TSS+59 kb,

(8) between TSS+59 kb to TSS+60 kb,

(9) between TSS+60 kb to TSS+61 kb,

(10) between TSS+61 kb to TSS+62 kb,

(11) between TSS+62 kb to TSS+63 kb,

(12) between TSS+63 kb to TSS+64 kb,

(13) between TSS+64 kb to TSS+64.4 kb,

(14) between TSS+64.4 kb to TSS+65 kb,

(15) between TSS+65 kb to TSS+65.1 kb,

(16) between TSS+65.1 kb to TSS+65.2 kb,

(17) between TSS+65.2 kb to TSS+65.3 kb,

(18) between TSS+65.3 kb to TSS+65.4 kb,

(19) between TSS+65.4 kb to TSS+65.5 kb,

(20) between TSS+65.5 kb to TSS+65.7 kb,

(21) between TSS+65.7 kb to TSS+65.8 kb,

(22) between TSS+65.8 kb to TSS+65.9 kb,

(23) between TSS+65.9 kb to TSS+66 kb,

(24) between TSS+66 kb to TSS+67 kb,

(25) between TSS+67 kb to TSS+68 kb,

(26) between TSS+68 kb to TSS+69 kb,

(27) between TSS+69 kb to TSS+70 kb,

(28) between TSS+70 kb to TSS+75 kb,

(29) between TSS+75 kb to TSS+80 kb, or

(30) between TSS+80 kb to TSS+84.4 kb.

While not wishing to be bound by theory, it is believed that the two sets of breaks (e.g., the two pair of single strand breaks) allow for NHEJ-mediated deletion of erythroid enhancer in the BCL11A gene.

Knocking Down the BCL11A Gene Mediated by an Enzymatically Inactive Cas9 (eiCas9) Molecule or an eiCas9-Fusion Protein by Targeting the Promoter Region of the Gene.

A targeted knockdown approach reduces or eliminates expression of functional BCL11A gene product. As described herein, a targeted knockdown is mediated by targeting an enzymatically inactive Cas9 (eiCas9) molecule or an eiCas9 fused to a transcription repressor domain or chromatin modifying protein to alter transcription, e.g., to block, reduce, or decrease transcription, of the BCL11A gene. In an embodiment, one or more eiCas9s may be used to block binding of one or more endogenous transcription factors. In another embodiment, an eiCas9 can be fused to a chromatin modifying protein. Altering chromatin status can result in decreased expression of the target gene. One or more eiCas9s fused to one or more chromatin modifying proteins may be used to alter chromatin status.

Methods and compositions discussed herein may be used to alter the expression of the BCL11A gene to treat or prevent SCD by targeting a promoter region of the BCL11A gene. In an embodiment, the promoter region, e.g., at least 2 kb, at least 1.5 kb, at least 1.0 kb, or at least 0.5 kb upstream or downstream of the TSS is targeted to knockdown expression of the BCL11A gene. In an embodiment, the methods and compositions discussed herein may be used to knock down the BCL11A gene to treat or prevent SCD by targeting 0.5 kb upstream or downstream of the TSS. A targeted knockdown approach reduces or eliminates expression of functional BCL11A gene product. As described herein, a targeted knockdown is mediated by targeting an enzymatically inactive Cas9 (eiCas9) molecule or an eiCas9 fused to a transcription repressor domain or chromatin modifying protein to alter transcription, e.g., to block, reduce, or decrease transcription, of the BCL11A gene.

Methods to Treat or Prevent Sickle Cell Disease (SCD)

Disclosed herein are the approaches to treat or prevent SCD, using the compositions and methods described herein.

One approach to treat or prevent SCD is to repair (i.e., correct) one or more mutations in the HBB gene, e.g., by HDR. In this approach, mutant HBB allele(s) are corrected and restored to wild type state. While not wishing to be bound by theory, it is believed that correction of the glutamic acid to valine substitution at amino acid 6 in the beta-globin gene restores wild type beta-globin production within erythroid cells. The method described herein can be performed in all cell types. Beta-globin is expressed in cells of erythroid cell lineage. In an embodiment, an erythroid cell is targeted.

In an embodiment, one HBB allele is repaired in the subject. In another embodiment, both HBB alleles are repaired in the subject. In either situation, the subjects can be cured of disease. As the disease only displays a phenotype when both alleles are mutated, repair of a single allele is adequate for a cure.

In one approach, the BCL11A gene is targeted as a targeted knockout or knockdown, e.g., to increase expression of fetal hemoglobin.

While not wishing to be bound by theory, it is considered that increasing levels of fetal hemoglobin (HbF) in subjects with SCD may ameliorate disease. Fetal hemoglobin can replace beta hemoglobin in the hemoglobin complex, form adequate tetramers with alpha hemoglobin, and effectively carry oxygen to tissues. Subjects with beta-thalassemia who express higher levels of fetal hemoglobin have been found to have a less severe phenotype. Hydroxyurea, often used in the treatment of beta-thalassemia, may exert its mechanism of action via increasing levels of HbF production.

In an embodiment, knockout or knockdown of the BCL11A gene increases fetal hemoglobin levels in beta-thalassemia subjects and improves phenotype and/or reduces or prevents disease progression. BCL11A is a zinc-finger repressor that is involved in the regulation of fetal hemoglobin and acts to repress the synthesis of fetal hemoglobin. Knockout of the BCL11A gene in erythroid cells induces increased fetal hemoglobin (HbF) synthesis and increased HbF can result in more effective oxygen carrying capacity in subjects with beta-thalassemia (HbF will form tetramers with hemoglobin alpha).

In an embodiment, the BCL11A knockout or knockdown is targeted specifically to cells of the erythroid lineage. BCL11A knockout in erythroid cells has been found in in vitro studies to have no effect on erythroid growth, maturation and function. In an embodiment, erythroid cells are preferentially targeted, e.g., at least 90%, 95%, 96%, 97%, 98%, 99%, or 100% of the targeted cells are erythroid cells. For example, in the case of in vivo delivery, erythroid cells are preferentially targeted, and if cells are treated ex vivo and returned to the subject, erythroid cells are preferentially modified.

In an embodiment, the methods described herein result in increased fetal hemoglobin synthesis in beta thalassemia subjects, thereby improving disease phenotype in subjects with SCD. For example, subjects with beta thalassemia major will suffer from less severe anemia and will need fewer blood transfusions. They will therefore have fewer complications arising from transfusions and chelation therapy. In an embodiment, the method described herein increases fetal hemoglobin synthesis and improves the oxygen carrying capacity of erythroid cells. For example, subjects are expected to demonstrate decreased rates of extramedullary erythropoiesis and decreased erythroid hypertrophy within the bone marrow compared to a subject who has not received the therapy. In an embodiment, the method described herein results in reduction of bone fractures, bone abnormalities, splenomegaly, and thrombosis compared to a subject who has not received the therapy.

Knockdown or knockout of one or both BCL11A alleles may be performed prior to disease onset or after disease onset, but preferably early in the disease course.

In an embodiment, the method comprises initiating treatment of a subject prior to disease onset.

In an embodiment, the method comprises initiating treatment of a subject after disease onset.

In an embodiment, the method comprises initiating treatment of a subject well after disease onset, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 16, 24, 36, 48 or more months after onset of SCD. While not wishing to be bound by theory it is believed that this treatment may be effective if subjects present well into the course of illness.

In an embodiment, the method comprises initiating treatment of a subject in an advanced stage of disease.

Overall, initiation of treatment for subjects at all stages of disease is expected to prevent negative consequences of disease and be of benefit to subjects.

In an embodiment, the method comprises initiating treatment of a subject prior to disease expression. In an embodiment, the method comprises initiating treatment of a subject in an early stage of disease, e.g., when a subject has tested positive for beta-thalassemia mutations but has no signs or symptoms associated with beta-thalassemia major, minor or intermedia.

In an embodiment, the method comprises initiating treatment of a subject at the appearance of microcytic anemia, e.g., in an infant, child, adult or young adult.

In an embodiment, the method comprises initiating treatment of a subject who is transfusion-dependent.

In an embodiment, the method comprises initiating treatment of a subject who has tested positive for a mutation in a beta globin gene.

In an embodiment, the method comprises initiating treatment at the appearance of any one or more of the following findings associated or consistent with beta-thalassemia major or beta-thalassemia minor: anemia, diarrhea, fever, failure to thrive, frontal bossing, broken long bones, hepatomegaly, splenomegaly, thrombosis, pulmonary embolus, stroke, leg ulcer, cardiomyopathy, cardiac arrhythmia, and evidence of extramedullary erythropoiesis.

In an embodiment, a cell is treated, e.g., ex vivo. In an embodiment, an ex vivo treated cell is returned to a subject.

In an embodiment, allogenic or autologous bone marrow or erythroid cells are treated ex vivo. In an embodiment, an ex vivo treated allogenic or autologous bone marrow or erythroid cells are administered to the subject. In an embodiment, an erythroid cell, e.g., an autologous erythroid cell, is treated ex vivo and returned to the subject. In an embodiment, an autologous stem cell, is treated ex vivo and returned to the subject. In an embodiment, the modified HSCs are administered to the patient following no myeloablative pre-conditioning. In an embodiment, the modified HSCs are administered to the patient following mild myeloablative pre-conditioning such that following engraftment, some of the hematopoietic cells are devied from the modified HSCs. In other aspects, the HSCs are administered after full myeloablation such that following engraftment, 100% of the hematopoietic cells are derived from the modified HSCs.

In an embodiment, the method comprises delivery of a gRNA molecule and Cas9 molecule by intravenous injection, intramuscular injection, subcutaneous injection, or intra-bone marrow (IBM) injection.

In an embodiment, the method comprises delivery of a gRNA molecule and/or a Cas9 molecule by an AAV. In an embodiment, the method comprises delivery of a gRNA molecule and/or a Cas9 molecule by a lentivirus. In an embodiment, the method comprises delivery of a gRNA molecule and/or a Cas9 molecule by a nanoparticle. In an embodiment, the method comprises delivery of a gRNA molecule by a parvovirus, e.g., a modified parvovirus specifically designed to target bone marrow cells and/or CD4 cells. In an embodiment, two or more gRNA molecules (e.g., a second, third or fourth gRNA molecules) are delivered.

I. gRNA Molecules

A gRNA molecule, as that term is used herein, refers to a nucleic acid that promotes the specific targeting or homing of a gRNA molecule/Cas9 molecule complex to a target nucleic acid. gRNA molecules can be unimolecular (having a single RNA molecule), sometimes referred to herein as “chimeric” gRNAs, or modular (comprising more than one, and typically two, separate RNA molecules). A gRNA molecule comprises a number of domains. The gRNA molecule domains are described in more detail below.

Several exemplary gRNA structures, with domains indicated thereon, are provided in FIGS. 1A-1G. While not wishing to be bound by theory, in an embodiment, with regard to the three dimensional form, or intra- or inter-strand interactions of an active form of a gRNA, regions of high complementarity are sometimes shown as duplexes in FIGS. 1A-1G and other depictions provided herein.

In an embodiment, a unimolecular, or chimeric, gRNA comprises, preferably from 5′ to 3′:

    • a targeting domain (which is complementary to a target nucleic acid in the HBB gene or BCL11A gene, e.g., a targeting domain from any of Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31;
    • a first complementarity domain;
    • a linking domain;
    • a second complementarity domain (which is complementary to the first complementarity domain);
    • a proximal domain; and
    • optionally, a tail domain.

In an embodiment, a modular gRNA comprises:

    • a first strand comprising, preferably from 5′ to 3′;
      • a targeting domain (which is complementary to a target nucleic acid in the HBB gene or BCL11A gene, e.g., a targeting domain from Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31; and
      • a first complementarity domain; and
    • a second strand, comprising, preferably from 5′ to 3′:
      • optionally, a 5′ extension domain;
      • a second complementarity domain;
      • a proximal domain; and
      • optionally, a tail domain.

The domains are discussed briefly below.

The Targeting Domain

FIGS. 1A-1G provide examples of the placement of targeting domains.

The targeting domain comprises a nucleotide sequence that is complementary, e.g., at least 80, 85, 90, or 95% complementary, e.g., fully complementary, to the target sequence on the target nucleic acid. The targeting domain is part of an RNA molecule and will therefore comprise the base uracil (U), while any DNA encoding the gRNA molecule will comprise the base thymine (T). While not wishing to be bound by theory, in an embodiment, it is believed that the complementarity of the targeting domain with the target sequence contributes to specificity of the interaction of the gRNA molecule/Cas9 molecule complex with a target nucleic acid. It is understood that in a targeting domain and target sequence pair, the uracil bases in the targeting domain will pair with the adenine bases in the target sequence. In an embodiment, the target domain itself comprises in the 5′ to 3′ direction, an optional secondary domain, and a core domain. In an embodiment, the core domain is fully complementary with the target sequence. In an embodiment, the targeting domain is 5 to 50 nucleotides in length. The strand of the target nucleic acid with which the targeting domain is complementary is referred to herein as the complementary strand. Some or all of the nucleotides of the domain can have a modification, e.g., a modification found in Section VIII herein.

In an embodiment, the targeting domain is 16 nucleotides in length.

In an embodiment, the targeting domain is 17 nucleotides in length.

In an embodiment, the targeting domain is 18 nucleotides in length.

In an embodiment, the targeting domain is 19 nucleotides in length.

In an embodiment, the targeting domain is 20 nucleotides in length.

In an embodiment, the targeting domain is 21 nucleotides in length.

In an embodiment, the targeting domain is 22 nucleotides in length.

In an embodiment, the targeting domain is 23 nucleotides in length.

In an embodiment, the targeting domain is 24 nucleotides in length.

In an embodiment, the targeting domain is 25 nucleotides in length.

In an embodiment, the targeting domain is 26 nucleotides in length.

In an embodiment, the targeting domain comprises 16 nucleotides.

In an embodiment, the targeting domain comprises 17 nucleotides.

In an embodiment, the targeting domain comprises 18 nucleotides.

In an embodiment, the targeting domain comprises 19 nucleotides.

In an embodiment, the targeting domain comprises 20 nucleotides.

In an embodiment, the targeting domain comprises 21 nucleotides.

In an embodiment, the targeting domain comprises 22 nucleotides.

In an embodiment, the targeting domain comprises 23 nucleotides.

In an embodiment, the targeting domain comprises 24 nucleotides.

In an embodiment, the targeting domain comprises 25 nucleotides.

In an embodiment, the targeting domain comprises 26 nucleotides.

Targeting domains are discussed in more detail below.

The First Complementarity Domain

FIGS. 1A-1G provide examples of first complementarity domains.

The first complementarity domain is complementary with the second complementarity domain, and in an embodiment, has sufficient complementarity to the second complementarity domain to form a duplexed region under at least some physiological conditions. In an embodiment, the first complementarity domain is 5 to 30 nucleotides in length. In an embodiment, the first complementarity domain is 5 to 25 nucleotides in length. In an embodiment, the first complementary domain is 7 to 25 nucleotides in length. In an embodiment, the first complementary domain is 7 to 22 nucleotides in length. In an embodiment, the first complementary domain is 7 to 18 nucleotides in length. In an embodiment, the first complementary domain is 7 to 15 nucleotides in length. In an embodiment, the first complementary domain is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 nucleotides in length.

In an embodiment, the first complementarity domain comprises 3 subdomains, which, in the 5′ to 3′ direction are: a 5′ subdomain, a central subdomain, and a 3′ subdomain. In an embodiment, the 5′ subdomain is 4 to 9, e.g., 4, 5, 6, 7, 8 or 9 nucleotides in length. In an embodiment, the central subdomain is 1, 2, or 3, e.g., 1, nucleotide in length. In an embodiment, the 3′ subdomain is 3 to 25, e.g., 4 to 22, 4 to 18, or 4 to 10, or 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 nucleotides in length.

The first complementarity domain can share homology with, or be derived from, a naturally occurring first complementarity domain. In an embodiment, it has at least 50% homology with a first complementarity domain disclosed herein, e.g., an S. pyogenes, S. aureus or S. thermophilus, first complementarity domain.

Some or all of the nucleotides of the domain can have a modification, e.g., a modification found in Section VIII herein.

First complementarity domains are discussed in more detail below.

The Linking Domain

FIGS. 1A-1G provide examples of linking domains.

A linking domain serves to link the first complementarity domain with the second complementarity domain of a unimolecular gRNA. The linking domain can link the first and second complementarity domains covalently or non-covalently. In an embodiment, the linkage is covalent. In an embodiment, the linking domain covalently couples the first and second complementarity domains, see, e.g., FIGS. 1B-1E. In an embodiment, the linking domain is, or comprises, a covalent bond interposed between the first complementarity domain and the second complementarity domain. Typically the linking domain comprises one or more, e.g., 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides.

In modular gRNA molecules the two molecules are associated by virtue of the hybridization of the complementarity domains see e.g., FIG. 1A.

A wide variety of linking domains are suitable for use in unimolecular gRNA molecules. Linking domains can consist of a covalent bond, or be as short as one or a few nucleotides, e.g., 1, 2, 3, 4, or 5 nucleotides in length. In an embodiment, a linking domain is 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, or 25 or more nucleotides in length. In an embodiment, a linking domain is 2 to 50, 2 to 40, 2 to 30, 2 to 20, 2 to 10, or 2 to 5 nucleotides in length. In an embodiment, a linking domain shares homology with, or is derived from, a naturally occurring sequence, e.g., the sequence of a tracrRNA that is 5′ to the second complementarity domain. In an embodiment, the linking domain has at least 50% homology with a linking domain disclosed herein.

Some or all of the nucleotides of the domain can have a modification, e.g., a modification found in Section VIII herein.

Linking domains are discussed in more detail below.

The 5′ Extension Domain

In an embodiment, a modular gRNA can comprise additional sequence, 5′ to the second complementarity domain, referred to herein as the 5′ extension domain, see, e.g., FIG. 1A. In an embodiment, the 5′ extension domain is, 2 to 10, 2 to 9, 2 to 8, 2 to 7, 2 to 6, 2 to 5, 2 to 4 nucleotides in length. In an embodiment, the 5′ extension domain is 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more nucleotides in length.

The Second Complementarity Domain

FIGS. 1A-1G provides examples of second complementarity domains.

The second complementarity domain is complementary with the first complementarity domain, and in an embodiment, has sufficient complementarity to the second complementarity domain to form a duplexed region under at least some physiological conditions. In an embodiment, e.g., as shown in FIGS. 1A-1B, the second complementarity domain can include sequence that lacks complementarity with the first complementarity domain, e.g., sequence that loops out from the duplexed region.

In an embodiment, the second complementarity domain is 5 to 27 nucleotides in length. In an embodiment, it is longer than the first complementarity region. In an embodiment the second complementary domain is 7 to 27 nucleotides in length. In an embodiment, the second complementary domain is 7 to 25 nucleotides in length. In an embodiment, the second complementary domain is 7 to 20 nucleotides in length. In an embodiment, the second complementary domain is 7 to 17 nucleotides in length. In an embodiment, the complementary domain is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, the second complementarity domain comprises 3 subdomains, which, in the 5′ to 3′ direction are: a 5′ subdomain, a central subdomain, and a 3′ subdomain. In an embodiment, the 5′ subdomain is 3 to 25, e.g., 4 to 22, 4 to 18, or 4 to 10, or 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 nucleotides in length. In an embodiment, the central subdomain is 1, 2, 3, 4 or 5, e.g., 3, nucleotides in length. In an embodiment, the 3′ subdomain is 4 to 9, e.g., 4, 5, 6, 7, 8 or 9 nucleotides in length.

In an embodiment, the 5′ subdomain and the 3′ subdomain of the first complementarity domain, are respectively, complementary, e.g., fully complementary, with the 3′ subdomain and the 5′ subdomain of the second complementarity domain.

The second complementarity domain can share homology with or be derived from a naturally occurring second complementarity domain. In an embodiment, it has at least 50% homology with a second complementarity domain disclosed herein, e.g., an S. pyogenes, S. aureus or S. thermophilus, first complementarity domain.

Some or all of the nucleotides of the domain can have a modification, e.g., a modification found in Section VIII herein.

A Proximal domain

FIGS. 1A-1G provide examples of proximal domains.

In an embodiment, the proximal domain is 5 to 20 nucleotides in length. In an embodiment, the proximal domain can share homology with or be derived from a naturally occurring proximal domain. In an embodiment, it has at least 50% homology with a proximal domain disclosed herein, e.g., an S. pyogenes, S. aureus or S. thermophilus, proximal domain.

Some or all of the nucleotides of the domain can have a modification, e.g., modification found in Section VIII herein.

A Tail Domain

FIGS. 1A-1G provide examples of tail domains.

As can be seen by inspection of the tail domains in FIGS. 1A-1E, a broad spectrum of tail domains are suitable for use in gRNA molecules. In an embodiment, the tail domain is 0 (absent), 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides in length. In embodiment, the tail domain nucleotides are from or share homology with sequence from the 5′ end of a naturally occurring tail domain, see e.g., panels 4a or 5a of FIG. 1D or FIG. 1E. In an embodiment, the tail domain includes sequences that are complementary to each other and which, under at least some physiological conditions, form a duplexed region.

In an embodiment, the tail domain is absent or is 1 to 50 nucleotides in length. In an embodiment, the tail domain can share homology with or be derived from a naturally occurring proximal tail domain. In an embodiment, it has at least 50% homology with a tail domain disclosed herein, e.g., an S. pyogenes, S. aureus or S. thermophilus, tail domain.

In an embodiment, the tail domain includes nucleotides at the 3′ end that are related to the method of in vitro or in vivo transcription. When a T7 promoter is used for in vitro transcription of the gRNA, these nucleotides may be any nucleotides present before the 3′ end of the DNA template. When a U6 promoter is used for in vivo transcription, these nucleotides may be the sequence UUUUUU. When alternate pol-III promoters are used, these nucleotides may be various numbers or uracil bases or may include alternate bases.

The domains of gRNA molecules are described in more detail below.

The Targeting Domain

The “targeting domain” of the gRNA is complementary to the “target domain” on the target nucleic acid. The strand of the target nucleic acid comprising the nucleotide sequence complementary to the core domain of the gRNA is referred to herein as the “complementary strand” of the target nucleic acid. Guidance on the selection of targeting domains can be found, e.g., in Fu Y et al., Nat Biotechnol 2014 (doi: 10.1038/nbt.2808) and Sternberg S H et al., Nature 2014 (doi: 10.1038/nature13011).

In an embodiment, the targeting domain is 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, the targeting domain is 16 nucleotides in length.

In an embodiment, the targeting domain is 17 nucleotides in length.

In an embodiment, the targeting domain is 18 nucleotides in length.

In an embodiment, the targeting domain is 19 nucleotides in length.

In an embodiment, the targeting domain is 20 nucleotides in length.

In an embodiment, the targeting domain is 21 nucleotides in length.

In an embodiment, the targeting domain is 22 nucleotides in length.

In an embodiment, the targeting domain is 23 nucleotides in length.

In an embodiment, the targeting domain is 24 nucleotides in length.

In an embodiment, the targeting domain is 25 nucleotides in length.

In an embodiment, the targeting domain is 26 nucleotides in length.

In an embodiment, the targeting domain comprises 16 nucleotides.

In an embodiment, the targeting domain comprises 17 nucleotides.

In an embodiment, the targeting domain comprises 18 nucleotides.

In an embodiment, the targeting domain comprises 19 nucleotides.

In an embodiment, the targeting domain comprises 20 nucleotides.

In an embodiment, the targeting domain comprises 21 nucleotides.

In an embodiment, the targeting domain comprises 22 nucleotides.

In an embodiment, the targeting domain comprises 23 nucleotides.

In an embodiment, the targeting domain comprises 24 nucleotides.

In an embodiment, the targeting domain comprises 25 nucleotides.

In an embodiment, the targeting domain comprises 26 nucleotides.

In an embodiment, the targeting domain is 10+/−5, 20+/−5, 30+/−5, 40+/−5, 50+/−5, 60+/−5, 70+/−5, 80+/−5, 90+/−5, or 100+/−5 nucleotides, in length.

In an embodiment, the targeting domain is 20+/−5 nucleotides in length.

In an embodiment, the targeting domain is 20+/−10, 30+/−10, 40+/−10, 50+/−10, 60+/−10, 70+/−10, 80+/−10, 90+/−10, or 100+/−10 nucleotides, in length.

In an embodiment, the targeting domain is 30+/−10 nucleotides in length.

In an embodiment, the targeting domain is 10 to 100, 10 to 90, 10 to 80, 10 to 70, 10 to 60, 10 to 50, 10 to 40, 10 to 30, 10 to 20 or 10 to 15 nucleotides in length.

In another embodiment, the targeting domain is 20 to 100, 20 to 90, 20 to 80, 20 to 70, 20 to 60, 20 to 50, 20 to 40, 20 to 30, or 20 to 25 nucleotides in length.

Typically the targeting domain has full complementarity with the target sequence. In an embodiment the targeting domain has or includes 1, 2, 3, 4, 5, 6, 7 or 8 nucleotides that are not complementary with the corresponding nucleotide of the targeting domain.

In an embodiment, the target domain includes 1, 2, 3, 4 or 5 nucleotides that are complementary with the corresponding nucleotide of the targeting domain within 5 nucleotides of its 5′ end. In an embodiment, the target domain includes 1, 2, 3, 4 or 5 nucleotides that are complementary with the corresponding nucleotide of the targeting domain within 5 nucleotides of its 3′ end.

In an embodiment, the target domain includes 1, 2, 3, or 4 nucleotides that are not complementary with the corresponding nucleotide of the targeting domain within 5 nucleotides of its 5′ end. In an embodiment, the target domain includes 1, 2, 3, or 4 nucleotides that are not complementary with the corresponding nucleotide of the targeting domain within 5 nucleotides of its 3′ end.

In an embodiment, the degree of complementarity, together with other properties of the gRNA, is sufficient to allow targeting of a Cas9 molecule to the target nucleic acid.

In an embodiment, the targeting domain comprises two consecutive nucleotides that are not complementary to the target domain (“non-complementary nucleotides”), e.g., two consecutive noncomplementary nucleotides that are within 5 nucleotides of the 5′ end of the targeting domain, within 5 nucleotides of the 3′ end of the targeting domain, or more than 5 nucleotides away from one or both ends of the targeting domain.

In an embodiment, no two consecutive nucleotides within 5 nucleotides of the 5′ end of the targeting domain, within 5 nucleotides of the 3′ end of the targeting domain, or within a region that is more than 5 nucleotides away from one or both ends of the targeting domain, are not complementary to the targeting domain.

In an embodiment, there are no noncomplementary nucleotides within 5 nucleotides of the 5′ end of the targeting domain, within 5 nucleotides of the 3′ end of the targeting domain, or within a region that is more than 5 nucleotides away from one or both ends of the targeting domain.

In an embodiment, the targeting domain nucleotides do not comprise modifications, e.g., modifications of the type provided in Section VIII. However, in an embodiment, the targeting domain comprises one or more modifications, e.g., modifications that it render it less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the targeting domain can be modified with a phosphorothioate, or other modification from Section VIII. In an embodiment, a nucleotide of the targeting domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification(s) from Section VIII.

In an embodiment, the targeting domain includes 1, 2, 3, 4, 5, 6, 7 or 8 or more modifications. In an embodiment, the targeting domain includes 1, 2, 3, or 4 modifications within 5 nucleotides of its 5′ end. In an embodiment, the targeting domain comprises as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 3′ end.

In an embodiment, the targeting domain comprises modifications at two consecutive nucleotides, e.g., two consecutive nucleotides that are within 5 nucleotides of the 5′ end of the targeting domain, within 5 nucleotides of the 3′ end of the targeting domain, or more than 5 nucleotides away from one or both ends of the targeting domain.

In an embodiment, no two consecutive nucleotides are modified within 5 nucleotides of the 5′ end of the targeting domain, within 5 nucleotides of the 3′ end of the targeting domain, or within a region that is more than 5 nucleotides away from one or both ends of the targeting domain. In an embodiment, no nucleotide is modified within 5 nucleotides of the 5′ end of the targeting domain, within 5 nucleotides of the 3′ end of the targeting domain, or within a region that is more than 5 nucleotides away from one or both ends of the targeting domain.

Modifications in the targeting domain can be selected to not interfere with targeting efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate targeting domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated in a system in Section IV. The candidate targeting domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, all of the modified nucleotides are complementary to and capable of hybridizing to corresponding nucleotides present in the target domain. In another embodiment, 1, 2, 3, 4, 5, 6, 7 or 8 or more modified nucleotides are not complementary to or capable of hybridizing to corresponding nucleotides present in the target domain.

In an embodiment, the targeting domain comprises, preferably in the 5′→3′ direction: a secondary domain and a core domain. These domains are discussed in more detail below.

The Core Domain and Secondary Domain of the Targeting Domain

The “core domain” of the targeting domain is complementary to the “core domain target” on the target nucleic acid. In an embodiment, the core domain comprises about 8 to about 13 nucleotides from the 3′ end of the targeting domain (e.g., the most 3′ 8 to 13 nucleotides of the targeting domain).

In an embodiment, the core domain and targeting domain, are independently, 6+/−2, 7+/−2, 8+/−2, 9+/−2, 10+/−2, 11+/−2, 12+/−2, 13+/−2, 14+/−2, 15+/−2, or 16+−2, nucleotides in length.

In an embodiment, the core domain and targeting domain, are independently, 10+/−2 nucleotides in length.

In an embodiment, the core domain and targeting domain, are independently, 10+/−4 nucleotides in length.

In an embodiment, the core domain and targeting domain are independently 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, or 18 nucleotides in length.

In an embodiment, the core domain and targeting domain are independently 3 to 20, 4 to 20, 5 to 20, 6 to 20, 7 to 20, 8 to 20, 9 to 20 10 to 20 or 15 to 20 nucleotides in length.

In an embodiment, the core domain and targeting domain are independently 3 to 15, e.g., 6 to 15, 7 to 14, 7 to 13, 6 to 12, 7 to 12, 7 to 11, 7 to 10, 8 to 14, 8 to 13, 8 to 12, 8 to 11, 8 to 10 or 8 to 9 nucleotides in length.

The core domain is complementary with the core domain target. Typically the core domain has exact complementarity with the core domain target. In an embodiment, the core domain can have 1, 2, 3, 4 or 5 nucleotides that are not complementary with the corresponding nucleotide of the core domain. In an embodiment, the degree of complementarity, together with other properties of the gRNA, is sufficient to allow targeting of a Cas9 molecule to the target nucleic acid.

The “secondary domain” of the targeting domain of the gRNA is complementary to the “secondary domain target” of the target nucleic acid.

In an embodiment, the secondary domain is positioned 5′ to the core domain.

In an embodiment, the secondary domain is absent or optional.

In an embodiment, if the targeting domain is 26 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 12 to 17 nucleotides in length.

In an embodiment, if the targeting domain is 25 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 12 to 17 nucleotides in length.

In an embodiment, if the targeting domain is 24 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 11 to 16 nucleotides in length.

In an embodiment, if the targeting domain is 23 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 10 to 15 nucleotides in length.

In an embodiment, if the targeting domain is 22 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 9 to 14 nucleotides in length.

In an embodiment, if the targeting domain is 21 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 8 to 13 nucleotides in length.

In an embodiment, if the targeting domain is 20 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 7 to 12 nucleotides in length.

In an embodiment, if the targeting domain is 19 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 6 to 11 nucleotides in length.

In an embodiment, if the targeting domain is 18 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 5 to 10 nucleotides in length.

In an embodiment, if the targeting domain is 17 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 4 to 9 nucleotides in length.

In an embodiment, if the targeting domain is 16 nucleotides in length and the core domain (counted from the 3′ end of the targeting domain) is 8 to 13 nucleotides in length, the secondary domain is 3 to 8 nucleotides in length.

In an embodiment, the secondary domain is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 nucleotides in length.

The secondary domain is complementary with the secondary domain target. Typically the secondary domain has exact complementarity with the secondary domain target. In an embodiment the secondary domain can have 1, 2, 3, 4 or 5 nucleotides that are not complementary with the corresponding nucleotide of the secondary domain. In an embodiment, the degree of complementarity, together with other properties of the gRNA, is sufficient to allow targeting of a Cas9 molecule to the target nucleic acid.

In an embodiment, the core domain nucleotides do not comprise modifications, e.g., modifications of the type provided in Section VIII. However, in an embodiment, the core domain comprises one or more modifications, e.g., modifications that it render it less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the core domain can be modified with a phosphorothioate, or other modification(s) from Section VIII. In an embodiment a nucleotide of the core domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification(s) from Section VIII. Typically, a core domain will contain no more than 1, 2, or 3 modifications.

Modifications in the core domain can be selected to not interfere with targeting efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate core domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated in the system described at Section IV. The candidate core domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, the secondary domain nucleotides do not comprise modifications, e.g., modifications of the type provided in Section VIII. However, in an embodiment, the secondary domain comprises one or more modifications, e.g., modifications that render it less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the secondary domain can be modified with a phosphorothioate, or other modification(s) from Section VIII. In an embodiment a nucleotide of the secondary domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification from Section VIII. Typically, a secondary domain will contain no more than 1, 2, or 3 modifications.

Modifications in the secondary domain can be selected to not interfere with targeting efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate secondary domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated in the system described at Section IV. The candidate secondary domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, (1) the degree of complementarity between the core domain and its target, and (2) the degree of complementarity between the secondary domain and its target, may differ. In an embodiment, (1) may be greater than (2). In an embodiment, (1) may be less than (2). In an embodiment, (1) and (2) are the same, e.g., each may be completely complementary with its target.

In an embodiment, (1) the number of modifications (e.g., modifications from Section VIII) of the nucleotides of the core domain and (2) the number of modification (e.g., modifications from Section VIII) of the nucleotides of the secondary domain, may differ. In an embodiment, (1) may be less than (2). In an embodiment, (1) may be greater than (2). In an embodiment, (1) and (2) may be the same, e.g., each may be free of modifications.

The First and Second Complementarity Domains

The first complementarity domain is complementary with the second complementarity domain.

Typically the first domain does not have exact complementarity with the second complementarity domain target. In an embodiment, the first complementarity domain can have 1, 2, 3, 4 or 5 nucleotides that are not complementary with the corresponding nucleotide of the second complementarity domain. In an embodiment, 1, 2, 3, 4, 5 or 6, e.g., 3 nucleotides, will not pair in the duplex, and, e.g., form a non-duplexed or looped-out region. In an embodiment, an unpaired, or loop-out, region, e.g., a loop-out of 3 nucleotides, is present on the second complementarity domain. In an embodiment, the unpaired region begins 1, 2, 3, 4, 5, or 6, e.g., 4, nucleotides from the 5′ end of the second complementarity domain.

In an embodiment, the degree of complementarity, together with other properties of the gRNA, is sufficient to allow targeting of a Cas9 molecule to the target nucleic acid.

In an embodiment, the first and second complementarity domains are:

independently, 6+/−2, 7+/−2, 8+/−2, 9+/−2, 10+/−2, 11+/−2, 12+/−2, 13+/−2, 14+/−2, 15+/−2, 16+/−2, 17+/−2, 18+/−2, 19+/−2, or 20+/−2, 21+/−2, 22+/−2, 23+/−2, or 24+/−2 nucleotides in length;

independently, 6, 7, 8, 9, 10, 11, 12, 13, 14, 14, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or 26, nucleotides in length; or

independently, 5 to 24, 5 to 23, 5 to 22, 5 to 21, 5 to 20, 7 to 18, 9 to 16, or 10 to 14 nucleotides in length.

In an embodiment, the second complementarity domain is longer than the first complementarity domain, e.g., 2, 3, 4, 5, or 6, e.g., 6, nucleotides longer.

In an embodiment, the first and second complementary domains, independently, do not comprise modifications, e.g., modifications of the type provided in Section VIII.

In an embodiment, the first and second complementary domains, independently, comprise one or more modifications, e.g., modifications that the render the domain less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the domain can be modified with a phosphorothioate, or other modification(s) from Section VIII. In an embodiment a nucleotide of the domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification(s) from Section VIII.

In an embodiment, the first and second complementary domains, independently, include 1, 2, 3, 4, 5, 6, 7 or 8 or more modifications. In an embodiment, the first and second complementary domains, independently, include 1, 2, 3, or 4 modifications within 5 nucleotides of its 5′ end. In an embodiment, the first and second complementary domains, independently, include as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 3′ end.

In an embodiment, the first and second complementary domains, independently, include modifications at two consecutive nucleotides, e.g., two consecutive nucleotides that are within 5 nucleotides of the 5′ end of the domain, within 5 nucleotides of the 3′ end of the domain, or more than 5 nucleotides away from one or both ends of the domain. In an embodiment, the first and second complementary domains, independently, include no two consecutive nucleotides that are modified, within 5 nucleotides of the 5′ end of the domain, within 5 nucleotides of the 3′ end of the domain, or within a region that is more than 5 nucleotides away from one or both ends of the domain. In an embodiment, the first and second complementary domains, independently, include no nucleotide that is modified within 5 nucleotides of the 5′ end of the domain, within 5 nucleotides of the 3′ end of the domain, or within a region that is more than 5 nucleotides away from one or both ends of the domain.

Modifications in a complementarity domain can be selected to not interfere with targeting efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate complementarity domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated in the system described in Section IV. The candidate complementarity domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, the first complementarity domain has at least 60, 70, 80, 85%, 90% or 95% homology with, or differs by no more than 1, 2, 3, 4, 5, or 6 nucleotides from, a reference first complementarity domain, e.g., a naturally occurring, e.g., an S. pyogenes, S. aureus or S. thermophilus, first complementarity domain, or a first complementarity domain described herein, e.g., from FIGS. 1A-1G.

In an embodiment, the second complementarity domain has at least 60, 70, 80, 85%, 90%, or 95% homology with, or differs by no more than 1, 2, 3, 4, 5, or 6 nucleotides from, a reference second complementarity domain, e.g., a naturally occurring, e.g., an S. pyogenes, S. aureus or S. thermophilus, second complementarity domain, or a second complementarity domain described herein, e.g., from FIGS. 1A-1G.

The duplexed region formed by first and second complementarity domains is typically 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 or 22 base pairs in length (excluding any looped out or unpaired nucleotides).

In an embodiment, the first and second complementarity domains, when duplexed, comprise 11 paired nucleotides, for example, in the gRNA sequence (one paired strand underlined, one bolded):

(SEQ ID NO: 5) NNNNNNNNNNNNNNNNNNNNGUUUUAGAGCUAGAAAUAGCAAGUUAAAA UAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUGC.

In an embodiment, the first and second complementarity domains, when duplexed, comprise 15 paired nucleotides, for example in the gRNA sequence (one paired strand underlined, one bolded):

(SEQ ID NO: 27) NNNNNNNNNNNNNNNNNNNNGUUUUAGAGCUAUGCUGAAAAGCAUAGCA AGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGU CGGUGC.

In an embodiment the first and second complementarity domains, when duplexed, comprise 16 paired nucleotides, for example in the gRNA sequence (one paired strand underlined, one bolded):

(SEQ ID NO: 28) NNNNNNNNNNNNNNNNNNNNGUUUUAGAGCUAUGCUGGAAACAGCAUAG CAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGA GUCGGUGC.

In an embodiment the first and second complementarity domains, when duplexed, comprise 21 paired nucleotides, for example in the gRNA sequence (one paired strand underlined, one bolded):

(SEQ ID NO: 29) NNNNNNNNNNNNNNNNNNNNGUUUUAGAGCUAUGCUGUUUUGGAAACAA AACAGCAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAA GUGGCACCGAGUCGGUGC.

In an embodiment, nucleotides are exchanged to remove poly-U tracts, for example in the gRNA sequences (exchanged nucleotides underlined):

(SEQ ID NO: 30) NNNNNNNNNNNNNNNNNNNNGUAUUAGAGCUAGAAAUAGCAAGUUAAUA UAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUGC; (SEQ ID NO: 31) NNNNNNNNNNNNNNNNNNNNGUUUAAGAGCUAGAAAUAGCAAGUUUAAA UAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUGC; or (SEQ ID NO: 32) NNNNNNNNNNNNNNNNNNNNGUAUUAGAGCUAUGCUGUAUUGGAAACAA UACAGCAUAGCAAGUUAAUAUAAGGCUAGUCCGUUAUCAACUUGAAAAA GUGGCACCGAGUCGGUGC.

The 5′ Extension Domain

In an embodiment, a modular gRNA can comprise additional sequence, 5′ to the second complementarity domain. In an embodiment, the 5′ extension domain is 2 to 10, 2 to 9, 2 to 8, 2 to 7, 2 to 6, 2 to 5, or 2 to 4 nucleotides in length. In an embodiment, the 5′ extension domain is 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more nucleotides in length.

In an embodiment, the 5′ extension domain nucleotides do not comprise modifications, e.g., modifications of the type provided in Section VIII. However, in an embodiment, the 5′ extension domain comprises one or more modifications, e.g., modifications that it render it less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the 5′ extension domain can be modified with a phosphorothioate, or other modification(s) from Section VIII. In an embodiment, a nucleotide of the 5′ extension domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification(s) from Section VIII.

In an embodiment, the 5′ extension domain can comprise as many as 1, 2, 3, 4, 5, 6, 7 or 8 modifications. In an embodiment, the 5′ extension domain comprises as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 5′ end, e.g., in a modular gRNA molecule. In an embodiment, the 5′ extension domain comprises as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 3′ end, e.g., in a modular gRNA molecule.

In an embodiment, the 5′ extension domain comprises modifications at two consecutive nucleotides, e.g., two consecutive nucleotides that are within 5 nucleotides of the 5′ end of the 5′ extension domain, within 5 nucleotides of the 3′ end of the 5′ extension domain, or more than 5 nucleotides away from one or both ends of the 5′ extension domain. In an embodiment, no two consecutive nucleotides are modified within 5 nucleotides of the 5′ end of the 5′ extension domain, within 5 nucleotides of the 3′ end of the 5′ extension domain, or within a region that is more than 5 nucleotides away from one or both ends of the 5′ extension domain. In an embodiment, no nucleotide is modified within 5 nucleotides of the 5′ end of the 5′ extension domain, within 5 nucleotides of the 3′ end of the 5′ extension domain, or within a region that is more than 5 nucleotides away from one or both ends of the 5′ extension domain.

Modifications in the 5′ extension domain can be selected so as to not interfere with gRNA molecule efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate 5′ extension domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated in the system described at Section IV. The candidate 5′ extension domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, the 5′ extension domain has at least 60, 70, 80, 85, 90 or 95% homology with, or differs by no more than 1, 2, 3, 4, 5, or 6 nucleotides from, a reference 5′ extension domain, e.g., a naturally occurring, e.g., an S. pyogenes, S. aureus or S. thermophilus, 5′ extension domain, or a 5′ extension domain described herein, e.g., from FIGS. 1A-1G.

The Linking Domain

In a unimolecular gRNA molecule the linking domain is disposed between the first and second complementarity domains. In a modular gRNA molecule, the two molecules are associated with one another by the complementarity domains.

In an embodiment, the linking domain is 10+/−5, 20+/−5, 30+/−5, 40+/−5, 50+/−5, 60+/−5, 70+/−5, 80+/−5, 90+/−5, or 100+/−5 nucleotides, in length.

In an embodiment, the linking domain is 20+/−10, 30+/−10, 40+/−10, 50+/−10, 60+/−10, 70+/−10, 80+/−10, 90+/−10, or 100+/−10 nucleotides, in length.

In an embodiment, the linking domain is 10 to 100, 10 to 90, 10 to 80, 10 to 70, 10 to 60, 10 to 50, 10 to 40, 10 to 30, 10 to 20 or 10 to 15 nucleotides in length.

In another embodiment, the linking domain is 20 to 100, 20 to 90, 20 to 80, 20 to 70, 20 to 60, 20 to 50, 20 to 40, 20 to 30, or 20 to 25 nucleotides in length.

In an embodiment, the linking domain is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 17, 18, 19, or 20 nucleotides in length.

In and embodiment, the linking domain is a covalent bond.

In an embodiment, the linking domain comprises a duplexed region, typically adjacent to or within 1, 2, or 3 nucleotides of the 3′ end of the first complementarity domain and/or the 5-end of the second complementarity domain. In an embodiment, the duplexed region can be 20+/−10 base pairs in length. In an embodiment, the duplexed region can be 10+/−5, 15+/−5, 20+/−5, or 30+/−5 base pairs in length. In an embodiment, the duplexed region can be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 base pairs in length.

Typically the sequences forming the duplexed region have exact complementarity with one another, though in an embodiment as many as 1, 2, 3, 4, 5, 6, 7 or 8 nucleotides are not complementary with the corresponding nucleotides.

In an embodiment, the linking domain nucleotides do not comprise modifications, e.g., modifications of the type provided in Section VIII. However, in an embodiment, the linking domain comprises one or more modifications, e.g., modifications that it render it less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the linking domain can be modified with a phosphorothioate, or other modification(s) from Section VIII. In an embodiment a nucleotide of the linking domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification(s) from Section VIII. In an embodiment, the linking domain can comprise as many as 1, 2, 3, 4, 5, 6, 7 or 8 modifications.

Modifications in a linking domain can be selected so as to not interfere with targeting efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate linking domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated a system described in Section IV. A candidate linking domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, the linking domain has at least 60, 70, 80, 85, 90 or 95% homology 30 with, or differs by no more than 1, 2, 3, 4, 5, or 6 nucleotides from, a reference linking domain, e.g., a linking domain described herein, e.g., from FIGS. 1A-1G.

The Proximal Domain

In an embodiment, the proximal domain is 6+/−2, 7+/−2, 8+/−2, 9+/−2, 10+/−2, 11+/−2, 12+/−2, 13+/−2, 14+/−2, 14+/−2, 16+/−2, 17+/−2, 18+/−2, 19+/−2, or 20+/−2 nucleotides in length.

In an embodiment, the proximal domain is 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length.

In an embodiment, the proximal domain is 5 to 20, 7, to 18, 9 to 16, or 10 to 14 nucleotides in length.

In an embodiment, the proximal domain nucleotides do not comprise modifications, e.g., modifications of the type provided in Section VIII. However, in an embodiment, the proximal domain comprises one or more modifications, e.g., modifications that it render it less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the proximal domain can be modified with a phosphorothioate, or other modification(s) from Section VIII. In an embodiment a nucleotide of the proximal domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification(s) from Section VIII.

In an embodiment, the proximal domain can comprise as many as 1, 2, 3, 4, 5, 6, 7 or 8 modifications. In an embodiment, the proximal domain comprises as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 5′ end, e.g., in a modular gRNA molecule. In an embodiment, the target domain comprises as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 3′ end, e.g., in a modular gRNA molecule.

In an embodiment, the proximal domain comprises modifications at two consecutive nucleotides, e.g., two consecutive nucleotides that are within 5 nucleotides of the 5′ end of the proximal domain, within 5 nucleotides of the 3′ end of the proximal domain, or more than 5 nucleotides away from one or both ends of the proximal domain. In an embodiment, no two consecutive nucleotides are modified within 5 nucleotides of the 5′ end of the proximal domain, within 5 nucleotides of the 3′ end of the proximal domain, or within a region that is more than 5 nucleotides away from one or both ends of the proximal domain. In an embodiment, no nucleotide is modified within 5 nucleotides of the 5′ end of the proximal domain, within 5 nucleotides of the 3′ end of the proximal domain, or within a region that is more than 5 nucleotides away from one or both ends of the proximal domain.

Modifications in the proximal domain can be selected so as to not interfere with gRNA molecule efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate proximal domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated in the system described at Section IV. The candidate proximal domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, the proximal domain has at least 60, 70, 80, 85 90 or 95% homology with, or differs by no more than 1, 2, 3, 4, 5, or 6 nucleotides from, a reference proximal domain, e.g., a naturally occurring, e.g., an S. pyogenes, S. aureus or S. thermophilus, proximal domain, or a proximal domain described herein, e.g., from FIGS. 1A-1G. The Tail Domain

In an embodiment, the tail domain is 10+/−5, 20+/−5, 30+/−5, 40+/−5, 50+/−5, 60+/−5, 70+/−5, 80+/−5, 90+/−5, or 100+/−5 nucleotides, in length.

In an embodiment, the tail domain is 20+/−5 nucleotides in length.

In an embodiment, the tail domain is 20+/−10, 30+/−10, 40+/−10, 50+/−10, 60+/−10, 70+/−10, 80+/−10, 90+/−10, or 100+/−10 nucleotides, in length.

In an embodiment, the tail domain is 25+/−10 nucleotides in length.

In an embodiment, the tail domain is 10 to 100, 10 to 90, 10 to 80, 10 to 70, 10 to 60, 10 to 50, 10 to 40, 10 to 30, 10 to 20 or 10 to 15 nucleotides in length.

In another embodiment, the tail domain is 20 to 100, 20 to 90, 20 to 80, 20 to 70, 20 to 60, 20 to 50, 20 to 40, 20 to 30, or 20 to 25 nucleotides in length.

In an embodiment, the tail domain is 1 to 20, 1 to 15, 1 to 10, or 1 to 5 nucleotides in length.

In an embodiment, the tail domain nucleotides do not comprise modifications, e.g., modifications of the type provided in Section VIII. However, in an embodiment, the tail domain comprises one or more modifications, e.g., modifications that it render it less susceptible to degradation or more bio-compatible, e.g., less immunogenic. By way of example, the backbone of the tail domain can be modified with a phosphorothioate, or other modification(s) from Section VIII. In an embodiment a nucleotide of the tail domain can comprise a 2′ modification (e.g., a modification at the 2′ position on ribose), e.g., a 2-acetylation, e.g., a 2′ methylation, or other modification(s) from Section VIII.

In an embodiment, the tail domain can have as many as 1, 2, 3, 4, 5, 6, 7 or 8 modifications. In an embodiment, the target domain comprises as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 5′ end. In an embodiment, the target domain comprises as many as 1, 2, 3, or 4 modifications within 5 nucleotides of its 3′ end.

In an embodiment, the tail domain comprises a tail duplex domain, which can form a tail duplexed region. In an embodiment, the tail duplexed region can be 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 base pairs in length. In an embodiment, a further single stranded domain, exists 3′ to the tail duplexed domain. In an embodiment, this domain is 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides in length. In an embodiment it is 4 to 6 nucleotides in length.

In an embodiment, the tail domain has at least 60, 70, 80, or 90% homology with, or differs by no more than 1, 2, 3, 4, 5, or 6 nucleotides from, a reference tail domain, e.g., a naturally occurring, e.g., an S. pyogenes, S. aureus or S. thermophilus, tail domain, or a tail domain described herein, e.g., from FIGS. 1A-1G.

In an embodiment, the proximal and tail domain, taken together comprise the following sequences:

(SEQ ID NO: 33) AAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUGCU, or (SEQ ID NO: 34) AAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUGGUG C, or (SEQ ID NO: 35) AAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUGCGGA UC, or (SEQ ID NO: 36) AAGGCUAGUCCGUUAUCAACUUGAAAAAGUG, or (SEQ ID NO: 37) AAGGCUAGUCCGUUAUCA, or (SEQ ID NO: 38) AAGGCUAGUCCG.

In an embodiment, the tail domain comprises the 3′ sequence UUUUUU, e.g., if a U6 promoter is used for transcription.

In an embodiment, the tail domain comprises the 3′ sequence UUUU, e.g., if an H1 promoter is used for transcription.

In an embodiment, tail domain comprises variable numbers of 3′ Us depending, e.g., on the termination signal of the pol-III promoter used.

In an embodiment, the tail domain comprises variable 3′ sequence derived from the DNA template if a T7 promoter is used.

In an embodiment, the tail domain comprises variable 3′ sequence derived from the DNA template, e.g., if in vitro transcription is used to generate the RNA molecule.

In an embodiment, the tail domain comprises variable 3′ sequence derived from the DNA template, e., if a pol-II promoter is used to drive transcription.

Modifications in the tail domain can be selected to not interfere with targeting efficacy, which can be evaluated by testing a candidate modification in the system described in Section IV. gRNAs having a candidate tail domain having a selected length, sequence, degree of complementarity, or degree of modification, can be evaluated in the system described in Section IV. The candidate tail domain can be placed, either alone, or with one or more other candidate changes in a gRNA molecule/Cas9 molecule system known to be functional with a selected target and evaluated.

In an embodiment, the tail domain comprises modifications at two consecutive nucleotides, e.g., two consecutive nucleotides that are within 5 nucleotides of the 5′ end of the tail domain, within 5 nucleotides of the 3′ end of the tail domain, or more than 5 nucleotides away from one or both ends of the tail domain. In an embodiment, no two consecutive nucleotides are modified within 5 nucleotides of the 5′ end of the tail domain, within 5 nucleotides of the 3′ end of the tail domain, or within a region that is more than 5 nucleotides away from one or both ends of the tail domain. In an embodiment, no nucleotide is modified within 5 nucleotides of the 5′ end of the tail domain, within 5 nucleotides of the 3′ end of the tail domain, or within a region that is more than 5 nucleotides away from one or both ends of the tail domain.

In an embodiment a gRNA has the following structure:

5′ [targeting domain]-[first complementarity domain]-[linking domain]-[second complementarity domain]-[proximal domain]-[tail domain]-3′

wherein, the targeting domain comprises a core domain and optionally a secondary domain, and is 10 to 50 nucleotides in length;

the first complementarity domain is 5 to 25 nucleotides in length and, In an embodiment has at least 50, 60, 70, 80, 85, 90 or 95% homology with a reference first complementarity domain disclosed herein;

the linking domain is 1 to 5 nucleotides in length;

the second complementarity domain is 5 to 27 nucleotides in length and, in an embodiment has at least 50, 60, 70, 80, 85, 90 or 95% homology with a reference second complementarity domain disclosed herein;

the proximal domain is 5 to 20 nucleotides in length and, in an embodiment has at least 50, 60, 70, 80, 85, 90 or 95% homology with a reference proximal domain disclosed herein; and

the tail domain is absent or a nucleotide sequence is 1 to 50 nucleotides in length and, in an embodiment has at least 50, 60, 70, 80, 85, 90 or 95% homology with a reference tail domain disclosed herein.

Exemplary Chimeric gRNAs

In an embodiment, a unimolecular, or chimeric, gRNA comprises, preferably from 5′ to 3′:

    • a targeting domain (which is complementary to a target nucleic acid);
    • a first complementarity domain, e.g., comprising 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or 26 nucleotides;
    • a linking domain;
    • a second complementarity domain (which is complementary to the first complementarity domain);
    • a proximal domain; and a tail domain,
    • wherein,
    • (a) the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides;
    • (b) there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain; or
    • (c) there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the sequence from (a), (b), or (c), has at least 60, 75, 80, 85, 90, 95, or 99% homology with the corresponding sequence of a naturally occurring gRNA, or with a gRNA described herein.

In an embodiment, the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides (e.g., 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or 26 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 25 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 25 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 25 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 25 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the unimolecular, or chimeric, gRNA molecule (comprising a targeting domain, a first complementary domain, a linking domain, a second complementary domain, a proximal domain and, optionally, a tail domain) comprises the following sequence in which the targeting domain is depicted as 20 Ns but could be any sequence and range in length from 16 to 26 nucleotides and in which the gRNA sequence is followed by 6 Us, which serve as a termination signal for the U6 promoter, but which could be either absent or fewer in number: NNNNNNNNNNNNNNNNNNNNGUUUUAGAGCUAGAAAUAGCAAGUUAAAAUAAGG CUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUGCUUUUUU (SEQ ID NO: 45). In an embodiment, the unimolecular, or chimeric, gRNA molecule is a S. pyogenes gRNA molecule.

In some embodiments, the unimolecular, or chimeric, gRNA molecule (comprising a targeting domain, a first complementary domain, a linking domain, a second complementary domain, a proximal domain and, optionally, a tail domain) comprises the following sequence in which the targeting domain is depicted as 20 Ns but could be any sequence and range in length from 16 to 26 nucleotides and in which the gRNA sequence is followed by 6 Us, which serve as a termination signal for the U6 promoter, but which could be either absent or fewer in number: NNNNNNNNNNNNNNNNNNNNGUUUUAGUACUCUGGAAACAGAAUCUACUAAAAC AAGGCAAAAUGCCGUGUUUAUCUCGUCAACUUGUUGGCGAGAUUUUUU (SEQ ID NO: 40). In an embodiment, the unimolecular, or chimeric, gRNA molecule is a S. aureus gRNA molecule.

The sequences and structures of exemplary chimeric gRNAs are also shown in FIGS. 1H-11.

Exemplary Modular gRNAs

In an embodiment, a modular gRNA comprises:

    • a first strand comprising, preferably from 5′ to 3′;
      • a targeting domain, e.g., comprising 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or 26 nucleotides;
      • a first complementarity domain; and
      • a second strand, comprising, preferably from 5′ to 3′:
      • optionally a 5′ extension domain;
      • a second complementarity domain;
      • a proximal domain; and
      • a tail domain,
    • wherein:
    • (a) the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides;
    • (b) there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain; or
    • (c) there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the sequence from (a), (b), or (c), has at least 60, 75, 80, 85, 90, 95, or 99% homology with the corresponding sequence of a naturally occurring gRNA, or with a gRNA described herein.

In an embodiment, the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides (e.g., 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or 26 nucleotides in length. In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length.

In an embodiment, the targeting domain has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length.

In an embodiment, the targeting domain has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 5 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length.

In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 16 nucleotides (e.g., 16 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 16 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain has, or consists of, 17 nucleotides (e.g., 17 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 17 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain has, or consists of, 18 nucleotides (e.g., 18 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 18 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 19 nucleotides (e.g., 19 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 19 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 20 nucleotides (e.g., 20 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 20 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 21 nucleotides (e.g., 21 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 21 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 22 nucleotides (e.g., 22 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 22 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 23 nucleotides (e.g., 23 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 23 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 24 nucleotides (e.g., 24 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 24 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 25 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 25 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 25 nucleotides (e.g., 25 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 25 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length; and the proximal and tail domain, when taken together, comprise at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length; and there are at least 15, 18, 20, 25, 30, 31, 35, 40, 45, 49, 50, or 53 nucleotides 3′ to the last nucleotide of the second complementarity domain.

In an embodiment, the targeting domain comprises, has, or consists of, 26 nucleotides (e.g., 26 consecutive nucleotides) having complementarity with the target domain, e.g., the targeting domain is 26 nucleotides in length; and there are at least 16, 19, 21, 26, 31, 32, 36, 41, 46, 50, 51, or 54 nucleotides 3′ to the last nucleotide of the second complementarity domain that is complementary to its corresponding nucleotide of the first complementarity domain.

II. Methods for Designing gRNAs

Methods for designing gRNAs are described herein, including methods for selecting, designing and validating target domains. Exemplary targeting domains are also provided herein. Targeting Domains discussed herein can be incorporated into the gRNAs described herein.

Methods for selection and validation of target sequences as well as off-target analyses are described, e.g., in Mali et al., 2013 Science 339(6121): 823-826; Hsu et al. Nat Biotechnol, 31(9): 827-32; Fu et al., 2014 Nat Biotechnol, doi: 10.1038/nbt.2808. PubMed PMID: 24463574; Heigwer et al., 2014 Nat Methods 11(2):122-3. doi: 10.1038/nmeth.2812. PubMed PMID: 24481216; Bae et al., 2014 Bioinformatics PubMed PMID: 24463181; Xiao A et al., 2014 Bioinformatics PubMed PMID: 24389662.

For example, a software tool can be used to optimize the choice of gRNA within a user's target sequence, e.g., to minimize total off-target activity across the genome. Off target activity may be other than cleavage. For each possible gRNA choice using S. pyogenes Cas9, software tools can identify all potential off-target sequences (preceding either NAG or NGG PAMs) across the genome that contain up to a certain number (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10) of mismatched base-pairs. The cleavage efficiency at each off-target sequence can be predicted, e.g., using an experimentally-derived weighting scheme. Each possible gRNA can then ranked according to its total predicted off-target cleavage; the top-ranked gRNAs represent those that are likely to have the greatest on-target and the least off-target cleavage. Other functions, e.g., automated reagent design for gRNA vector construction, primer design for the on-target Surveyor assay, and primer design for high-throughput detection and quantification of off-target cleavage via next-generation sequencing, can also be included in the tool. Candidate gRNA molecules can be evaluated by art-known methods or as described in Section IV herein.

Guide RNAs (gRNAs) for use with S. pyogenes, S. aureus and N. meningitidis Cas9s were identified using a DNA sequence searching algorithm. Guide RNA design was carried out using a custom guide RNA design software based on the public tool cas-offinder (reference:Cas-OFFinder: a fast and versatile algorithm that searches for potential off-target sites of Cas9 RNA-guided endonucleases., Bioinformatics. 2014 Feb. 17. Bae S, Park J, Kim J S. PMID:24463181). Said custom guide RNA design software scores guides after calculating their genomewide off-target propensity. Typically matches ranging from perfect matches to 7 mismatches are considered for guides ranging in length from 17 to 24. Once the off-target sites are computationally determined, an aggregate score is calculated for each guide and summarized in a tabular output using a web-interface. In addition to identifying potential gRNA sites adjacent to PAM sequences, the software also identifies all PAM adjacent sequences that differ by 1, 2, 3 or more nucleotides from the selected gRNA sites. Genomic DNA sequence for each gene was obtained from the UCSC Genome browser and sequences were screened for repeat elements using the publically available RepeatMasker program. RepeatMasker searches input DNA sequences for repeated elements and regions of low complexity. The output is a detailed annotation of the repeats present in a given query sequence.

Following identification, gRNAs were ranked into tiers based on their distance to the target site, their orthogonality or presence of a 5′ G (based on identification of close matches in the human genome containing a relavant PAM (e.g., in the case of S. pyogenes, a NGG PAM, in the case of S. aureus, a NNGRRT or NNGRRV PAM, and in the case of N. meningitidis, a NNNNGATT or NNNNGCTT PAM). Orthogonality refers to the number of sequences in the human genome that contain a minimum number of mismatches to the target sequence. A “high level of orthogonality” or “good orthogonality” may, for example, refer to 20-mer gRNAs that have no identical sequences in the human genome besides the intended target, nor any sequences that contain one or two mismatches in the target sequence. Targeting domains with good orthogonality are selected to minimize off-target DNA cleavage.

As an example, for S. pyogenes and N. meningitidis targets, 17-mer, or 20-mer gRNAs were designed. As another example, for S. aureus targets, 18-mer, 19-mer, 20-mer, 21-mer, 22-mer, 23-mer and 24-mer gRNAs were designed. Targeting domains, disclosed herein, may comprise the 17-mer described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 18 or more nucleotides may comprise the 17-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. Targeting domains, disclosed herein, may comprises the 18-mer described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 19 or more nucleotides may comprise the 18-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. Targeting domains, disclosed herein, may comprises the 19-mer described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 20 or more nucleotides may comprise the 19-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. Targeting domains, disclosed herein, may comprises the 20-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 21 or more nucleotides may comprise the 20-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. Targeting domains, disclosed herein, may comprises the 21-mer described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 22 or more nucleotides may comprise the 21-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. Targeting domains, disclosed herein, may comprises the 22-mer described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 23 or more nucleotides may comprise the 22-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. Targeting domains, disclosed herein, may comprises the 23-mer described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 24 or more nucleotides may comprise the 23-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31. Targeting domains, disclosed herein, may comprises the 24-mer described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31, e.g., the targeting domains of 25 or more nucleotides may comprise the 24-mer gRNAs described in Tables 1A-1D, 2A-2F, 3A-3C, 4A-4E, 5A-5E, 6A-6B, 7A-7D, 8A-8D, 9, 15 10A-10D, 11A-11D, 12, 13A-13D, 14A-14C, 15A-15D, 16A-16E, 17A-17B, 18A-18C, 19A-19E, 20A-20C, 21A-21E, 22A-22E, 23A-23C, 24A-24D, 25A-25B, 26, or 31.

gRNAs were identified for both single-gRNA nuclease cleavage and for a dual-gRNA paired “nickase” strategy. Criteria for selecting gRNAs and the determination for which gRNAs can be used for the dual-gRNA paired “nickase” strategy is based on two considerations:

    • 1. gRNA pairs should be oriented on the DNA such that PAMs are facing out and cutting with the D10A Cas9 nickase will result in 5′ overhangs.
    • 2. An assumption that cleaving with dual nickase pairs will result in deletion of the entire intervening sequence at a reasonable frequency. However, cleaving with dual nickase pairs can also result in indel mutations at the site of only one of the gRNAs. Candidate pair members can be tested for how efficiently they remove the entire sequence versus causing indel mutations at the site of one gRNA.

The targeting domains discussed herein can be incorporated into the gRNAs described herein.

Strategies to Identify gRNAs for S. pyogenes, S. aureus, and N. meningitidis to Correct a Mutation in the HBB Gene

gRNAs were designed for use with S. pyogenes, and S. aureus Cas9 enzymes to target the E6V mutation in the HBB gene. As an example, three strategies were utilized to identify gRNAs for use with S. pyogenes, S. aureus and N. meningitidis Cas9 enzymes.

In one strategy, the gRNAs were identified and ranked into 3 tiers for S. pyogenes (Tables 1A-1C). The targeting domains for tier 1 gRNA molecules for use with the S. pyogenes Cas9 to target the E6V mutation in the HBB gene were selected based on (1) a reasonable distance to the target position, and (2) a high level of orthogonality. Tier 2 gRNAs were selected based on (1), a reasonable distance to the target position, and (2) presence of a 5′G. Tier 3 used the same distance restriction, but removed the requirement of good orthogonality and the 5′G. Note that tiers are non-inclusive (each gRNA is listed only once). gRNAs for use with the S. aureus (Table 1D), Cas9s were identified manually by scanning genomic DNA sequence for the presence of PAM sequences. These gRNAs were not separated into tiers, but were listed in a single list.

In a second strategy, the gRNAs were identified and ranked into 4 tiers for S. pyogenes (Tables 13A-13D) and 5 tiers for S. aureus (Tables 14A-14C). The targeting domain for tier 1 gRNA molecules to use with S. pyogenes Cas9 were selected based on (1) a short distance to the target position, e.g., within 100 bp upstream and 100 bp downstream of the mutation, (2) a high level of orthogonality, and (3) the presence of a 5′ G. For selection of tier 2 gRNAs, a short distance and high orthogonality were required but the presence of a 5′G was not required. Tier 3 uses the same distance restriction and the requirement for a 5′G, but removes the requirement of good orthogonality. Tier 4 uses the same distance restriction but removes the requirement of good orthogonality and the 5′G. The targeting domain for tier 1 gRNA molecules to use with S. aureus Cas9 were selected based on (1) a short distance to the target position, e.g., within 100 bp upstream and 100 bp downstream of the mutation, (2) a high level of orthogonality, and (3) the presence of a 5′ G. For selection of tier 2 gRNAs, a short distance and high orthogonality were required but the presence of a 5′G was not required. Tier 3 uses the same distance restriction and the requirement for a 5′G, but removes the requirement of good orthogonality. Tier 4 uses the same distance restriction but removes the requirement of good orthogonality and the 5′G. Tier 5 is selected based on (1) a short distance to the target position, e.g., within 100 bp upstream and 100 bp downstream of the mutation and (2) PAM is NNGRRV. Note that tiers are non-inclusive (each gRNA is listed only once for the strategy). In certain instances, no gRNA was identified based on the criteria of the particular tier. In some instances, there are no corresponding exemplary gRNAs in certain tiers.

In a third strategy, the gRNAs were identified and ranked into 3 tiers for S. pyogenes (Tables 24A-24D), 4 tiers for S. aureus (Tables 25A-25B) and 3 tiers for N. meningitidis (Tables 26). The targeting domain for tier 1 gRNA molecules to use with S. pyogenes Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation and (2) a high level of orthogonality. The targeting domain for tier 2 gRNA molecules to use with S. pyogenes Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation and (2) the presence of a 5′G. The targeting domain for tier 3 gRNA molecules to use with S. pyogenes Cas9 were selected based on distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation. The targeting domain for tier 1 gRNA molecules to use with S. aureus Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation, (2) a high level of orthogonality and (3) PAM is NNGRRT. The targeting domain for tier 2 gRNA molecules to use with S. aureus Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation, (2) the presence of a 5′G, and (3) PAM is NNGRRT. The targeting domain for tier 3 gRNA molecules to use with S. aureus Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation and (2) PAM is NNGRRT. The targeting domain for tier 4 gRNA molecules to use with S. aureus Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation and (2) PAM is NNGRRV. The targeting domain for tier 1 gRNA molecules to use with N. meningitidis Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation and (2) a high level of orthogonality. The targeting domain for tier 2 gRNA molecules to use with N. meningitidis Cas9 were selected based on (1) distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation and (2) the presence of a 5′G. The targeting domain for tier 3 gRNA molecules to use with N. meningitidis Cas9 were selected based on distance to the target position, e.g., within 200 bp upstream and 200 bp downstream of the mutation.

In an embodiment, dual targeting (e.g., dual nicking) is used to create two nicks on opposite DNA strands by using S. pyogenes, S. aureus and N. meningitidis Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp. Exemplary nickase pairs including selecting a targeting domain from Group A and a second targeting domain from Group B in Table 24D (for S. pyogenes). It is contemplated herein that in an embodiment a targeting domain of Group A can be combined with any of the targeting domains of Group B in Table 24D (for S. pyogenes). For example, HBB-9, HBB-20can be combined with HBB-11, HBB-39.

Strategies to Identify gRNAs for S. pyogenes, S. aureus, and N. meningitidis to Knock Out the BCL11A Gene

gRNAs were designed for use with S. pyogenes, S. aureus and N. meningitidis Cas9 enzymes to induce an insertion or deletion of one or more nucleotides mediated by NHEJ in close proximity to or within the early coding region. As an example, three strategies were utilized to identify gRNAs for use with S. pyogenes, S. aureus and N. meningitidis Cas9 enzymes.

In one strategy, the gRNAs were identified and ranked into 4 tires for S. pyogenes (Tables 2A-2D). The targeting domains for tier 1 gRNA molecules for use with the S. pyogenes Cas9 to knockout the BCL11A gene were selected based on (1) a reasonable distance to the target position, and (2) a high level of orthogonality. Tier 2 gRNAs were selected based on (1), a reasonable distance to the target position, and (2) presence of a 5′G. Tier 3 used the same distance restriction, but removed the requirement of good orthogonality and the 5′G. Tier 4 only required the presence in the coding sequence. Note that tiers are non-inclusive (each gRNA is listed only once). gRNAs for use with the S. aureus (Table 2E), and N. meningitidis (Table 2F) Cas9s were identified manually by scanning genomic DNA sequence for the presence of PAM sequences. These gRNAs were not separated into tiers, but were listed in a single list. Note that tiers are non-inclusive (each gRNA is listed only once for the strategy). In certain instances, no gRNA was identified based on the criteria of the particular tier.

In a second strategy, the gRNAs were identified and ranked into 5 tiers for S. pyogenes (Tables 4A-4E), and S. aureus (Tables 5A-5E); and 2 tiers for N. meningitidis (Tables 6A-6B). For S. pyogenes, and S. aureus, the targeting domain for tier 1 gRNA molecules were selected based on (1) distance to a target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon), (2) a high level of orthogonality and (3) the presence of 5′G. The targeting domain for tier 2 gRNA molecules were selected based on (1) distance to a target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon) and (2) a high level of orthogonality. The targeting domain for tier 3 gRNA molecules were selected based on (1) distance to a target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon) and (2) the presence of 5′G. The targeting domain for tier 4 gRNA molecules were selected based on distance to a target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon). The targeting domain for tier 5 gRNA molecules were selected based on distance to the target site (e.g., start codon), e.g., within reminder of the coding sequence, e.g., downstream of the first 500 bp of coding sequence (e.g., anywhere from +500 (relative to the start codon) to the stop codon). For N. meningitidis, the targeting domain for tier 1 gRNA molecules were selected based on (1) distance to a target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon). The targeting domain for tier 2 gRNA molecules were selected based on distance to the target site (e.g., start codon), e.g., within reminder of the coding sequence, e.g., downstream of the first 500 bp of coding sequence (e.g., anywhere from +500 (relative to the start codon) to the stop codon). Note that tiers are non-inclusive (each gRNA is listed only once for the strategy). In certain instances, no gRNA was identified based on the criteria of the particular tier.

In a third strategy, the gRNAs were identified and ranked into 3 tiers for S. pyogenes (Tables 15A-15D), and N. meningitidis (Tables 17A-17B); and 5 tiers for S. aureus (Tables 16A-16D). The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) distance to a target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon) and (2) a high level of orthogonality. The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) distance to the target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon). The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 3 gRNA molecules were selected based on distance to the target site (e.g., start codon), e.g., within reminder of the coding sequence, e.g., downstream of the first 500 bp of coding sequence (e.g., anywhere from +500 (relative to the start codon) to the stop codon). The gRNAs were identified and ranked into 5 tiers for S. aureus, when the relevant PAM was NNGRRT or NNGRRV. The targeting domain to be used with S. aureus Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) distance to the target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon), (2) a high level of orthogonality, and (3) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) distance to the target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon), and (2) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 3 gRNA molecules were selected based on (1) distance to a the target site (e.g., start codon) mutation, e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon), and (2) PAM is NNGRRV. The targeting domain to be used with S. aureus Cas9 enzymes for tier 4 gRNA molecules were selected based on (1) distance to the target site (e.g., start codon), e.g., within reminder of the coding sequence, e.g., downstream of the first 500 bp of coding sequence (e.g., anywhere from +500 (relative to the start codon) to the stop codon), and (2) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 5 gRNA molecules were selected based on (1) distance to the target site (e.g., start codon), e.g., within reminder of the coding sequence, e.g., downstream of the first 500 bp of coding sequence (e.g., anywhere from +500 (relative to the start codon) to the stop codon), and (2) PAM is NNGRRV. The gRNAs were identified and ranked into 3 tiers for N. meningitidis. The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) distance to the target site, e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon) and (2) a high level of orthogonality. The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) distance to the target site (e.g., start codon), e.g., within 500 bp (e.g., downstream) of the target site (e.g., start codon). The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 3 gRNA molecules were selected based on distance to the target site (e.g., start codon), e.g., within reminder of the coding sequence, e.g., downstream of the first 500 bp of coding sequence (e.g., anywhere from +500 (relative to the start codon) to the stop codon). Note that tiers are non-inclusive (each gRNA is listed only once for the strategy). In certain instances, no gRNA was identified based on the criteria of the particular tier.

In an embodiment, when a single gRNA molecule is used to target a Cas9 nickase to create a single strand break in close proximity to the BCL11A target position, e.g., the gRNA is used to target either upstream of (e.g., within 500 bp, e.g., within 200 bp upstream of the BCL11A target position), or downstream of (e.g., within 500 bp, e.g., within 200 bp downstream of the BCL11A target position) in the BCL11A gene.

In an embodiment, when a single gRNA molecule is used to target a Cas9 nuclease to create a double strand break to in close proximity to the BCL11A target position, e.g., the gRNA is used to target either upstream of (e.g., within 500 bp, e.g., within 200 bp upstream of the BCL11A target position), or downstream of (e.g., within 500 bp, e.g., within 200 bp downstream of the BCL11A target position) in the BCL11A gene.

In an embodiment, dual targeting is used to create two double strand breaks to in close proximity to the mutation, e.g., the gRNA is used to target either upstream of (e.g., within 500 bp, e.g., within 200 bp upstream of the BCL11A target position), or downstream of (e.g., within 500 bp, e.g., within 200 bp downstream of the BCL11A target position) in the BCL11A gene. In an embodiment, the first and second gRNAs are used to target two Cas9 nucleases to flank, e.g., the first of gRNA is used to target upstream of (e.g., within 500 bp, e.g., within 200 bp upstream of the BCL11A target position), and the second gRNA is used to target downstream of (e.g., within 500 bp, e.g., within 200 bp downstream of the BCL11A target position) in the BCL11A gene.

In an embodiment, dual targeting is used to create a double strand break and a pair of single strand breaks to delete a genomic sequence including the BCL11A target position. In an embodiment, the first, second and third gRNAs are used to target one Cas9 nuclease and two Cas9 nickases to flank, e.g., the first gRNA that will be used with the Cas9 nuclease is used to target upstream of (e.g., within 500 bp, e.g., within 200 bp upstream of the BCL11A target position) or downstream of (e.g., within 500 bp, e.g., within 200 bp downstream of the BCL11A target position), and the second and third gRNAs that will be used with the Cas9 nickase pair are used to target the opposite side of the mutation (e.g., within 200 bp upstream or downstream of the BCL11A target position) in the BCL11A gene.

In an embodiment, when four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four single strand breaks to delete genomic sequence including the mutation, the first pair and second pair of gRNAs are used to target four Cas9 nickases to flank, e.g., the first pair of gRNAs are used to target upstream of (e.g., within 500 bp, e.g., within 200 bp upstream of the BCL11A target position), and the second pair of gRNAs are used to target downstream of (e.g., within 500 bp, e.g., within 200 bp downstream of the BCL11A target position) in the BCL11A gene.

In an embodiment, dual targeting (e.g., dual nicking) is used to create two nicks on opposite DNA strands by using S. pyogenes, S. aureus and N. meningitidis Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp. Exemplary nickase pairs including selecting a targeting domain from Group A and a second targeting domain from Group B, or including selecting a targeting domain from Group C and a second targeting domain from Group D in Table 15D (for S. pyogenes). It is contemplated herein that in an embodiment a targeting domain of Group A can be combined with any of the targeting domains of Group B; in an embodiment a targeting domain of Group C can be combined with any of the targeting domains of Group D in Table 15D (for S. pyogenes). For example, BCL11A-5355 or BCL11A-5380 can be combined with BCL11A-5321 or BCL11A-5416; or BCL11A-5333, BCL11A-5354, or BCL11A-5329 can be combined with BCL11A-5367 or BCL11A-5341.

Strategies to Identify gRNAs for S. pyogenes, S. aureus, and N. meningitidis to Knock Down the BCL11A Gene

gRNAs were designed for use with S. pyogenes, S. aureus and N. meningitidis one or more Cas9 molecules, e.g., enzymatically inactive Cas9 (eiCas9) molecules or Cas9 fusion proteins (e.g., an eiCas9 fused to a transcription repressor domain or chromatin modifying protein to alter (e.g., to block, reduce, or decrease) the transcription of the BCL11A gene. As an example, three strategies were utilized to identify gRNAs for use with S. pyogenes, S. aureus and N. meningitidis one or more Cas9 molecules.

In one strategy, the targeting domains for gRNA molecules to knockdown the BCL11A gene were designed to target the 1 kb of sequence 3′ of the start codon. They were listed in a single list for S. pyogenes (Table 3A), S. aureus (Table 3B) and N. meningitidis (Table 3C).

In a second strategy, the gRNAs were identified and ranked into 4 tiers for S. pyogenes (Tables 10A-10D), and S. aureus (Tables 11A-11D). The gRNAs were identified and listed in a single list for N. meningitidis (Table 12). For S. pyogenes, and S. aureus, the targeting domain for tier 1 gRNA molecules were selected based on (1) distance to a target site (e.g., a transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site), (2) a high level of orthogonality and (3) the presence of 5′G. The targeting domain for tier 2 gRNA molecules were selected based on (1) distance to a target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site) and (2) a high level of orthogonality. The targeting domain for tier 3 gRNA molecules were selected based on (1) distance to a target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site) and (2) the presence of 5′G. The targeting domain for tier 4 gRNA molecules were selected based on distance to a target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site).

In a third strategy, gRNAs were designed for use with S. pyogenes, S. aureus and N. meningitidis Cas9 molecules. The gRNAs were identified and ranked into 3 tiers for S. pyogenes (Tables 18A-18C). The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) distance to a target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site) and (2) a high level of orthogonality. The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) distance to the target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site). The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 3 gRNA molecules were selected based on distance to the target site (e.g., the transcription start site), e.g., within the additional 500 bp upstream and downstream of the transcription start site (i.e., extending to 1 kb upstream and downstream of the transcription start site. The gRNAs were identified and ranked into 5 tiers for S. aureus, when the relevant PAM was NNGRRT or NNGRRV (Tables 19A-19B). The targeting domain to be used with S. aureus Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) distance to the target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site), (2) a high level of orthogonality, and (3) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) distance to the target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site), and (2) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 3 gRNA molecules were selected based on (1) distance to a target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site), and (2) PAM is NNGRRV. The targeting domain to be used with S. aureus Cas9 enzymes for tier 4 gRNA molecules were selected based on (1) distance to the target site (e.g., the transcription start site), e.g., within the additional 500 bp upstream and downstream of the transcription start site (i.e., extending to 1 kb upstream and downstream of the transcription start site, and (2) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 5 gRNA molecules were selected based on (1) distance to the target site (e.g., the transcription start site), e.g., within the additional 500 bp upstream and downstream of the transcription start site (i.e., extending to 1 kb upstream and downstream of the transcription start site, and (2) PAM is NNGRRV. The gRNAs were identified and ranked into 3 tiers for N. meningitidis (Tables 20A-20C). The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) distance to a target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site) and (2) a high level of orthogonality. The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) distance to the target site (e.g., the transcription start site), e.g., within 500 bp (e.g., upstream or downstream) of the target site (e.g., the transcription start site). The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 3 gRNA molecules were selected based on distance to the target site (e.g., the transcription start site), e.g., within the additional 500 bp upstream and downstream of the transcription start site (i.e., extending to 1 kb upstream and downstream of the transcription start site. Note that tiers are non-inclusive (each gRNA is listed only once for the strategy). In certain instances, no gRNA was identified based on the criteria of the particular tier.

Strategies to Identify gRNAs for S. pyogenes, S. aureus, and N. meningitidis to Remove (e.g., Delete) the Enhancer Region the BCL11A Gene

gRNAs were designed for use with S. pyogenes, S. aureus and N. meningitidis Cas9 enzymes to remove (e.g., delete) the enhancer region in the BCL11A gene. As an example, two strategies were utilized to identify gRNAs for use with S. pyogenes, S. aureus and N. meningitidis one or more Cas9 molecules.

In an strategy, the gRNAs were identified and ranked into 4 tiers for S. pyogenes (Tables 7A-7D) and for S. aureus (Tables 8A-8D). The gRNAs were identified and listed in a single list for N. meningitidis (Table 9). The targeting domains for tier 1 gRNA molecules for use with the S. pyogenes, S. aureus Cas9 were selected based on (1) a reasonable distance to the target position, e.g., within a region 5′ (51.5 to 51.7 kb downstream of transcription start site, TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), (2) a high level of orthogonality and (3) presence of a 5′G. For selection of tier 2 gRNAs, reasonable distance and high orthogonality were required but the presence of a 5′G was not required. Tier 3 uses the same distance restriction and the requirement for a 5′G, but removes the requirement of good orthogonality. Tier 4 uses the same distance restriction but removes the requirement of good orthogonality and the 5′G. Note that tiers are non-inclusive (each gRNA is listed only once for the strategy). In certain instances, no gRNA was identified based on the criteria of the particular tier.

In a second strategy, gRNAs were designed for use with S. pyogenes, S. aureus and N. meningitidis Cas9 molecules. The gRNAs were identified and ranked into 4 tiers for S. pyogenes (Tables 21A-21E). The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), (2) a high level of orthogonality and (3) presence of 5′G. The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS) and (2) a high level of orthogonality. The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 3 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS) and (2) presence of 5′G. The targeting domain to be used with S. pyogenes Cas9 enzymes for tier 4 gRNA molecules were selected based on within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS). The gRNAs were identified and ranked into 5 tiers for S. aureus, when the relevant PAM was NNGRRT or NNGRRV (Tables 22A-22E). The targeting domain to be used with S. aureus Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), (2) a high level of orthogonality, (3)) presence of 5′G and (4) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), (2) a high level of orthogonality, and (3) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 3 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), (2) presence of 5′G and (3) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 4 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), and (2) PAM is NNGRRT. The targeting domain to be used with S. aureus Cas9 enzymes for tier 5 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), and (2) PAM is NNGRRV. The gRNAs were identified and ranked into 3 tiers for N. meningitidis (Tables 23A-23C). The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 1 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS), (2) a high level of orthogonality and (3) presence of 5′G. The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 2 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS) and (2) a high level of orthogonality. The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 3 gRNA molecules were selected based on (1) within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS) and (2) presence of 5′G. The targeting domain to be used with N. meningitidis Cas9 enzymes for tier 4 gRNA molecules were selected based on within a region 5′ (51.5 to 51.7 kb downstream of TSS) or 3′ (65.1 to 65.3 kb downstream of TSS). Note that tiers are non-inclusive (each gRNA is listed only once for the strategy). In certain instances, no gRNA was identified based on the criteria of the particular tier.

In an embodiment, dual targeting (e.g., dual nicking) is used to create two nicks on opposite DNA strands by using S. pyogenes, S. aureus and N. meningitidis Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp. Exemplary nickase pairs including selecting a targeting domain from Group A and a second targeting domain from Group B, or including selecting a targeting domain from Group C and a second targeting domain from Group D in Table 20E (for S. pyogenes). It is contemplated herein that in an embodiment a targeting domain of Group A can be combined with any of the targeting domains of Group B; in an embodiment a targeting domain of Group C can be combined with any of the targeting domains of Group D in Table 20E (for S. pyogenes). For example, BCL11A-13271 or BCL11A-13264 can be combined with BCL11A-13276; or BCL11A-13262 or BCL11A-13282 can be combined with BCL11A-13290 or BCL11A-13280.

In an embodiment, two or more (e.g., three or four) gRNA molecules are used with one Cas9 molecule. In another embodiment, when two or more (e.g., three or four) gRNAs are used with two or more Cas9 molecules, at least one Cas9 molecule is from a different species than the other Cas9 molecule(s). For example, when two gRNA molecules are used with two Cas9 molecules, one Cas9 molecule can be from one species and the other Cas9 molecule can be from a different species. Both Cas9 species are used to generate a single or double-strand break, as desired.

Any of the targeting domains in the tables described herein can be used with a Cas9 nickase molecule to generate a single strand break.

Any of the targeting domains in the tables described herein can be used with a Cas9 nuclease molecule to generate a double strand break.

When two gRNAs designed for use to target two Cas9 molecules, one Cas9 can be one species, the second Cas9 can be from a different species. Both Cas9 species are used to generate a single or double-strand break, as desired.

It is contemplated herein that any upstream gRNA described herein may be paired with any downstream gRNA described herein. When an upstream gRNA designed for use with one species of Cas9 is paired with a downstream gRNA designed for use from a different species of Cas9, both Cas9 species are used to generate a single or double-strand break, as desired.

Exemplary Targeting Domains

Table 1A provides exemplary targeting domains for the E6V target site in the HBB gene selected according to the first tier parameters, and are selected based on the close proximity and orientation to mutation and orthogonality in the human genome. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a Cas9 molecule (e.g., a S. pyogenes Cas9 molecule) that gives double stranded cleavage. Any of the targeting domains in the table can be used with a Cas9 (e.g., a S. pyogenes Cas9 nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using Cas9 nickases (e.g., a S. pyogenes Cas9 nickase) with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position. In an embodiment, two 20-mer guide RNAs are used to target two Cas9 nucleases (e.g., two S. pyogenes Cas9 nucleases) or two Cas9 nickases (e.g., two S. pyogenes Cas9 nickases), e.g., HBB-8 and HBB-25 are used. In an embodiment, two 17-mer RNAs are used to target two Cas9 nucleases or two Cas9 nickases, e.g., HBB-35 and HBB-53 are used.

TABLE 1A Target SEQ 1st Tier DNA Site ID gRNA Name Strand Targeting Domain Length NO HBB-8 AAGGUGAACGUGGAUGAAGU 20 387 HBB-25 + GUAACGGCAGACUUCUCCUC 20 388 HBB-35 GUGAACGUGGAUGAAGU 17 389 HBB-53 + ACGGCAGACUUCUCCUC 17 390

Table 1B provides exemplary targeting domains for the E6V target site in the HBB gene selected according to the second tier parameters and are selected based on the presence of a 5′ G and reasonable proximity to mutation. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with S. pyogenes single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE 1B Target SEQ 2nd Tier DNA Site ID gRNA Name Strand Targeting Domain Length NO HBB-12 GAAGUUGGUGGUGAGGCCCU 20 391 HBB-1 GCAACCUCAAACAGACACCA 20 392 HBB-52 + GCCCCACAGGGCAGUAA 17 393 HBB-32 GCCGUUACUGCCCUGUG 17 394 HBB-46 GGAGACCAAUAGAAACU 17 395 HBB-37 GGAUGAAGUUGGUGGUG 17 396 HBB-29 GGUGCAUCUGACUCCUG 17 397 HBB-4 GUCUGCCGUUACUGCCCUGU 20 398 HBB-9 GUGAACGUGGAUGAAGUUGG 20 399 HBB-34 GUGGGGCAAGGUGAACG 17 400 HBB-40 GUGGUGAGGCCCUGGGC 17 401 HBB-44 GUUACAAGACAGGUUUA 17 402 HBB-51 + GUUCACCUUGCCCCACA 17 403 HBB-39 GUUGGUGGUGAGGCCCU 17 404

Table 1C provides exemplary targeting domains for the E6V target site in the HBB gene selected according to the third tier parameters and are selected based on reasonable proximity to mutation. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with S. pyogenes single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE 1C Target SEQ 3rd Tier DNA Site ID gRNA Name Strand Targeting Domain Length NO HBB-36 AACGUGGAUGAAGUUGG 17 405 HBB-17 AAGGUUACAAGACAGGUUUA 20 406 HBB-47 + ACAUGCCCAGUUUCUAU 17 407 HBB-55 + ACCAUGGUGUCUGUUUG 17 408 HBB-28 ACCUCAAACAGACACCA 17 409 HBB-20 + ACCUUGAUACCAACCUGCCC 20 410 HBB-45 AGGAGACCAAUAGAAAC 17 411 HBB-54 + AGGAGUCAGAUGCACCA 17 412 HBB-3 AGUCUGCCGUUACUGCCCUG 20 413 HBB-38 AGUUGGUGGUGAGGCCC 17 414 HBB-23 + CACGUUCACCUUGCCCCACA 20 415 HBB-2 CAUGGUGCAUCUGACUCCUG 20 416 HBB-22 + CCACGUUCACCUUGCCCCAC 20 417 HBB-15 CCCUGGGCAGGUUGGUAUCA 20 418 HBB-7 CCUGUGGGGCAAGGUGAACG 20 419 HBB-21 + CCUUGAUACCAACCUGCCCA 20 420 HBB-10 CGUGGAUGAAGUUGGUGGUG 20 421 HBB-6 CGUUACUGCCCUGUGGGGCA 20 422 HBB-50 + CGUUCACCUUGCCCCAC 17 423 HBB-26 + CUCAGGAGUCAGAUGCACCA 20 424 HBB-30 CUGCCGUUACUGCCCUG 17 425 HBB-24 + CUUGCCCCACAGGGCAGUAA 20 426 HBB-19 UAAGGAGACCAAUAGAAACU 20 427 HBB-33 UACUGCCCUGUGGGGCA 17 428 HBB-43 UAUCAAGGUUACAAGAC 17 429 HBB-5 UCUGCCGUUACUGCCCUGUG 20 430 HBB-11 UGAAGUUGGUGGUGAGGCCC 20 431 HBB-41 UGAGGCCCUGGGCAGGU 17 432 HBB-49 + UGAUACCAACCUGCCCA 17 433 HBB-27 + UGCACCAUGGUGUCUGUUUG 20 434 HBB-31 UGCCGUUACUGCCCUGU 17 435 HBB-42 UGGGCAGGUUGGUAUCA 17 436 HBB-16 UGGUAUCAAGGUUACAAGAC 20 437 HBB-14 UGGUGAGGCCCUGGGCAGGU 20 438 HBB-18 UUAAGGAGACCAAUAGAAAC 20 439 HBB-48 + UUGAUACCAACCUGCCC 17 440 HBB-13 UUGGUGGUGAGGCCCUGGGC 20 441

Table 1D provides exemplary targeting domains for the E6V target site in the HBB gene selected based on close proximity to mutation. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. aureus Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with S. aureus single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE ID Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO HBB-56 CACCAUGGUGCAUCUGACUC 20 442 HBB-57 CCAUGGUGCAUCUGACUCCU 20 443 HBB-58 CAUGGUGCAUCUGACUCCUG 20 444 HBB-59 UGGUGCAUCUGACUCCUGAG 20 445 HBB-60 AAGUCUGCCGUUACUGCCCU 20 446 HBB-61 AGUCUGCCGUUACUGCCCUG 20 447 HBB-62 UUACUGCCCUGUGGGGCAAG 20 448 HBB-63 CCCUGUGGGGCAAGGUGAAC 20 449 HBB-64 GUGGGGCAAGGUGAACGUGG 20 450 HBB-65 GAACGUGGAUGAAGUUGGUG 20 451 HBB-66 AUGAAGUUGGUGGUGAGGCC 20 452 HBB-67 CAAGGUUACAAGACAGGUUU 20 453 HBB-68 AAGGUUACAAGACAGGUUUA 20 454 HBB-69 GACAGGUUUAAGGAGACCAA 20 455 HBB-70 UUUAAGGAGACCAAUAGAAA 20 456 HBB-71 CAUGGUGCAUCUGACUC 20 457 HBB-72 UGGUGCAUCUGACUCCU 17 458 HBB-73 GGUGCAUCUGACUCCUG 17 459 HBB-74 UGCAUCUGACUCCUGAG 17 460 HBB-75 UCUGCCGUUACUGCCCU 17 461 HBB-76 CUGCCGUUACUGCCCUG 17 462 HBB-77 CUGCCCUGUGGGGCAAG 17 463 HBB-78 UGUGGGGCAAGGUGAAC 17 464 HBB-79 GGGCAAGGUGAACGUGG 17 465 HBB-80 CGUGGAUGAAGUUGGUG 17 466 HBB-81 AAGUUGGUGGUGAGGCC 17 467 HBB-82 GGUUACAAGACAGGUUU 17 468 HBB-83 GUUACAAGACAGGUUUA 17 469 HBB-84 AGGUUUAAGGAGACCAA 17 470 HBB-85 AAGGAGACCAAUAGAAA 17 471 HBB-86 + GCUAGUGAACACAGUUGUGU 20 472 HBB-87 + GUGUCUGUUUGAGGUUGCUA 20 473 HBB-88 + AGAUGCACCAUGGUGUCUGU 20 474 HBB-89 + GUAACGGCAGACUUCUCCUC 20 475 HBB-90 + AGUAACGGCAGACUUCUCCU 20 476 HBB-91 + UCCACGUUCACCUUGCCCCA 20 477 HBB-92 + AACCUUGAUACCAACCUGCC 20 478 HBB-93 + AGUGAACACAGUUGUGU 17 479 HBB-94 + UCUGUUUGAGGUUGCUA 17 480 HBB-95 + UGCACCAUGGUGUCUGU 17 481 HBB-96 + ACGGCAGACUUCUCCUC 17 482 HBB-97 + AACGGCAGACUUCUCCU 17 483 HBB-98 + ACGUUCACCUUGCCCCA 17 484 HBB-99 + CUUGAUACCAACCUGCC 17 485

Table 2A provides exemplary targeting domains for knocking out the BCL11A gene selected according to first tier parameters, and are selected based on close proximity to start of the coding sequence and orthogonality in the human genome. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position. In an embodiment, two 20-mer guide RNAs are used to target two S. pyogenes Cas9 nucleases or two S. pyogenes Cas9 nickases, e.g., BCL11A-31 and BCL11A-40, BCL11A-30 and BCL11A-42, or BCL11A-24 and BCL11A-53 are used. In an embodiment, two 17-mer RNAs are used to target two Cas9 nucleases or two Cas9 nickases, e.g., BCL11A-79 and BCL11A-90, BCL11A-77 and BCL11A-92, or BCL11A-71 and BCL11A-103 are used.

TABLE 2A 1st Tier DNA Target Site SEQ ID gRNA Name Strand Targeting Domain Length NO BCL11A-32 - UGGCAUCCAGGUCACGCCAG 20 486 BCL11A-40 + GAUGCUUUUUUCAUCUCGAU 20 487 BCL11A-30 - GCAUCCAAUCCCGUGGAGGU 20 488 BCL11A-42 + UUUUCAUCUCGAUUGGUGAA 20 489 BCL11A-24 - CCAGAUGAACUUCCCAUUGG 20 490 BCL11A-53 + AGGAGGUCAUGAUCCCCUUC 20 491 BCL11A-79 - CAUCCAGGUCACGCCAG 17 492 BCL11A-90 + GCUUUUUUCAUCUCGAU 17 493 BCL11A-77 - UCCAAUCCCGUGGAGGU 17 494 BCL11A-92 + UCAUCUCGAUUGGUGAA 17 495 BCL11A-71 - GAUGAACUUCCCAUUGG 17 496 BCL11A-103 + AGGUCAUGAUCCCCUUC 17 497

Table 2B provides exemplary targeting domains for knocking out the BCL11A gene selected according to the second tier parameters and are selected based on close proximity to start of the coding sequence and presence of a 5′ G. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE 2B 2nd Tier DNA Target Site SEQ ID gRNA Name Strand Targeting Domain Length NO BCL11A-28 - GAAAAAAGCAUCCAAUCCCG 20 498 BCL11A-15 - GAACCAGACCACGGCCCGUU 20 499 BCL11A-37 + GACCUGGAUGCCAACCUCCA 20 500 BCL11A-120 + GAGCUCCAUGUGCAGAACGA 20 501 BCL11A-106 + GAGCUCCCAACGGGCCG 17 502 BCL11A-112 - GAGCUCUAAUCCCCACGCCU 20 503 BCL11A-113 - GAGUGCAGAAUAUGCCCCGC 20 504 BCL11A-35 + GAUAAACAAUCGUCAUCCUC 20 505 BCL11A-19 - GAUCAUGACCUCCUCACCUG 20 506 BCL11A-60 - GAUGAUGAACCAGACCA 17 507 BCL11A-39 + GAUGCCAACCUCCACGGGAU 20 508 BCL11A-133 + GCACUCAUCCCAGGCGU 17 509 BCL11A-130 - GCAGAAUAUGCCCCGCA 17 510 BCL11A-115 + GCAUAUUCUGCACUCAUCCC 20 511 BCL11A-89 + GCCAACCUCCACGGGAU 17 512 BCL11A-23 - GCCAGAUGAACUUCCCAUUG 20 513 BCL11A-17 - GCCCGUUGGGAGCUCCAGAA 20 514 BCL11A-83 + GCUAUGUGUUCCUGUUU 17 515 BCL11A-135 + GCUCCAUGUGCAGAACG 17 516 BCL11A-57 + GCUCCCAACGGGCCGUGGUC 20 517 BCL11A-127 - GCUCUAAUCCCCACGCC 17 518 BCL11A-6 + GCUGGGGUUUGCCUUGCUUG 20 519 BCL11A-111 - GGAGCUCUAAUCCCCACGCC 20 520 BCL11A-101 + GGCACUGCCCACAGGUG 17 521 BCL11A-52 + GGCACUGCCCACAGGUGAGG 20 522 BCL11A-16 - GGCCCGUUGGGAGCUCCAGA 20 523 BCL11A-12 + GGGGUUUGCCUUGCUUG 17 524 BCL11A-109 + GUAAGAAUGGCUUCAAG 17 525 BCL11A-123 + GUGCAGAACGAGGGGAGGAG 20 526 BCL11A-21 - GUGCCAGAUGAACUUCCCAU 20 527 BCL11A-50 + GUUCAUCUGGCACUGCCCAC 20 528 BCL11A-65 - GUUGGGAGCUCCAGAAG 17 529

Table 2C provides exemplary targeting domains for knocking out the BCL11A gene selected according to the third tier parameters and are selected based on close proximity to start of the coding sequence. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE 2C 3rd Tier DNA Target Site SEQ ID gRNA Name Strand Targeting Domain Length NO BCL11A-75 - AAAAGCAUCCAAUCCCG 17 530 BCL11A-29 - AAAAGCAUCCAAUCCCGUGG 20 531 BCL11A-47 + AAAAUAAGAAUGUCCCCCAA 20 532 BCL11A-85 + AAACAAUCGUCAUCCUC 17 533 BCL11A-73 - AAACGGAAACAAUGCAA 17 534 BCL11A-125 - AAACUUCUGCACUGGAG 17 535 BCL11A-48 + AAAUAAGAAUGUCCCCCAAU 20 536 BCL11A-1 - AACCCCAGCACUUAAGCAAA 20 537 BCL11A-13 - ACAGAUGAUGAACCAGACCA 20 538 BCL11A-61 - ACCAGACCACGGCCCGU 17 539 BCL11A-2 - ACCCCAGCACUUAAGCAAAC 20 540 BCL11A-38 + ACCUGGAUGCCAACCUCCAC 20 541 BCL11A-102 + ACUGCCCACAGGUGAGG 17 542 BCL11A-119 + AGAGCUCCAUGUGCAGAACG 20 543 BCL11A-70 - AGAUGAACUUCCCAUUG 17 544 BCL11A-76 - AGCAUCCAAUCCCGUGG 17 545 BCL11A-121 + AGCUCCAUGUGCAGAACGAG 20 546 BCL11A-81 - AGGAAUUUGCCCCAAAC 17 547 BCL11A-114 - AGUGCAGAAUAUGCCCCGCA 20 548 BCL11A-97 + AUAAGAAUGUCCCCCAA 17 549 BCL11A-20 - AUCAUGACCUCCUCACCUGU 20 550 BCL11A-44 + AUCUCGAUUGGUGAAGGGGA 20 551 BCL11A-67 - AUGACCUCCUCACCUGU 17 552 BCL11A-138 + AUGUGCAGAACGAGGGG 17 553 BCL11A-3 + AUUCCCGUUUGCUUAAGUGC 20 554 BCL11A-95 + AUUGGUGAAGGGGAAGG 17 555 BCL11A-26 - CACAAACGGAAACAAUGCAA 20 556 BCL11A-134 + CACUCAUCCCAGGCGUG 17 557 BCL11A-139 + CAGAACGAGGGGAGGAG 17 558 BCL11A-69 - CAGAUGAACUUCCCAUU 17 559 BCL11A-96 + CAGCUUUUUCUAAGCAG 17 560 BCL11A-86 + CAUCCUCUGGCGUGACC 17 561 BCL11A-93 + CAUCUCGAUUGGUGAAG 17 562 BCL11A-100 + CAUCUGGCACUGCCCAC 17 563 BCL11A-66 - CAUGACCUCCUCACCUG 17 564 BCL11A-99 + CCAAUGGGAAGUUCAUC 17 565 BCL11A-46 + CCACAGCUUUUUCUAAGCAG 20 566 BCL11A-62 - CCAGACCACGGCCCGUU 17 567 BCL11A-68 - CCAGAUGAACUUCCCAU 17 568 BCL11A-8 - CCAGCACUUAAGCAAAC 17 569 BCL11A-107 + CCCAACGGGCCGUGGUC 17 570 BCL11A-7 - CCCAGCACUUAAGCAAA 17 571 BCL11A-49 + CCCCCAAUGGGAAGUUCAUC 20 572 BCL11A-55 + CCCCUUCUGGAGCUCCCAAC 20 573 BCL11A-18 - CCCGUUGGGAGCUCCAGAAG 20 574 BCL11A-9 + CCCGUUUGCUUAAGUGC 17 575 BCL11A-63 - CCGUUGGGAGCUCCAGA 17 576 BCL11A-10 + CCGUUUGCUUAAGUGCU 17 577 BCL11A-27 - CCUCUGCUUAGAAAAAGCUG 20 578 BCL11A-104 + CCUUCUGGAGCUCCCAA 17 579 BCL11A-36 + CGUCAUCCUCUGGCGUGACC 20 580 BCL11A-78 - CGUGGAGGUUGGCAUCC 17 581 BCL11A-64 - CGUUGGGAGCUCCAGAA 17 582 BCL11A-11 + CGUUUGCUUAAGUGCUG 17 583 BCL11A-84 + CUAUGUGUUCCUGUUUG 17 584 BCL11A-136 + CUCCAUGUGCAGAACGA 17 585 BCL11A-128 - CUCUAAUCCCCACGCCU 17 586 BCL11A-118 + CUGCACUCAUCCCAGGCGUG 20 587 BCL11A-74 - CUGCUUAGAAAAAGCUG 17 588 BCL11A-56 + CUGGAGCUCCCAACGGGCCG 20 589 BCL11A-87 + CUGGAUGCCAACCUCCA 17 590 BCL11A-105 + CUUCUGGAGCUCCCAAC 17 591 BCL11A-124 - UAAACUUCUGCACUGGA 17 592 BCL11A-98 + UAAGAAUGUCCCCCAAU 17 593 BCL11A-34 - UAGAGGAAUUUGCCCCAAAC 20 594 BCL11A-131 + UAUUCUGCACUCAUCCC 17 595 BCL11A-137 + UCCAUGUGCAGAACGAG 17 596 BCL11A-122 + UCCAUGUGCAGAACGAGGGG 20 597 BCL11A-126 - UCCCCUCGUUCUGCACA 17 598 BCL11A-54 + UCCCCUUCUGGAGCUCCCAA 20 599 BCL11A-31 - UCCCGUGGAGGUUGGCAUCC 20 600 BCL11A-5 + UCCCGUUUGCUUAAGUGCUG 20 601 BCL11A-110 - UCCUCCCCUCGUUCUGCACA 20 602 BCL11A-94 + UCGAUUGGUGAAGGGGA 17 603 BCL11A-45 + UCGAUUGGUGAAGGGGAAGG 20 604 BCL11A-117 + UCUGCACUCAUCCCAGGCGU 20 605 BCL11A-51 + UCUGGCACUGCCCACAGGUG 20 606 BCL11A-59 + UCUGUAAGAAUGGCUUCAAG 20 607 BCL11A-14 - UGAACCAGACCACGGCCCGU 20 608 BCL11A-132 + UGCACUCAUCCCAGGCG 17 609 BCL11A-129 - UGCAGAAUAUGCCCCGC 17 610 BCL11A-22 - UGCCAGAUGAACUUCCCAUU 20 611 BCL11A-82 + UGCUAUGUGUUCCUGUU 17 612 BCL11A-88 + UGGAUGCCAACCUCCAC 17 613 BCL11A-58 + UGGUUCAUCAUCUGUAAGAA 20 614 BCL11A-33 - UGUUUAUCAACGUCAUCUAG 20 615 BCL11A-80 - UUAUCAACGUCAUCUAG 17 616 BCL11A-25 - UUAUUUUUAUCGAGCACAAA 20 617 BCL11A-108 + UUCAUCAUCUGUAAGAA 17 618 BCL11A-91 + UUCAUCUCGAUUGGUGA 17 619 BCL11A-4 + UUCCCGUUUGCUUAAGUGCU 20 620 BCL11A-116 + UUCUGCACUCAUCCCAGGCG 20 621 BCL11A-43 + UUUCAUCUCGAUUGGUGAAG 20 622 BCL11A-72 - UUUUUAUCGAGCACAAA 17 623 BCL11A-41 + UUUUUCAUCUCGAUUGGUGA 20 624

Table 2D) provides exemplary targeting domains for knocking out the BCL11A gene selected according to the fourth tier parameters and are selected based on presence in the coding sequence. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE 2D 4th Tier DNA Target Site SEQ ID gRNA Name Strand Targeting domain Length NO BCL11A-140 - AACAGCCAUUCACCAGUGCA 20 625 BCL11A-141 - CAACACGCACAGAACACUCA 20 626 BCL11A-142 - AUCUACUUAGAAAGCGAACA 20 627 BCL11A-143 - ACGGAAGUCCCCUGACCCCG 20 628 BCL11A-144 - CGGAAGUCCCCUGACCCCGC 20 629 BCL11A-145 - AGUCCCCUGACCCCGCGGGU 20 630 BCL11A-146 - CCGCGGGUUGGUAUCCCUUC 20 631 BCL11A-147 - GUUGGUAUCCCUUCAGGACU 20 632 BCL11A-148 - CCUUCCCAGCCACCUCUCCA 20 633 BCL11A-149 - CUUCCCAGCCACCUCUCCAU 20 634 BCL11A-150 - UUUAACCUGCUAAGAAUACC 20 635 BCL11A-151 - ACCAGGAUCAGUAUCGAGAG 20 636 BCL11A-152 - UCAGUAUCGAGAGAGGCUUC 20 637 BCL11A-153 - AUCGAGAGAGGCUUCCGGCC 20 638 BCL11A-154 - GAGGCUUCCGGCCUGGCAGA 20 639 BCL11A-155 - AGGCUUCCGGCCUGGCAGAA 20 640 BCL11A-156 - UCCACCACCGAGACAUCACU 20 641 BCL11A-157 - CCCCCACCGCAUAGAGCGCC 20 642 BCL11A-158 - CCCCACCGCAUAGAGCGCCU 20 643 BCL11A-159 - CCCACCGCAUAGAGCGCCUG 20 644 BCL11A-160 - CCACCGCAUAGAGCGCCUGG 20 645 BCL11A-161 - CCGCAUAGAGCGCCUGGGGG 20 646 BCL11A-162 - GCGCCUGGGGGCGGAAGAGA 20 647 BCL11A-163 - GGGGGCGGAAGAGAUGGCCC 20 648 BCL11A-164 - AUCACCCGAGUGCCUUUGAC 20 649 BCL11A-165 - UCACCCGAGUGCCUUUGACA 20 650 BCL11A-166 - GUGCCUUUGACAGGGUGCUG 20 651 BCL11A-167 - GGUGCUGCGGUUGAAUCCAA 20 652 BCL11A-168 - GCGGUUGAAUCCAAUGGCUA 20 653 BCL11A-169 - GGCUAUGGAGCCUCCCGCCA 20 654 BCL11A-170 - CUCCCGCCAUGGAUUUCUCU 20 655 BCL11A-171 - CUCUAGGAGACUUAGAGAGC 20 656 BCL11A-172 - AGGAGACUUAGAGAGCUGGC 20 657 BCL11A-173 - GGAGACUUAGAGAGCUGGCA 20 658 BCL11A-174 - UCUAGCCCACCGCUGUCCCC 20 659 BCL11A-175 - GCCCACCGCUGUCCCCAGGC 20 660 BCL11A-176 - GCCGGCCCAGCCCUAUGCAA 20 661 BCL11A-177 - UUACUGCAACCAUUCCAGCC 20 662 BCL11A-178 - AGGUAGCAAGCCGCCCUUCC 20 663 BCL11A-179 - CCCUCCUCCCUCCCAGCCCC 20 664 BCL11A-180 - UCCAAGUCAUGCGAGUUCUG 20 665 BCL11A-181 - GUUCAAAUUUCAGAGCAACC 20 666 BCL11A-182 - CAAAUUUCAGAGCAACCUGG 20 667 BCL11A-183 - AGAGCAACCUGGUGGUGCAC 20 668 BCL11A-184 - GGUGCACCGGCGCAGCCACA 20 669 BCL11A-185 - GUGCACCGGCGCAGCCACAC 20 670 BCL11A-186 - GUGCGACCACGCGUGCACCC 20 671 BCL11A-187 - GCACAAAUCGUCCCCCAUGA 20 672 BCL11A-188 - AUGACGGUCAAGUCCGACGA 20 673 BCL11A-189 - UCUCUCCACCGCCAGCUCCC 20 674 BCL11A-190 - ACCGCCAGCUCCCCGGAACC 20 675 BCL11A-191 - GGAACCCGGCACCAGCGACU 20 676 BCL11A-192 - ACCCGGCACCAGCGACUUGG 20 677 BCL11A-193 - CCCGGCACCAGCGACUUGGU 20 678 BCL11A-194 - CAGCAGCGCGCUCAAGUCCG 20 679 BCL11A-195 - CAGCGCGCUCAAGUCCGUGG 20 680 BCL11A-196 - GAACGACCCCAACCUGAUCC 20 681 BCL11A-197 - CCCAACCUGAUCCCGGAGAA 20 682 BCL11A-198 - CCAACCUGAUCCCGGAGAAC 20 683 BCL11A-199 - CAACCUGAUCCCGGAGAACG 20 684 BCL11A-200 - GAUCCCGGAGAACGGGGACG 20 685 BCL11A-201 - CCCGGAGAACGGGGACGAGG 20 686 BCL11A-202 - GAACGGGGACGAGGAGGAAG 20 687 BCL11A-203 - CGGGGACGAGGAGGAAGAGG 20 688 BCL11A-204 - GGAGGAAGAGGAGGACGACG 20 689 BCL11A-205 - AGAGGAGGACGACGAGGAAG 20 690 BCL11A-206 - CGACGAGGAAGAGGAAGAAG 20 691 BCL11A-207 - CGAGGAAGAGGAAGAAGAGG 20 692 BCL11A-208 - AGAGGAAGAAGAGGAGGAAG 20 693 BCL11A-209 - GGAAGAAGAGGAGGAAGAGG 20 694 BCL11A-210 - AGAAGAGGAGGAAGAGGAGG 20 695 BCL11A-211 - AGAGGAGGAAGAGGAGGAGG 20 696 BCL11A-212 + UCCUCCUCGUCCCCGUUCUC 20 697 BCL11A-213 + CCUCCUCGUCCCCGUUCUCC 20 698 BCL11A-214 + CGUCCCCGUUCUCCGGGAUC 20 699 BCL11A-215 + CCCGUUCUCCGGGAUCAGGU 20 700 BCL11A-216 + CCGUUCUCCGGGAUCAGGUU 20 701 BCL11A-217 + CGUUCUCCGGGAUCAGGUUG 20 702 BCL11A-218 + GUCGUUCUCGCUCUUGAACU 20 703 BCL11A-219 + GCUCUUGAACUUGGCCACCA 20 704 BCL11A-220 + CACGGACUUGAGCGCGCUGC 20 705 BCL11A-221 + GGCGCUGCCCACCAAGUCGC 20 706 BCL11A-222 + GCCCACCAAGUCGCUGGUGC 20 707 BCL11A-223 + CCCACCAAGUCGCUGGUGCC 20 708 BCL11A-224 + AAGUCGCUGGUGCCGGGUUC 20 709 BCL11A-225 + AGUCGCUGGUGCCGGGUUCC 20 710 BCL11A-226 + GUCGCUGGUGCCGGGUUCCG 20 711 BCL11A-227 + GGUGCCGGGUUCCGGGGAGC 20 712 BCL11A-228 + GCCGGGUUCCGGGGAGCUGG 20 713 BCL11A-229 + GGGUUCCGGGGAGCUGGCGG 20 714 BCL11A-230 + GGCGGUGGAGAGACCGUCGU 20 715 BCL11A-231 + GUCGUCGGACUUGACCGUCA 20 716 BCL11A-232 + UCGUCGGACUUGACCGUCAU 20 717 BCL11A-233 + CGUCGGACUUGACCGUCAUG 20 718 BCL11A-234 + GUCGGACUUGACCGUCAUGG 20 719 BCL11A-235 + UGUGCAUGUGCGUCUUCAUG 20 720 BCL11A-236 + CAUGUGGCGCUUCAGCUUGC 20 721 BCL11A-237 + GGCGCUUCAGCUUGCUGGCC 20 722 BCL11A-238 + GCGCUUCAGCUUGCUGGCCU 20 723 BCL11A-239 + UGCUGGCCUGGGUGCACGCG 20 724 BCL11A-240 + GGGUGCACGCGUGGUCGCAC 20 725 BCL11A-241 + GUCGCACAGGUUGCACUUGU 20 726 BCL11A-242 + UCGCACAGGUUGCACUUGUA 20 727 BCL11A-243 + UGUAGGGCUUCUCGCCCGUG 20 728 BCL11A-244 + UCUCGCCCGUGUGGCUGCGC 20 729 BCL11A-245 + GGCUGCGCCGGUGCACCACC 20 730 BCL11A-246 + GCCGCAGAACUCGCAUGACU 20 731 BCL11A-247 + UCGCAUGACUUGGACUUGAC 20 732 BCL11A-248 + CGCAUGACUUGGACUUGACC 20 733 BCL11A-249 + GCAUGACUUGGACUUGACCG 20 734 BCL11A-250 + CAUGACUUGGACUUGACCGG 20 735 BCL11A-251 + ACUUGGACUUGACCGGGGGC 20 736 BCL11A-252 + CUUGGACUUGACCGGGGGCU 20 737 BCL11A-253 + GGACUUGACCGGGGGCUGGG 20 738 BCL11A-254 + GACUUGACCGGGGGCUGGGA 20 739 BCL11A-255 + UUGACCGGGGGCUGGGAGGG 20 740 BCL11A-256 + ACCGGGGGCUGGGAGGGAGG 20 741 BCL11A-257 + CCGGGGGCUGGGAGGGAGGA 20 742 BCL11A-258 + CGGGGGCUGGGAGGGAGGAG 20 743 BCL11A-259 + GGGCUGGGAGGGAGGAGGGG 20 744 BCL11A-260 + GGAGGAGGGGCGGAUUGCAG 20 745 BCL11A-261 + GGAGGGGCGGAUUGCAGAGG 20 746 BCL11A-262 + GAGGGGCGGAUUGCAGAGGA 20 747 BCL11A-263 + GGGCGGAUUGCAGAGGAGGG 20 748 BCL11A-264 + GGCGGAUUGCAGAGGAGGGA 20 749 BCL11A-265 + GCGGAUUGCAGAGGAGGGAG 20 750 BCL11A-266 + CGGAUUGCAGAGGAGGGAGG 20 751 BCL11A-267 + GGAUUGCAGAGGAGGGAGGG 20 752 BCL11A-268 + GAUUGCAGAGGAGGGAGGGG 20 753 BCL11A-269 + GAGGGAGGGGGGGCGUCGCC 20 754 BCL11A-270 + GAGGGGGGGCGUCGCCAGGA 20 755 BCL11A-271 + AGGGGGGGCGUCGCCAGGAA 20 756 BCL11A-272 + GGGGGCGUCGCCAGGAAGGG 20 757 BCL11A-273 + AGGAAGGGCGGCUUGCUACC 20 758 BCL11A-274 + AGGGCGGCUUGCUACCUGGC 20 759 BCL11A-275 + GGCUUGCUACCUGGCUGGAA 20 760 BCL11A-276 + GGUUGCAGUAACCUUUGCAU 20 761 BCL11A-277 + GUUGCAGUAACCUUUGCAUA 20 762 BCL11A-278 + CAGUAACCUUUGCAUAGGGC 20 763 BCL11A-279 + AGUAACCUUUGCAUAGGGCU 20 764 BCL11A-280 + ACCUUUGCAUAGGGCUGGGC 20 765 BCL11A-281 + UGCAUAGGGCUGGGCCGGCC 20 766 BCL11A-282 + GCAUAGGGCUGGGCCGGCCU 20 767 BCL11A-283 + CAUAGGGCUGGGCCGGCCUG 20 768 BCL11A-284 + CUGGGCCGGCCUGGGGACAG 20 769 BCL11A-285 + GGCCGGCCUGGGGACAGCGG 20 770 BCL11A-286 + GCCGGCCUGGGGACAGCGGU 20 771 BCL11A-287 + AAGUCUCCUAGAGAAAUCCA 20 772 BCL11A-288 + UCUCCUAGAGAAAUCCAUGG 20 773 BCL11A-289 + CUCCUAGAGAAAUCCAUGGC 20 774 BCL11A-290 + CUAGAGAAAUCCAUGGCGGG 20 775 BCL11A-291 + GCGGGAGGCUCCAUAGCCAU 20 776 BCL11A-292 + CAACCGCAGCACCCUGUCAA 20 777 BCL11A-293 + AGCACCCUGUCAAAGGCACU 20 778 BCL11A-294 + GCACCCUGUCAAAGGCACUC 20 779 BCL11A-295 + UGUCAAAGGCACUCGGGUGA 20 780 BCL11A-296 + GUCAAAGGCACUCGGGUGAU 20 781 BCL11A-297 + AAAGGCACUCGGGUGAUGGG 20 782 BCL11A-298 + CACUCGGGUGAUGGGUGGCC 20 783 BCL11A-299 + ACUCGGGUGAUGGGUGGCCA 20 784 BCL11A-300 + GGGCCAUCUCUUCCGCCCCC 20 785 BCL11A-301 + CCGCCCCCAGGCGCUCUAUG 20 786 BCL11A-302 + CCCCCAGGCGCUCUAUGCGG 20 787 BCL11A-303 + CCCCAGGCGCUCUAUGCGGU 20 788 BCL11A-304 + CCCAGGCGCUCUAUGCGGUG 20 789 BCL11A-305 + CCAGGCGCUCUAUGCGGUGG 20 790 BCL11A-306 + UGGGGGUCCAAGUGAUGUCU 20 791 BCL11A-307 + GGGUCCAAGUGAUGUCUCGG 20 792 BCL11A-308 + UCCAAGUGAUGUCUCGGUGG 20 793 BCL11A-309 + GUCUCGGUGGUGGACUAAAC 20 794 BCL11A-310 + UCUCGGUGGUGGACUAAACA 20 795 BCL11A-311 + CUCGGUGGUGGACUAAACAG 20 796 BCL11A-312 + UCGGUGGUGGACUAAACAGG 20 797 BCL11A-313 + CGGUGGUGGACUAAACAGGG 20 798 BCL11A-314 + GGUGGUGGACUAAACAGGGG 20 799 BCL11A-315 + UGGACUAAACAGGGGGGGAG 20 800 BCL11A-316 + GGACUAAACAGGGGGGGAGU 20 801 BCL11A-317 + CUAAACAGGGGGGGAGUGGG 20 802 BCL11A-318 + GUGGAAAGCGCCCUUCUGCC 20 803 BCL11A-319 + AAAGCGCCCUUCUGCCAGGC 20 804 BCL11A-320 + GCCUCUCUCGAUACUGAUCC 20 805 BCL11A-321 + CUGAUCCUGGUAUUCUUAGC 20 806 BCL11A-322 + UGGUAUUCUUAGCAGGUUAA 20 807 BCL11A-323 + GGUAUUCUUAGCAGGUUAAA 20 808 BCL11A-324 + GUAUUCUUAGCAGGUUAAAG 20 809 BCL11A-325 + UGUCUGCAAUAUGAAUCCCA 20 810 BCL11A-326 + GCAAUAUGAAUCCCAUGGAG 20 811 BCL11A-327 + AUAUGAAUCCCAUGGAGAGG 20 812 BCL11A-328 + GAAUCCCAUGGAGAGGUGGC 20 813 BCL11A-329 + AAUCCCAUGGAGAGGUGGCU 20 814 BCL11A-330 + CCAUGGAGAGGUGGCUGGGA 20 815 BCL11A-331 + CAUUCUGCACCUAGUCCUGA 20 816 BCL11A-332 + AUUCUGCACCUAGUCCUGAA 20 817 BCL11A-333 + CCUGAAGGGAUACCAACCCG 20 818 BCL11A-334 + CUGAAGGGAUACCAACCCGC 20 819 BCL11A-335 + UGAAGGGAUACCAACCCGCG 20 820 BCL11A-336 + GGAUACCAACCCGCGGGGUC 20 821 BCL11A-337 + GAUACCAACCCGCGGGGUCA 20 822 BCL11A-338 + AUACCAACCCGCGGGGUCAG 20 823 BCL11A-339 + UUGCAAGAGAAACCAUGCAC 20 824 BCL11A-340 + AGAAACCAUGCACUGGUGAA 20 825 BCL11A-341 + AGUUGUACAUGUGUAGCUGC 20 826 BCL11A-342 + GUUGUACAUGUGUAGCUGCU 20 827 BCL11A-343 - AGCCAUUCACCAGUGCA 17 828 BCL11A-344 - CACGCACAGAACACUCA 17 829 BCL11A-345 - UACUUAGAAAGCGAACA 17 830 BCL11A-346 - GAAGUCCCCUGACCCCG 17 831 BCL11A-347 - AAGUCCCCUGACCCCGC 17 832 BCL11A-348 - CCCCUGACCCCGCGGGU 17 833 BCL11A-349 - CGGGUUGGUAUCCCUUC 17 834 BCL11A-350 - GGUAUCCCUUCAGGACU 17 835 BCL11A-351 - UCCCAGCCACCUCUCCA 17 836 BCL11A-352 - CCCAGCCACCUCUCCAU 17 837 BCL11A-353 - AACCUGCUAAGAAUACC 17 838 BCL11A-354 - AGGAUCAGUAUCGAGAG 17 839 BCL11A-355 - GUAUCGAGAGAGGCUUC 17 840 BCL11A-356 - GAGAGAGGCUUCCGGCC 17 841 BCL11A-357 - GCUUCCGGCCUGGCAGA 17 842 BCL11A-358 - CUUCCGGCCUGGCAGAA 17 843 BCL11A-359 - ACCACCGAGACAUCACU 17 844 BCL11A-360 - CCACCGCAUAGAGCGCC 17 845 BCL11A-361 - CACCGCAUAGAGCGCCU 17 846 BCL11A-362 - ACCGCAUAGAGCGCCUG 17 847 BCL11A-363 - CCGCAUAGAGCGCCUGG 17 848 BCL11A-364 - CAUAGAGCGCCUGGGGG 17 849 BCL11A-365 - CCUGGGGGCGGAAGAGA 17 850 BCL11A-366 - GGCGGAAGAGAUGGCCC 17 851 BCL11A-367 - ACCCGAGUGCCUUUGAC 17 852 BCL11A-368 - CCCGAGUGCCUUUGACA 17 853 BCL11A-369 - CCUUUGACAGGGUGCUG 17 854 BCL11A-370 - GCUGCGGUUGAAUCCAA 17 855 BCL11A-371 - GUUGAAUCCAAUGGCUA 17 856 BCL11A-372 - UAUGGAGCCUCCCGCCA 17 857 BCL11A-373 - CCGCCAUGGAUUUCUCU 17 858 BCL11A-374 - UAGGAGACUUAGAGAGC 17 859 BCL11A-375 - AGACUUAGAGAGCUGGC 17 860 BCL11A-376 - GACUUAGAGAGCUGGCA 17 861 BCL11A-377 - AGCCCACCGCUGUCCCC 17 862 BCL11A-378 - CACCGCUGUCCCCAGGC 17 863 BCL11A-379 - GGCCCAGCCCUAUGCAA 17 864 BCL11A-380 - CUGCAACCAUUCCAGCC 17 865 BCL11A-381 - UAGCAAGCCGCCCUUCC 17 866 BCL11A-382 - UCCUCCCUCCCAGCCCC 17 867 BCL11A-383 - AAGUCAUGCGAGUUCUG 17 868 BCL11A-384 - CAAAUUUCAGAGCAACC 17 869 BCL11A-385 - AUUUCAGAGCAACCUGG 17 870 BCL11A-386 - GCAACCUGGUGGUGCAC 17 871 BCL11A-387 - GCACCGGCGCAGCCACA 17 872 BCL11A-388 - CACCGGCGCAGCCACAC 17 873 BCL11A-389 - CGACCACGCGUGCACCC 17 874 BCL11A-390 - CAAAUCGUCCCCCAUGA 17 875 BCL11A-391 - ACGGUCAAGUCCGACGA 17 876 BCL11A-392 - CUCCACCGCCAGCUCCC 17 877 BCL11A-393 - GCCAGCUCCCCGGAACC 17 878 BCL11A-394 - ACCCGGCACCAGCGACU 17 879 BCL11A-395 - CGGCACCAGCGACUUGG 17 880 BCL11A-396 - GGCACCAGCGACUUGGU 17 881 BCL11A-397 - CAGCGCGCUCAAGUCCG 17 882 BCL11A-398 - CGCGCUCAAGUCCGUGG 17 883 BCL11A-399 - CGACCCCAACCUGAUCC 17 884 BCL11A-400 - AACCUGAUCCCGGAGAA 17 885 BCL11A-401 - ACCUGAUCCCGGAGAAC 17 886 BCL11A-402 - CCUGAUCCCGGAGAACG 17 887 BCL11A-403 - CCCGGAGAACGGGGACG 17 888 BCL11A-404 - GGAGAACGGGGACGAGG 17 889 BCL11A-405 - CGGGGACGAGGAGGAAG 17 890 BCL11A-406 - GGACGAGGAGGAAGAGG 17 891 BCL11A-407 - GGAAGAGGAGGACGACG 17 892 BCL11A-408 - GGAGGACGACGAGGAAG 17 893 BCL11A-409 - CGAGGAAGAGGAAGAAG 17 894 BCL11A-410 - GGAAGAGGAAGAAGAGG 17 895 BCL11A-411 - GGAAGAAGAGGAGGAAG 17 896 BCL11A-412 - AGAAGAGGAGGAAGAGG 17 897 BCL11A-413 - AGAGGAGGAAGAGGAGG 17 898 BCL11A-414 - GGAGGAAGAGGAGGAGG 17 899 BCL11A-415 + UCCUCGUCCCCGUUCUC 17 900 BCL11A-416 + CCUCGUCCCCGUUCUCC 17 901 BCL11A-417 + CCCCGUUCUCCGGGAUC 17 902 BCL11A-418 + GUUCUCCGGGAUCAGGU 17 903 BCL11A-419 + UUCUCCGGGAUCAGGUU 17 904 BCL11A-420 + UCUCCGGGAUCAGGUUG 17 905 BCL11A-421 + GUUCUCGCUCUUGAACU 17 906 BCL11A-422 + CUUGAACUUGGCCACCA 17 907 BCL11A-423 + GGACUUGAGCGCGCUGC 17 908 BCL11A-424 + GCUGCCCACCAAGUCGC 17 909 BCL11A-425 + CACCAAGUCGCUGGUGC 17 910 BCL11A-426 + ACCAAGUCGCUGGUGCC 17 911 BCL11A-427 + UCGCUGGUGCCGGGUUC 17 912 BCL11A-428 + CGCUGGUGCCGGGUUCC 17 913 BCL11A-429 + GCUGGUGCCGGGUUCCG 17 914 BCL11A-430 + GCCGGGUUCCGGGGAGC 17 915 BCL11A-431 + GGGUUCCGGGGAGCUGG 17 916 BCL11A-432 + UUCCGGGGAGCUGGCGG 17 917 BCL11A-433 + GGUGGAGAGACCGUCGU 17 918 BCL11A-434 + GUCGGACUUGACCGUCA 17 919 BCL11A-435 + UCGGACUUGACCGUCAU 17 920 BCL11A-436 + CGGACUUGACCGUCAUG 17 921 BCL11A-437 + GGACUUGACCGUCAUGG 17 922 BCL11A-438 + GCAUGUGCGUCUUCAUG 17 923 BCL11A-439 + GUGGCGCUUCAGCUUGC 17 924 BCL11A-440 + GCUUCAGCUUGCUGGCC 17 925 BCL11A-441 + CUUCAGCUUGCUGGCCU 17 926 BCL11A-442 + UGGCCUGGGUGCACGCG 17 927 BCL11A-443 + UGCACGCGUGGUCGCAC 17 928 BCL11A-444 + GCACAGGUUGCACUUGU 17 929 BCL11A-445 + CACAGGUUGCACUUGUA 17 930 BCL11A-446 + AGGGCUUCUCGCCCGUG 17 931 BCL11A-447 + CGCCCGUGUGGCUGCGC 17 932 BCL11A-448 + UGCGCCGGUGCACCACC 17 933 BCL11A-449 + GCAGAACUCGCAUGACU 17 934 BCL11A-450 + CAUGACUUGGACUUGAC 17 935 BCL11A-451 + AUGACUUGGACUUGACC 17 936 BCL11A-452 + UGACUUGGACUUGACCG 17 937 BCL11A-453 + GACUUGGACUUGACCGG 17 938 BCL11A-454 + UGGACUUGACCGGGGGC 17 939 BCL11A-455 + GGACUUGACCGGGGGCU 17 940 BCL11A-456 + CUUGACCGGGGGCUGGG 17 941 BCL11A-457 + UUGACCGGGGGCUGGGA 17 942 BCL11A-458 + ACCGGGGGCUGGGAGGG 17 943 BCL11A-459 + GGGGGCUGGGAGGGAGG 17 944 BCL11A-460 + GGGGCUGGGAGGGAGGA 17 945 BCL11A-461 + GGGCUGGGAGGGAGGAG 17 946 BCL11A-462 + CUGGGAGGGAGGAGGGG 17 947 BCL11A-463 + GGAGGGGCGGAUUGCAG 17 948 BCL11A-464 + GGGGCGGAUUGCAGAGG 17 949 BCL11A-465 + GGGCGGAUUGCAGAGGA 17 950 BCL11A-466 + CGGAUUGCAGAGGAGGG 17 951 BCL11A-467 + GGAUUGCAGAGGAGGGA 17 952 BCL11A-468 + GAUUGCAGAGGAGGGAG 17 953 BCL11A-469 + AUUGCAGAGGAGGGAGG 17 954 BCL11A-470 + UUGCAGAGGAGGGAGGG 17 955 BCL11A-471 + UGCAGAGGAGGGAGGGG 17 956 BCL11A-472 + GGAGGGGGGGCGUCGCC 17 957 BCL11A-473 + GGGGGGCGUCGCCAGGA 17 958 BCL11A-474 + GGGGGCGUCGCCAGGAA 17 959 BCL11A-475 + GGCGUCGCCAGGAAGGG 17 960 BCL11A-476 + AAGGGCGGCUUGCUACC 17 961 BCL11A-477 + GCGGCUUGCUACCUGGC 17 962 BCL11A-478 + UUGCUACCUGGCUGGAA 17 963 BCL11A-479 + UGCAGUAACCUUUGCAU 17 964 BCL11A-480 + GCAGUAACCUUUGCAUA 17 965 BCL11A-481 + UAACCUUUGCAUAGGGC 17 966 BCL11A-482 + AACCUUUGCAUAGGGCU 17 967 BCL11A-483 + UUUGCAUAGGGCUGGGC 17 968 BCL11A-484 + AUAGGGCUGGGCCGGCC 17 969 BCL11A-485 + UAGGGCUGGGCCGGCCU 17 970 BCL11A-486 + AGGGCUGGGCCGGCCUG 17 971 BCL11A-487 + GGCCGGCCUGGGGACAG 17 972 BCL11A-488 + CGGCCUGGGGACAGCGG 17 973 BCL11A-489 + GGCCUGGGGACAGCGGU 17 974 BCL11A-490 + UCUCCUAGAGAAAUCCA 17 975 BCL11A-491 + CCUAGAGAAAUCCAUGG 17 976 BCL11A-492 + CUAGAGAAAUCCAUGGC 17 977 BCL11A-493 + GAGAAAUCCAUGGCGGG 17 978 BCL11A-494 + GGAGGCUCCAUAGCCAU 17 979 BCL11A-495 + CCGCAGCACCCUGUCAA 17 980 BCL11A-496 + ACCCUGUCAAAGGCACU 17 981 BCL11A-497 + CCCUGUCAAAGGCACUC 17 982 BCL11A-498 + CAAAGGCACUCGGGUGA 17 983 BCL11A-499 + AAAGGCACUCGGGUGAU 17 984 BCL11A-500 + GGCACUCGGGUGAUGGG 17 985 BCL11A-501 + UCGGGUGAUGGGUGGCC 17 986 BCL11A-502 + CGGGUGAUGGGUGGCCA 17 987 BCL11A-503 + CCAUCUCUUCCGCCCCC 17 988 BCL11A-504 + CCCCCAGGCGCUCUAUG 17 989 BCL11A-505 + CCAGGCGCUCUAUGCGG 17 990 BCL11A-506 + CAGGCGCUCUAUGCGGU 17 991 BCL11A-507 + AGGCGCUCUAUGCGGUG 17 992 BCL11A-508 + GGCGCUCUAUGCGGUGG 17 993 BCL11A-509 + GGGUCCAAGUGAUGUCU 17 994 BCL11A-510 + UCCAAGUGAUGUCUCGG 17 995 BCL11A-511 + AAGUGAUGUCUCGGUGG 17 996 BCL11A-512 + UCGGUGGUGGACUAAAC 17 997 BCL11A-513 + CGGUGGUGGACUAAACA 17 998 BCL11A-514 + GGUGGUGGACUAAACAG 17 999 BCL11A-515 + GUGGUGGACUAAACAGG 17 1000 BCL11A-516 + UGGUGGACUAAACAGGG 17 1001 BCL11A-517 + GGUGGACUAAACAGGGG 17 1002 BCL11A-518 + ACUAAACAGGGGGGGAG 17 1003 BCL11A-519 + CUAAACAGGGGGGGAGU 17 1004 BCL11A-520 + AACAGGGGGGGAGUGGG 17 1005 BCL11A-521 + GAAAGCGCCCUUCUGCC 17 1006 BCL11A-522 + GCGCCCUUCUGCCAGGC 17 1007 BCL11A-523 + UCUCUCGAUACUGAUCC 17 1008 BCL11A-524 + AUCCUGGUAUUCUUAGC 17 1009 BCL11A-525 + UAUUCUUAGCAGGUUAA 17 1010 BCL11A-526 + AUUCUUAGCAGGUUAAA 17 1011 BCL11A-527 + UUCUUAGCAGGUUAAAG 17 1012 BCL11A-528 + CUGCAAUAUGAAUCCCA 17 1013 BCL11A-529 + AUAUGAAUCCCAUGGAG 17 1014 BCL11A-530 + UGAAUCCCAUGGAGAGG 17 1015 BCL11A-531 + UCCCAUGGAGAGGUGGC 17 1016 BCL11A-532 + CCCAUGGAGAGGUGGCU 17 1017 BCL11A-533 + UGGAGAGGUGGCUGGGA 17 1018 BCL11A-534 + UCUGCACCUAGUCCUGA 17 1019 BCL11A-535 + CUGCACCUAGUCCUGAA 17 1020 BCL11A-536 + GAAGGGAUACCAACCCG 17 1021 BCL11A-537 + AAGGGAUACCAACCCGC 17 1022 BCL11A-538 + AGGGAUACCAACCCGCG 17 1023 BCL11A-539 + UACCAACCCGCGGGGUC 17 1024 BCL11A-540 + ACCAACCCGCGGGGUCA 17 1025 BCL11A-541 + CCAACCCGCGGGGUCAG 17 1026 BCL11A-542 + CAAGAGAAACCAUGCAC 17 1027 BCL11A-543 + AACCAUGCACUGGUGAA 17 1028 BCL11A-544 + UGUACAUGUGUAGCUGC 17 1029 BCL11A-545 + GUACAUGUGUAGCUGCU 17 1030 BCL11A-546 - AGAGGAGGAGGAGGAGCUGA 20 1031 BCL11A-547 - AGGAGCUGACGGAGAGCGAG 20 1032 BCL11A-548 - GGAGCUGACGGAGAGCGAGA 20 1033 BCL11A-549 - GCUGACGGAGAGCGAGAGGG 20 1034 BCL11A-550 - GAGAGCGAGAGGGUGGACUA 20 1035 BCL11A-551 - GAGAGGGUGGACUACGGCUU 20 1036 BCL11A-552 - AGAGGGUGGACUACGGCUUC 20 1037 BCL11A-553 - CUACGGCUUCGGGCUGAGCC 20 1038 BCL11A-554 - CGGCUUCGGGCUGAGCCUGG 20 1039 BCL11A-555 - CUUCGGGCUGAGCCUGGAGG 20 1040 BCL11A-556 - GCCACCACGAGAACAGCUCG 20 1041 BCL11A-557 - CCACCACGAGAACAGCUCGC 20 1042 BCL11A-558 - CACCACGAGAACAGCUCGCG 20 1043 BCL11A-559 - CGAGAACAGCUCGCGGGGCG 20 1044 BCL11A-560 - CAGCUCGCGGGGCGCGGUCG 20 1045 BCL11A-561 - AGCUCGCGGGGCGCGGUCGU 20 1046 BCL11A-562 - GCGGGGCGCGGUCGUGGGCG 20 1047 BCL11A-563 - CGGGGCGCGGUCGUGGGCGU 20 1048 BCL11A-564 - CGCCCUGCCCGACGUCAUGC 20 1049 BCL11A-565 - GCCCUGCCCGACGUCAUGCA 20 1050 BCL11A-566 - GCCCGACGUCAUGCAGGGCA 20 1051 BCL11A-567 - CUCCAUGCAGCACUUCAGCG 20 1052 BCL11A-568 - CUUCAGCGAGGCCUUCCACC 20 1053 BCL11A-569 - CGAGGCCUUCCACCAGGUCC 20 1054 BCL11A-570 - GAGGCCUUCCACCAGGUCCU 20 1055 BCL11A-571 - CUGGGCGAGAAGCAUAAGCG 20 1056 BCL11A-572 - GAAGCAUAAGCGCGGCCACC 20 1057 BCL11A-573 - UAAGCGCGGCCACCUGGCCG 20 1058 BCL11A-574 - CGGCCACCUGGCCGAGGCCG 20 1059 BCL11A-575 - GGCCACCUGGCCGAGGCCGA 20 1060 BCL11A-576 - UGGCCGAGGCCGAGGGCCAC 20 1061 BCL11A-577 - GGCCGAGGCCGAGGGCCACA 20 1062 BCL11A-578 - GGACACUUGCGACGAAGACU 20 1063 BCL11A-579 - CACUUGCGACGAAGACUCGG 20 1064 BCL11A-580 - UGCGACGAAGACUCGGUGGC 20 1065 BCL11A-581 - AGACUCGGUGGCCGGCGAGU 20 1066 BCL11A-582 - GAGUCGGACCGCAUAGACGA 20 1067 BCL11A-583 - AUAGACGAUGGCACUGUUAA 20 1068 BCL11A-584 - GAUGGCACUGUUAAUGGCCG 20 1069 BCL11A-585 - UAAUGGCCGCGGCUGCUCCC 20 1070 BCL11A-586 - AAUGGCCGCGGCUGCUCCCC 20 1071 BCL11A-587 - CGGCUGCUCCCCGGGCGAGU 20 1072 BCL11A-588 - CUCCCCGGGCGAGUCGGCCU 20 1073 BCL11A-589 - UCCCCGGGCGAGUCGGCCUC 20 1074 BCL11A-590 - CCCCGGGCGAGUCGGCCUCG 20 1075 BCL11A-591 - CCCGGGCGAGUCGGCCUCGG 20 1076 BCL11A-592 - CCGGGCGAGUCGGCCUCGGG 20 1077 BCL11A-593 - CCUGUCCAAAAAGCUGCUGC 20 1078 BCL11A-594 - CUGUCCAAAAAGCUGCUGCU 20 1079 BCL11A-595 - UAAGCGCAUCAAGCUCGAGA 20 1080 BCL11A-596 - GAAGGAGUUCGACCUGCCCC 20 1081 BCL11A-597 - CCCGGCCGCGAUGCCCAACA 20 1082 BCL11A-598 - CGGAGAACGUGUACUCGCAG 20 1083 BCL11A-599 - GUGUACUCGCAGUGGCUCGC 20 1084 BCL11A-600 - GCAGUGGCUCGCCGGCUACG 20 1085 BCL11A-601 - UCGCCGGCUACGCGGCCUCC 20 1086 BCL11A-602 - AAAGAUCCCUUCCUUAGCUU 20 1087 BCL11A-603 - AUCGCCUUUUGCCUCCUCGU 20 1088 BCL11A-604 - CUCCUCGUCGGAGCACUCCU 20 1089 BCL11A-605 - UCGGAGCACUCCUCGGAGAA 20 1090 BCL11A-606 - CGGAGCACUCCUCGGAGAAC 20 1091 BCL11A-607 - UUGCGCUUCUCCACACCGCC 20 1092 BCL11A-608 - UGCGCUUCUCCACACCGCCC 20 1093 BCL11A-609 - GCGCUUCUCCACACCGCCCG 20 1094 BCL11A-610 - CUCCACACCGCCCGGGGAGC 20 1095 BCL11A-611 - ACACCGCCCGGGGAGCUGGA 20 1096 BCL11A-612 - CCGCCCGGGGAGCUGGACGG 20 1097 BCL11A-613 - CGCCCGGGGAGCUGGACGGA 20 1098 BCL11A-614 - GGAGCUGGACGGAGGGAUCU 20 1099 BCL11A-615 - GAGCUGGACGGAGGGAUCUC 20 1100 BCL11A-616 - AGCUGGACGGAGGGAUCUCG 20 1101 BCL11A-617 - GGAGGGAUCUCGGGGCGCAG 20 1102 BCL11A-618 - GAUCUCGGGGCGCAGCGGCA 20 1103 BCL11A-619 - AUCUCGGGGCGCAGCGGCAC 20 1104 BCL11A-620 - GGGCGCAGCGGCACGGGAAG 20 1105 BCL11A-621 - CGCAGCGGCACGGGAAGUGG 20 1106 BCL11A-622 - GCAGCGGCACGGGAAGUGGA 20 1107 BCL11A-623 - GGGAGCACGCCCCAUAUUAG 20 1108 BCL11A-624 - CACGCCCCAUAUUAGUGGUC 20 1109 BCL11A-625 - ACGCCCCAUAUUAGUGGUCC 20 1110 BCL11A-626 - CCAUAUUAGUGGUCCGGGCC 20 1111 BCL11A-627 - CAUAUUAGUGGUCCGGGCCC 20 1112 BCL11A-628 - UUAGUGGUCCGGGCCCGGGC 20 1113 BCL11A-629 - GGGCAGGCCCAGCUCAAAAG 20 1114 BCL11A-630 - GGCAGGCCCAGCUCAAAAGA 20 1115 BCL11A-631 + GCGUCUGCCCUCUUUUGAGC 20 1116 BCL11A-632 + CGUCUGCCCUCUUUUGAGCU 20 1117 BCL11A-633 + UCUUUUGAGCUGGGCCUGCC 20 1118 BCL11A-634 + CUUUUGAGCUGGGCCUGCCC 20 1119 BCL11A-635 + GAGCUGGGCCUGCCCGGGCC 20 1120 BCL11A-636 + CCGGGCCCGGACCACUAAUA 20 1121 BCL11A-637 + CGGGCCCGGACCACUAAUAU 20 1122 BCL11A-638 + GGGCCCGGACCACUAAUAUG 20 1123 BCL11A-639 + GAUCCCUCCGUCCAGCUCCC 20 1124 BCL11A-640 + AUCCCUCCGUCCAGCUCCCC 20 1125 BCL11A-641 + CCUCCGUCCAGCUCCCCGGG 20 1126 BCL11A-642 + GUCCAGCUCCCCGGGCGGUG 20 1127 BCL11A-643 + GCGCAAACUCCCGUUCUCCG 20 1128 BCL11A-644 + CUCCGAGGAGUGCUCCGACG 20 1129 BCL11A-645 + CGAGGAGUGCUCCGACGAGG 20 1130 BCL11A-646 + UGCUCCGACGAGGAGGCAAA 20 1131 BCL11A-647 + GGAGGCAAAAGGCGAUUGUC 20 1132 BCL11A-648 + GUCUGGAGUCUCCGAAGCUA 20 1133 BCL11A-649 + GGAGUCUCCGAAGCUAAGGA 20 1134 BCL11A-650 + GAGUCUCCGAAGCUAAGGAA 20 1135 BCL11A-651 + GAAGGGAUCUUUGAGCUGCC 20 1136 BCL11A-652 + GGGAUCUUUGAGCUGCCUGG 20 1137 BCL11A-653 + CUGCCUGGAGGCCGCGUAGC 20 1138 BCL11A-654 + CGAGUACACGUUCUCCGUGU 20 1139 BCL11A-655 + GAGUACACGUUCUCCGUGUU 20 1140 BCL11A-656 + GUUCUCCGUGUUGGGCAUCG 20 1141 BCL11A-657 + UCCGUGUUGGGCAUCGCGGC 20 1142 BCL11A-658 + CCGUGUUGGGCAUCGCGGCC 20 1143 BCL11A-659 + CGUGUUGGGCAUCGCGGCCG 20 1144 BCL11A-660 + GUGUUGGGCAUCGCGGCCGG 20 1145 BCL11A-661 + UGGGCAUCGCGGCCGGGGGC 20 1146 BCL11A-662 + GAGCUUGAUGCGCUUAGAGA 20 1147 BCL11A-663 + AGCUUGAUGCGCUUAGAGAA 20 1148 BCL11A-664 + GCUUGAUGCGCUUAGAGAAG 20 1149 BCL11A-665 + AGAGAAGGGGCUCAGCGAGC 20 1150 BCL11A-666 + GAGAAGGGGCUCAGCGAGCU 20 1151 BCL11A-667 + AGAAGGGGCUCAGCGAGCUG 20 1152 BCL11A-668 + GCUGCCCAGCAGCAGCUUUU 20 1153 BCL11A-669 + CCAGCAGCAGCUUUUUGGAC 20 1154 BCL11A-670 + CUUUUUGGACAGGCCCCCCG 20 1155 BCL11A-671 + CCCCCCGAGGCCGACUCGCC 20 1156 BCL11A-672 + CCCCCGAGGCCGACUCGCCC 20 1157 BCL11A-673 + CCCCGAGGCCGACUCGCCCG 20 1158 BCL11A-674 + ACUCGCCCGGGGAGCAGCCG 20 1159 BCL11A-675 + UAACAGUGCCAUCGUCUAUG 20 1160 BCL11A-676 + GUCUAUGCGGUCCGACUCGC 20 1161 BCL11A-677 + CUUCGUCGCAAGUGUCCCUG 20 1162 BCL11A-678 + GCAAGUGUCCCUGUGGCCCU 20 1163 BCL11A-679 + GUCCCUGUGGCCCUCGGCCU 20 1164 BCL11A-680 + UGUGGCCCUCGGCCUCGGCC 20 1165 BCL11A-681 + GGCCCUCGGCCUCGGCCAGG 20 1166 BCL11A-682 + CGCGCUUAUGCUUCUCGCCC 20 1167 BCL11A-683 + UAUGCUUCUCGCCCAGGACC 20 1168 BCL11A-684 + GCUUCUCGCCCAGGACCUGG 20 1169 BCL11A-685 + CUCGCCCAGGACCUGGUGGA 20 1170 BCL11A-686 + GGCCUCGCUGAAGUGCUGCA 20 1171 BCL11A-687 + CACCAUGCCCUGCAUGACGU 20 1172 BCL11A-688 + ACCAUGCCCUGCAUGACGUC 20 1173 BCL11A-689 + UGCCCUGCAUGACGUCGGGC 20 1174 BCL11A-690 + GCCCUGCAUGACGUCGGGCA 20 1175 BCL11A-691 + GCAUGACGUCGGGCAGGGCG 20 1176 BCL11A-692 + CGCCCCGCGAGCUGUUCUCG 20 1177 BCL11A-693 + CCCGCGAGCUGUUCUCGUGG 20 1178 BCL11A-694 + CGUGGUGGCGCGCCGCCUCC 20 1179 BCL11A-695 - GGAGGAAGAGGAGGAGG 17 1180 BCL11A-696 - GGAGGAGGAGGAGCUGA 17 1181 BCL11A-697 - AGCUGACGGAGAGCGAG 17 1182 BCL11A-698 - GCUGACGGAGAGCGAGA 17 1183 BCL11A-699 - GACGGAGAGCGAGAGGG 17 1184 BCL11A-700 - AGCGAGAGGGUGGACUA 17 1185 BCL11A-701 - AGGGUGGACUACGGCUU 17 1186 BCL11A-702 - GGGUGGACUACGGCUUC 17 1187 BCL11A-703 - CGGCUUCGGGCUGAGCC 17 1188 BCL11A-704 - CUUCGGGCUGAGCCUGG 17 1189 BCL11A-705 - CGGGCUGAGCCUGGAGG 17 1190 BCL11A-706 - ACCACGAGAACAGCUCG 17 1191 BCL11A-707 - CCACGAGAACAGCUCGC 17 1192 BCL11A-708 - CACGAGAACAGCUCGCG 17 1193 BCL11A-709 - GAACAGCUCGCGGGGCG 17 1194 BCL11A-710 - CUCGCGGGGCGCGGUCG 17 1195 BCL11A-711 - UCGCGGGGCGCGGUCGU 17 1196 BCL11A-712 - GGGCGCGGUCGUGGGCG 17 1197 BCL11A-713 - GGCGCGGUCGUGGGCGU 17 1198 BCL11A-714 - CCUGCCCGACGUCAUGC 17 1199 BCL11A-715 - CUGCCCGACGUCAUGCA 17 1200 BCL11A-716 - CGACGUCAUGCAGGGCA 17 1201 BCL11A-717 - CAUGCAGCACUUCAGCG 17 1202 BCL11A-718 - CAGCGAGGCCUUCCACC 17 1203 BCL11A-719 - GGCCUUCCACCAGGUCC 17 1204 BCL11A-720 - GCCUUCCACCAGGUCCU 17 1205 BCL11A-721 - GGCGAGAAGCAUAAGCG 17 1206 BCL11A-722 - GCAUAAGCGCGGCCACC 17 1207 BCL11A-723 - GCGCGGCCACCUGGCCG 17 1208 BCL11A-724 - CCACCUGGCCGAGGCCG 17 1209 BCL11A-725 - CACCUGGCCGAGGCCGA 17 1210 BCL11A-726 - CCGAGGCCGAGGGCCAC 17 1211 BCL11A-727 - CGAGGCCGAGGGCCACA 17 1212 BCL11A-728 - CACUUGCGACGAAGACU 17 1213 BCL11A-729 - UUGCGACGAAGACUCGG 17 1214 BCL11A-730 - GACGAAGACUCGGUGGC 17 1215 BCL11A-731 - CUCGGUGGCCGGCGAGU 17 1216 BCL11A-732 - UCGGACCGCAUAGACGA 17 1217 BCL11A-733 - GACGAUGGCACUGUUAA 17 1218 BCL11A-734 - GGCACUGUUAAUGGCCG 17 1219 BCL11A-735 - UGGCCGCGGCUGCUCCC 17 1220 BCL11A-736 - GGCCGCGGCUGCUCCCC 17 1221 BCL11A-737 - CUGCUCCCCGGGCGAGU 17 1222 BCL11A-738 - CCCGGGCGAGUCGGCCU 17 1223 BCL11A-739 - CCGGGCGAGUCGGCCUC 17 1224 BCL11A-740 - CGGGCGAGUCGGCCUCG 17 1225 BCL11A-741 - GGGCGAGUCGGCCUCGG 17 1226 BCL11A-742 - GGCGAGUCGGCCUCGGG 17 1227 BCL11A-743 - GUCCAAAAAGCUGCUGC 17 1228 BCL11A-744 - UCCAAAAAGCUGCUGCU 17 1229 BCL11A-745 - GCGCAUCAAGCUCGAGA 17 1230 BCL11A-746 - GGAGUUCGACCUGCCCC 17 1231 BCL11A-747 - GGCCGCGAUGCCCAACA 17 1232 BCL11A-748 - AGAACGUGUACUCGCAG 17 1233 BCL11A-749 - UACUCGCAGUGGCUCGC 17 1234 BCL11A-750 - GUGGCUCGCCGGCUACG 17 1235 BCL11A-751 - CCGGCUACGCGGCCUCC 17 1236 BCL11A-752 - GAUCCCUUCCUUAGCUU 17 1237 BCL11A-753 - GCCUUUUGCCUCCUCGU 17 1238 BCL11A-754 - CUCGUCGGAGCACUCCU 17 1239 BCL11A-755 - GAGCACUCCUCGGAGAA 17 1240 BCL11A-756 - AGCACUCCUCGGAGAAC 17 1241 BCL11A-757 - CGCUUCUCCACACCGCC 17 1242 BCL11A-758 - GCUUCUCCACACCGCCC 17 1243 BCL11A-759 - CUUCUCCACACCGCCCG 17 1244 BCL11A-760 - CACACCGCCCGGGGAGC 17 1245 BCL11A-761 - CCGCCCGGGGAGCUGGA 17 1246 BCL11A-762 - CCCGGGGAGCUGGACGG 17 1247 BCL11A-763 - CCGGGGAGCUGGACGGA 17 1248 BCL11A-764 - GCUGGACGGAGGGAUCU 17 1249 BCL11A-765 - CUGGACGGAGGGAUCUC 17 1250 BCL11A-766 - UGGACGGAGGGAUCUCG 17 1251 BCL11A-767 - GGGAUCUCGGGGCGCAG 17 1252 BCL11A-768 - CUCGGGGCGCAGCGGCA 17 1253 BCL11A-769 - UCGGGGCGCAGCGGCAC 17 1254 BCL11A-770 - CGCAGCGGCACGGGAAG 17 1255 BCL11A-771 - AGCGGCACGGGAAGUGG 17 1256 BCL11A-772 - GCGGCACGGGAAGUGGA 17 1257 BCL11A-773 - AGCACGCCCCAUAUUAG 17 1258 BCL11A-774 - GCCCCAUAUUAGUGGUC 17 1259 BCL11A-775 - CCCCAUAUUAGUGGUCC 17 1260 BCL11A-776 - UAUUAGUGGUCCGGGCC 17 1261 BCL11A-777 - AUUAGUGGUCCGGGCCC 17 1262 BCL11A-778 - GUGGUCCGGGCCCGGGC 17 1263 BCL11A-779 - CAGGCCCAGCUCAAAAG 17 1264 BCL11A-780 - AGGCCCAGCUCAAAAGA 17 1265 BCL11A-781 + UCUGCCCUCUUUUGAGC 17 1266 BCL11A-782 + CUGCCCUCUUUUGAGCU 17 1267 BCL11A-783 + UUUGAGCUGGGCCUGCC 17 1268 BCL11A-784 + UUGAGCUGGGCCUGCCC 17 1269 BCL11A-785 + CUGGGCCUGCCCGGGCC 17 1270 BCL11A-786 + GGCCCGGACCACUAAUA 17 1271 BCL11A-787 + GCCCGGACCACUAAUAU 17 1272 BCL11A-788 + CCCGGACCACUAAUAUG 17 1273 BCL11A-789 + CCCUCCGUCCAGCUCCC 17 1274 BCL11A-790 + CCUCCGUCCAGCUCCCC 17 1275 BCL11A-791 + CCGUCCAGCUCCCCGGG 17 1276 BCL11A-792 + CAGCUCCCCGGGCGGUG 17 1277 BCL11A-793 + CAAACUCCCGUUCUCCG 17 1278 BCL11A-794 + CGAGGAGUGCUCCGACG 17 1279 BCL11A-795 + GGAGUGCUCCGACGAGG 17 1280 BCL11A-796 + UCCGACGAGGAGGCAAA 17 1281 BCL11A-797 + GGCAAAAGGCGAUUGUC 17 1282 BCL11A-798 + UGGAGUCUCCGAAGCUA 17 1283 BCL11A-799 + GUCUCCGAAGCUAAGGA 17 1284 BCL11A-800 + UCUCCGAAGCUAAGGAA 17 1285 BCL11A-801 + GGGAUCUUUGAGCUGCC 17 1286 BCL11A-802 + AUCUUUGAGCUGCCUGG 17 1287 BCL11A-803 + CCUGGAGGCCGCGUAGC 17 1288 BCL11A-804 + GUACACGUUCUCCGUGU 17 1289 BCL11A-805 + UACACGUUCUCCGUGUU 17 1290 BCL11A-806 + CUCCGUGUUGGGCAUCG 17 1291 BCL11A-807 + GUGUUGGGCAUCGCGGC 17 1292 BCL11A-808 + UGUUGGGCAUCGCGGCC 17 1293 BCL11A-809 + GUUGGGCAUCGCGGCCG 17 1294 BCL11A-810 + UUGGGCAUCGCGGCCGG 17 1295 BCL11A-811 + GCAUCGCGGCCGGGGGC 17 1296 BCL11A-812 + CUUGAUGCGCUUAGAGA 17 1297 BCL11A-813 + UUGAUGCGCUUAGAGAA 17 1298 BCL11A-814 + UGAUGCGCUUAGAGAAG 17 1299 BCL11A-815 + GAAGGGGCUCAGCGAGC 17 1300 BCL11A-816 + AAGGGGCUCAGCGAGCU 17 1301 BCL11A-817 + AGGGGCUCAGCGAGCUG 17 1302 BCL11A-818 + GCCCAGCAGCAGCUUUU 17 1303 BCL11A-819 + GCAGCAGCUUUUUGGAC 17 1304 BCL11A-820 + UUUGGACAGGCCCCCCG 17 1305 BCL11A-821 + CCCGAGGCCGACUCGCC 17 1306 BCL11A-822 + CCGAGGCCGACUCGCCC 17 1307 BCL11A-823 + CGAGGCCGACUCGCCCG 17 1308 BCL11A-824 + CGCCCGGGGAGCAGCCG 17 1309 BCL11A-825 + CAGUGCCAUCGUCUAUG 17 1310 BCL11A-826 + UAUGCGGUCCGACUCGC 17 1311 BCL11A-827 + CGUCGCAAGUGUCCCUG 17 1312 BCL11A-828 + AGUGUCCCUGUGGCCCU 17 1313 BCL11A-829 + CCUGUGGCCCUCGGCCU 17 1314 BCL11A-830 + GGCCCUCGGCCUCGGCC 17 1315 BCL11A-831 + CCUCGGCCUCGGCCAGG 17 1316 BCL11A-832 + GCUUAUGCUUCUCGCCC 17 1317 BCL11A-833 + GCUUCUCGCCCAGGACC 17 1318 BCL11A-834 + UCUCGCCCAGGACCUGG 17 1319 BCL11A-835 + GCCCAGGACCUGGUGGA 17 1320 BCL11A-836 + CUCGCUGAAGUGCUGCA 17 1321 BCL11A-837 + CAUGCCCUGCAUGACGU 17 1322 BCL11A-838 + AUGCCCUGCAUGACGUC 17 1323 BCL11A-839 + CCUGCAUGACGUCGGGC 17 1324 BCL11A-840 + CUGCAUGACGUCGGGCA 17 1325 BCL11A-841 + UGACGUCGGGCAGGGCG 17 1326 BCL11A-842 + CCCGCGAGCUGUUCUCG 17 1327 BCL11A-843 + GCGAGCUGUUCUCGUGG 17 1328 BCL11A-844 + GGUGGCGCGCCGCCUCC 17 1329 BCL11A-845 - CCCAGAGAGCUCAAGAUGUG 20 1330 BCL11A-846 - UCAAGAUGUGUGGCAGUUUU 20 1331 BCL11A-847 - GAUGUGUGGCAGUUUUCGGA 20 1332 BCL11A-848 + GCCACACAUCUUGAGCUCUC 20 1333 BCL11A-849 + CCACACAUCUUGAGCUCUCU 20 1334 BCL11A-850 + UCUCUGGGUACUACGCCGAA 20 1335 BCL11A-851 + CUCUGGGUACUACGCCGAAU 20 1336 BCL11A-852 + UCUGGGUACUACGCCGAAUG 20 1337 BCL11A-853 + CUGGGUACUACGCCGAAUGG 20 1338 BCL11A-854 - CUUCACACACCCCCAUU 17 1339 BCL11A-855 - AGAGAGCUCAAGAUGUG 17 1340 BCL11A-856 - AGAUGUGUGGCAGUUUU 17 1341 BCL11A-857 - GUGUGGCAGUUUUCGGA 17 1342 BCL11A-858 + ACACAUCUUGAGCUCUC 17 1343 BCL11A-859 + CACAUCUUGAGCUCUCU 17 1344 BCL11A-860 + CUGGGUACUACGCCGAA 17 1345 BCL11A-861 + UGGGUACUACGCCGAAU 17 1346 BCL11A-862 + GGGUACUACGCCGAAUG 17 1347 BCL11A-863 + GGUACUACGCCGAAUGG 17 1348

Table 2E provides exemplary targeting domains for knocking out the BCL11A gene. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. aureus Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with a S. aureus Cas9 single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE 2E S. aureus gRNA targets for BCL11A knockout DNA Target Site SEQ ID gRNA Name Strand Targeting Domain Length NO BCL11A-864 - AAACCCCAGCACUUAAGCAA 20 1349 BCL11A-865 - AACCCCAGCACUUAAGCAAA 20 1350 BCL11A-866 - ACCCCAGCACUUAAGCAAAC 20 1351 BCL11A-867 - CCCCAGCACUUAAGCAA 17 1352 BCL11A-868 - CCCAGCACUUAAGCAAA 17 1353 BCL11A-869 - CCAGCACUUAAGCAAAC 17 1354 BCL11A-870 + UGGGGUUUGCCUUGCUUGCG 20 1355 BCL11A-871 + AUUCCCGUUUGCUUAAGUGC 20 1356 BCL11A-872 + AAUUCCCGUUUGCUUAAGUG 20 1357 BCL11A-873 + GGUUUGCCUUGCUUGCG 17 1358 BCL11A-874 + CCCGUUUGCUUAAGUGC 17 1359 BCL11A-875 + UCCCGUUUGCUUAAGUG 17 1360 BCL11A-876 - UGAAGCCAUUCUUACAGAUG 20 1361 BCL11A-877 - AUGAACCAGACCACGGCCCG 20 1362 BCL11A-878 - UGAACCAGACCACGGCCCGU 20 1363 BCL11A-879 - GAACCAGACCACGGCCCGUU 20 1364 BCL11A-880 - CCACGGCCCGUUGGGAGCUC 20 1365 BCL11A-881 - CGGCCCGUUGGGAGCUCCAG 20 1366 BCL11A-882 - GGCCCGUUGGGAGCUCCAGA 20 1367 BCL11A-883 - GCCCGUUGGGAGCUCCAGAA 20 1368 BCL11A-884 - GGAUCAUGACCUCCUCACCU 20 1369 BCL11A-885 - UCACCUGUGGGCAGUGCCAG 20 1370 BCL11A-886 - AGUGCCAGAUGAACUUCCCA 20 1371 BCL11A-887 - GUGCCAGAUGAACUUCCCAU 20 1372 BCL11A-888 - UGCCAGAUGAACUUCCCAUU 20 1373 BCL11A-889 - GCCAGAUGAACUUCCCAUUG 20 1374 BCL11A-890 - GGGGGACAUUCUUAUUUUUA 20 1375 BCL11A-891 - CUUAUUUUUAUCGAGCACAA 20 1376 BCL11A-892 - UUAUUUUUAUCGAGCACAAA 20 1377 BCL11A-893 - AUGCAAUGGCAGCCUCUGCU 20 1378 BCL11A-894 - GCCUCUGCUUAGAAAAAGCU 20 1379 BCL11A-895 - GCCACCUUCCCCUUCACCAA 20 1380 BCL11A-896 - CUUCCCCUUCACCAAUCGAG 20 1381 BCL11A-897 - UGAAAAAAGCAUCCAAUCCC 20 1382 BCL11A-898 - GAAAAAAGCAUCCAAUCCCG 20 1383 BCL11A-899 - GGUUGGCAUCCAGGUCACGC 20 1384 BCL11A-900 - UUGGCAUCCAGGUCACGCCA 20 1385 BCL11A-901 - GAUUGUUUAUCAACGUCAUC 20 1386 BCL11A-902 - UUGUUUAUCAACGUCAUCUA 20 1387 BCL11A-903 - UGUUUAUCAACGUCAUCUAG 20 1388 BCL11A-904 - CUAGAGGAAUUUGCCCCAAA 20 1389 BCL11A-905 - UAGAGGAAUUUGCCCCAAAC 20 1390 BCL11A-906 - AGCCAUUCUUACAGAUG 17 1391 BCL11A-907 - AACCAGACCACGGCCCG 17 1392 BCL11A-908 - ACCAGACCACGGCCCGU 17 1393 BCL11A-909 - CCAGACCACGGCCCGUU 17 1394 BCL11A-910 - CGGCCCGUUGGGAGCUC 17 1395 BCL11A-911 - CCCGUUGGGAGCUCCAG 17 1396 BCL11A-912 - CCGUUGGGAGCUCCAGA 17 1397 BCL11A-913 - CGUUGGGAGCUCCAGAA 17 1398 BCL11A-914 - UCAUGACCUCCUCACCU 17 1399 BCL11A-915 - CCUGUGGGCAGUGCCAG 17 1400 BCL11A-916 - GCCAGAUGAACUUCCCA 17 1401 BCL11A-917 - CCAGAUGAACUUCCCAU 17 1402 BCL11A-918 - CAGAUGAACUUCCCAUU 17 1403 BCL11A-919 - AGAUGAACUUCCCAUUG 17 1404 BCL11A-920 - GGACAUUCUUAUUUUUA 17 1405 BCL11A-921 - AUUUUUAUCGAGCACAA 17 1406 BCL11A-922 - UUUUUAUCGAGCACAAA 17 1407 BCL11A-923 - CAAUGGCAGCCUCUGCU 17 1408 BCL11A-924 - UCUGCUUAGAAAAAGCU 17 1409 BCL11A-925 - ACCUUCCCCUUCACCAA 17 1410 BCL11A-926 - CCCCUUCACCAAUCGAG 17 1411 BCL11A-927 - AAAAAGCAUCCAAUCCC 17 1412 BCL11A-928 - AAAAGCAUCCAAUCCCG 17 1413 BCL11A-929 - UGGCAUCCAGGUCACGC 17 1414 BCL11A-930 - GCAUCCAGGUCACGCCA 17 1415 BCL11A-931 - UGUUUAUCAACGUCAUC 17 1416 BCL11A-932 - UUUAUCAACGUCAUCUA 17 1417 BCL11A-933 - UUAUCAACGUCAUCUAG 17 1418 BCL11A-934 - GAGGAAUUUGCCCCAAA 17 1419 BCL11A-935 - AGGAAUUUGCCCCAAAC 17 1420 BCL11A-936 + UCAUCUGUAAGAAUGGCUUC 20 1421 BCL11A-937 + UGGUCUGGUUCAUCAUCUGU 20 1422 BCL11A-938 + AUCCCCUUCUGGAGCUCCCA 20 1423 BCL11A-939 + AGGAGGUCAUGAUCCCCUUC 20 1424 BCL11A-940 + GAGGAGGUCAUGAUCCCCUU 20 1425 BCL11A-941 + UCUGGCACUGCCCACAGGUG 20 1426 BCL11A-942 + AUCUGGCACUGCCCACAGGU 20 1427 BCL11A-943 + UCAUCUGGCACUGCCCACAG 20 1428 BCL11A-944 + AAAUAAGAAUGUCCCCCAAU 20 1429 BCL11A-945 + AAAAUAAGAAUGUCCCCCAA 20 1430 BCL11A-946 + AAAAAUAAGAAUGUCCCCCA 20 1431 BCL11A-947 + CGUUUGUGCUCGAUAAAAAU 20 1432 BCL11A-948 + UAUCCACAGCUUUUUCUAAG 20 1433 BCL11A-949 + UUUCAUCUCGAUUGGUGAAG 20 1434 BCL11A-950 + UUUUCAUCUCGAUUGGUGAA 20 1435 BCL11A-951 + UUUUUCAUCUCGAUUGGUGA 20 1436 BCL11A-952 + UUUUUUCAUCUCGAUUGGUG 20 1437 BCL11A-953 + UGCUUUUUUCAUCUCGAUUG 20 1438 BCL11A-954 + GGAUGCCAACCUCCACGGGA 20 1439 BCL11A-955 + GACCUGGAUGCCAACCUCCA 20 1440 BCL11A-956 + UGACCUGGAUGCCAACCUCC 20 1441 BCL11A-957 + UCGUCAUCCUCUGGCGUGAC 20 1442 BCL11A-958 + CUGCUAUGUGUUCCUGUUUG 20 1443 BCL11A-959 + CUGCUAUGUGUUCCUGUUUG 20 1444 BCL11A-960 + UCUGUAAGAAUGGCUUC 17 1445 BCL11A-961 + UCUGGUUCAUCAUCUGU 17 1446 BCL11A-962 + CCCUUCUGGAGCUCCCA 17 1447 BCL11A-963 + AGGUCAUGAUCCCCUUC 17 1448 BCL11A-964 + GAGGUCAUGAUCCCCUU 17 1449 BCL11A-965 + GGCACUGCCCACAGGUG 17 1450 BCL11A-966 + UGGCACUGCCCACAGGU 17 1451 BCL11A-967 + UCUGGCACUGCCCACAG 17 1452 BCL11A-968 + UAAGAAUGUCCCCCAAU 17 1453 BCL11A-969 + AUAAGAAUGUCCCCCAA 17 1454 BCL11A-970 + AAUAAGAAUGUCCCCCA 17 1455 BCL11A-971 + UUGUGCUCGAUAAAAAU 17 1456 BCL11A-972 + CCACAGCUUUUUCUAAG 17 1457 BCL11A-973 + CAUCUCGAUUGGUGAAG 17 1458 BCL11A-974 + UCAUCUCGAUUGGUGAA 17 1459 BCL11A-975 + UUCAUCUCGAUUGGUGA 17 1460 BCL11A-976 + UUUCAUCUCGAUUGGUG 17 1461 BCL11A-977 + UUUUUUCAUCUCGAUUG 17 1462 BCL11A-978 + UGCCAACCUCCACGGGA 17 1463 BCL11A-979 + CUGGAUGCCAACCUCCA 17 1464 BCL11A-980 + CCUGGAUGCCAACCUCC 17 1465 BCL11A-981 + UCAUCCUCUGGCGUGAC 17 1466 BCL11A-982 + UGCUAUGUGUUCCUGUU 17 1467 BCL11A-983 + CUGCUAUGUGUUCCUGU 17 1468 BCL11A-984 - CUCCUCCCCUCGUUCUGCAC 20 1469 BCL11A-985 - UCCUCCCCUCGUUCUGCACA 20 1470 BCL11A-986 - UGGAGCUCUAAUCCCCACGC 20 1471 BCL11A-987 - GGAGCUCUAAUCCCCACGCC 20 1472 BCL11A-988 - CUCUAAUCCCCACGCCUGGG 20 1473 BCL11A-989 - CCCCACGCCUGGGAUGAGUG 20 1474 BCL11A-990 - UGAGUGCAGAAUAUGCCCCG 20 1475 BCL11A-991 - CUCCCCUCGUUCUGCAC 17 1476 BCL11A-992 - UCCCCUCGUUCUGCACA 17 1477 BCL11A-993 - AGCUCUAAUCCCCACGC 17 1478 BCL11A-994 - GCUCUAAUCCCCACGCC 17 1479 BCL11A-995 - UAAUCCCCACGCCUGGG 17 1480 BCL11A-996 - CACGCCUGGGAUGAGUG 17 1481 BCL11A-997 - GUGCAGAAUAUGCCCCG 17 1482 BCL11A-998 + GAGGAGAGGCCCCUCCAGUG 20 1483 BCL11A-999 + CAUGUGCAGAACGAGGGGAG 20 1484 BCL11A-1000 + UCCAUGUGCAGAACGAGGGG 20 1485 BCL11A-1001 + CUCCAUGUGCAGAACGAGGG 20 1486 BCL11A-1002 + AGCUCCAUGUGCAGAACGAG 20 1487 BCL11A-1003 + GAGCUCCAUGUGCAGAACGA 20 1488 BCL11A-1004 + AGAGCUCCAUGUGCAGAACG 20 1489 BCL11A-1005 + UAGAGCUCCAUGUGCAGAAC 20 1490 BCL11A-1006 + AUUAGAGCUCCAUGUGCAGA 20 1491 BCL11A-1007 + GGGGAUUAGAGCUCCAUGUG 20 1492 BCL11A-1008 + CUCAUCCCAGGCGUGGGGAU 20 1493 BCL11A-1009 + UCUGCACUCAUCCCAGGCGU 20 1494 BCL11A-1010 + UUCUGCACUCAUCCCAGGCG 20 1495 BCL11A-1011 + AUUCUGCACUCAUCCCAGGC 20 1496 BCL11A-1012 + GAGAGGCCCCUCCAGUG 17 1497 BCL11A-1013 + GUGCAGAACGAGGGGAG 17 1498 BCL11A-1014 + AUGUGCAGAACGAGGGG 17 1499 BCL11A-1015 + CAUGUGCAGAACGAGGG 17 1500 BCL11A-1016 + UCCAUGUGCAGAACGAG 17 1501 BCL11A-1017 + CUCCAUGUGCAGAACGA 17 1502 BCL11A-1018 + GCUCCAUGUGCAGAACG 17 1503 BCL11A-1019 + AGCUCCAUGUGCAGAAC 17 1504 BCL11A-1020 + AGAGCUCCAUGUGCAGA 17 1505 BCL11A-1021 + GAUUAGAGCUCCAUGUG 17 1506 BCL11A-1022 + AUCCCAGGCGUGGGGAU 17 1507 BCL11A-1023 + GCACUCAUCCCAGGCGU 17 1508 BCL11A-1024 + UGCACUCAUCCCAGGCG 17 1509 BCL11A-1025 + CUGCACUCAUCCCAGGC 17 1510 BCL11A-1026 - GGUUUCUCUUGCAACACGCA 20 1511 BCL11A-1027 - GCAACACGCACAGAACACUC 20 1512 BCL11A-1028 - GCACAGAACACUCAUGGAUU 20 1513 BCL11A-1029 - UCAUGGAUUAAGAAUCUACU 20 1514 BCL11A-1030 - AUUAAGAAUCUACUUAGAAA 20 1515 BCL11A-1031 - AAUCUACUUAGAAAGCGAAC 20 1516 BCL11A-1032 - AUCUACUUAGAAAGCGAACA 20 1517 BCL11A-1033 - CACGGAAGUCCCCUGACCCC 20 1518 BCL11A-1034 - CCCGCGGGUUGGUAUCCCUU 20 1519 BCL11A-1035 - UAUCCCUUCAGGACUAGGUG 20 1520 BCL11A-1036 - UCCUUCCCAGCCACCUCUCC 20 1521 BCL11A-1037 - CCUUCCCAGCCACCUCUCCA 20 1522 BCL11A-1038 - AAUAACCCCUUUAACCUGCU 20 1523 BCL11A-1039 - CUUUAACCUGCUAAGAAUAC 20 1524 BCL11A-1040 - UAAGAAUACCAGGAUCAGUA 20 1525 BCL11A-1041 - AGAAUACCAGGAUCAGUAUC 20 1526 BCL11A-1042 - AAUACCAGGAUCAGUAUCGA 20 1527 BCL11A-1043 - GAGAGAGGCUUCCGGCCUGG 20 1528 BCL11A-1044 - AGAGGCUUCCGGCCUGGCAG 20 1529 BCL11A-1045 - CCCCCCUGUUUAGUCCACCA 20 1530 BCL11A-1046 - GUCCACCACCGAGACAUCAC 20 1531 BCL11A-1047 - UCACUUGGACCCCCACCGCA 20 1532 BCL11A-1048 - ACCCCCACCGCAUAGAGCGC 20 1533 BCL11A-1049 - CCCCCACCGCAUAGAGCGCC 20 1534 BCL11A-1050 - CCCCACCGCAUAGAGCGCCU 20 1535 BCL11A-1051 - ACCGCAUAGAGCGCCUGGGG 20 1536 BCL11A-1052 - CCGCAUAGAGCGCCUGGGGG 20 1537 BCL11A-1053 - CAUAGAGCGCCUGGGGGCGG 20 1538 BCL11A-1054 - UGGCCCUGGCCACCCAUCAC 20 1539 BCL11A-1055 - CAUCACCCGAGUGCCUUUGA 20 1540 BCL11A-1056 - CCUUUGACAGGGUGCUGCGG 20 1541 BCL11A-1057 - UGCGGUUGAAUCCAAUGGCU 20 1542 BCL11A-1058 - GCGGUUGAAUCCAAUGGCUA 20 1543 BCL11A-1059 - UGGCUAUGGAGCCUCCCGCC 20 1544 BCL11A-1060 - CCUCCCGCCAUGGAUUUCUC 20 1545 BCL11A-1061 - CUCCCGCCAUGGAUUUCUCU 20 1546 BCL11A-1062 - AUGGAUUUCUCUAGGAGACU 20 1547 BCL11A-1063 - GGAUUUCUCUAGGAGACUUA 20 1548 BCL11A-1064 - UAGGAGACUUAGAGAGCUGG 20 1549 BCL11A-1065 - AGGAGACUUAGAGAGCUGGC 20 1550 BCL11A-1066 - GGAGACUUAGAGAGCUGGCA 20 1551 BCL11A-1067 - CCCGGUCAAGUCCAAGUCAU 20 1552 BCL11A-1068 - GCGGCAAGACGUUCAAAUUU 20 1553 BCL11A-1069 - UGGUGCACCGGCGCAGCCAC 20 1554 BCL11A-1070 - GCACCGGCGCAGCCACACGG 20 1555 BCL11A-1071 - ACCGGCGCAGCCACACGGGC 20 1556 BCL11A-1072 - CGUGCACCCAGGCCAGCAAG 20 1557 BCL11A-1073 - CCAGCAAGCUGAAGCGCCAC 20 1558 BCL11A-1074 - GUCUCUCCACCGCCAGCUCC 20 1559 BCL11A-1075 - UCUCUCCACCGCCAGCUCCC 20 1560 BCL11A-1076 - AACCCGGCACCAGCGACUUG 20 1561 BCL11A-1077 - AGUCCGUGGUGGCCAAGUUC 20 1562 BCL11A-1078 - CGUGGUGGCCAAGUUCAAGA 20 1563 BCL11A-1079 - UGGUGGCCAAGUUCAAGAGC 20 1564 BCL11A-1080 - AGAACGACCCCAACCUGAUC 20 1565 BCL11A-1081 - GAACGACCCCAACCUGAUCC 20 1566 BCL11A-1082 - ACGACCCCAACCUGAUCCCG 20 1567 BCL11A-1083 - CCCCAACCUGAUCCCGGAGA 20 1568 BCL11A-1084 - CCCAACCUGAUCCCGGAGAA 20 1569 BCL11A-1085 - CCAACCUGAUCCCGGAGAAC 20 1570 BCL11A-1086 - CCUGAUCCCGGAGAACGGGG 20 1571 BCL11A-1087 - UGAUCCCGGAGAACGGGGAC 20 1572 BCL11A-1088 - GAUCCCGGAGAACGGGGACG 20 1573 BCL11A-1089 - UCCCGGAGAACGGGGACGAG 20 1574 BCL11A-1090 - CCCGGAGAACGGGGACGAGG 20 1575 BCL11A-1091 - GGAGAACGGGGACGAGGAGG 20 1576 BCL11A-1092 - AGAACGGGGACGAGGAGGAA 20 1577 BCL11A-1093 - GAACGGGGACGAGGAGGAAG 20 1578 BCL11A-1094 - ACGGGGACGAGGAGGAAGAG 20 1579 BCL11A-1095 - CGAGGAGGAAGAGGAGGACG 20 1580 BCL11A-1096 - AGGAGGAAGAGGAGGACGAC 20 1581 BCL11A-1097 - GGAGGAAGAGGAGGACGACG 20 1582 BCL11A-1098 - GGAAGAGGAGGACGACGAGG 20 1583 BCL11A-1099 - AAGAGGAGGACGACGAGGAA 20 1584 BCL11A-1100 - AGAGGAGGACGACGAGGAAG 20 1585 BCL11A-1101 - GGAGGACGACGAGGAAGAGG 20 1586 BCL11A-1102 - GGACGACGAGGAAGAGGAAG 20 1587 BCL11A-1103 - ACGACGAGGAAGAGGAAGAA 20 1588 BCL11A-1104 - CGACGAGGAAGAGGAAGAAG 20 1589 BCL11A-1105 - ACGAGGAAGAGGAAGAAGAG 20 1590 BCL11A-1106 - CGAGGAAGAGGAAGAAGAGG 20 1591 BCL11A-1107 - GGAAGAGGAAGAAGAGGAGG 20 1592 BCL11A-1108 - AAGAGGAAGAAGAGGAGGAA 20 1593 BCL11A-1109 - AGAGGAAGAAGAGGAGGAAG 20 1594 BCL11A-1110 - AGGAAGAAGAGGAGGAAGAG 20 1595 BCL11A-1111 - GGAAGAAGAGGAGGAAGAGG 20 1596 BCL11A-1112 - AAGAAGAGGAGGAAGAGGAG 20 1597 BCL11A-1113 - AGAAGAGGAGGAAGAGGAGG 20 1598 BCL11A-1114 - AAGAGGAGGAAGAGGAGGAG 20 1599 BCL11A-1115 - AGAGGAGGAAGAGGAGGAGG 20 1600 BCL11A-1116 - AAGAGGAGGAGGAGGAGCUG 20 1601 BCL11A-1117 - AGAGGAGGAGGAGGAGCUGA 20 1602 BCL11A-1118 - AGGAGGAGGAGGAGCUGACG 20 1603 BCL11A-1119 - GGAGGAGGAGCUGACGGAGA 20 1604 BCL11A-1120 - AGGAGGAGCUGACGGAGAGC 20 1605 BCL11A-1121 - GAGGAGCUGACGGAGAGCGA 20 1606 BCL11A-1122 - AGCUGACGGAGAGCGAGAGG 20 1607 BCL11A-1123 - CGAGAGGGUGGACUACGGCU 20 1608 BCL11A-1124 - GGGUGGACUACGGCUUCGGG 20 1609 BCL11A-1125 - ACUACGGCUUCGGGCUGAGC 20 1610 BCL11A-1126 - CUACGGCUUCGGGCUGAGCC 20 1611 BCL11A-1127 - CCUGGAGGCGGCGCGCCACC 20 1612 BCL11A-1128 - UGGAGGCGGCGCGCCACCAC 20 1613 BCL11A-1129 - CGCCACCACGAGAACAGCUC 20 1614 BCL11A-1130 - GCCACCACGAGAACAGCUCG 20 1615 BCL11A-1131 - ACAGCUCGCGGGGCGCGGUC 20 1616 BCL11A-1132 - CGCGGGGCGCGGUCGUGGGC 20 1617 BCL11A-1133 - CGCGGUCGUGGGCGUGGGCG 20 1618 BCL11A-1134 - CGGUCGUGGGCGUGGGCGAC 20 1619 BCL11A-1135 - GCGCCCUGCCCGACGUCAUG 20 1620 BCL11A-1136 - CAGCUCCAUGCAGCACUUCA 20 1621 BCL11A-1137 - GCGAGGCCUUCCACCAGGUC 20 1622 BCL11A-1138 - GGCCUUCCACCAGGUCCUGG 20 1623 BCL11A-1139 - CCUUCCACCAGGUCCUGGGC 20 1624 BCL11A-1140 - GCAUAAGCGCGGCCACCUGG 20 1625 BCL11A-1141 - GCGCGGCCACCUGGCCGAGG 20 1626 BCL11A-1142 - GCGGCCACCUGGCCGAGGCC 20 1627 BCL11A-1143 - CUGGCCGAGGCCGAGGGCCA 20 1628 BCL11A-1144 - UGGCCGAGGCCGAGGGCCAC 20 1629 BCL11A-1145 - GGGCCACAGGGACACUUGCG 20 1630 BCL11A-1146 - CGACGAAGACUCGGUGGCCG 20 1631 BCL11A-1147 - AAGACUCGGUGGCCGGCGAG 20 1632 BCL11A-1148 - UUAAUGGCCGCGGCUGCUCC 20 1633 BCL11A-1149 - UGGCCGCGGCUGCUCCCCGG 20 1634 BCL11A-1150 - GCUCCCCGGGCGAGUCGGCC 20 1635 BCL11A-1151 - CUCCCCGGGCGAGUCGGCCU 20 1636 BCL11A-1152 - UCCCCGGGCGAGUCGGCCUC 20 1637 BCL11A-1153 - CCCCGGGCGAGUCGGCCUCG 20 1638 BCL11A-1154 - GCCUGUCCAAAAAGCUGCUG 20 1639 BCL11A-1155 - UGCUGGGCAGCCCCAGCUCG 20 1640 BCL11A-1156 - CUUCUCUAAGCGCAUCAAGC 20 1641 BCL11A-1157 - UCUCUAAGCGCAUCAAGCUC 20 1642 BCL11A-1158 - CUAAGCGCAUCAAGCUCGAG 20 1643 BCL11A-1159 - UAAGCGCAUCAAGCUCGAGA 20 1644 BCL11A-1160 - CCCCGGCCGCGAUGCCCAAC 20 1645 BCL11A-1161 - CCCGGCCGCGAUGCCCAACA 20 1646 BCL11A-1162 - CGGCCGCGAUGCCCAACACG 20 1647 BCL11A-1163 - CAAAGAUCCCUUCCUUAGCU 20 1648 BCL11A-1164 - AAAGAUCCCUUCCUUAGCUU 20 1649 BCL11A-1165 - AAUCGCCUUUUGCCUCCUCG 20 1650 BCL11A-1166 - AUCGCCUUUUGCCUCCUCGU 20 1651 BCL11A-1167 - CCUCCUCGUCGGAGCACUCC 20 1652 BCL11A-1168 - CUCCUCGUCGGAGCACUCCU 20 1653 BCL11A-1169 - CCUCGUCGGAGCACUCCUCG 20 1654 BCL11A-1170 - GUCGGAGCACUCCUCGGAGA 20 1655 BCL11A-1171 - UCGGAGCACUCCUCGGAGAA 20 1656 BCL11A-1172 - CGGAGCACUCCUCGGAGAAC 20 1657 BCL11A-1173 - UUUGCGCUUCUCCACACCGC 20 1658 BCL11A-1174 - UUGCGCUUCUCCACACCGCC 20 1659 BCL11A-1175 - UGCGCUUCUCCACACCGCCC 20 1660 BCL11A-1176 - GCGCUUCUCCACACCGCCCG 20 1661 BCL11A-1177 - UCUCCACACCGCCCGGGGAG 20 1662 BCL11A-1178 - CACACCGCCCGGGGAGCUGG 20 1663 BCL11A-1179 - ACACCGCCCGGGGAGCUGGA 20 1664 BCL11A-1180 - ACCGCCCGGGGAGCUGGACG 20 1665 BCL11A-1181 - CCGCCCGGGGAGCUGGACGG 20 1666 BCL11A-1182 - GGGAGCUGGACGGAGGGAUC 20 1667 BCL11A-1183 - GGAGCUGGACGGAGGGAUCU 20 1668 BCL11A-1184 - GGAUCUCGGGGCGCAGCGGC 20 1669 BCL11A-1185 - GAUCUCGGGGCGCAGCGGCA 20 1670 BCL11A-1186 - AUCUCGGGGCGCAGCGGCAC 20 1671 BCL11A-1187 - GGGGCGCAGCGGCACGGGAA 20 1672 BCL11A-1188 - GGGCGCAGCGGCACGGGAAG 20 1673 BCL11A-1189 - GCGCAGCGGCACGGGAAGUG 20 1674 BCL11A-1190 - CGCAGCGGCACGGGAAGUGG 20 1675 BCL11A-1191 - GCAGCGGCACGGGAAGUGGA 20 1676 BCL11A-1192 - GCACGCCCCAUAUUAGUGGU 20 1677 BCL11A-1193 - CCCAUAUUAGUGGUCCGGGC 20 1678 BCL11A-1194 - CCCGGGCAGGCCCAGCUCAA 20 1679 BCL11A-1195 - CGGGCAGGCCCAGCUCAAAA 20 1680 BCL11A-1196 - UUCUCUUGCAACACGCA 17 1681 BCL11A-1197 - ACACGCACAGAACACUC 17 1682 BCL11A-1198 - CAGAACACUCAUGGAUU 17 1683 BCL11A-1199 - UGGAUUAAGAAUCUACU 17 1684 BCL11A-1200 - AAGAAUCUACUUAGAAA 17 1685 BCL11A-1201 - CUACUUAGAAAGCGAAC 17 1686 BCL11A-1202 - UACUUAGAAAGCGAACA 17 1687 BCL11A-1203 - GGAAGUCCCCUGACCCC 17 1688 BCL11A-1204 - GCGGGUUGGUAUCCCUU 17 1689 BCL11A-1205 - CCCUUCAGGACUAGGUG 17 1690 BCL11A-1206 - UUCCCAGCCACCUCUCC 17 1691 BCL11A-1207 - UCCCAGCCACCUCUCCA 17 1692 BCL11A-1208 - AACCCCUUUAACCUGCU 17 1693 BCL11A-1209 - UAACCUGCUAAGAAUAC 17 1694 BCL11A-1210 - GAAUACCAGGAUCAGUA 17 1695 BCL11A-1211 - AUACCAGGAUCAGUAUC 17 1696 BCL11A-1212 - ACCAGGAUCAGUAUCGA 17 1697 BCL11A-1213 - AGAGGCUUCCGGCCUGG 17 1698 BCL11A-1214 - GGCUUCCGGCCUGGCAG 17 1699 BCL11A-1215 - CCCUGUUUAGUCCACCA 17 1700 BCL11A-1216 - CACCACCGAGACAUCAC 17 1701 BCL11A-1217 - CUUGGACCCCCACCGCA 17 1702 BCL11A-1218 - CCCACCGCAUAGAGCGC 17 1703 BCL11A-1219 - CCACCGCAUAGAGCGCC 17 1704 BCL11A-1220 - CACCGCAUAGAGCGCCU 17 1705 BCL11A-1221 - GCAUAGAGCGCCUGGGG 17 1706 BCL11A-1222 - CAUAGAGCGCCUGGGGG 17 1707 BCL11A-1223 - AGAGCGCCUGGGGGCGG 17 1708 BCL11A-1224 - CCCUGGCCACCCAUCAC 17 1709 BCL11A-1225 - CACCCGAGUGCCUUUGA 17 1710 BCL11A-1226 - UUGACAGGGUGCUGCGG 17 1711 BCL11A-1227 - GGUUGAAUCCAAUGGCU 17 1712 BCL11A-1228 - GUUGAAUCCAAUGGCUA 17 1713 BCL11A-1229 - CUAUGGAGCCUCCCGCC 17 1714 BCL11A-1230 - CCCGCCAUGGAUUUCUC 17 1715 BCL11A-1231 - CCGCCAUGGAUUUCUCU 17 1716 BCL11A-1232 - GAUUUCUCUAGGAGACU 17 1717 BCL11A-1233 - UUUCUCUAGGAGACUUA 17 1718 BCL11A-1234 - GAGACUUAGAGAGCUGG 17 1719 BCL11A-1235 - AGACUUAGAGAGCUGGC 17 1720 BCL11A-1236 - GACUUAGAGAGCUGGCA 17 1721 BCL11A-1237 - GGUCAAGUCCAAGUCAU 17 1722 BCL11A-1238 - GCAAGACGUUCAAAUUU 17 1723 BCL11A-1239 - UGCACCGGCGCAGCCAC 17 1724 BCL11A-1240 - CCGGCGCAGCCACACGG 17 1725 BCL11A-1241 - GGCGCAGCCACACGGGC 17 1726 BCL11A-1242 - GCACCCAGGCCAGCAAG 17 1727 BCL11A-1243 - GCAAGCUGAAGCGCCAC 17 1728 BCL11A-1244 - UCUCCACCGCCAGCUCC 17 1729 BCL11A-1245 - CUCCACCGCCAGCUCCC 17 1730 BCL11A-1246 - CCGGCACCAGCGACUUG 17 1731 BCL11A-1247 - CCGUGGUGGCCAAGUUC 17 1732 BCL11A-1248 - GGUGGCCAAGUUCAAGA 17 1733 BCL11A-1249 - UGGCCAAGUUCAAGAGC 17 1734 BCL11A-1250 - ACGACCCCAACCUGAUC 17 1735 BCL11A-1251 - CGACCCCAACCUGAUCC 17 1736 BCL11A-1252 - ACCCCAACCUGAUCCCG 17 1737 BCL11A-1253 - CAACCUGAUCCCGGAGA 17 1738 BCL11A-1254 - AACCUGAUCCCGGAGAA 17 1739 BCL11A-1255 - ACCUGAUCCCGGAGAAC 17 1740 BCL11A-1256 - GAUCCCGGAGAACGGGG 17 1741 BCL11A-1257 - UCCCGGAGAACGGGGAC 17 1742 BCL11A-1258 - CCCGGAGAACGGGGACG 17 1743 BCL11A-1259 - CGGAGAACGGGGACGAG 17 1744 BCL11A-1260 - GGAGAACGGGGACGAGG 17 1745 BCL11A-1261 - GAACGGGGACGAGGAGG 17 1746 BCL11A-1262 - ACGGGGACGAGGAGGAA 17 1747 BCL11A-1263 - CGGGGACGAGGAGGAAG 17 1748 BCL11A-1264 - GGGACGAGGAGGAAGAG 17 1749 BCL11A-1265 - GGAGGAAGAGGAGGACG 17 1750 BCL11A-1266 - AGGAAGAGGAGGACGAC 17 1751 BCL11A-1267 - GGAAGAGGAGGACGACG 17 1752 BCL11A-1268 - AGAGGAGGACGACGAGG 17 1753 BCL11A-1269 - AGGAGGACGACGAGGAA 17 1754 BCL11A-1270 - GGAGGACGACGAGGAAG 17 1755 BCL11A-1271 - GGACGACGAGGAAGAGG 17 1756 BCL11A-1272 - CGACGAGGAAGAGGAAG 17 1757 BCL11A-1273 - ACGAGGAAGAGGAAGAA 17 1758 BCL11A-1274 - CGAGGAAGAGGAAGAAG 17 1759 BCL11A-1275 - AGGAAGAGGAAGAAGAG 17 1760 BCL11A-1276 - GGAAGAGGAAGAAGAGG 17 1761 BCL11A-1277 - AGAGGAAGAAGAGGAGG 17 1762 BCL11A-1278 - AGGAAGAAGAGGAGGAA 17 1763 BCL11A-1279 - GGAAGAAGAGGAGGAAG 17 1764 BCL11A-1280 - AAGAAGAGGAGGAAGAG 17 1765 BCL11A-1281 - AGAAGAGGAGGAAGAGG 17 1766 BCL11A-1282 - AAGAGGAGGAAGAGGAG 17 1767 BCL11A-1283 - AGAGGAGGAAGAGGAGG 17 1768 BCL11A-1284 - AGGAGGAAGAGGAGGAG 17 1769 BCL11A-1285 - GGAGGAAGAGGAGGAGG 17 1770 BCL11A-1286 - AGGAGGAGGAGGAGCUG 17 1771 BCL11A-1287 - GGAGGAGGAGGAGCUGA 17 1772 BCL11A-1288 - AGGAGGAGGAGCUGACG 17 1773 BCL11A-1289 - GGAGGAGCUGACGGAGA 17 1774 BCL11A-1290 - AGGAGCUGACGGAGAGC 17 1775 BCL11A-1291 - GAGCUGACGGAGAGCGA 17 1776 BCL11A-1292 - UGACGGAGAGCGAGAGG 17 1777 BCL11A-1293 - GAGGGUGGACUACGGCU 17 1778 BCL11A-1294 - UGGACUACGGCUUCGGG 17 1779 BCL11A-1295 - ACGGCUUCGGGCUGAGC 17 1780 BCL11A-1296 - CGGCUUCGGGCUGAGCC 17 1781 BCL11A-1297 - GGAGGCGGCGCGCCACC 17 1782 BCL11A-1298 - AGGCGGCGCGCCACCAC 17 1783 BCL11A-1299 - CACCACGAGAACAGCUC 17 1784 BCL11A-1300 - ACCACGAGAACAGCUCG 17 1785 BCL11A-1301 - GCUCGCGGGGCGCGGUC 17 1786 BCL11A-1302 - GGGGCGCGGUCGUGGGC 17 1787 BCL11A-1303 - GGUCGUGGGCGUGGGCG 17 1788 BCL11A-1304 - UCGUGGGCGUGGGCGAC 17 1789 BCL11A-1305 - CCCUGCCCGACGUCAUG 17 1790 BCL11A-1306 - CUCCAUGCAGCACUUCA 17 1791 BCL11A-1307 - AGGCCUUCCACCAGGUC 17 1792 BCL11A-1308 - CUUCCACCAGGUCCUGG 17 1793 BCL11A-1309 - UCCACCAGGUCCUGGGC 17 1794 BCL11A-1310 - UAAGCGCGGCCACCUGG 17 1795 BCL11A-1311 - CGGCCACCUGGCCGAGG 17 1796 BCL11A-1312 - GCCACCUGGCCGAGGCC 17 1797 BCL11A-1313 - GCCGAGGCCGAGGGCCA 17 1798 BCL11A-1314 - CCGAGGCCGAGGGCCAC 17 1799 BCL11A-1315 - CCACAGGGACACUUGCG 17 1800 BCL11A-1316 - CGAAGACUCGGUGGCCG 17 1801 BCL11A-1317 - ACUCGGUGGCCGGCGAG 17 1802 BCL11A-1318 - AUGGCCGCGGCUGCUCC 17 1803 BCL11A-1319 - CCGCGGCUGCUCCCCGG 17 1804 BCL11A-1320 - CCCCGGGCGAGUCGGCC 17 1805 BCL11A-1321 - CCCGGGCGAGUCGGCCU 17 1806 BCL11A-1322 - CCGGGCGAGUCGGCCUC 17 1807 BCL11A-1323 - CGGGCGAGUCGGCCUCG 17 1808 BCL11A-1324 - UGUCCAAAAAGCUGCUG 17 1809 BCL11A-1325 - UGGGCAGCCCCAGCUCG 17 1810 BCL11A-1326 - CUCUAAGCGCAUCAAGC 17 1811 BCL11A-1327 - CUAAGCGCAUCAAGCUC 17 1812 BCL11A-1328 - AGCGCAUCAAGCUCGAG 17 1813 BCL11A-1329 - GCGCAUCAAGCUCGAGA 17 1814 BCL11A-1330 - CGGCCGCGAUGCCCAAC 17 1815 BCL11A-1331 - GGCCGCGAUGCCCAACA 17 1816 BCL11A-1332 - CCGCGAUGCCCAACACG 17 1817 BCL11A-1333 - AGAUCCCUUCCUUAGCU 17 1818 BCL11A-1334 - GAUCCCUUCCUUAGCUU 17 1819 BCL11A-1335 - CGCCUUUUGCCUCCUCG 17 1820 BCL11A-1336 - GCCUUUUGCCUCCUCGU 17 1821 BCL11A-1337 - CCUCGUCGGAGCACUCC 17 1822 BCL11A-1338 - CUCGUCGGAGCACUCCU 17 1823 BCL11A-1339 - CGUCGGAGCACUCCUCG 17 1824 BCL11A-1340 - GGAGCACUCCUCGGAGA 17 1825 BCL11A-1341 - GAGCACUCCUCGGAGAA 17 1826 BCL11A-1342 - AGCACUCCUCGGAGAAC 17 1827 BCL11A-1343 - GCGCUUCUCCACACCGC 17 1828 BCL11A-1344 - CGCUUCUCCACACCGCC 17 1829 BCL11A-1345 - GCUUCUCCACACCGCCC 17 1830 BCL11A-1346 - CUUCUCCACACCGCCCG 17 1831 BCL11A-1347 - CCACACCGCCCGGGGAG 17 1832 BCL11A-1348 - ACCGCCCGGGGAGCUGG 17 1833 BCL11A-1349 - CCGCCCGGGGAGCUGGA 17 1834 BCL11A-1350 - GCCCGGGGAGCUGGACG 17 1835 BCL11A-1351 - CCCGGGGAGCUGGACGG 17 1836 BCL11A-1352 - AGCUGGACGGAGGGAUC 17 1837 BCL11A-1353 - GCUGGACGGAGGGAUCU 17 1838 BCL11A-1354 - UCUCGGGGCGCAGCGGC 17 1839 BCL11A-1355 - CUCGGGGCGCAGCGGCA 17 1840 BCL11A-1356 - UCGGGGCGCAGCGGCAC 17 1841 BCL11A-1357 - GCGCAGCGGCACGGGAA 17 1842 BCL11A-1358 - CGCAGCGGCACGGGAAG 17 1843 BCL11A-1359 - CAGCGGCACGGGAAGUG 17 1844 BCL11A-1360 - AGCGGCACGGGAAGUGG 17 1845 BCL11A-1361 - GCGGCACGGGAAGUGGA 17 1846 BCL11A-1362 - CGCCCCAUAUUAGUGGU 17 1847 BCL11A-1363 - AUAUUAGUGGUCCGGGC 17 1848 BCL11A-1364 - GGGCAGGCCCAGCUCAA 17 1849 BCL11A-1365 - GCAGGCCCAGCUCAAAA 17 1850 BCL11A-1366 + AAGUUGUACAUGUGUAGCUG 20 1851 BCL11A-1367 + GCAAGAGAAACCAUGCACUG 20 1852 BCL11A-1368 + GUGUUCUGUGCGUGUUGCAA 20 1853 BCL11A-1369 + GAGUGUUCUGUGCGUGUUGC 20 1854 BCL11A-1370 + UCUAAGUAGAUUCUUAAUCC 20 1855 BCL11A-1371 + GAUACCAACCCGCGGGGUCA 20 1856 BCL11A-1372 + GGAUACCAACCCGCGGGGUC 20 1857 BCL11A-1373 + GGGAUACCAACCCGCGGGGU 20 1858 BCL11A-1374 + CCUGAAGGGAUACCAACCCG 20 1859 BCL11A-1375 + UCCUGAAGGGAUACCAACCC 20 1860 BCL11A-1376 + CAUUCUGCACCUAGUCCUGA 20 1861 BCL11A-1377 + ACAUUCUGCACCUAGUCCUG 20 1862 BCL11A-1378 + AGGACAUUCUGCACCUAGUC 20 1863 BCL11A-1379 + CCCAUGGAGAGGUGGCUGGG 20 1864 BCL11A-1380 + AAUCCCAUGGAGAGGUGGCU 20 1865 BCL11A-1381 + GAAUCCCAUGGAGAGGUGGC 20 1866 BCL11A-1382 + UGAAUCCCAUGGAGAGGUGG 20 1867 BCL11A-1383 + UCUGCAAUAUGAAUCCCAUG 20 1868 BCL11A-1384 + UGUCUGCAAUAUGAAUCCCA 20 1869 BCL11A-1385 + UUGUCUGCAAUAUGAAUCCC 20 1870 BCL11A-1386 + AAGGGGUUAUUGUCUGCAAU 20 1871 BCL11A-1387 + UGGUAUUCUUAGCAGGUUAA 20 1872 BCL11A-1388 + CUGGUAUUCUUAGCAGGUUA 20 1873 BCL11A-1389 + AAAGCGCCCUUCUGCCAGGC 20 1874 BCL11A-1390 + GAAAGCGCCCUUCUGCCAGG 20 1875 BCL11A-1391 + CUAAACAGGGGGGGAGUGGG 20 1876 BCL11A-1392 + ACUAAACAGGGGGGGAGUGG 20 1877 BCL11A-1393 + GUGGACUAAACAGGGGGGGA 20 1878 BCL11A-1394 + GGUGGUGGACUAAACAGGGG 20 1879 BCL11A-1395 + CGGUGGUGGACUAAACAGGG 20 1880 BCL11A-1396 + UCGGUGGUGGACUAAACAGG 20 1881 BCL11A-1397 + CUCGGUGGUGGACUAAACAG 20 1882 BCL11A-1398 + UCUCGGUGGUGGACUAAACA 20 1883 BCL11A-1399 + GUCUCGGUGGUGGACUAAAC 20 1884 BCL11A-1400 + UGUCUCGGUGGUGGACUAAA 20 1885 BCL11A-1401 + GUCCAAGUGAUGUCUCGGUG 20 1886 BCL11A-1402 + CCCCAGGCGCUCUAUGCGGU 20 1887 BCL11A-1403 + CCCCCAGGCGCUCUAUGCGG 20 1888 BCL11A-1404 + GCCCCCAGGCGCUCUAUGCG 20 1889 BCL11A-1405 + GCACUCGGGUGAUGGGUGGC 20 1890 BCL11A-1406 + CUGUCAAAGGCACUCGGGUG 20 1891 BCL11A-1407 + CAGCACCCUGUCAAAGGCAC 20 1892 BCL11A-1408 + GGCGGGAGGCUCCAUAGCCA 20 1893 BCL11A-1409 + CUCCUAGAGAAAUCCAUGGC 20 1894 BCL11A-1410 + UCUCCUAGAGAAAUCCAUGG 20 1895 BCL11A-1411 + GUCUCCUAGAGAAAUCCAUG 20 1896 BCL11A-1412 + CCAGCUCUCUAAGUCUCCUA 20 1897 BCL11A-1413 + UGCCAGCUCUCUAAGUCUCC 20 1898 BCL11A-1414 + GGGCCGGCCUGGGGACAGCG 20 1899 BCL11A-1415 + GCAUAGGGCUGGGCCGGCCU 20 1900 BCL11A-1416 + UGCAUAGGGCUGGGCCGGCC 20 1901 BCL11A-1417 + UUGCAUAGGGCUGGGCCGGC 20 1902 BCL11A-1418 + GCAGUAACCUUUGCAUAGGG 20 1903 BCL11A-1419 + UGGUUGCAGUAACCUUUGCA 20 1904 BCL11A-1420 + AGGGCGGCUUGCUACCUGGC 20 1905 BCL11A-1421 + AAGGGCGGCUUGCUACCUGG 20 1906 BCL11A-1422 + GGAGGGGGGGCGUCGCCAGG 20 1907 BCL11A-1423 + GAGGGAGGGGGGGCGUCGCC 20 1908 BCL11A-1424 + GGAGGGAGGGGGGGCGUCGC 20 1909 BCL11A-1425 + CGGAUUGCAGAGGAGGGAGG 20 1910 BCL11A-1426 + GCGGAUUGCAGAGGAGGGAG 20 1911 BCL11A-1427 + GGCGGAUUGCAGAGGAGGGA 20 1912 BCL11A-1428 + GGGCGGAUUGCAGAGGAGGG 20 1913 BCL11A-1429 + GGGGCGGAUUGCAGAGGAGG 20 1914 BCL11A-1430 + GAGGGGCGGAUUGCAGAGGA 20 1915 BCL11A-1431 + GGAGGGGCGGAUUGCAGAGG 20 1916 BCL11A-1432 + AGGAGGGGCGGAUUGCAGAG 20 1917 BCL11A-1433 + GGAGGAGGGGCGGAUUGCAG 20 1918 BCL11A-1434 + GGGAGGAGGGGCGGAUUGCA 20 1919 BCL11A-1435 + GAGGGAGGAGGGGCGGAUUG 20 1920 BCL11A-1436 + GGGGCUGGGAGGGAGGAGGG 20 1921 BCL11A-1437 + ACCGGGGGCUGGGAGGGAGG 20 1922 BCL11A-1438 + GACCGGGGGCUGGGAGGGAG 20 1923 BCL11A-1439 + UUGACCGGGGGCUGGGAGGG 20 1924 BCL11A-1440 + CUUGACCGGGGGCUGGGAGG 20 1925 BCL11A-1441 + GACUUGACCGGGGGCUGGGA 20 1926 BCL11A-1442 + GGACUUGACCGGGGGCUGGG 20 1927 BCL11A-1443 + UGGACUUGACCGGGGGCUGG 20 1928 BCL11A-1444 + CUUGGACUUGACCGGGGGCU 20 1929 BCL11A-1445 + ACUUGGACUUGACCGGGGGC 20 1930 BCL11A-1446 + GACUUGGACUUGACCGGGGG 20 1931 BCL11A-1447 + CGCAUGACUUGGACUUGACC 20 1932 BCL11A-1448 + UCGCAUGACUUGGACUUGAC 20 1933 BCL11A-1449 + CUCGCAUGACUUGGACUUGA 20 1934 BCL11A-1450 + UGCCGCAGAACUCGCAUGAC 20 1935 BCL11A-1451 + GAAAUUUGAACGUCUUGCCG 20 1936 BCL11A-1452 + CCACCAGGUUGCUCUGAAAU 20 1937 BCL11A-1453 + CGGUGCACCACCAGGUUGCU 20 1938 BCL11A-1454 + GGUCGCACAGGUUGCACUUG 20 1939 BCL11A-1455 + UGGCGCUUCAGCUUGCUGGC 20 1940 BCL11A-1456 + CGUCGGACUUGACCGUCAUG 20 1941 BCL11A-1457 + UCGUCGGACUUGACCGUCAU 20 1942 BCL11A-1458 + GUCGUCGGACUUGACCGUCA 20 1943 BCL11A-1459 + CGUCGUCGGACUUGACCGUC 20 1944 BCL11A-1460 + UGGCGGUGGAGAGACCGUCG 20 1945 BCL11A-1461 + GUUCCGGGGAGCUGGCGGUG 20 1946 BCL11A-1462 + GGGUUCCGGGGAGCUGGCGG 20 1947 BCL11A-1463 + CGGGUUCCGGGGAGCUGGCG 20 1948 BCL11A-1464 + GUCGCUGGUGCCGGGUUCCG 20 1949 BCL11A-1465 + AGUCGCUGGUGCCGGGUUCC 20 1950 BCL11A-1466 + AAGUCGCUGGUGCCGGGUUC 20 1951 BCL11A-1467 + CAAGUCGCUGGUGCCGGGUU 20 1952 BCL11A-1468 + UGCCCACCAAGUCGCUGGUG 20 1953 BCL11A-1469 + UGAACUUGGCCACCACGGAC 20 1954 BCL11A-1470 + CGCUCUUGAACUUGGCCACC 20 1955 BCL11A-1471 + GGUUGGGGUCGUUCUCGCUC 20 1956 BCL11A-1472 + CCCGUUCUCCGGGAUCAGGU 20 1957 BCL11A-1473 + CCCCGUUCUCCGGGAUCAGG 20 1958 BCL11A-1474 + UCCUCCUCGUCCCCGUUCUC 20 1959 BCL11A-1475 + UUCCUCCUCGUCCCCGUUCU 20 1960 BCL11A-1476 + GCGCCGCCUCCAGGCUCAGC 20 1961 BCL11A-1477 + CACGCCCACGACCGCGCCCC 20 1962 BCL11A-1478 + AUGCCCUGCAUGACGUCGGG 20 1963 BCL11A-1479 + GCACCAUGCCCUGCAUGACG 20 1964 BCL11A-1480 + CGCUGAAGUGCUGCAUGGAG 20 1965 BCL11A-1481 + GGCCUCGCUGAAGUGCUGCA 20 1966 BCL11A-1482 + AGGCCUCGCUGAAGUGCUGC 20 1967 BCL11A-1483 + GGACCUGGUGGAAGGCCUCG 20 1968 BCL11A-1484 + GCUUCUCGCCCAGGACCUGG 20 1969 BCL11A-1485 + UGCUUCUCGCCCAGGACCUG 20 1970 BCL11A-1486 + CCGCGCUUAUGCUUCUCGCC 20 1971 BCL11A-1487 + GCGGUCCGACUCGCCGGCCA 20 1972 BCL11A-1488 + CCCCGAGGCCGACUCGCCCG 20 1973 BCL11A-1489 + CCCCCGAGGCCGACUCGCCC 20 1974 BCL11A-1490 + CCCCCCGAGGCCGACUCGCC 20 1975 BCL11A-1491 + GCCCCCCGAGGCCGACUCGC 20 1976 BCL11A-1492 + CAGCUUUUUGGACAGGCCCC 20 1977 BCL11A-1493 + GGCUGCCCAGCAGCAGCUUU 20 1978 BCL11A-1494 + AGAGAAGGGGCUCAGCGAGC 20 1979 BCL11A-1495 + UAGAGAAGGGGCUCAGCGAG 20 1980 BCL11A-1496 + GCGCUUAGAGAAGGGGCUCA 20 1981 BCL11A-1497 + GAGCUUGAUGCGCUUAGAGA 20 1982 BCL11A-1498 + CGAGCUUGAUGCGCUUAGAG 20 1983 BCL11A-1499 + UCUCGAGCUUGAUGCGCUUA 20 1984 BCL11A-1500 + CUUCUCGAGCUUGAUGCGCU 20 1985 BCL11A-1501 + GGGGCAGGUCGAACUCCUUC 20 1986 BCL11A-1502 + GCAUCGCGGCCGGGGGCAGG 20 1987 BCL11A-1503 + CCGUGUUGGGCAUCGCGGCC 20 1988 BCL11A-1504 + UCCGUGUUGGGCAUCGCGGC 20 1989 BCL11A-1505 + CUCCGUGUUGGGCAUCGCGG 20 1990 BCL11A-1506 + GCGAGUACACGUUCUCCGUG 20 1991 BCL11A-1507 + CGCGUAGCCGGCGAGCCACU 20 1992 BCL11A-1508 + GCCUGGAGGCCGCGUAGCCG 20 1993 BCL11A-1509 + GAAGGGAUCUUUGAGCUGCC 20 1994 BCL11A-1510 + GGAAGGGAUCUUUGAGCUGC 20 1995 BCL11A-1511 + CGAAGCUAAGGAAGGGAUCU 20 1996 BCL11A-1512 + GGAGUCUCCGAAGCUAAGGA 20 1997 BCL11A-1513 + UGGAGUCUCCGAAGCUAAGG 20 1998 BCL11A-1514 + GUCUGGAGUCUCCGAAGCUA 20 1999 BCL11A-1515 + UGUCUGGAGUCUCCGAAGCU 20 2000 BCL11A-1516 + AAGGCGAUUGUCUGGAGUCU 20 2001 BCL11A-1517 + GGAGGCAAAAGGCGAUUGUC 20 2002 BCL11A-1518 + AGGAGGCAAAAGGCGAUUGU 20 2003 BCL11A-1519 + CUCCGAGGAGUGCUCCGACG 20 2004 BCL11A-1520 + UCUCCGAGGAGUGCUCCGAC 20 2005 BCL11A-1521 + GUUCUCCGAGGAGUGCUCCG 20 2006 BCL11A-1522 + GCGCAAACUCCCGUUCUCCG 20 2007 BCL11A-1523 + AGCGCAAACUCCCGUUCUCC 20 2008 BCL11A-1524 + GAAGCGCAAACUCCCGUUCU 20 2009 BCL11A-1525 + CCAGCUCCCCGGGCGGUGUG 20 2010 BCL11A-1526 + GUCCAGCUCCCCGGGCGGUG 20 2011 BCL11A-1527 + CGUCCAGCUCCCCGGGCGGU 20 2012 BCL11A-1528 + AGAUCCCUCCGUCCAGCUCC 20 2013 BCL11A-1529 + ACUUCCCGUGCCGCUGCGCC 20 2014 BCL11A-1530 + CCGGGCCCGGACCACUAAUA 20 2015 BCL11A-1531 + CCCGGGCCCGGACCACUAAU 20 2016 BCL11A-1532 + UGAGCUGGGCCUGCCCGGGC 20 2017 BCL11A-1533 + CUCUUUUGAGCUGGGCCUGC 20 2018 BCL11A-1534 + UGCGUCUGCCCUCUUUUGAG 20 2019 BCL11A-1535 + GUCGCUGCGUCUGCCCUCUU 20 2020 BCL11A-1536 + UUGUACAUGUGUAGCUG 17 2021 BCL11A-1537 + AGAGAAACCAUGCACUG 17 2022 BCL11A-1538 + UUCUGUGCGUGUUGCAA 17 2023 BCL11A-1539 + UGUUCUGUGCGUGUUGC 17 2024 BCL11A-1540 + AAGUAGAUUCUUAAUCC 17 2025 BCL11A-1541 + ACCAACCCGCGGGGUCA 17 2026 BCL11A-1542 + UACCAACCCGCGGGGUC 17 2027 BCL11A-1543 + AUACCAACCCGCGGGGU 17 2028 BCL11A-1544 + GAAGGGAUACCAACCCG 17 2029 BCL11A-1545 + UGAAGGGAUACCAACCC 17 2030 BCL11A-1546 + UCUGCACCUAGUCCUGA 17 2031 BCL11A-1547 + UUCUGCACCUAGUCCUG 17 2032 BCL11A-1548 + ACAUUCUGCACCUAGUC 17 2033 BCL11A-1549 + AUGGAGAGGUGGCUGGG 17 2034 BCL11A-1550 + CCCAUGGAGAGGUGGCU 17 2035 BCL11A-1551 + UCCCAUGGAGAGGUGGC 17 2036 BCL11A-1552 + AUCCCAUGGAGAGGUGG 17 2037 BCL11A-1553 + GCAAUAUGAAUCCCAUG 17 2038 BCL11A-1554 + CUGCAAUAUGAAUCCCA 17 2039 BCL11A-1555 + UCUGCAAUAUGAAUCCC 17 2040 BCL11A-1556 + GGGUUAUUGUCUGCAAU 17 2041 BCL11A-1557 + UAUUCUUAGCAGGUUAA 17 2042 BCL11A-1558 + GUAUUCUUAGCAGGUUA 17 2043 BCL11A-1559 + GCGCCCUUCUGCCAGGC 17 2044 BCL11A-1560 + AGCGCCCUUCUGCCAGG 17 2045 BCL11A-1561 + AACAGGGGGGGAGUGGG 17 2046 BCL11A-1562 + AAACAGGGGGGGAGUGG 17 2047 BCL11A-1563 + GACUAAACAGGGGGGGA 17 2048 BCL11A-1564 + GGUGGACUAAACAGGGG 17 2049 BCL11A-1565 + UGGUGGACUAAACAGGG 17 2050 BCL11A-1566 + GUGGUGGACUAAACAGG 17 2051 BCL11A-1567 + GGUGGUGGACUAAACAG 17 2052 BCL11A-1568 + CGGUGGUGGACUAAACA 17 2053 BCL11A-1569 + UCGGUGGUGGACUAAAC 17 2054 BCL11A-1570 + CUCGGUGGUGGACUAAA 17 2055 BCL11A-1571 + CAAGUGAUGUCUCGGUG 17 2056 BCL11A-1572 + CAGGCGCUCUAUGCGGU 17 2057 BCL11A-1573 + CCAGGCGCUCUAUGCGG 17 2058 BCL11A-1574 + CCCAGGCGCUCUAUGCG 17 2059 BCL11A-1575 + CUCGGGUGAUGGGUGGC 17 2060 BCL11A-1576 + UCAAAGGCACUCGGGUG 17 2061 BCL11A-1577 + CACCCUGUCAAAGGCAC 17 2062 BCL11A-1578 + GGGAGGCUCCAUAGCCA 17 2063 BCL11A-1579 + CUAGAGAAAUCCAUGGC 17 2064 BCL11A-1580 + CCUAGAGAAAUCCAUGG 17 2065 BCL11A-1581 + UCCUAGAGAAAUCCAUG 17 2066 BCL11A-1582 + GCUCUCUAAGUCUCCUA 17 2067 BCL11A-1583 + CAGCUCUCUAAGUCUCC 17 2068 BCL11A-1584 + CCGGCCUGGGGACAGCG 17 2069 BCL11A-1585 + UAGGGCUGGGCCGGCCU 17 2070 BCL11A-1586 + AUAGGGCUGGGCCGGCC 17 2071 BCL11A-1587 + CAUAGGGCUGGGCCGGC 17 2072 BCL11A-1588 + GUAACCUUUGCAUAGGG 17 2073 BCL11A-1589 + UUGCAGUAACCUUUGCA 17 2074 BCL11A-1590 + GCGGCUUGCUACCUGGC 17 2075 BCL11A-1591 + GGCGGCUUGCUACCUGG 17 2076 BCL11A-1592 + GGGGGGGCGUCGCCAGG 17 2077 BCL11A-1593 + GGAGGGGGGGCGUCGCC 17 2078 BCL11A-1594 + GGGAGGGGGGGCGUCGC 17 2079 BCL11A-1595 + AUUGCAGAGGAGGGAGG 17 2080 BCL11A-1596 + GAUUGCAGAGGAGGGAG 17 2081 BCL11A-1597 + GGAUUGCAGAGGAGGGA 17 2082 BCL11A-1598 + CGGAUUGCAGAGGAGGG 17 2083 BCL11A-1599 + GCGGAUUGCAGAGGAGG 17 2084 BCL11A-1600 + GGGCGGAUUGCAGAGGA 17 2085 BCL11A-1601 + GGGGCGGAUUGCAGAGG 17 2086 BCL11A-1602 + AGGGGCGGAUUGCAGAG 17 2087 BCL11A-1603 + GGAGGGGCGGAUUGCAG 17 2088 BCL11A-1604 + AGGAGGGGCGGAUUGCA 17 2089 BCL11A-1605 + GGAGGAGGGGCGGAUUG 17 2090 BCL11A-1606 + GCUGGGAGGGAGGAGGG 17 2091 BCL11A-1607 + GGGGGCUGGGAGGGAGG 17 2092 BCL11A-1608 + CGGGGGCUGGGAGGGAG 17 2093 BCL11A-1609 + ACCGGGGGCUGGGAGGG 17 2094 BCL11A-1610 + GACCGGGGGCUGGGAGG 17 2095 BCL11A-1611 + UUGACCGGGGGCUGGGA 17 2096 BCL11A-1612 + CUUGACCGGGGGCUGGG 17 2097 BCL11A-1613 + ACUUGACCGGGGGCUGG 17 2098 BCL11A-1614 + GGACUUGACCGGGGGCU 17 2099 BCL11A-1615 + UGGACUUGACCGGGGGC 17 2100 BCL11A-1616 + UUGGACUUGACCGGGGG 17 2101 BCL11A-1617 + AUGACUUGGACUUGACC 17 2102 BCL11A-1618 + CAUGACUUGGACUUGAC 17 2103 BCL11A-1619 + GCAUGACUUGGACUUGA 17 2104 BCL11A-1620 + CGCAGAACUCGCAUGAC 17 2105 BCL11A-1621 + AUUUGAACGUCUUGCCG 17 2106 BCL11A-1622 + CCAGGUUGCUCUGAAAU 17 2107 BCL11A-1623 + UGCACCACCAGGUUGCU 17 2108 BCL11A-1624 + CGCACAGGUUGCACUUG 17 2109 BCL11A-1625 + CGCUUCAGCUUGCUGGC 17 2110 BCL11A-1626 + CGGACUUGACCGUCAUG 17 2111 BCL11A-1627 + UCGGACUUGACCGUCAU 17 2112 BCL11A-1628 + GUCGGACUUGACCGUCA 17 2113 BCL11A-1629 + CGUCGGACUUGACCGUC 17 2114 BCL11A-1630 + CGGUGGAGAGACCGUCG 17 2115 BCL11A-1631 + CCGGGGAGCUGGCGGUG 17 2116 BCL11A-1632 + UUCCGGGGAGCUGGCGG 17 2117 BCL11A-1633 + GUUCCGGGGAGCUGGCG 17 2118 BCL11A-1634 + GCUGGUGCCGGGUUCCG 17 2119 BCL11A-1635 + CGCUGGUGCCGGGUUCC 17 2120 BCL11A-1636 + UCGCUGGUGCCGGGUUC 17 2121 BCL11A-1637 + GUCGCUGGUGCCGGGUU 17 2122 BCL11A-1638 + CCACCAAGUCGCUGGUG 17 2123 BCL11A-1639 + ACUUGGCCACCACGGAC 17 2124 BCL11A-1640 + UCUUGAACUUGGCCACC 17 2125 BCL11A-1641 + UGGGGUCGUUCUCGCUC 17 2126 BCL11A-1642 + GUUCUCCGGGAUCAGGU 17 2127 BCL11A-1643 + CGUUCUCCGGGAUCAGG 17 2128 BCL11A-1644 + UCCUCGUCCCCGUUCUC 17 2129 BCL11A-1645 + CUCCUCGUCCCCGUUCU 17 2130 BCL11A-1646 + CCGCCUCCAGGCUCAGC 17 2131 BCL11A-1647 + GCCCACGACCGCGCCCC 17 2132 BCL11A-1648 + CCCUGCAUGACGUCGGG 17 2133 BCL11A-1649 + CCAUGCCCUGCAUGACG 17 2134 BCL11A-1650 + UGAAGUGCUGCAUGGAG 17 2135 BCL11A-1651 + CUCGCUGAAGUGCUGCA 17 2136 BCL11A-1652 + CCUCGCUGAAGUGCUGC 17 2137 BCL11A-1653 + CCUGGUGGAAGGCCUCG 17 2138 BCL11A-1654 + UCUCGCCCAGGACCUGG 17 2139 BCL11A-1655 + UUCUCGCCCAGGACCUG 17 2140 BCL11A-1656 + CGCUUAUGCUUCUCGCC 17 2141 BCL11A-1657 + GUCCGACUCGCCGGCCA 17 2142 BCL11A-1658 + CGAGGCCGACUCGCCCG 17 2143 BCL11A-1659 + CCGAGGCCGACUCGCCC 17 2144 BCL11A-1660 + CCCGAGGCCGACUCGCC 17 2145 BCL11A-1661 + CCCCGAGGCCGACUCGC 17 2146 BCL11A-1662 + CUUUUUGGACAGGCCCC 17 2147 BCL11A-1663 + UGCCCAGCAGCAGCUUU 17 2148 BCL11A-1664 + GAAGGGGCUCAGCGAGC 17 2149 BCL11A-1665 + AGAAGGGGCUCAGCGAG 17 2150 BCL11A-1666 + CUUAGAGAAGGGGCUCA 17 2151 BCL11A-1667 + CUUGAUGCGCUUAGAGA 17 2152 BCL11A-1668 + GCUUGAUGCGCUUAGAG 17 2153 BCL11A-1669 + CGAGCUUGAUGCGCUUA 17 2154 BCL11A-1670 + CUCGAGCUUGAUGCGCU 17 2155 BCL11A-1671 + GCAGGUCGAACUCCUUC 17 2156 BCL11A-1672 + UCGCGGCCGGGGGCAGG 17 2157 BCL11A-1673 + UGUUGGGCAUCGCGGCC 17 2158 BCL11A-1674 + GUGUUGGGCAUCGCGGC 17 2159 BCL11A-1675 + CGUGUUGGGCAUCGCGG 17 2160 BCL11A-1676 + AGUACACGUUCUCCGUG 17 2161 BCL11A-1677 + GUAGCCGGCGAGCCACU 17 2162 BCL11A-1678 + UGGAGGCCGCGUAGCCG 17 2163 BCL11A-1679 + GGGAUCUUUGAGCUGCC 17 2164 BCL11A-1680 + AGGGAUCUUUGAGCUGC 17 2165 BCL11A-1681 + AGCUAAGGAAGGGAUCU 17 2166 BCL11A-1682 + GUCUCCGAAGCUAAGGA 17 2167 BCL11A-1683 + AGUCUCCGAAGCUAAGG 17 2168 BCL11A-1684 + UGGAGUCUCCGAAGCUA 17 2169 BCL11A-1685 + CUGGAGUCUCCGAAGCU 17 2170 BCL11A-1686 + GCGAUUGUCUGGAGUCU 17 2171 BCL11A-1687 + GGCAAAAGGCGAUUGUC 17 2172 BCL11A-1688 + AGGCAAAAGGCGAUUGU 17 2173 BCL11A-1689 + CGAGGAGUGCUCCGACG 17 2174 BCL11A-1690 + CCGAGGAGUGCUCCGAC 17 2175 BCL11A-1691 + CUCCGAGGAGUGCUCCG 17 2176 BCL11A-1692 + CAAACUCCCGUUCUCCG 17 2177 BCL11A-1693 + GCAAACUCCCGUUCUCC 17 2178 BCL11A-1694 + GCGCAAACUCCCGUUCU 17 2179 BCL11A-1695 + GCUCCCCGGGCGGUGUG 17 2180 BCL11A-1696 + CAGCUCCCCGGGCGGUG 17 2181 BCL11A-1697 + CCAGCUCCCCGGGCGGU 17 2182 BCL11A-1698 + UCCCUCCGUCCAGCUCC 17 2183 BCL11A-1699 + UCCCGUGCCGCUGCGCC 17 2184 BCL11A-1700 + GGCCCGGACCACUAAUA 17 2185 BCL11A-1701 + GGGCCCGGACCACUAAU 17 2186 BCL11A-1702 + GCUGGGCCUGCCCGGGC 17 2187 BCL11A-1703 + UUUUGAGCUGGGCCUGC 17 2188 BCL11A-1704 + GUCUGCCCUCUUUUGAG 17 2189 BCL11A-1705 + GCUGCGUCUGCCCUCUU 17 2190 BCL11A-1706 - CCCCCAUUCGGCGUAGUACC 20 2191 BCL11A-1707 - CCCAUUCGGCGUAGUACCCA 20 2192 BCL11A-1708 - CUCAAGAUGUGUGGCAGUUU 20 2193 BCL11A-1709 - AGAUGUGUGGCAGUUUUCGG 20 2194 BCL11A-1710 - GAUGUGUGGCAGUUUUCGGA 20 2195 BCL11A-1711 - GGCAGUUUUCGGAUGGAAGC 20 2196 BCL11A-1712 - CAGUUUUCGGAUGGAAGCUC 20 2197 BCL11A-1713 - CCAUUCGGCGUAGUACC 17 2198 BCL11A-1714 - AUUCGGCGUAGUACCCA 17 2199 BCL11A-1715 - AAGAUGUGUGGCAGUUU 17 2200 BCL11A-1716 - UGUGUGGCAGUUUUCGG 17 2201 BCL11A-1717 - GUGUGGCAGUUUUCGGA 17 2202 BCL11A-1718 - AGUUUUCGGAUGGAAGC 17 2203 BCL11A-1719 - UUUUCGGAUGGAAGCUC 17 2204 BCL11A-1720 + ACGCCGAAUGGGGGUGUGUG 20 2205 BCL11A-1721 + ACUACGCCGAAUGGGGGUGU 20 2206 BCL11A-1722 + CUCUGGGUACUACGCCGAAU 20 2207 BCL11A-1723 + UCUCUGGGUACUACGCCGAA 20 2208 BCL11A-1724 + CUCUCUGGGUACUACGCCGA 20 2209 BCL11A-1725 + UGAGCUCUCUGGGUACUACG 20 2210 BCL11A-1726 + UGCCACACAUCUUGAGCUCU 20 2211 BCL11A-1727 + UCCGAAAACUGCCACACAUC 20 2212 BCL11A-1728 + AAGGGCUCUCGAGCUUCCAU 20 2213 BCL11A-1729 + CCGAAUGGGGGUGUGUG 17 2214 BCL11A-1730 + ACGCCGAAUGGGGGUGU 17 2215 BCL11A-1731 + UGGGUACUACGCCGAAU 17 2216 BCL11A-1732 + CUGGGUACUACGCCGAA 17 2217 BCL11A-1733 + UCUGGGUACUACGCCGA 17 2218 BCL11A-1734 + GCUCUCUGGGUACUACG 17 2219 BCL11A-1735 + CACACAUCUUGAGCUCU 17 2220 BCL11A-1736 + GAAAACUGCCACACAUC 17 2221 BCL11A-1737 + GGCUCUCGAGCUUCCAU 17 2222

Table 2F provides exemplary targeting domains for knocking out the BCL11A gene. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with an N. meningitidis Cas9 molecule that gives double stranded cleavage. Any of the targeting domains in the table can be used with an N. meningitidis Cas9 single-stranded break nucleases (nickases). In an embodiment, dual targeting is used to create two nicks. When selecting gRNAs for use in a nickase pair, one gRNA targets a domain in the complementary strand and the second gRNA targets a domain in the non-complementary strand, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain targeting the same target position.

TABLE 2F N. meningitidis gRNA targets for BCL11A knockout Tar- get gRNA DNA Targeting Site Name Strand Domain Length BCL11A-1738 AUCCAGGUCACGCCAGAGGA 20 2223 BCL11A-1739 UGCAACACGCACAGAACACU 20 2224 BCL11A-1740 UCCUUCCCAGCCACCUCUCC 20 2225 BCL11A-1741 AUGGCUAUGGAGCCUCCCGC 20 2226 BCL11A-1742 CAGGUCACGCCAGAGGA 17 2227 BCL11A-1743 AACACGCACAGAACACU 17 2228 BCL11A-1744 UUCCCAGCCACCUCUCC 17 2229 BCL11A-1745 GCUAUGGAGCCUCCCGC 17 2230 BCL11A-1746 + UGAAAAAAGCAUCCAAUCCC 20 2231 BCL11A-1747 + GGAGGUUGGCAUCCAGGUCA 20 2232 BCL11A-1748 + CGCCUGGGAUGAGUGCAGAA 20 2233 BCL11A-1749 + UAGAAAGCGAACACGGAAGU 20 2234 BCL11A-1750 + GGCUAUGGAGCCUCCCGCCA 20 2235 BCL11A-1751 + CCUCCUCCCUCCCAGCCCCC 20 2236 BCL11A-1752 + CCCAUGACGGUCAAGUCCGA 20 2237 BCL11A-1753 + UUUGCCUCCUCGUCGGAGCA 20 2238 BCL11A-1754 + UGAAAAAAGCAUCCAAU 17 2239 BCL11A-1755 + GGAGGUUGGCAUCCAGG 17 2240 BCL11A-1756 + CGCCUGGGAUGAGUGCA 17 2241 BCL11A-1757 + UAGAAAGCGAACACGGA 17 2242 BCL11A-1758 + GGCUAUGGAGCCUCCCG 17 2243 BCL11A-1759 + CCUCCUCCCUCCCAGCC 17 2244 BCL11A-1760 + CCCAUGACGGUCAAGUC 17 2245 BCL11A-1761 + UUUGCCUCCUCGUCGGA 17 2246

Table 3A provides exemplary targeting domains for repressing (i.e., knocking down or decreasing) expression of the BCL11A gene. In an embodiment, the targeting domain is the exact complement of the target domain. Any of the targeting domains in the table can be used with a S. pyogenes eiCas9 molecule to cause a steric block at the promoter region to block transcription resulting in the repression of the BCL11A gene. Alternatively, any of the targeting domains in the table can be used with a S. pyogenes eiCas9 fused to a transcriptional repressor to decrease transcription and therefore downregulate gene expression.

TABLE 3A S. pyogenes gRNA targets for BCL11A knockdown Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO BCL11A-1762 UCUUCUCCUUGCUGCCUCUG 20 2247 BCL11A-1763 UCCUUGCUGCCUCUGAGGUU 20 2248 BCL11A-1764 UGCUGCCUCUGAGGUUCGGU 20 2249 BCL11A-1765 GCUGCCUCUGAGGUUCGGUC 20 2250 BCL11A-1766 GCCUCUGAGGUUCGGUCGGG 20 2251 BCL11A-1767 CCUCUGAGGUUCGGUCGGGA 20 2252 BCL11A-1768 CUCUGAGGUUCGGUCGGGAG 20 2253 BCL11A-1769 UGAGGUUCGGUCGGGAGGGG 20 2254 BCL11A-1770 GAGGUUCGGUCGGGAGGGGA 20 2255 BCL11A-1771 CGGUCGGGAGGGGAGGGCAG 20 2256 BCL11A-1772 GGGGAGGGCAGCGGCAACCC 20 2257 BCL11A-1773 GAGGGCAGCGGCAACCCAGG 20 2258 BCL11A-1774 CAACCCAGGAGGCAGCAGUC 20 2259 BCL11A-1775 AACCCAGGAGGCAGCAGUCC 20 2260 BCL11A-1776 CUCCCUCUCCCGCGUGCCCC 20 2261 BCL11A-1777 CCCCCGGCCGCCUCCUCCCC 20 2262 BCL11A-1778 CGGCCCUAGCUCCUGCCCUU 20 2263 BCL11A-1779 CCCUAGCUCCUGCCCUUCGG 20 2264 BCL11A-1780 UAGCUCCUGCCCUUCGGCGG 20 2265 BCL11A-1781 CUCCUGCCCUUCGGCGGCGG 20 2266 BCL11A-1782 CUGCCCUUCGGCGGCGGCGG 20 2267 BCL11A-1783 CCCUUCGGCGGCGGCGGCGG 20 2268 BCL11A-1784 UUCGGCGGCGGCGGCGGCGG 20 2269 BCL11A-1785 CGGCGGCGGCGGCGGCGGCG 20 2270 BCL11A-1786 GGCGGCGGCGGCGGCGGCGC 20 2271 BCL11A-1787 GGCGGCGGCGGCGGCGCGGG 20 2272 BCL11A-1788 GCGGCGGCGGCGGCGCGGGA 20 2273 BCL11A-1789 GGCGCGGGAGGGCAAGCGCG 20 2274 BCL11A-1790 GGAGGGCAAGCGCGAGGAGC 20 2275 BCL11A-1791 GCGCGAGGAGCCGGCACAAA 20 2276 BCL11A-1792 GGAGCCGGCACAAAAGGCAG 20 2277 BCL11A-1793 GAGCCGGCACAAAAGGCAGC 20 2278 BCL11A-1794 GCGGGACAAACACCCACCUC 20 2279 BCL11A-1795 GACAAACACCCACCUCUGGC 20 2280 BCL11A-1796 CCACCUCUGGCCGGAACAAA 20 2281 BCL11A-1797 CCUCUGGCCGGAACAAAAGG 20 2282 BCL11A-1798 GGAACAAAAGGCGGCAGUGC 20 2283 BCL11A-1799 GCCGCGUCUCCCGUCCUUCC 20 2284 BCL11A-1800 UCCCGUCCUUCCCGGUCCCA 20 2285 BCL11A-1801 CACGGCUCUCCCCGUCGCCG 20 2286 BCL11A-1802 CGGCCCCUCUCCCGACUCCG 20 2287 BCL11A-1803 UCUCCCGACUCCGCGGACUC 20 2288 BCL11A-1804 CUCCGCGGACUCAGGAGCGC 20 2289 BCL11A-1805 UCCGCGGACUCAGGAGCGCC 20 2290 BCL11A-1806 CCGCGGACUCAGGAGCGCCG 20 2291 BCL11A-1807 CGCGGACUCAGGAGCGCCGG 20 2292 BCL11A-1808 GUGCCACUUUCUCACUAUUG 20 2293 BCL11A-1809 UGCCACUUUCUCACUAUUGU 20 2294 BCL11A-1810 GCCACUUUCUCACUAUUGUG 20 2295 BCL11A-1811 ACACUUGACCGUGAGCGCGC 20 2296 BCL11A-1812 AGUCUCACCUCUUUUCUCCC 20 2297 BCL11A-1813 GUCUCACCUCUUUUCUCCCC 20 2298 BCL11A-1814 CCUACCCCCCCAUUUUCUUA 20 2299 BCL11A-1815 CCCCAUUUUCUUACGGUGAG 20 2300 BCL11A-1816 CCCAUUUUCUUACGGUGAGU 20 2301 BCL11A-1817 CCCCACCAGCUCCCACCCCC 20 2302 BCL11A-1818 UGUUCAUUAUUUUGCAAAAC 20 2303 BCL11A-1819 UCAUUAUUUUGCAAAACUGG 20 2304 BCL11A-1820 CAUUAUUUUGCAAAACUGGC 20 2305 BCL11A-1821 AUUAUUUUGCAAAACUGGCG 20 2306 BCL11A-1822 AUUUUGCAAAACUGGCGGGG 20 2307 BCL11A-1823 UUUUGCAAAACUGGCGGGGC 20 2308 BCL11A-1824 UUUGCAAAACUGGCGGGGCG 20 2309 BCL11A-1825 UUGCAAAACUGGCGGGGCGG 20 2310 BCL11A-1826 UGCAAAACUGGCGGGGCGGG 20 2311 BCL11A-1827 GCAAAACUGGCGGGGCGGGG 20 2312 BCL11A-1828 CAAAACUGGCGGGGCGGGGG 20 2313 BCL11A-1829 CUGGCGGGGCGGGGGGGGAG 20 2314 BCL11A-1830 UUUCGAAAAGAGAAAUAAAG 20 2315 BCL11A-1831 CGAAAAGAGAAAUAAAGCGG 20 2316 BCL11A-1832 AGAGAAAUAAAGCGGCGGAA 20 2317 BCL11A-1833 GAAAUAAAGCGGCGGAAAGG 20 2318 BCL11A-1834 AGCGGCGGAAAGGAGGAAAG 20 2319 BCL11A-1835 GGCGGAAAGGAGGAAAGAGG 20 2320 BCL11A-1836 UAAAAUUAAAUAAAAUUAAA 20 2321 BCL11A-1837 CUGUCUCAAAAGUGCAUACA 20 2322 BCL11A-1838 CAAAAGUGCAUACACGGCAA 20 2323 BCL11A-1839 UACACGGCAAUGGUUCCAGA 20 2324 BCL11A-1840 ACACGGCAAUGGUUCCAGAU 20 2325 BCL11A-1841 CAAUGGUUCCAGAUGGGAUG 20 2326 BCL11A-1842 AAUGGUUCCAGAUGGGAUGA 20 2327 BCL11A-1843 AUCUCUUUUACCUCGACUCU 20 2328 BCL11A-1844 UCUUUUACCUCGACUCUCGG 20 2329 BCL11A-1845 AUAAUUAUUAUUACUAUUAU 20 2330 BCL11A-1846 UAAUUAUUAUUACUAUUAUU 20 2331 BCL11A-1847 + UAAUAAUCACGAGAGCGCGC 20 2332 BCL11A-1848 + CAGGACUAGAAGCAAAAGCG 20 2333 BCL11A-1849 + AGGACUAGAAGCAAAAGCGA 20 2334 BCL11A-1850 + GGACUAGAAGCAAAAGCGAG 20 2335 BCL11A-1851 + GACUAGAAGCAAAAGCGAGG 20 2336 BCL11A-1852 + AGCAAAAGCGAGGGGGAGAG 20 2337 BCL11A-1853 + GCAAAAGCGAGGGGGAGAGA 20 2338 BCL11A-1854 + CAAAAGCGAGGGGGAGAGAG 20 2339 BCL11A-1855 + AGAAAAACCUCCGAGAGUCG 20 2340 BCL11A-1856 + AGUCGAGGUAAAAGAGAUAA 20 2341 BCL11A-1857 + GUCGAGGUAAAAGAGAUAAA 20 2342 BCL11A-1858 + UCGAGGUAAAAGAGAUAAAG 20 2343 BCL11A-1859 + CGAGGUAAAAGAGAUAAAGG 20 2344 BCL11A-1860 + GAAAAAACCCUCAUCCCAUC 20 2345 BCL11A-1861 + CUUUAUUUCUCUUUUCGAAA 20 2346 BCL11A-1862 + CAAAAUAAUGAACAAUGCUA 20 2347 BCL11A-1863 + GAACAACUCACAUGCAAACC 20 2348 BCL11A-1864 + AACAACUCACAUGCAAACCU 20 2349 BCL11A-1865 + ACAACUCACAUGCAAACCUG 20 2350 BCL11A-1866 + CAACUCACAUGCAAACCUGG 20 2351 BCL11A-1867 + CUCACAUGCAAACCUGGGGG 20 2352 BCL11A-1868 + UCACAUGCAAACCUGGGGGU 20 2353 BCL11A-1869 + GCAAACCUGGGGGUGGGAGC 20 2354 BCL11A-1870 + AACCUGGGGGUGGGAGCUGG 20 2355 BCL11A-1871 + ACCUGGGGGUGGGAGCUGGU 20 2356 BCL11A-1872 + CCUGGGGGUGGGAGCUGGUG 20 2357 BCL11A-1873 + GGGUGGGAGCUGGUGGGGAA 20 2358 BCL11A-1874 + GGUGGGAGCUGGUGGGGAAA 20 2359 BCL11A-1875 + GGGAGCUGGUGGGGAAAGGG 20 2360 BCL11A-1876 + UCCCACUCACCGUAAGAAAA 20 2361 BCL11A-1877 + CCCACUCACCGUAAGAAAAU 20 2362 BCL11A-1878 + CCACUCACCGUAAGAAAAUG 20 2363 BCL11A-1879 + CACUCACCGUAAGAAAAUGG 20 2364 BCL11A-1880 + ACUCACCGUAAGAAAAUGGG 20 2365 BCL11A-1881 + CUCACCGUAAGAAAAUGGGG 20 2366 BCL11A-1882 + CCGUAAGAAAAUGGGGGGGU 20 2367 BCL11A-1883 + CGUAAGAAAAUGGGGGGGUA 20 2368 BCL11A-1884 + AAGAAAAUGGGGGGGUAGGG 20 2369 BCL11A-1885 + AGAAAAUGGGGGGGUAGGGA 20 2370 BCL11A-1886 + CAAGUCUAAAAAACGAUUCC 20 2371 BCL11A-1887 + AAGUCUAAAAAACGAUUCCC 20 2372 BCL11A-1888 + AGUCUAAAAAACGAUUCCCG 20 2373 BCL11A-1889 + ACGAUUCCCGGGGAGAAAAG 20 2374 BCL11A-1890 + GGGGAGAAAAGAGGUGAGAC 20 2375 BCL11A-1891 + AAAGAGGUGAGACUGGCUUU 20 2376 BCL11A-1892 + UUUGGACACCAGCGCGCUCA 20 2377 BCL11A-1893 + GCUCACGGUCAAGUGUGCAG 20 2378 BCL11A-1894 + CUCACGGUCAAGUGUGCAGC 20 2379 BCL11A-1895 + ACGGUCAAGUGUGCAGCGGG 20 2380 BCL11A-1896 + UCCCCACAAUAGUGAGAAAG 20 2381 BCL11A-1897 + AUAGUGAGAAAGUGGCACUG 20 2382 BCL11A-1898 + GAGAAAGUGGCACUGUGGAA 20 2383 BCL11A-1899 + AGAAAGUGGCACUGUGGAAA 20 2384 BCL11A-1900 + GAAAGUGGCACUGUGGAAAG 20 2385 BCL11A-1901 + GCACUGUGGAAAGGGGCCCC 20 2386 BCL11A-1902 + CCCCGGCGCUCCUGAGUCCG 20 2387 BCL11A-1903 + CGCUCCUGAGUCCGCGGAGU 20 2388 BCL11A-1904 + GCUCCUGAGUCCGCGGAGUC 20 2389 BCL11A-1905 + UGAGUCCGCGGAGUCGGGAG 20 2390 BCL11A-1906 + GAGUCCGCGGAGUCGGGAGA 20 2391 BCL11A-1907 + AGUCCGCGGAGUCGGGAGAG 20 2392 BCL11A-1908 + CGGAGUCGGGAGAGGGGCCG 20 2393 BCL11A-1909 + CGGGAGAGGGGCCGCGGCGA 20 2394 BCL11A-1910 + GGGAGAGGGGCCGCGGCGAC 20 2395 BCL11A-1911 + GGAGAGGGGCCGCGGCGACG 20 2396 BCL11A-1912 + CGCGGCGACGGGGAGAGCCG 20 2397 BCL11A-1913 + GCGGCGACGGGGAGAGCCGU 20 2398 BCL11A-1914 + GACGGGGAGAGCCGUGGGAC 20 2399 BCL11A-1915 + ACGGGGAGAGCCGUGGGACC 20 2400 BCL11A-1916 + GGAGAGCCGUGGGACCGGGA 20 2401 BCL11A-1917 + AGCCGUGGGACCGGGAAGGA 20 2402 BCL11A-1918 + GCCGUGGGACCGGGAAGGAC 20 2403 BCL11A-1919 + ACCGGGAAGGACGGGAGACG 20 2404 BCL11A-1920 + GGAAGGACGGGAGACGCGGC 20 2405 BCL11A-1921 + GGCACUGCCGCCUUUUGUUC 20 2406 BCL11A-1922 + CCGCCUUUUGUUCCGGCCAG 20 2407 BCL11A-1923 + CCUUUUGUUCCGGCCAGAGG 20 2408 BCL11A-1924 + CUUUUGUUCCGGCCAGAGGU 20 2409 BCL11A-1925 + UGUCCCGCUGCCUUUUGUGC 20 2410 BCL11A-1926 + GCCGCCGCCGCCGCCGCCGA 20 2411 BCL11A-1927 + CCGCCGCCGCCGCCGCCGAA 20 2412 BCL11A-1928 + CGCCGCCGCCGCCGAAGGGC 20 2413 BCL11A-1929 + GCCGCCGAAGGGCAGGAGCU 20 2414 BCL11A-1930 + CCGCCGAAGGGCAGGAGCUA 20 2415 BCL11A-1931 + CGAAGGGCAGGAGCUAGGGC 20 2416 BCL11A-1932 + GAAGGGCAGGAGCUAGGGCC 20 2417 BCL11A-1933 + AAGGGCAGGAGCUAGGGCCG 20 2418 BCL11A-1934 + AGGGCAGGAGCUAGGGCCGG 20 2419 BCL11A-1935 + GCAGGAGCUAGGGCCGGGGG 20 2420 BCL11A-1936 + GGAGCUAGGGCCGGGGGAGG 20 2421 BCL11A-1937 + GCUAGGGCCGGGGGAGGAGG 20 2422 BCL11A-1938 + GGGCCGGGGGAGGAGGCGGC 20 2423 BCL11A-1939 + GGCCGGGGGAGGAGGCGGCC 20 2424 BCL11A-1940 + GCCGGGGGAGGAGGCGGCCG 20 2425 BCL11A-1941 + CCGGGGGAGGAGGCGGCCGG 20 2426 BCL11A-1942 + AGGAGGCGGCCGGGGGCACG 20 2427 BCL11A-1943 + GGAGGCGGCCGGGGGCACGC 20 2428 BCL11A-1944 + CGGCCGGGGGCACGCGGGAG 20 2429 BCL11A-1945 + GGCCGGGGGCACGCGGGAGA 20 2430 BCL11A-1946 + CGGGGGCACGCGGGAGAGGG 20 2431 BCL11A-1947 + GGGGGCACGCGGGAGAGGGA 20 2432 BCL11A-1948 + GGCACGCGGGAGAGGGAGGG 20 2433 BCL11A-1949 + GCACGCGGGAGAGGGAGGGA 20 2434 BCL11A-1950 + GGAGAGGGAGGGAGGGAGCC 20 2435 BCL11A-1951 + GAGCCCGGACUGCUGCCUCC 20 2436 BCL11A-1952 + AGCCCGGACUGCUGCCUCCU 20 2437 BCL11A-1953 + CCCUCCCGACCGAACCUCAG 20 2438 BCL11A-1954 + ACCGAACCUCAGAGGCAGCA 20 2439 BCL11A-1955 + AGAGGCAGCAAGGAGAAGAC 20 2440 BCL11A-1956 + AAAAUAAAAUAAAUAAAACA 20 2441 BCL11A-1957 UCUCCUUGCUGCCUCUG 17 2442 BCL11A-1958 UUGCUGCCUCUGAGGUU 17 2443 BCL11A-1959 UGCCUCUGAGGUUCGGU 17 2444 BCL11A-1960 GCCUCUGAGGUUCGGUC 17 2445 BCL11A-1961 UCUGAGGUUCGGUCGGG 17 2446 BCL11A-1962 CUGAGGUUCGGUCGGGA 17 2447 BCL11A-1963 UGAGGUUCGGUCGGGAG 17 2448 BCL11A-1964 GGUUCGGUCGGGAGGGG 17 2449 BCL11A-1965 GUUCGGUCGGGAGGGGA 17 2450 BCL11A-1966 UCGGGAGGGGAGGGCAG 17 2451 BCL11A-1967 GAGGGCAGCGGCAACCC 17 2452 BCL11A-1968 GGCAGCGGCAACCCAGG 17 2453 BCL11A-1969 CCCAGGAGGCAGCAGUC 17 2454 BCL11A-1970 CCAGGAGGCAGCAGUCC 17 2455 BCL11A-1971 CCUCUCCCGCGUGCCCC 17 2456 BCL11A-1972 CCGGCCGCCUCCUCCCC 17 2457 BCL11A-1973 CCCUAGCUCCUGCCCUU 17 2458 BCL11A-1974 UAGCUCCUGCCCUUCGG 17 2459 BCL11A-1975 CUCCUGCCCUUCGGCGG 17 2460 BCL11A-1976 CUGCCCUUCGGCGGCGG 17 2461 BCL11A-1977 CCCUUCGGCGGCGGCGG 17 2462 BCL11A-1978 UUCGGCGGCGGCGGCGG 17 2463 BCL11A-1979 GGCGGCGGCGGCGGCGG 17 2464 BCL11A-1980 CGGCGGCGGCGGCGGCG 17 2465 BCL11A-1981 GGCGGCGGCGGCGGCGG 17 2466 BCL11A-1982 GGCGGCGGCGGCGCGGG 17 2467 BCL11A-1983 GCGGCGGCGGCGCGGGA 17 2468 BCL11A-1984 GCGGGAGGGCAAGCGCG 17 2469 BCL11A-1985 GGGCAAGCGCGAGGAGC 17 2470 BCL11A-1986 CGAGGAGCCGGCACAAA 17 2471 BCL11A-1987 GCCGGCACAAAAGGCAG 17 2472 BCL11A-1988 CCGGCACAAAAGGCAGC 17 2473 BCL11A-1989 GGACAAACACCCACCUC 17 2474 BCL11A-1990 AAACACCCACCUCUGGC 17 2475 BCL11A-1991 CCUCUGGCCGGAACAAA 17 2476 BCL11A-1992 CUGGCCGGAACAAAAGG 17 2477 BCL11A-1993 ACAAAAGGCGGCAGUGC 17 2478 BCL11A-1994 GCGUCUCCCGUCCUUCC 17 2479 BCL11A-1995 CGUCCUUCCCGGUCCCA 17 2480 BCL11A-1996 GGCUCUCCCCGUCGCCG 17 2481 BCL11A-1997 CCCCUCUCCCGACUCCG 17 2482 BCL11A-1998 CCCGACUCCGCGGACUC 17 2483 BCL11A-1999 CGCGGACUCAGGAGCGC 17 2484 BCL11A-2000 GCGGACUCAGGAGCGCC 17 2485 BCL11A-2001 CGGACUCAGGAGCGCCG 17 2486 BCL11A-2002 GGACUCAGGAGCGCCGG 17 2487 BCL11A-2003 CCACUUUCUCACUAUUG 17 2488 BCL11A-2004 CACUUUCUCACUAUUGU 17 2489 BCL11A-2005 ACUUUCUCACUAUUGUG 17 2490 BCL11A-2006 CUUGACCGUGAGCGCGC 17 2491 BCL11A-2007 CUCACCUCUUUUCUCCC 17 2492 BCL11A-2008 UCACCUCUUUUCUCCCC 17 2493 BCL11A-2009 ACCCCCCCAUUUUCUUA 17 2494 BCL11A-2010 CAUUUUCUUACGGUGAG 17 2495 BCL11A-2011 AUUUUCUUACGGUGAGU 17 2496 BCL11A-2012 CACCAGCUCCCACCCCC 17 2497 BCL11A-2013 UCAUUAUUUUGCAAAAC 17 2498 BCL11A-2014 UUAUUUUGCAAAACUGG 17 2499 BCL11A-2015 UAUUUUGCAAAACUGGC 17 2500 BCL11A-2016 AUUUUGCAAAACUGGCG 17 2501 BCL11A-2017 UUGCAAAACUGGCGGGG 17 2502 BCL11A-2018 UGCAAAACUGGCGGGGC 17 2503 BCL11A-2019 GCAAAACUGGCGGGGCG 17 2504 BCL11A-2020 CAAAACUGGCGGGGCGG 17 2505 BCL11A-2021 AAAACUGGCGGGGCGGG 17 2506 BCL11A-2022 AAACUGGCGGGGCGGGG 17 2507 BCL11A-2023 AACUGGCGGGGCGGGGG 17 2508 BCL11A-2024 GCGGGGCGGGGGGGGAG 17 2509 BCL11A-2025 CGAAAAGAGAAAUAAAG 17 2510 BCL11A-2026 AAAGAGAAAUAAAGCGG 17 2511 BCL11A-2027 GAAAUAAAGCGGCGGAA 17 2512 BCL11A-2028 AUAAAGCGGCGGAAAGG 17 2513 BCL11A-2029 GGCGGAAAGGAGGAAAG 17 2514 BCL11A-2030 GGAAAGGAGGAAAGAGG 17 2515 BCL11A-2031 AAUUAAAUAAAAUUAAA 17 2516 BCL11A-2032 UCUCAAAAGUGCAUACA 17 2517 BCL11A-2033 AAGUGCAUACACGGCAA 17 2518 BCL11A-2034 ACGGCAAUGGUUCCAGA 17 2519 BCL11A-2035 CGGCAAUGGUUCCAGAU 17 2520 BCL11A-2036 UGGUUCCAGAUGGGAUG 17 2521 BCL11A-2037 GGUUCCAGAUGGGAUGA 17 2522 BCL11A-2038 UCUUUUACCUCGACUCU 17 2523 BCL11A-2039 UUUACCUCGACUCUCGG 17 2524 BCL11A-2040 AUUAUUAUUACUAUUAU 17 2525 BCL11A-2041 UUAUUAUUACUAUUAUU 17 2526 BCL11A-2042 + UAAUCACGAGAGCGCGC 17 2527 BCL11A-2043 + GACUAGAAGCAAAAGCG 17 2528 BCL11A-2044 + ACUAGAAGCAAAAGCGA 17 2529 BCL11A-2045 + CUAGAAGCAAAAGCGAG 17 2530 BCL11A-2046 + UAGAAGCAAAAGCGAGG 17 2531 BCL11A-2047 + AAAAGCGAGGGGGAGAG 17 2532 BCL11A-2048 + AAAGCGAGGGGGAGAGA 17 2533 BCL11A-2049 + AAGCGAGGGGGAGAGAG 17 2534 BCL11A-2050 + AAAACCUCCGAGAGUCG 17 2535 BCL11A-2051 + CGAGGUAAAAGAGAUAA 17 2536 BCL11A-2052 + GAGGUAAAAGAGAUAAA 17 2537 BCL11A-2053 + AGGUAAAAGAGAUAAAG 17 2538 BCL11A-2054 + GGUAAAAGAGAUAAAGG 17 2539 BCL11A-2055 + AAAACCCUCAUCCCAUC 17 2540 BCL11A-2056 + UAUUUCUCUUUUCGAAA 17 2541 BCL11A-2057 + AAUAAUGAACAAUGCUA 17 2542 BCL11A-2058 + CAACUCACAUGCAAACC 17 2543 BCL11A-2059 + AACUCACAUGCAAACCU 17 2544 BCL11A-2060 + ACUCACAUGCAAACCUG 17 2545 BCL11A-2061 + CUCACAUGCAAACCUGG 17 2546 BCL11A-2062 + ACAUGCAAACCUGGGGG 17 2547 BCL11A-2063 + CAUGCAAACCUGGGGGU 17 2548 BCL11A-2064 + AACCUGGGGGUGGGAGC 17 2549 BCL11A-2065 + CUGGGGGUGGGAGCUGG 17 2550 BCL11A-2066 + UGGGGGUGGGAGCUGGU 17 2551 BCL11A-2067 + GGGGGUGGGAGCUGGUG 17 2552 BCL11A-2068 + UGGGAGCUGGUGGGGAA 17 2553 BCL11A-2069 + GGGAGCUGGUGGGGAAA 17 2554 BCL11A-2070 + AGCUGGUGGGGAAAGGG 17 2555 BCL11A-2071 + CACUCACCGUAAGAAAA 17 2556 BCL11A-2072 + ACUCACCGUAAGAAAAU 17 2557 BCL11A-2073 + CUCACCGUAAGAAAAUG 17 2558 BCL11A-2074 + UCACCGUAAGAAAAUGG 17 2559 BCL11A-2075 + CACCGUAAGAAAAUGGG 17 2560 BCL11A-2076 + ACCGUAAGAAAAUGGGG 17 2561 BCL11A-2077 + UAAGAAAAUGGGGGGGU 17 2562 BCL11A-2078 + AAGAAAAUGGGGGGGUA 17 2563 BCL11A-2079 + AAAAUGGGGGGGUAGGG 17 2564 BCL11A-2080 + AAAUGGGGGGGUAGGGA 17 2565 BCL11A-2081 + GUCUAAAAAACGAUUCC 17 2566 BCL11A-2082 + UCUAAAAAACGAUUCCC 17 2567 BCL11A-2083 + CUAAAAAACGAUUCCCG 17 2568 BCL11A-2084 + AUUCCCGGGGAGAAAAG 17 2569 BCL11A-2085 + GAGAAAAGAGGUGAGAC 17 2570 BCL11A-2086 + GAGGUGAGACUGGCUUU 17 2571 BCL11A-2087 + GGACACCAGCGCGCUCA 17 2572 BCL11A-2088 + CACGGUCAAGUGUGCAG 17 2573 BCL11A-2089 + ACGGUCAAGUGUGCAGC 17 2574 BCL11A-2090 + GUCAAGUGUGCAGCGGG 17 2575 BCL11A-2091 + CCACAAUAGUGAGAAAG 17 2576 BCL11A-2092 + GUGAGAAAGUGGCACUG 17 2577 BCL11A-2093 + AAAGUGGCACUGUGGAA 17 2578 BCL11A-2094 + AAGUGGCACUGUGGAAA 17 2579 BCL11A-2095 + AGUGGCACUGUGGAAAG 17 2580 BCL11A-2096 + CUGUGGAAAGGGGCCCC 17 2581 BCL11A-2097 + CGGCGCUCCUGAGUCCG 17 2582 BCL11A-2098 + UCCUGAGUCCGCGGAGU 17 2583 BCL11A-2099 + CCUGAGUCCGCGGAGUC 17 2584 BCL11A-2100 + GUCCGCGGAGUCGGGAG 17 2585 BCL11A-2101 + UCCGCGGAGUCGGGAGA 17 2586 BCL11A-2102 + CCGCGGAGUCGGGAGAG 17 2587 BCL11A-2103 + AGUCGGGAGAGGGGCCG 17 2588 BCL11A-2104 + GAGAGGGGCCGCGGCGA 17 2589 BCL11A-2105 + AGAGGGGCCGCGGCGAC 17 2590 BCL11A-2106 + GAGGGGCCGCGGCGACG 17 2591 BCL11A-2107 + GGCGACGGGGAGAGCCG 17 2592 BCL11A-2108 + GCGACGGGGAGAGCCGU 17 2593 BCL11A-2109 + GGGGAGAGCCGUGGGAC 17 2594 BCL11A-2110 + GGGAGAGCCGUGGGACC 17 2595 BCL11A-2111 + GAGCCGUGGGACCGGGA 17 2596 BCL11A-2112 + CGUGGGACCGGGAAGGA 17 2597 BCL11A-2113 + GUGGGACCGGGAAGGAC 17 2598 BCL11A-2114 + GGGAAGGACGGGAGACG 17 2599 BCL11A-2115 + AGGACGGGAGACGCGGC 17 2600 BCL11A-2116 + ACUGCCGCCUUUUGUUC 17 2601 BCL11A-2117 + CCUUUUGUUCCGGCCAG 17 2602 BCL11A-2118 + UUUGUUCCGGCCAGAGG 17 2603 BCL11A-2119 + UUGUUCCGGCCAGAGGU 17 2604 BCL11A-2120 + CCCGCUGCCUUUUGUGC 17 2605 BCL11A-2121 + GCCGCCGCCGCCGCCGA 17 2606 BCL11A-2122 + CCGCCGCCGCCGCCGAA 17 2607 BCL11A-2123 + CGCCGCCGCCGAAGGGC 17 2608 BCL11A-2124 + GCCGAAGGGCAGGAGCU 17 2609 BCL11A-2125 + CCGAAGGGCAGGAGCUA 17 2610 BCL11A-2126 + AGGGCAGGAGCUAGGGC 17 2611 BCL11A-2127 + GGGCAGGAGCUAGGGCC 17 2612 BCL11A-2128 + GGCAGGAGCUAGGGCCG 17 2613 BCL11A-2129 + GCAGGAGCUAGGGCCGG 17 2614 BCL11A-2130 + GGAGCUAGGGCCGGGGG 17 2615 BCL11A-2131 + GCUAGGGCCGGGGGAGG 17 2616 BCL11A-2132 + AGGGCCGGGGGAGGAGG 17 2617 BCL11A-2133 + CCGGGGGAGGAGGCGGC 17 2618 BCL11A-2134 + CGGGGGAGGAGGCGGCC 17 2619 BCL11A-2135 + GGGGGAGGAGGCGGCCG 17 2620 BCL11A-2136 + GGGGAGGAGGCGGCCGG 17 2621 BCL11A-2137 + AGGCGGCCGGGGGCACG 17 2622 BCL11A-2138 + GGCGGCCGGGGGCACGC 17 2623 BCL11A-2139 + CCGGGGGCACGCGGGAG 17 2624 BCL11A-2140 + CGGGGGCACGCGGGAGA 17 2625 BCL11A-2141 + GGGCACGCGGGAGAGGG 17 2626 BCL11A-2142 + GGCACGCGGGAGAGGGA 17 2627 BCL11A-2143 + ACGCGGGAGAGGGAGGG 17 2628 BCL11A-2144 + CGCGGGAGAGGGAGGGA 17 2629 BCL11A-2145 + GAGGGAGGGAGGGAGCC 17 2630 BCL11A-2146 + CCCGGACUGCUGCCUCC 17 2631 BCL11A-2147 + CCGGACUGCUGCCUCCU 17 2632 BCL11A-2148 + UCCCGACCGAACCUCAG 17 2633 BCL11A-2149 + GAACCUCAGAGGCAGCA 17 2634 BCL11A-2150 + GGCAGCAAGGAGAAGAC 17 2635 BCL11A-2151 + AUAAAAUAAAUAAAACA 17 2636

Table 3B provides exemplary targeting domains for repressing (i.e., knocking down or decreasing) expression of the BCL11A gene. Any of the targeting domains in the table can be used with a S. aureus eiCas9 molecule to cause a steric block in the promoter region to block transcription elongation resulting in the repression of the BCL6A gene. Any of the targeting domains in the table can be used with a S. aureus eiCas9 fused to a transcriptional repressor to decrease transcription and therefore downregulate gene expression.

TABLE 3B S. aureus gRNA targets for BCL11A knockdown Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO BCL11A-2152 CAGUCUUCUCCUUGCUGCCU 20 2637 BCL11A-2153 UUGCUGCCUCUGAGGUUCGG 20 2638 BCL11A-2154 UGCUGCCUCUGAGGUUCGGU 20 2639 BCL11A-2155 GCUGCCUCUGAGGUUCGGUC 20 2640 BCL11A-2156 UGCCUCUGAGGUUCGGUCGG 20 2641 BCL11A-2157 GCCUCUGAGGUUCGGUCGGG 20 2642 BCL11A-2158 CCUCUGAGGUUCGGUCGGGA 20 2643 BCL11A-2159 CUCUGAGGUUCGGUCGGGAG 20 2644 BCL11A-216O CUGAGGUUCGGUCGGGAGGG 20 2645 BCL11A-2161 AGGGGAGGGCAGCGGCAACC 20 2646 BCL11A-2162 GGGGAGGGCAGCGGCAACCC 20 2647 BCL11A-2163 GCAACCCAGGAGGCAGCAGU 20 2648 BCL11A-2164 GCGGCGGCGGCGGCGGCGGC 20 2649 BCL11A-2165 CGGCGGCGGCGGCGGCGGCG 20 2650 BCL11A-2166 GGCGGCGGCGGCGGCGGCGC 20 2651 BCL11A-2167 CGGCGGCGGCGGCGGCGCGG 20 2652 BCL11A-2168 GGCGGCGCGGGAGGGCAAGC 20 2653 BCL11A-2169 CGGCGCGGGAGGGCAAGCGC 20 2654 BCL11A-2170 GGCGCGGGAGGGCAAGCGCG 20 2655 BCL11A-2171 AGGAGCCGGCACAAAAGGCA 20 2656 BCL11A-2172 GGAGCCGGCACAAAAGGCAG 20 2657 BCL11A-2173 GGACAAACACCCACCUCUGG 20 2658 BCL11A-2174 GACAAACACCCACCUCUGGC 20 2659 BCL11A-2175 GCGGCCCCUCUCCCGACUCC 20 2660 BCL11A-2176 CUCUCCCGACUCCGCGGACU 20 2661 BCL11A-2177 UCUCCCGACUCCGCGGACUC 20 2662 BCL11A-2178 ACUCCGCGGACUCAGGAGCG 20 2663 BCL11A-2179 CUCCGCGGACUCAGGAGCGC 20 2664 BCL11A-2180 UCCGCGGACUCAGGAGCGCC 20 2665 BCL11A-2181 AGUGCCACUUUCUCACUAUU 20 2666 BCL11A-2182 GUGCCACUUUCUCACUAUUG 20 2667 BCL11A-2183 UGCCACUUUCUCACUAUUGU 20 2668 BCL11A-2184 CUCCCGCUGCACACUUGACC 20 2669 BCL11A-2185 CAGUCUCACCUCUUUUCUCC 20 2670 BCL11A-2186 AGUCUCACCUCUUUUCUCCC 20 2671 BCL11A-2187 GUCUCACCUCUUUUCUCCCC 20 2672 BCL11A-2188 UACCCCCCCAUUUUCUUACG 20 2673 BCL11A-2189 CCCCCAUUUUCUUACGGUGA 20 2674 BCL11A-2190 CCCCAUUUUCUUACGGUGAG 20 2675 BCL11A-2191 CCCAUUUUCUUACGGUGAGU 20 2676 BCL11A-2192 UCCCACCCCCAGGUUUGCAU 20 2677 BCL11A-2193 UUCAUUAUUUUGCAAAACUG 20 2678 BCL11A-2194 UCAUUAUUUUGCAAAACUGG 20 2679 BCL11A-2195 UAUUUUGCAAAACUGGCGGG 20 2680 BCL11A-2196 AUUUUGCAAAACUGGCGGGG 20 2681 BCL11A-2197 UUUUGCAAAACUGGCGGGGC 20 2682 BCL11A-2198 UUUGCAAAACUGGCGGGGCG 20 2683 BCL11A-2199 UUGCAAAACUGGCGGGGCGG 20 2684 BCL11A-2200 UGCAAAACUGGCGGGGCGGG 20 2685 BCL11A-2201 GCAAAACUGGCGGGGCGGGG 20 2686 BCL11A-2202 CAAAACUGGCGGGGCGGGGG 20 2687 BCL11A-2203 ACUGGCGGGGCGGGGGGGGA 20 2688 BCL11A-2204 CUGGCGGGGCGGGGGGGGAG 20 2689 BCL11A-2205 UGGAAUCAUUGCAUUCCUUU 20 2690 BCL11A-2206 UCAUUGCAUUCCUUUUCGAA 20 2691 BCL11A-2207 AUUGCAUUCCUUUUCGAAAA 20 2692 BCL11A-2208 UCGAAAAGAGAAAUAAAGCG 20 2693 BCL11A-2209 CGAAAAGAGAAAUAAAGCGG 20 2694 BCL11A-2210 AAGAGAAAUAAAGCGGCGGA 20 2695 BCL11A-2211 AGAGAAAUAAAGCGGCGGAA 20 2696 BCL11A-2212 AGAAAUAAAGCGGCGGAAAG 20 2697 BCL11A-2213 GAAAUAAAGCGGCGGAAAGG 20 2698 BCL11A-2214 UAAAGCGGCGGAAAGGAGGA 20 2699 BCL11A-2215 AAGCGGCGGAAAGGAGGAAA 20 2700 BCL11A-2216 AGCGGCGGAAAGGAGGAAAG 20 2701 BCL11A-2217 CGGCGGAAAGGAGGAAAGAG 20 2702 BCL11A-2218 GGCGGAAAGGAGGAAAGAGG 20 2703 BCL11A-2219 AUACACGGCAAUGGUUCCAG 20 2704 BCL11A-2220 UACACGGCAAUGGUUCCAGA 20 2705 BCL11A-2221 CGGCAAUGGUUCCAGAUGGG 20 2706 BCL11A-2222 GCAAUGGUUCCAGAUGGGAU 20 2707 BCL11A-2223 UAUCUCUUUUACCUCGACUC 20 2708 BCL11A-2224 AUCUCUUUUACCUCGACUCU 20 2709 BCL11A-2225 GACUCUCGGAGGUUUUUCUC 20 2710 BCL11A-2226 AAUAAUUAUUAUUACUAUUA 20 2711 BCL11A-2227 ACUAUUAUUGGGUUACUUAC 20 2712 BCL11A-2228 UAUUAUUGGGUUACUUACGC 20 2713 BCL11A-2229 UCUUCUCCUUGCUGCCU 17 2714 BCL11A-2230 CUGCCUCUGAGGUUCGG 17 2715 BCL11A-2231 UGCCUCUGAGGUUCGGU 17 2716 BCL11A-2232 GCCUCUGAGGUUCGGUC 17 2717 BCL11A-2233 CUCUGAGGUUCGGUCGG 17 2718 BCL11A-2234 UCUGAGGUUCGGUCGGG 17 2719 BCL11A-2235 CUGAGGUUCGGUCGGGA 17 2720 BCL11A-2236 UGAGGUUCGGUCGGGAG 17 2721 BCL11A-2237 AGGUUCGGUCGGGAGGG 17 2722 BCL11A-2238 GGAGGGCAGCGGCAACC 17 2723 BCL11A-2239 GAGGGCAGCGGCAACCC 17 2724 BCL11A-2240 ACCCAGGAGGCAGCAGU 17 2725 BCL11A-2241 GCGGCGGCGGCGGCGGC 17 2726 BCL11A-2242 CGGCGGCGGCGGCGGCG 17 2727 BCL11A-2243 GGCGGCGGCGGCGGCGC 17 2728 BCL11A-2244 CGGCGGCGGCGGCGCGG 17 2729 BCL11A-2245 GGCGCGGGAGGGCAAGC 17 2730 BCL11A-2246 CGCGGGAGGGCAAGCGC 17 2731 BCL11A-2247 GCGGGAGGGCAAGCGCG 17 2732 BCL11A-2248 AGCCGGCACAAAAGGCA 17 2733 BCL11A-2249 GCCGGCACAAAAGGCAG 17 2734 BCL11A-2250 CAAACACCCACCUCUGG 17 2735 BCL11A-2251 AAACACCCACCUCUGGC 17 2736 BCL11A-2252 GCCCCUCUCCCGACUCC 17 2737 BCL11A-2253 UCCCGACUCCGCGGACU 17 2738 BCL11A-2254 CCCGACUCCGCGGACUC 17 2739 BCL11A-2255 CCGCGGACUCAGGAGCG 17 2740 BCL11A-2256 CGCGGACUCAGGAGCGC 17 2741 BCL11A-2257 GCGGACUCAGGAGCGCC 17 2742 BCL11A-2258 GCCACUUUCUCACUAUU 17 2743 BCL11A-2259 CCACUUUCUCACUAUUG 17 2744 BCL11A-2260 CACUUUCUCACUAUUGU 17 2745 BCL11A-2261 CCGCUGCACACUUGACC 17 2746 BCL11A-2262 UCUCACCUCUUUUCUCC 17 2747 BCL11A-2263 CUCACCUCUUUUCUCCC 17 2748 BCL11A-2264 UCACCUCUUUUCUCCCC 17 2749 BCL11A-2265 CCCCCCAUUUUCUUACG 17 2750 BCL11A-2266 CCAUUUUCUUACGGUGA 17 2751 BCL11A-2267 CAUUUUCUUACGGUGAG 17 2752 BCL11A-2268 AUUUUCUUACGGUGAGU 17 2753 BCL11A-2269 CACCCCCAGGUUUGCAU 17 2754 BCL11A-2270 AUUAUUUUGCAAAACUG 17 2755 BCL11A-2271 UUAUUUUGCAAAACUGG 17 2756 BCL11A-2272 UUUGCAAAACUGGCGGG 17 2757 BCL11A-2273 UUGCAAAACUGGCGGGG 17 2758 BCL11A-2274 UGCAAAACUGGCGGGGC 17 2759 BCL11A-2275 GCAAAACUGGCGGGGCG 17 2760 BCL11A-2276 CAAAACUGGCGGGGCGG 17 2761 BCL11A-2277 AAAACUGGCGGGGCGGG 17 2762 BCL11A-2278 AAACUGGCGGGGCGGGG 17 2763 BCL11A-2279 AACUGGCGGGGCGGGGG 17 2764 BCL11A-2280 GGCGGGGCGGGGGGGGA 17 2765 BCL11A-2281 GCGGGGCGGGGGGGGAG 17 2766 BCL11A-2282 AAUCAUUGCAUUCCUUU 17 2767 BCL11A-2283 UUGCAUUCCUUUUCGAA 17 2768 BCL11A-2284 GCAUUCCUUUUCGAAAA 17 2769 BCL11A-2285 AAAAGAGAAAUAAAGCG 17 2770 BCL11A-2286 AAAGAGAAAUAAAGCGG 17 2771 BCL11A-2287 AGAAAUAAAGCGGCGGA 17 2772 BCL11A-2288 GAAAUAAAGCGGCGGAA 17 2773 BCL11A-2289 AAUAAAGCGGCGGAAAG 17 2774 BCL11A-2290 AUAAAGCGGCGGAAAGG 17 2775 BCL11A-2291 AGCGGCGGAAAGGAGGA 17 2776 BCL11A-2292 CGGCGGAAAGGAGGAAA 17 2777 BCL11A-2293 GGCGGAAAGGAGGAAAG 17 2778 BCL11A-2294 CGGAAAGGAGGAAAGAG 17 2779 BCL11A-2295 GGAAAGGAGGAAAGAGG 17 2780 BCL11A-2296 CACGGCAAUGGUUCCAG 17 2781 BCL11A-2297 ACGGCAAUGGUUCCAGA 17 2782 BCL11A-2298 CAAUGGUUCCAGAUGGG 17 2783 BCL11A-2299 AUGGUUCCAGAUGGGAU 17 2784 BCL11A-2300 CUCUUUUACCUCGACUC 17 2785 BCL11A-2301 UCUUUUACCUCGACUCU 17 2786 BCL11A-2302 UCUCGGAGGUUUUUCUC 17 2787 BCL11A-2303 AAUUAUUAUUACUAUUA 17 2788 BCL11A-2304 AUUAUUGGGUUACUUAC 17 2789 BCL11A-2305 UAUUGGGUUACUUACGC 17 2790 BCL11A-2306 + CGAACCUCAGAGGCAGCAAG 20 2791 BCL11A-2307 + ACCGAACCUCAGAGGCAGCA 20 2792 BCL11A-2308 + GACCGAACCUCAGAGGCAGC 20 2793 BCL11A-2309 + CUCCCCUCCCGACCGAACCU 20 2794 BCL11A-2310 + CCGCUGCCCUCCCCUCCCGA 20 2795 BCL11A-2311 + GGAGCCCGGACUGCUGCCUC 20 2796 BCL11A-2312 + GGGAGAGGGAGGGAGGGAGC 20 2797 BCL11A-2313 + GCACGCGGGAGAGGGAGGGA 20 2798 BCL11A-2314 + GGCACGCGGGAGAGGGAGGG 20 2799 BCL11A-2315 + GGGCACGCGGGAGAGGGAGG 20 2800 BCL11A-2316 + GGGGGCACGCGGGAGAGGGA 20 2801 BCL11A-2317 + CGGGGGCACGCGGGAGAGGG 20 2802 BCL11A-2318 + CCGGGGGCACGCGGGAGAGG 20 2803 BCL11A-2319 + GGCCGGGGGCACGCGGGAGA 20 2804 BCL11A-2320 + CGGCCGGGGGCACGCGGGAG 20 2805 BCL11A-2321 + GCGGCCGGGGGCACGCGGGA 20 2806 BCL11A-2322 + AGGCGGCCGGGGGCACGCGG 20 2807 BCL11A-2323 + GGAGGCGGCCGGGGGCACGC 20 2808 BCL11A-2324 + AGGAGGCGGCCGGGGGCACG 20 2809 BCL11A-2325 + GAGGAGGCGGCCGGGGGCAC 20 2810 BCL11A-2326 + GGCCGGGGGAGGAGGCGGCC 20 2811 BCL11A-2327 + GGGCCGGGGGAGGAGGCGGC 20 2812 BCL11A-2328 + AGGGCCGGGGGAGGAGGCGG 20 2813 BCL11A-2329 + GCAGGAGCUAGGGCCGGGGG 20 2814 BCL11A-2330 + GGCAGGAGCUAGGGCCGGGG 20 2815 BCL11A-2331 + AGGGCAGGAGCUAGGGCCGG 20 2816 BCL11A-2332 + AAGGGCAGGAGCUAGGGCCG 20 2817 BCL11A-2333 + GAAGGGCAGGAGCUAGGGCC 20 2818 BCL11A-2334 + CGAAGGGCAGGAGCUAGGGC 20 2819 BCL11A-2335 + CCGAAGGGCAGGAGCUAGGG 20 2820 BCL11A-2336 + CGCCGCCGAAGGGCAGGAGC 20 2821 BCL11A-2337 + CGCCGCCGCCGCCGAAGGGC 20 2822 BCL11A-2338 + CCGCCGCCGCCGCCGAAGGG 20 2823 BCL11A-2339 + CGCCGCCGCCGCCGCCGCCG 20 2824 BCL11A-2340 + CGCCGCCGCCGCCGCCGCCG 20 2825 BCL11A-2341 + GCCUUUUGUUCCGGCCAGAG 20 2826 BCL11A-2342 + CUGCCGCCUUUUGUUCCGGC 20 2827 BCL11A-2343 + GCCGUGGGACCGGGAAGGAC 20 2828 BCL11A-2344 + AGCCGUGGGACCGGGAAGGA 20 2829 BCL11A-2345 + GAGCCGUGGGACCGGGAAGG 20 2830 BCL11A-2346 + GGGAGAGCCGUGGGACCGGG 20 2831 BCL11A-2347 + ACGGGGAGAGCCGUGGGACC 20 2832 BCL11A-2348 + GACGGGGAGAGCCGUGGGAC 20 2833 BCL11A-2349 + CGACGGGGAGAGCCGUGGGA 20 2834 BCL11A-2350 + CGCGGCGACGGGGAGAGCCG 20 2835 BCL11A-2351 + CCGCGGCGACGGGGAGAGCC 20 2836 BCL11A-2352 + AGAGGGGCCGCGGCGACGGG 20 2837 BCL11A-2353 + GGAGAGGGGCCGCGGCGACG 20 2838 BCL11A-2354 + GGGAGAGGGGCCGCGGCGAC 20 2839 BCL11A-2355 + CGGGAGAGGGGCCGCGGCGA 20 2840 BCL11A-2356 + UCGGGAGAGGGGCCGCGGCG 20 2841 BCL11A-2357 + UGAGUCCGCGGAGUCGGGAG 20 2842 BCL11A-2358 + CUGAGUCCGCGGAGUCGGGA 20 2843 BCL11A-2359 + UCCUGAGUCCGCGGAGUCGG 20 2844 BCL11A-2360 + GCUCCUGAGUCCGCGGAGUC 20 2845 BCL11A-2361 + CGCUCCUGAGUCCGCGGAGU 20 2846 BCL11A-2362 + GCGCUCCUGAGUCCGCGGAG 20 2847 BCL11A-2363 + CCCCGGCGCUCCUGAGUCCG 20 2848 BCL11A-2364 + CCCCCGGCGCUCCUGAGUCC 20 2849 BCL11A-2365 + GAAAGGGGCCCCCGGCGCUC 20 2850 BCL11A-2366 + GAGAAAGUGGCACUGUGGAA 20 2851 BCL11A-2367 + UGAGAAAGUGGCACUGUGGA 20 2852 BCL11A-2368 + AUAGUGAGAAAGUGGCACUG 20 2853 BCL11A-2369 + AAUAGUGAGAAAGUGGCACU 20 2854 BCL11A-2370 + GUAGUCAUCCCCACAAUAGU 20 2855 BCL11A-2371 + AAGUAGUCAUCCCCACAAUA 20 2856 BCL11A-2372 + ACGGUCAAGUGUGCAGCGGG 20 2857 BCL11A-2373 + CACGGUCAAGUGUGCAGCGG 20 2858 BCL11A-2374 + CUCACGGUCAAGUGUGCAGC 20 2859 BCL11A-2375 + GCUCACGGUCAAGUGUGCAG 20 2860 BCL11A-2376 + CGCUCACGGUCAAGUGUGCA 20 2861 BCL11A-2377 + AAAAGAGGUGAGACUGGCUU 20 2862 BCL11A-2378 + GAUUCCCGGGGAGAAAAGAG 20 2863 BCL11A-2379 + AAAACGAUUCCCGGGGAGAA 20 2864 BCL11A-2380 + UCUAAAAAACGAUUCCCGGG 20 2865 BCL11A-2381 + AGUCUAAAAAACGAUUCCCG 20 2866 BCL11A-2382 + AAGUCUAAAAAACGAUUCCC 20 2867 BCL11A-2383 + CAAGUCUAAAAAACGAUUCC 20 2868 BCL11A-2384 + ACAAGUCUAAAAAACGAUUC 20 2869 BCL11A-2385 + AAUGGGGGGGUAGGGAGGGA 20 2870 BCL11A-2386 + AGAAAAUGGGGGGGUAGGGA 20 2871 BCL11A-2387 + AAGAAAAUGGGGGGGUAGGG 20 2872 BCL11A-2388 + UAAGAAAAUGGGGGGGUAGG 20 2873 BCL11A-2389 + CGUAAGAAAAUGGGGGGGUA 20 2874 BCL11A-2390 + CCGUAAGAAAAUGGGGGGGU 20 2875 BCL11A-2391 + ACCGUAAGAAAAUGGGGGGG 20 2876 BCL11A-2392 + CACUCACCGUAAGAAAAUGG 20 2877 BCL11A-2393 + CCACUCACCGUAAGAAAAUG 20 2878 BCL11A-2394 + CCCACUCACCGUAAGAAAAU 20 2879 BCL11A-2395 + UCCCACUCACCGUAAGAAAA 20 2880 BCL11A-2396 + UUCCCACUCACCGUAAGAAA 20 2881 BCL11A-2397 + GGUUGCUUCCCACUCACCGU 20 2882 BCL11A-2398 + GGUGGGAGCUGGUGGGGAAA 20 2883 BCL11A-2399 + GGGUGGGAGCUGGUGGGGAA 20 2884 BCL11A-2400 + GGGGUGGGAGCUGGUGGGGA 20 2885 BCL11A-2401 + CCUGGGGGUGGGAGCUGGUG 20 2886 BCL11A-2402 + ACCUGGGGGUGGGAGCUGGU 20 2887 BCL11A-2403 + AACCUGGGGGUGGGAGCUGG 20 2888 BCL11A-2404 + AAACCUGGGGGUGGGAGCUG 20 2889 BCL11A-2405 + UCACAUGCAAACCUGGGGGU 20 2890 BCL11A-2406 + CUCACAUGCAAACCUGGGGG 20 2891 BCL11A-2407 + ACUCACAUGCAAACCUGGGG 20 2892 BCL11A-2408 + AACAACUCACAUGCAAACCU 20 2893 BCL11A-2409 + GAACAACUCACAUGCAAACC 20 2894 BCL11A-2410 + CGAACAACUCACAUGCAAAC 20 2895 BCL11A-2411 + UAAUGAACAAUGCUAAGGUU 20 2896 BCL11A-2412 + CCCGCCAGUUUUGCAAAAUA 20 2897 BCL11A-2413 + CUUUAUUUCUCUUUUCGAAA 20 2898 BCL11A-2414 + GCUUUAUUUCUCUUUUCGAA 20 2899 BCL11A-2415 + CCGCCGCUUUAUUUCUCUUU 20 2900 BCL11A-2416 + CCAUUGCCGUGUAUGCACUU 20 2901 BCL11A-2417 + GAAAAAACCCUCAUCCCAUC 20 2902 BCL11A-2418 + GGAAAAAACCCUCAUCCCAU 20 2903 BCL11A-2419 + CGAGGUAAAAGAGAUAAAGG 20 2904 BCL11A-2420 + UCGAGGUAAAAGAGAUAAAG 20 2905 BCL11A-2421 + GUCGAGGUAAAAGAGAUAAA 20 2906 BCL11A-2422 + AGUCGAGGUAAAAGAGAUAA 20 2907 BCL11A-2423 + GAGUCGAGGUAAAAGAGAUA 20 2908 BCL11A-2424 + ACCUCCGAGAGUCGAGGUAA 20 2909 BCL11A-2425 + ACGAGAAAAACCUCCGAGAG 20 2910 BCL11A-2426 + UUUUCACGAGAAAAACCUCC 20 2911 BCL11A-2427 + AUUUUUCACGAGAAAAACCU 20 2912 BCL11A-2428 + UGCAUUUUUAAAUUUUUCAC 20 2913 BCL11A-2429 + CAUGCAUUUUUAAAUUUUUC 20 2914 BCL11A-2430 + AGCAAAAGCGAGGGGGAGAG 20 2915 BCL11A-2431 + AAGCAAAAGCGAGGGGGAGA 20 2916 BCL11A-2432 + AGAAGCAAAAGCGAGGGGGA 20 2917 BCL11A-2433 + CUAGAAGCAAAAGCGAGGGG 20 2918 BCL11A-2434 + GACUAGAAGCAAAAGCGAGG 20 2919 BCL11A-2435 + GGACUAGAAGCAAAAGCGAG 20 2920 BCL11A-2436 + AGGACUAGAAGCAAAAGCGA 20 2921 BCL11A-2437 + CAGGACUAGAAGCAAAAGCG 20 2922 BCL11A-2438 + GCAGGACUAGAAGCAAAAGC 20 2923 BCL11A-2439 + GCGCAGGACUAGAAGCAAAA 20 2924 BCL11A-2440 + AUCACGAGAGCGCGCAGGAC 20 2925 BCL11A-2441 + UUAAUAAUCACGAGAGCGCG 20 2926 BCL11A-2442 + UAAUAAUUAUUAAUAAUCAC 20 2927 BCL11A-2443 + AAUAAUAAUUAUUAAUAAUC 20 2928 BCL11A-2444 + ACCUCAGAGGCAGCAAG 17 2929 BCL11A-2445 + GAACCUCAGAGGCAGCA 17 2930 BCL11A-2446 + CGAACCUCAGAGGCAGC 17 2931 BCL11A-2447 + CCCUCCCGACCGAACCU 17 2932 BCL11A-2448 + CUGCCCUCCCCUCCCGA 17 2933 BCL11A-2449 + GCCCGGACUGCUGCCUC 17 2934 BCL11A-2450 + AGAGGGAGGGAGGGAGC 17 2935 BCL11A-2451 + CGCGGGAGAGGGAGGGA 17 2936 BCL11A-2452 + ACGCGGGAGAGGGAGGG 17 2937 BCL11A-2453 + CACGCGGGAGAGGGAGG 17 2938 BCL11A-2454 + GGCACGCGGGAGAGGGA 17 2939 BCL11A-2455 + GGGCACGCGGGAGAGGG 17 2940 BCL11A-2456 + GGGGCACGCGGGAGAGG 17 2941 BCL11A-2457 + CGGGGGCACGCGGGAGA 17 2942 BCL11A-2458 + CCGGGGGCACGCGGGAG 17 2943 BCL11A-2459 + GCCGGGGGCACGCGGGA 17 2944 BCL11A-2460 + CGGCCGGGGGCACGCGG 17 2945 BCL11A-2461 + GGCGGCCGGGGGCACGC 17 2946 BCL11A-2462 + AGGCGGCCGGGGGCACG 17 2947 BCL11A-2463 + GAGGCGGCCGGGGGCAC 17 2948 BCL11A-2464 + CGGGGGAGGAGGCGGCC 17 2949 BCL11A-2465 + CCGGGGGAGGAGGCGGC 17 2950 BCL11A-2466 + GCCGGGGGAGGAGGCGG 17 2951 BCL11A-2467 + GGAGCUAGGGCCGGGGG 17 2952 BCL11A-2468 + AGGAGCUAGGGCCGGGG 17 2953 BCL11A-2469 + GCAGGAGCUAGGGCCGG 17 2954 BCL11A-2470 + GGCAGGAGCUAGGGCCG 17 2955 BCL11A-2471 + GGGCAGGAGCUAGGGCC 17 2956 BCL11A-2472 + AGGGCAGGAGCUAGGGC 17 2957 BCL11A-2473 + AAGGGCAGGAGCUAGGG 17 2958 BCL11A-2474 + CGCCGAAGGGCAGGAGC 17 2959 BCL11A-2475 + CGCCGCCGCCGAAGGGC 17 2960 BCL11A-2476 + CCGCCGCCGCCGAAGGG 17 2961 BCL11A-2477 + CGCCGCCGCCGCCGCCG 17 2962 BCL11A-2478 + CGCCGCCGCCGCCGCCG 17 2963 BCL11A-2479 + UUUUGUUCCGGCCAGAG 17 2964 BCL11A-2480 + CCGCCUUUUGUUCCGGC 17 2965 BCL11A-2481 + GUGGGACCGGGAAGGAC 17 2966 BCL11A-2482 + CGUGGGACCGGGAAGGA 17 2967 BCL11A-2483 + CCGUGGGACCGGGAAGG 17 2968 BCL11A-2484 + AGAGCCGUGGGACCGGG 17 2969 BCL11A-2485 + GGGAGAGCCGUGGGACC 17 2970 BCL11A-2486 + GGGGAGAGCCGUGGGAC 17 2971 BCL11A-2487 + CGGGGAGAGCCGUGGGA 17 2972 BCL11A-2488 + GGCGACGGGGAGAGCCG 17 2973 BCL11A-2489 + CGGCGACGGGGAGAGCC 17 2974 BCL11A-2490 + GGGGCCGCGGCGACGGG 17 2975 BCL11A-2491 + GAGGGGCCGCGGCGACG 17 2976 BCL11A-2492 + AGAGGGGCCGCGGCGAC 17 2977 BCL11A-2493 + GAGAGGGGCCGCGGCGA 17 2978 BCL11A-2494 + GGAGAGGGGCCGCGGCG 17 2979 BCL11A-2495 + GUCCGCGGAGUCGGGAG 17 2980 BCL11A-2496 + AGUCCGCGGAGUCGGGA 17 2981 BCL11A-2497 + UGAGUCCGCGGAGUCGG 17 2982 BCL11A-2498 + CCUGAGUCCGCGGAGUC 17 2983 BCL11A-2499 + UCCUGAGUCCGCGGAGU 17 2984 BCL11A-2500 + CUCCUGAGUCCGCGGAG 17 2985 BCL11A-2501 + CGGCGCUCCUGAGUCCG 17 2986 BCL11A-2502 + CCGGCGCUCCUGAGUCC 17 2987 BCL11A-2503 + AGGGGCCCCCGGCGCUC 17 2988 BCL11A-2504 + AAAGUGGCACUGUGGAA 17 2989 BCL11A-2505 + GAAAGUGGCACUGUGGA 17 2990 BCL11A-2506 + GUGAGAAAGUGGCACUG 17 2991 BCL11A-2507 + AGUGAGAAAGUGGCACU 17 2992 BCL11A-2508 + GUCAUCCCCACAAUAGU 17 2993 BCL11A-2509 + UAGUCAUCCCCACAAUA 17 2994 BCL11A-2510 + GUCAAGUGUGCAGCGGG 17 2995 BCL11A-2511 + GGUCAAGUGUGCAGCGG 17 2996 BCL11A-2512 + ACGGUCAAGUGUGCAGC 17 2997 BCL11A-2513 + CACGGUCAAGUGUGCAG 17 2998 BCL11A-2514 + UCACGGUCAAGUGUGCA 17 2999 BCL11A-2515 + AGAGGUGAGACUGGCUU 17 3000 BCL11A-2516 + UCCCGGGGAGAAAAGAG 17 3001 BCL11A-2517 + ACGAUUCCCGGGGAGAA 17 3002 BCL11A-2518 + AAAAAACGAUUCCCGGG 17 3003 BCL11A-2519 + CUAAAAAACGAUUCCCG 17 3004 BCL11A-2520 + UCUAAAAAACGAUUCCC 17 3005 BCL11A-2521 + GUCUAAAAAACGAUUCC 17 3006 BCL11A-2522 + AGUCUAAAAAACGAUUC 17 3007 BCL11A-2523 + GGGGGGGUAGGGAGGGA 17 3008 BCL11A-2524 + AAAUGGGGGGGUAGGGA 17 3009 BCL11A-2525 + AAAAUGGGGGGGUAGGG 17 3010 BCL11A-2526 + GAAAAUGGGGGGGUAGG 17 3011 BCL11A-2527 + AAGAAAAUGGGGGGGUA 17 3012 BCL11A-2528 + UAAGAAAAUGGGGGGGU 17 3013 BCL11A-2529 + GUAAGAAAAUGGGGGGG 17 3014 BCL11A-2530 + UCACCGUAAGAAAAUGG 17 3015 BCL11A-2531 + CUCACCGUAAGAAAAUG 17 3016 BCL11A-2532 + ACUCACCGUAAGAAAAU 17 3017 BCL11A-2533 + CACUCACCGUAAGAAAA 17 3018 BCL11A-2534 + CCACUCACCGUAAGAAA 17 3019 BCL11A-2535 + UGCUUCCCACUCACCGU 17 3020 BCL11A-2536 + GGGAGCUGGUGGGGAAA 17 3021 BCL11A-2537 + UGGGAGCUGGUGGGGAA 17 3022 BCL11A-2538 + GUGGGAGCUGGUGGGGA 17 3023 BCL11A-2539 + GGGGGUGGGAGCUGGUG 17 3024 BCL11A-2540 + UGGGGGUGGGAGCUGGU 17 3025 BCL11A-2541 + CUGGGGGUGGGAGCUGG 17 3026 BCL11A-2542 + CCUGGGGGUGGGAGCUG 17 3027 BCL11A-2543 + CAUGCAAACCUGGGGGU 17 3028 BCL11A-2544 + ACAUGCAAACCUGGGGG 17 3029 BCL11A-2545 + CACAUGCAAACCUGGGG 17 3030 BCL11A-2546 + AACUCACAUGCAAACCU 17 3031 BCL11A-2547 + CAACUCACAUGCAAACC 17 3032 BCL11A-2548 + ACAACUCACAUGCAAAC 17 3033 BCL11A-2549 + UGAACAAUGCUAAGGUU 17 3034 BCL11A-2550 + GCCAGUUUUGCAAAAUA 17 3035 BCL11A-2551 + UAUUUCUCUUUUCGAAA 17 3036 BCL11A-2552 + UUAUUUCUCUUUUCGAA 17 3037 BCL11A-2553 + CCGCUUUAUUUCUCUUU 17 3038 BCL11A-2554 + UUGCCGUGUAUGCACUU 17 3039 BCL11A-2555 + AAAACCCUCAUCCCAUC 17 3040 BCL11A-2556 + AAAAACCCUCAUCCCAU 17 3041 BCL11A-2557 + GGUAAAAGAGAUAAAGG 17 3042 BCL11A-2558 + AGGUAAAAGAGAUAAAG 17 3043 BCL11A-2559 + GAGGUAAAAGAGAUAAA 17 3044 BCL11A-2560 + CGAGGUAAAAGAGAUAA 17 3045 BCL11A-2561 + UCGAGGUAAAAGAGAUA 17 3046 BCL11A-2562 + UCCGAGAGUCGAGGUAA 17 3047 BCL11A-2563 + AGAAAAACCUCCGAGAG 17 3048 BCL11A-2564 + UCACGAGAAAAACCUCC 17 3049 BCL11A-2565 + UUUCACGAGAAAAACCU 17 3050 BCL11A-2566 + AUUUUUAAAUUUUUCAC 17 3051 BCL11A-2567 + GCAUUUUUAAAUUUUUC 17 3052 BCL11A-2568 + AAAAGCGAGGGGGAGAG 17 3053 BCL11A-2569 + CAAAAGCGAGGGGGAGA 17 3054 BCL11A-2570 + AGCAAAAGCGAGGGGGA 17 3055 BCL11A-2571 + GAAGCAAAAGCGAGGGG 17 3056 BCL11A-2572 + UAGAAGCAAAAGCGAGG 17 3057 BCL11A-2573 + CUAGAAGCAAAAGCGAG 17 3058 BCL11A-2574 + ACUAGAAGCAAAAGCGA 17 3059 BCL11A-2575 + GACUAGAAGCAAAAGCG 17 3060 BCL11A-2576 + GGACUAGAAGCAAAAGC 17 3061 BCL11A-2577 + CAGGACUAGAAGCAAAA 17 3062 BCL11A-2578 + ACGAGAGCGCGCAGGAC 17 3063 BCL11A-2579 + AUAAUCACGAGAGCGCG 17 3064 BCL11A-2580 + UAAUUAUUAAUAAUCAC 17 3065 BCL11A-2581 + AAUAAUUAUUAAUAAUC 17 3066

Table 3C provides exemplary targeting domains for repressing (i.e., knocking down or decreasing) expression of the BCL11A gene. Any of the targeting domains in the table can be used with an N. meningitidis eiCas9 molecule to cause a steric block in the promoter region to block transcription elongation resulting in the repression of the BCL11A gene. Any of the targeting domains in the table can be used with an N. meningitidis eiCas9 fused to a transcriptional repressor to decrease transcription and therefore downregulate gene expression.

TABLE 3C N. meningitidis gRNA targets for BCL11A knockdown Target SEQ DNA Targeting Site ID gRNA Name Strand Domain Length NO BCL11A-2582 GCUUCUAGUC 20 3067 CUGCGCGCUC BCL11A-2583 UCUAGUCCUG 17 3068 CGCGCUC BCL11A-2584 + UUUAGACUUG 20 3069 UACUCACUCC BCL11A-2585 + CAUUCCUUUU 20 3070 CGAAAAGAGA BCL11A-2586 + UUUAGACUUG 17 3071 UACUCAC BCL11A-2587 + CAUUCCUUUU 17 3072 CGAAAAG

Table 4A provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to first tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon, good orthogonality, start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. pyogenes Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. pyogenes Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp. Exemplary gRNA pairs are: BCL11A-2607 and BCL11A-2593, BCL11A-2607 and BCL11A-2598, BCL11A-264 and BCL11A-2593, BCL11A-2614 and BCL11A-2598, BCL11A-2589 and BCL11A-2664, BCL11A-2589 and BCL11A-2666, BCL11A-2596 and BCL11A-2664, BCL11A-2596 and BCL11A-2666, BCL11A-2603 and BCL11A-2664, of BCL11A-2603 and BCL11A-2666.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene. For example, gRNA pairs that target upstream (i.e., 5′) of the enhancer region in the BCL11A gene (e.g., 2607 and BCL11A-2593, BCL11A-2607 and BCL11A-2598, BCL11A-264 and BCL11A-2593, or BCL11A-2614 and BCL11A-2598) can be paired with gRNA pairs that target downstream (i.e., 3′) of the enhancer region in the BCL11A gene (e.g., BCL11A-2589 and BCL11A-2664, BCL11A-2589 and BCL11A-2666, BCL11A-2596 and BCL11A-2664, BCL11A-2596 and BCL11A-2666, BCL11A-2603 and BCL11A-2664, of BCL11A-2603 and BCL11A-2666).

TABLE 4A Target SEQ 1st Tier DNA Targeting Site ID gRNA Name Strand Domain Length NO BCL11A-2588 + GAGCUCCAUG 20 3073 UGCAGAACGA BCL11A-2589 + GAGCUCCCAA 17 3074 CGGGCCG BCL11A-2590 GAGUGCAGAA 20 3075 UAUGCCCCGC BCL11A-2591 + GAUAAACAAU 20 3076 CGUCAUCCUC BCL11A-2592 + GAUGCCAACC 20 3077 UCCACGGGAU BCL11A-2593 GCAGAAUAUG 17 3078 CCCCGCA BCL11A-2594 GCAUCCAAUC 20 3079 CCGUGGAGGU BCL11A-2595 + GCCAACCUCC 17 3080 ACGGGAU BCL11A-2596 + GCUCCCAACG 20 3081 GGCCGUGGUC BCL11A-2597 GGAGCUCUAA 20 3082 UCCCCACGCC

Table 4B provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to second tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon, good orthogonality, and do not start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. pyogenes Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. pyogenes Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 4B Target SEQ 2nd Tier DNA Targeting Site ID gRNA Name Strand Domain Length NO BCL11A-2598 AGCAUCCAAU 17 3083 CCCGUGG BCL11A-2599 AGUGCAGAAU 20 3084 AUGCCCCGCA BCL11A-2600 AUGUCUCGCC 17 3085 GCAAGCA BCL11A-2601 + AUUCCCGUUU 20 3086 GCUUAAGUGC BCL11A-2602 + CAUCCUCUGG 17 3087 CGUGACC BCL11A-2603 + CCCAACGGGC 17 3088 CGUGGUC BCL11A-2604 + CCCCCAAUGG 20 3089 GAAGUUCAUC BCL11A-2605 + CCCGUUUGCU 17 3090 UAAGUGC BCL11A-2606 + CGUCAUCCUC 20 3091 UGGCGUGACC BCL11A-2607 + UCAUCUCGAU 17 3092 UGGUGAA BCL11A-2608 UCCAAUCCCG 17 3093 UGGAGGU BCL11A-2609 + UCCCGUUUGC 20 3094 UUAAGUGCUG BCL11A-2610 UGAACCAGAC 20 3095 CACGGCCCGU BCL11A-2611 UGCAGAAUAU 17 3096 GCCCCGC BCL11A-2612 UGGCAUCCAG 20 3097 GUCACGCCAG BCL11A-2613 UUAUCAACGU 17 3098 CAUCUAG BCL11A-2614 + UUCAUCUCGA 17 3099 UUGGUGA

Table 4C provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to third tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon and start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. pyogenes Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. pyogenes Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 4C 3rd Tier Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO BCL11A-2615 GAAAAAAGCAUCCAAUCCCG 20 3100 BCL11A-2616 GAACCAGACCACGGCCCGUU 20 3101 BCL11A-2617 + GACCUGGAUGCCAACCUCCA 20 3102 BCL11A-2618 GAGCUCUAAUCCCCACGCCU 20 3103 BCL11A-2619 GAUCAUGACCUCCUCACCUG 20 3104 BCL11A-2620 GAUGAACUUCCCAUUGG 17 3105 BCL11A-2621 GAUGAUGAACCAGACCA 17 3106 BCL11A-2622 + GAUGCUUUUUUCAUCUCGAU 20 3107 BCL11A-2623 + GCACUCAUCCCAGGCGU 17 3108 BCL11A-2624 + GCAUAUUCUGCACUCAUCCC 20 3109 BCL11A-2625 GCCAGAUGAACUUCCCAUUG 20 3110 BCL11A-2626 GCCCGUUGGGAGCUCCAGAA 20 3111 BCL11A-2627 + GCUAUGUGUUCCUGUUU 17 3112 BCL11A-2628 + GCUCCAUGUGCAGAACG 17 3113 BCL11A-2629 GCUCUAAUCCCCACGCC 17 3114 BCL11A-2630 + GCUGGGGUUUGCCUUGCUUG 20 3115 BCL11A-2631 + GCUUUUUUCAUCUCGAU 17 3116 BCL11A-2632 + GGCACUGCCCACAGGUG 17 3117 BCL11A-2633 + GGCACUGCCCACAGGUGAGG 20 3118 BCL11A-2634 GGCCCGUUGGGAGCUCCAGA 20 3119 BCL11A-2635 + GGGGUUUGCCUUGCUUG 17 3120 BCL11A-2636 + GUAAGAAUGGCUUCAAG 17 3121 BCL11A-2637 + GUGCAGAACGAGGGGAGGAG 20 3122 BCL11A-2638 GUGCCAGAUGAACUUCCCAU 20 3123 BCL11A-2639 + GUUCAUCUGGCACUGCCCAC 20 3124 BCL11A-2640 GUUGGGAGCUCCAGAAG 17 3125

Table 4D provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to forth tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon and do not start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. pyogenes Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. pyogenes Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL0A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 4D 4th Tier Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO BCL11A-2641 AAAAGCAUCCAAUCCCG 17 3126 BCL11A-2642 AAAAGCAUCCAAUCCCGUGG 20 3127 BCL11A-2643 + AAAAUAAGAAUGUCCCCCAA 20 3128 BCL11A-2644 + AAACAAUCGUCAUCCUC 17 3129 BCL11A-2645 AAACGGAAACAAUGCAA 17 3130 BCL11A-2646 AAACUUCUGCACUGGAG 17 3131 BCL11A-2647 + AAAUAAGAAUGUCCCCCAAU 20 3132 BCL11A-2648 AACCCCAGCACUUAAGCAAA 20 3133 BCL11A-2649 + AAGAAUGGCUUCAAGAGGCU 20 3134 BCL11A-2650 + AAUGGCUUCAAGAGGCU 17 3135 BCL11A-2651 ACAGAUGAUGAACCAGACCA 20 3136 BCL11A-2652 ACCAGACCACGGCCCGU 17 3137 BCL11A-2653 ACCCCAGCACUUAAGCAAAC 20 3138 BCL11A-2654 + ACCUGGAUGCCAACCUCCAC 20 3139 BCL11A-2655 + ACUGCCCACAGGUGAGG 17 3140 BCL11A-2656 + AGAGCUCCAUGUGCAGAACG 20 3141 BCL11A-2657 AGAUGAACUUCCCAUUG 17 3142 BCL11A-2658 + AGCUCCAUGUGCAGAACGAG 20 3143 BCL11A-2659 AGGAAUUUGCCCCAAAC 17 3144 BCL11A-2660 + AGGAGGUCAUGAUCCCCUUC 20 3145 BCL11A-2661 + AGGUCAUGAUCCCCUUC 17 3146 BCL11A-2662 AUAAACUUCUGCACUGG 17 3147 BCL11A-2663 + AUAAGAAUGUCCCCCAA 17 3148 BCL11A-2664 AUCAUGACCUCCUCACCUGU 20 3149 BCL11A-2665 + AUCUCGAUUGGUGAAGGGGA 20 3150 BCL11A-2666 AUGACCUCCUCACCUGU 17 3151 BCL11A-2667 + AUGUGCAGAACGAGGGG 17 3152 BCL11A-2668 + AUUGGUGAAGGGGAAGG 17 3153 BCL11A-2669 CACAAACGGAAACAAUGCAA 20 3154 BCL11A-2670 + CACUCAUCCCAGGCGUG 17 3155 BCL11A-2671 + CAGAACGAGGGGAGGAG 17 3156 BCL11A-2672 CAGAUGAACUUCCCAUU 17 3157 BCL11A-2673 + CAGCUUUUUCUAAGCAG 17 3158 BCL11A-2674 CAUCCAGGUCACGCCAG 17 3159 BCL11A-2675 + CAUCUCGAUUGGUGAAG 17 3160 BCL11A-2676 + CAUCUGGCACUGCCCAC 17 3161 BCL11A-2677 CAUGACCUCCUCACCUG 17 3162 BCL11A-2678 + CCAAUGGGAAGUUCAUC 17 3163 BCL11A-2679 + CCACAGCUUUUUCUAAGCAG 20 3164 BCL11A-2680 CCAGACCACGGCCCGUU 17 3165 BCL11A-2681 CCAGAUGAACUUCCCAU 17 3166 BCL11A-2682 CCAGAUGAACUUCCCAUUGG 20 3167 BCL11A-2683 CCAGCACUUAAGCAAAC 17 3168 BCL11A-2684 CCCAGCACUUAAGCAAA 17 3169 BCL11A-2685 + CCCCUUCUGGAGCUCCCAAC 20 3170 BCL11A-2686 CCCGUUGGGAGCUCCAGAAG 20 3171 BCL11A-2687 CCGUUGGGAGCUCCAGA 17 3172 BCL11A-2688 + CCGUUUGCUUAAGUGCU 17 3173 BCL11A-2689 CCUCUGCUUAGAAAAAGCUG 20 3174 BCL11A-2690 + CCUUCUGGAGCUCCCAA 17 3175 BCL11A-2691 CGUGGAGGUUGGCAUCC 17 3176 BCL11A-2692 CGUUGGGAGCUCCAGAA 17 3177 BCL11A-2693 + CGUUUGCUUAAGUGCUG 17 3178 BCL11A-2694 + CUAUGUGUUCCUGUUUG 17 3179 BCL11A-2695 + CUCCAUGUGCAGAACGA 17 3180 BCL11A-2696 CUCUAAUCCCCACGCCU 17 3181 BCL11A-2697 + CUGCACUCAUCCCAGGCGUG 20 3182 BCL11A-2698 + CUGCUAUGUGUUCCUGUUUG 20 3183 BCL11A-2699 CUGCUUAGAAAAAGCUG 17 3184 BCL11A-2700 + CUGGAGCUCCCAACGGGCCG 20 3185 BCL11A-2701 + CUGGAUGCCAACCUCCA 17 3186 BCL11A-2702 + CUUCUGGAGCUCCCAAC 17 3187 BCL11A-2703 UAAACUUCUGCACUGGA 17 3188 BCL11A-2704 + UAAGAAUGUCCCCCAAU 17 3189 BCL11A-2705 UAGAGGAAUUUGCCCCAAAC 20 3190 BCL11A-2706 + UAUUCUGCACUCAUCCC 17 3191 BCL11A-2707 + UCCAUGUGCAGAACGAG 17 3192 BCL11A-2708 + UCCAUGUGCAGAACGAGGGG 20 3193 BCL11A-2709 UCCCCUCGUUCUGCACA 17 3194 BCL11A-2710 + UCCCCUUCUGGAGCUCCCAA 20 3195 BCL11A-2711 UCCCGUGGAGGUUGGCAUCC 20 3196 BCL11A-2712 UCCUCCCCUCGUUCUGCACA 20 3197 BCL11A-2713 + UCGAUUGGUGAAGGGGA 17 3198 BCL11A-2714 + UCGAUUGGUGAAGGGGAAGG 20 3199 BCL11A-2715 + UCUGCACUCAUCCCAGGCGU 20 3200 BCL11A-2716 + UCUGGCACUGCCCACAGGUG 20 3201 BCL11A-2717 + UCUGUAAGAAUGGCUUCAAG 20 3202 BCL11A-2718 + UGCACUCAUCCCAGGCG 17 3203 BCL11A-2719 UGCCAGAUGAACUUCCCAUU 20 3204 BCL11A-2720 + UGCUAUGUGUUCCUGUU 17 3205 BCL11A-2721 + UGGAUGCCAACCUCCAC 17 3206 BCL11A-2722 + UGGUUCAUCAUCUGUAAGAA 20 3207 BCL11A-2723 UGUUUAUCAACGUCAUCUAG 20 3208 BCL11A-2724 UUAUUUUUAUCGAGCACAAA 20 3209 BCL11A-2725 + UUCAUCAUCUGUAAGAA 17 3210 BCL11A-2726 + UUCCCGUUUGCUUAAGUGCU 20 3211 BCL11A-2727 + UUCUGCACUCAUCCCAGGCG 20 3212 BCL11A-2728 + UUUCAUCUCGAUUGGUGAAG 20 3213 BCL11A-2729 + UUUUCAUCUCGAUUGGUGAA 20 3214 BCL11A-2730 UUUUUAUCGAGCACAAA 17 3215 BCL11A-2731 + UUUUUCAUCUCGAUUGGUGA 20 3216

Table 4E provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to fifth tier parameters. The targeting domains outside the first 500 bp of coding sequence downstream of start codon. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. pyogenes Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. pyogenes Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. pyogenes Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL23A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL3A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 4E 5th Tier Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO BCL11A-2732 + UAUGCGGUCCGACUCGC 17 3217 BCL11A-2733 UCGGACCGCAUAGACGA 17 3218 BCL11A-2734 + UGGGUACUACGCCGAAU 17 3219 BCL11A-2735 + GGUACUACGCCGAAUGG 17 3220 BCL11A-2736 UUGCGACGAAGACUCGG 17 3221 BCL11A-2737 + CUGGGUACUACGCCGAA 17 3222 BCL11A-2738 + GGGUACUACGCCGAAUG 17 3223 BCL11A-2739 + UCGGACUUGACCGUCAU 17 3224 BCL11A-2740 + AGGGAUACCAACCCGCG 17 3225 BCL11A-2741 CGCGCUCAAGUCCGUGG 17 3226 BCL11A-2742 + CGAGGAGUGCUCCGACG 17 3227 BCL11A-2743 + GUCGGACUUGACCGUCA 17 3228 BCL11A-2744 + UGCACGCGUGGUCGCAC 17 3229 BCL11A-2745 CAGCGCGCUCAAGUCCG 17 3230 BCL11A-2746 + UACCAACCCGCGGGGUC 17 3231 BCL11A-2747 GUGGCUCGCCGGCUACG 17 3232 BCL11A-2748 + CGGACUUGACCGUCAUG 17 3233 BCL11A-2749 CACCGCAUAGAGCGCCU 17 3234 BCL11A-2750 GCGCAUCAAGCUCGAGA 17 3235 BCL11A-2751 + GGCCCGGACCACUAAUA 17 3236 BCL11A-2752 + GCCCGGACCACUAAUAU 17 3237 BCL11A-2753 GCAUAAGCGCGGCCACC 17 3238 BCL11A-2754 + AGGCGCUCUAUGCGGUG 17 3239 BCL11A-2755 ACGGUCAAGUCCGACGA 17 3240 BCL11A-2756 + CGAGGCCGACUCGCCCG 17 3241 BCL11A-2757 ACCGCAUAGAGCGCCUG 17 3242 BCL11A-2758 CGACCACGCGUGCACCC 17 3243 BCL11A-2759 + GUACACGUUCUCCGUGU 17 3244 BCL11A-2760 CACUUGCGACGAAGACU 17 3245 BCL11A-2761 CGGGUUGGUAUCCCUUC 17 3246 BCL11A-2762 CUCGUCGGAGCACUCCU 17 3247 BCL11A-2763 + CCCGGACCACUAAUAUG 17 3248 BCL11A-2764 + UCGGUGGUGGACUAAAC 17 3249 BCL11A-2765 + CAGGCGCUCUAUGCGGU 17 3250 BCL11A-2766 + AAGGGAUACCAACCCGC 17 3251 BCL11A-2767 + GGCGCUCUAUGCGGUGG 17 3252 BCL11A-2768 CCACCGCAUAGAGCGCC 17 3253 BCL11A-2769 UACUCGCAGUGGCUCGC 17 3254 BCL11A-2770 CGGGCGAGUCGGCCUCG 17 3255 BCL11A-2771 + UACACGUUCUCCGUGUU 17 3256 BCL11A-2772 AGCACGCCCCAUAUUAG 17 3257 BCL11A-2773 + GAAGGGAUACCAACCCG 17 3258 BCL11A-2774 + UUGGGCAUCGCGGCCGG 17 3259 BCL11A-2775 CCGGGCGAGUCGGCCUC 17 3260 BCL11A-2776 + GGUGGAGAGACCGUCGU 17 3261 BCL11A-2777 + GUUGGGCAUCGCGGCCG 17 3262 BCL11A-2778 AGAACGUGUACUCGCAG 17 3263 BCL11A-2779 + ACCAACCCGCGGGGUCA 17 3264 BCL11A-2780 CACGAGAACAGCUCGCG 17 3265 BCL11A-2781 UAUUAGUGGUCCGGGCC 17 3266 BCL11A-2782 + CGUCGCAAGUGUCCCUG 17 3267 BCL11A-2783 + CCCGCGAGCUGUUCUCG 17 3268 BCL11A-2784 + UGCGCCGGUGCACCACC 17 3269 BCL11A-2785 CUGCCCGACGUCAUGCA 17 3270 BCL11A-2786 GACGAAGACUCGGUGGC 17 3271 BCL11A-2787 CCUGCCCGACGUCAUGC 17 3272 BCL11A-2788 + AAGGGCGGCUUGCUACC 17 3273 BCL11A-2789 GGGUGGACUACGGCUUC 17 3274 BCL11A-2790 + UCGCUGGUGCCGGGUUC 17 3275 BCL11A-2791 GGCGAGAAGCAUAAGCG 17 3276 BCL11A-2792 + GGACUUGAGCGCGCUGC 17 3277 BCL11A-2793 CUCGGUGGCCGGCGAGU 17 3278 BCL11A-2794 + CCCGAGGCCGACUCGCC 17 3279 BCL11A-2795 CCCGGGCGAGUCGGCCU 17 3280 BCL11A-2796 CCGCAUAGAGCGCCUGG 17 3281 BCL11A-2797 + UGUUGGGCAUCGCGGCC 17 3282 BCL11A-2798 + GUGUUGGGCAUCGCGGC 17 3283 BCL11A-2799 + UCUCUCGAUACUGAUCC 17 3284 BCL11A-2800 ACCCGAGUGCCUUUGAC 17 3285 BCL11A-2801 + UCCGACGAGGAGGCAAA 17 3286 BCL11A-2802 ACCCGGCACCAGCGACU 17 3287 BCL11A-2803 + CCCCGUUCUCCGGGAUC 17 3288 BCL11A-2804 + CCGAGGCCGACUCGCCC 17 3289 BCL11A-2805 CCCCAUAUUAGUGGUCC 17 3290 BCL11A-2806 + GACUUGGACUUGACCGG 17 3291 BCL11A-2807 GCCCCAUAUUAGUGGUC 17 3292 BCL11A-2808 AGGGUGGACUACGGCUU 17 3293 BCL11A-2809 CAAAUCGUCCCCCAUGA 17 3294 BCL11A-2810 CGACGUCAUGCAGGGCA 17 3295 BCL11A-2811 GGCCGCGAUGCCCAACA 17 3296 BCL11A-2812 + CCAGGCGCUCUAUGCGG 17 3297 BCL11A-2813 CCUGAUCCCGGAGAACG 17 3298 BCL11A-2814 + CCAACCCGCGGGGUCAG 17 3299 BCL11A-2815 GGCGAGUCGGCCUCGGG 17 3300 BCL11A-2816 + GGCAAAAGGCGAUUGUC 17 3301 BCL11A-2817 + UUUGGACAGGCCCCCCG 17 3302 BCL11A-2818 + GCGGCUUGCUACCUGGC 17 3303 BCL11A-2819 + GGACUUGACCGUCAUGG 17 3304 BCL11A-2820 + GGAGUGCUCCGACGAGG 17 3305 BCL11A-2821 AUUAGUGGUCCGGGCCC 17 3306 BCL11A-2822 CCACGAGAACAGCUCGC 17 3307 BCL11A-2823 GUAUCGAGAGAGGCUUC 17 3308 BCL11A-2824 + CUCCGUGUUGGGCAUCG 17 3309 BCL11A-2825 + CAAACUCCCGUUCUCCG 17 3310 BCL11A-2826 ACCUGAUCCCGGAGAAC 17 3311 BCL11A-2827 GGCACUGUUAAUGGCCG 17 3312 BCL11A-2828 + UUCUCCGGGAUCAGGUU 17 3313 BCL11A-2829 UAUGGAGCCUCCCGCCA 17 3314 BCL11A-2830 + CUUGAUGCGCUUAGAGA 17 3315 BCL11A-2831 UAGCAAGCCGCCCUUCC 17 3316 BCL11A-2832 CCGGCUACGCGGCCUCC 17 3317 BCL11A-2833 + UCCAAGUGAUGUCUCGG 17 3318 BCL11A-2834 GAACAGCUCGCGGGGCG 17 3319 BCL11A-2835 GCUGCGGUUGAAUCCAA 17 3320 BCL11A-2836 + UGACUUGGACUUGACCG 17 3321 BCL11A-2837 CCCGGAGAACGGGGACG 17 3322 BCL11A-2838 + GUGGCGCUUCAGCUUGC 17 3323 BCL11A-2839 + GUUCUCCGGGAUCAGGU 17 3324 BCL11A-2840 + CAGUGCCAUCGUCUAUG 17 3325 BCL11A-2841 + UCUCCGGGAUCAGGUUG 17 3326 BCL11A-2842 GACGAUGGCACUGUUAA 17 3327 BCL11A-2843 CUGCUCCCCGGGCGAGU 17 3328 BCL11A-2844 + CGGUGGUGGACUAAACA 17 3329 BCL11A-2845 CUCGCGGGGCGCGGUCG 17 3330 BCL11A-2846 + AUGCCCUGCAUGACGUC 17 3331 BCL11A-2847 + UGGACUUGACCGGGGGC 17 3332 BCL11A-2848 ACCACCGAGACAUCACU 17 3333 BCL11A-2849 GGAGUUCGACCUGCCCC 17 3334 BCL11A-2850 + CCUGCAUGACGUCGGGC 17 3335 BCL11A-2851 + CUGCAUGACGUCGGGCA 17 3336 BCL11A-2852 AGGAUCAGUAUCGAGAG 17 3337 BCL11A-2853 + GGACUUGACCGGGGGCU 17 3338 BCL11A-2854 + AAAGGCACUCGGGUGAU 17 3339 BCL11A-2855 UGGACGGAGGGAUCUCG 17 3340 BCL11A-2856 + CCCCCAGGCGCUCUAUG 17 3341 BCL11A-2857 CCGCCAUGGAUUUCUCU 17 3342 BCL11A-2858 GGCGCGGUCGUGGGCGU 17 3343 BCL11A-2859 AACCUGAUCCCGGAGAA 17 3344 BCL11A-2860 + CAUGCCCUGCAUGACGU 17 3345 BCL11A-2861 + CGCUGGUGCCGGGUUCC 17 3346 BCL11A-2862 + CCUGGAGGCCGCGUAGC 17 3347 BCL11A-2863 CCCCUGACCCCGCGGGU 17 3348 BCL11A-2864 + GCUUAUGCUUCUCGCCC 17 3349 BCL11A-2865 AAGUCAUGCGAGUUCUG 17 3350 BCL11A-2866 + CACCAAGUCGCUGGUGC 17 3351 BCL11A-2867 CCCGAGUGCCUUUGACA 17 3352 BCL11A-2868 + CAUGACUUGGACUUGAC 17 3353 BCL11A-2869 CGACCCCAACCUGAUCC 17 3354 BCL11A-2870 + ACCAAGUCGCUGGUGCC 17 3355 BCL11A-2871 + AAGUGAUGUCUCGGUGG 17 3356 BCL11A-2872 CUUCUCCACACCGCCCG 17 3357 BCL11A-2873 + UGGAGUCUCCGAAGCUA 17 3358 BCL11A-2874 CGCUUCUCCACACCGCC 17 3359 BCL11A-2875 + GCUGGUGCCGGGUUCCG 17 3360 BCL11A-2876 CGCAGCGGCACGGGAAG 17 3361 BCL11A-2877 + GCAUCGCGGCCGGGGGC 17 3362 BCL11A-2878 GAGCACUCCUCGGAGAA 17 3363 BCL11A-2879 + GGGGGGCGUCGCCAGGA 17 3364 BCL11A-2880 + GAAAGCGCCCUUCUGCC 17 3365 BCL11A-2881 CUGGACGGAGGGAUCUC 17 3366 BCL11A-2882 CGGCUUCGGGCUGAGCC 17 3367 BCL11A-2883 + GGGGGCGUCGCCAGGAA 17 3368 BCL11A-2884 + UAACCUUUGCAUAGGGC 17 3369 BCL11A-2885 GGGCGAGUCGGCCUCGG 17 3370 BCL11A-2886 CACACCGCCCGGGGAGC 17 3371 BCL11A-2887 GGGAUCUCGGGGCGCAG 17 3372 BCL11A-2888 + CUCGCUGAAGUGCUGCA 17 3373 BCL11A-2889 UCGGGGCGCAGCGGCAC 17 3374 BCL11A-2890 AAGUCCCCUGACCCCGC 17 3375 BCL11A-2891 GCCUUUUGCCUCCUCGU 17 3376 BCL11A-2892 CACCUGGCCGAGGCCGA 17 3377 BCL11A-2893 GGUAUCCCUUCAGGACU 17 3378 BCL11A-2894 + GUGGUGGACUAAACAGG 17 3379 BCL11A-2895 + GCGAGCUGUUCUCGUGG 17 3380 BCL11A-2896 AGCACUCCUCGGAGAAC 17 3381 BCL11A-2897 CAUGCAGCACUUCAGCG 17 3382 BCL11A-2898 + UGGCCUGGGUGCACGCG 17 3383 BCL11A-2899 AGCGAGAGGGUGGACUA 17 3384 BCL11A-2900 + GCACAGGUUGCACUUGU 17 3385 BCL11A-2901 + GAGAAAUCCAUGGCGGG 17 3386 BCL11A-2902 + GCAGAACUCGCAUGACU 17 3387 BCL11A-2903 + UCUCCGAAGCUAAGGAA 17 3388 BCL11A-2904 + UGACGUCGGGCAGGGCG 17 3389 BCL11A-2905 + GGGUCCAAGUGAUGUCU 17 3390 BCL11A-2906 GCAACCUGGUGGUGCAC 17 3391 BCL11A-2907 + GGUGGCGCGCCGCCUCC 17 3392 BCL11A-2908 + GCUGCCCACCAAGUCGC 17 3393 BCL11A-2909 + GUUCUCGCUCUUGAACU 17 3394 BCL11A-2910 + CCGCAGCACCCUGUCAA 17 3395 BCL11A-2911 GAAGUCCCCUGACCCCG 17 3396 BCL11A-2912 GCGCGGCCACCUGGCCG 17 3397 BCL11A-2913 + GGCGUCGCCAGGAAGGG 17 3398 BCL11A-2914 GUUGAAUCCAAUGGCUA 17 3399 BCL11A-2915 CUCGGGGCGCAGCGGCA 17 3400 BCL11A-2916 CCGAGGCCGAGGGCCAC 17 3401 BCL11A-2917 + CUAAACAGGGGGGGAGU 17 3402 BCL11A-2918 GCGGCACGGGAAGUGGA 17 3403 BCL11A-2919 + CACAGGUUGCACUUGUA 17 3404 BCL11A-2920 CAGCGAGGCCUUCCACC 17 3405 BCL11A-2921 AACCUGCUAAGAAUACC 17 3406 BCL11A-2922 + AUCCUGGUAUUCUUAGC 17 3407 BCL11A-2923 + GGUGGUGGACUAAACAG 17 3408 BCL11A-2924 CGAGGCCGAGGGCCACA 17 3409 BCL11A-2925 + GUACAUGUGUAGCUGCU 17 3410 BCL11A-2926 + UUGAUGCGCUUAGAGAA 17 3411 BCL11A-2927 + UCCUCGUCCCCGUUCUC 17 3412 BCL11A-2928 + AUGACUUGGACUUGACC 17 3413 BCL11A-2929 + GUCUCCGAAGCUAAGGA 17 3414 BCL11A-2930 + GGUGGACUAAACAGGGG 17 3415 BCL11A-2931 + GCAUGUGCGUCUUCAUG 17 3416 BCL11A-2932 + GGCACUCGGGUGAUGGG 17 3417 BCL11A-2933 + AUAGGGCUGGGCCGGCC 17 3418 BCL11A-2934 + CCGUCCAGCUCCCCGGG 17 3419 BCL11A-2935 + GCAGUAACCUUUGCAUA 17 3420 BCL11A-2936 GAUCCCUUCCUUAGCUU 17 3421 BCL11A-2937 + AAGGGGCUCAGCGAGCU 17 3422 BCL11A-2938 AGCUGACGGAGAGCGAG 17 3423 BCL11A-2939 UCGCGGGGCGCGGUCGU 17 3424 BCL11A-2940 AGCGGCACGGGAAGUGG 17 3425 BCL11A-2941 + CAAAGGCACUCGGGUGA 17 3426 BCL11A-2942 + CUGCACCUAGUCCUGAA 17 3427 BCL11A-2943 GCUGGACGGAGGGAUCU 17 3428 BCL11A-2944 + CCCUGUCAAAGGCACUC 17 3429 BCL11A-2945 + AACCUUUGCAUAGGGCU 17 3430 BCL11A-2946 + CGCCCGGGGAGCAGCCG 17 3431 BCL11A-2947 + UGGUGGACUAAACAGGG 17 3432 BCL11A-2948 GGCCCAGCCCUAUGCAA 17 3433 BCL11A-2949 + CCUCGUCCCCGUUCUCC 17 3434 BCL11A-2950 GCCAGCUCCCCGGAACC 17 3435 BCL11A-2951 + GCCGGGUUCCGGGGAGC 17 3436 BCL11A-2952 + UGCAGUAACCUUUGCAU 17 3437 BCL11A-2953 + GCUUCUCGCCCAGGACC 17 3438 BCL11A-2954 CCGCCCGGGGAGCUGGA 17 3439 BCL11A-2955 CCGGGGAGCUGGACGGA 17 3440 BCL11A-2956 CUUCCGGCCUGGCAGAA 17 3441 BCL11A-2957 + CCUAGAGAAAUCCAUGG 17 3442 BCL11A-2958 + GGAGGGGGGGCGUCGCC 17 3443 BCL11A-2959 UACUUAGAAAGCGAACA 17 3444 BCL11A-2960 + GGAGGCUCCAUAGCCAU 17 3445 BCL11A-2961 + ACACAUCUUGAGCUCUC 17 3446 BCL11A-2962 GGCACCAGCGACUUGGU 17 3447 BCL11A-2963 + GGGAUCUUUGAGCUGCC 17 3448 BCL11A-2964 + GCAGCAGCUUUUUGGAC 17 3449 BCL11A-2965 + CUGCAAUAUGAAUCCCA 17 3450 BCL11A-2966 + UCUGCACCUAGUCCUGA 17 3451 BCL11A-2967 + GAAGGGGCUCAGCGAGC 17 3452 BCL11A-2968 + UUCCGGGGAGCUGGCGG 17 3453 BCL11A-2969 GCACCGGCGCAGCCACA 17 3454 BCL11A-2970 + AUAUGAAUCCCAUGGAG 17 3455 BCL11A-2971 GUGGUCCGGGCCCGGGC 17 3456 BCL11A-2972 CUUCACACACCCCCAUU 17 3457 BCL11A-2973 GUCCAAAAAGCUGCUGC 17 3458 BCL11A-2974 CGGCACCAGCGACUUGG 17 3459 BCL11A-2975 GCUUCUCCACACCGCCC 17 3460 BCL11A-2976 + CGCCCGUGUGGCUGCGC 17 3461 BCL11A-2977 CACGCACAGAACACUCA 17 3462 BCL11A-2978 + UGUACAUGUGUAGCUGC 17 3463 BCL11A-2979 CACCGGCGCAGCCACAC 17 3464 BCL11A-2980 + UUGCUACCUGGCUGGAA 17 3465 BCL11A-2981 + ACCCUGUCAAAGGCACU 17 3466 BCL11A-2982 CCACCUGGCCGAGGCCG 17 3467 BCL11A-2983 + GGGCGGAUUGCAGAGGA 17 3468 BCL11A-2984 + CUAGAGAAAUCCAUGGC 17 3469 BCL11A-2985 GGCGGAAGAGAUGGCCC 17 3470 BCL11A-2986 + GGGGCGGAUUGCAGAGG 17 3471 BCL11A-2987 GUGUGGCAGUUUUCGGA 17 3472 BCL11A-2988 GAGAGAGGCUUCCGGCC 17 3473 BCL11A-2989 + CGGGUGAUGGGUGGCCA 17 3474 BCL11A-2990 CCCGGGGAGCUGGACGG 17 3475 BCL11A-2991 UAGGAGACUUAGAGAGC 17 3476 BCL11A-2992 + CACAUCUUGAGCUCUCU 17 3477 BCL11A-2993 + CCUCGGCCUCGGCCAGG 17 3478 BCL11A-2994 GGCCUUCCACCAGGUCC 17 3479 BCL11A-2995 + UCUCGCCCAGGACCUGG 17 3480 BCL11A-2996 + UCUGCCCUCUUUUGAGC 17 3481 BCL11A-2997 + ACUAAACAGGGGGGGAG 17 3482 BCL11A-2998 + CUUGACCGGGGGCUGGG 17 3483 BCL11A-2999 + UUGACCGGGGGCUGGGA 17 3484 BCL11A-3000 AGACUUAGAGAGCUGGC 17 3485 BCL11A-3001 AGCCCACCGCUGUCCCC 17 3486 BCL11A-3002 AGCCAUUCACCAGUGCA 17 3487 BCL11A-3003 GCUUCCGGCCUGGCAGA 17 3488 BCL11A-3004 GACUUAGAGAGCUGGCA 17 3489 BCL11A-3005 AGGCCCAGCUCAAAAGA 17 3490 BCL11A-3006 + UCGGGUGAUGGGUGGCC 17 3491 BCL11A-3007 + CAAGAGAAACCAUGCAC 17 3492 BCL11A-3008 + AUCUUUGAGCUGCCUGG 17 3493 BCL11A-3009 + UAUUCUUAGCAGGUUAA 17 3494 BCL11A-3010 + CUGCCCUCUUUUGAGCU 17 3495 BCL11A-3011 + CCAUCUCUUCCGCCCCC 17 3496 BCL11A-3012 UGGCCGCGGCUGCUCCC 17 3497 BCL11A-3013 + CCUGUGGCCCUCGGCCU 17 3498 BCL11A-3014 + CAGCUCCCCGGGCGGUG 17 3499 BCL11A-3015 + UUUGCAUAGGGCUGGGC 17 3500 BCL11A-3016 + GGCCCUCGGCCUCGGCC 17 3501 BCL11A-3017 GCUGACGGAGAGCGAGA 17 3502 BCL11A-3018 AGAUGUGUGGCAGUUUU 17 3503 BCL11A-3019 + AUUCUUAGCAGGUUAAA 17 3504 BCL11A-3020 + UCUCCUAGAGAAAUCCA 17 3505 BCL11A-3021 CCUUUGACAGGGUGCUG 17 3506 BCL11A-3022 + GGAGGGGCGGAUUGCAG 17 3507 BCL11A-3023 + UUCUUAGCAGGUUAAAG 17 3508 BCL11A-3024 + CGGAUUGCAGAGGAGGG 17 3509 BCL11A-3025 + UUUGAGCUGGGCCUGCC 17 3510 BCL11A-3026 + CUUCAGCUUGCUGGCCU 17 3511 BCL11A-3027 + CUUGAACUUGGCCACCA 17 3512 BCL11A-3028 CUGCAACCAUUCCAGCC 17 3513 BCL11A-3029 CAUAGAGCGCCUGGGGG 17 3514 BCL11A-3030 GGGCGCGGUCGUGGGCG 17 3515 BCL11A-3031 + UCCCAUGGAGAGGUGGC 17 3516 BCL11A-3032 GGCCGCGGCUGCUCCCC 17 3517 BCL11A-3033 AUUUCAGAGCAACCUGG 17 3518 BCL11A-3034 GCCUUCCACCAGGUCCU 17 3519 BCL11A-3035 + UGAAUCCCAUGGAGAGG 17 3520 BCL11A-3036 + UUGAGCUGGGCCUGCCC 17 3521 BCL11A-3037 + AGGGGCUCAGCGAGCUG 17 3522 BCL11A-3038 + AGGGCUUCUCGCCCGUG 17 3523 BCL11A-3039 CACCGCUGUCCCCAGGC 17 3524 BCL11A-3040 CAAAUUUCAGAGCAACC 17 3525 BCL11A-3041 AGAGAGCUCAAGAUGUG 17 3526 BCL11A-3042 + AACCAUGCACUGGUGAA 17 3527 BCL11A-3043 + CCUCCGUCCAGCUCCCC 17 3528 BCL11A-3044 + AGUGUCCCUGUGGCCCU 17 3529 BCL11A-3045 + CCCUCCGUCCAGCUCCC 17 3530 BCL11A-3046 + GGCCUGGGGACAGCGGU 17 3531 BCL11A-3047 + GCCCAGCAGCAGCUUUU 17 3532 BCL11A-3048 CAGGCCCAGCUCAAAAG 17 3533 BCL11A-3049 CUUCGGGCUGAGCCUGG 17 3534 BCL11A-3050 + CCCAUGGAGAGGUGGCU 17 3535 BCL11A-3051 CCCAGCCACCUCUCCAU 17 3536 BCL11A-3052 + GGGUUCCGGGGAGCUGG 17 3537 BCL11A-3053 + UAGGGCUGGGCCGGCCU 17 3538 BCL11A-3054 CCUGGGGGCGGAAGAGA 17 3539 BCL11A-3055 + GCCCAGGACCUGGUGGA 17 3540 BCL11A-3056 CGGGCUGAGCCUGGAGG 17 3541 BCL11A-3057 ACCACGAGAACAGCUCG 17 3542 BCL11A-3058 + CGGCCUGGGGACAGCGG 17 3543 BCL11A-3059 UCCAAAAAGCUGCUGCU 17 3544 BCL11A-3060 + GCGCCCUUCUGCCAGGC 17 3545 BCL11A-3061 UCCCAGCCACCUCUCCA 17 3546 BCL11A-3062 CUCCACCGCCAGCUCCC 17 3547 BCL11A-3063 + CUGGGCCUGCCCGGGCC 17 3548 BCL11A-3064 + AGGGCUGGGCCGGCCUG 17 3549 BCL11A-3065 + AACAGGGGGGGAGUGGG 17 3550 BCL11A-3066 GGAGAACGGGGACGAGG 17 3551 BCL11A-3067 + UGAUGCGCUUAGAGAAG 17 3552 BCL11A-3068 + GGAUUGCAGAGGAGGGA 17 3553 BCL11A-3069 + GGCCGGCCUGGGGACAG 17 3554 BCL11A-3070 + GAUUGCAGAGGAGGGAG 17 3555 BCL11A-3071 + AUUGCAGAGGAGGGAGG 17 3556 BCL11A-3072 + ACCGGGGGCUGGGAGGG 17 3557 BCL11A-3073 + UGGAGAGGUGGCUGGGA 17 3558 BCL11A-3074 + UUGCAGAGGAGGGAGGG 17 3559 BCL11A-3075 CGGGGACGAGGAGGAAG 17 3560 BCL11A-3076 GACGGAGAGCGAGAGGG 17 3561 BCL11A-3077 UCCUCCCUCCCAGCCCC 17 3562 BCL11A-3078 + GCUUCAGCUUGCUGGCC 17 3563 BCL11A-3079 + UGCAGAGGAGGGAGGGG 17 3564 BCL11A-3080 + GGGCUGGGAGGGAGGAG 17 3565 BCL11A-3081 GGAAGAGGAGGACGACG 17 3566 BCL11A-3082 + GGGGCUGGGAGGGAGGA 17 3567 BCL11A-3083 GGAGGACGACGAGGAAG 17 3568 BCL11A-3084 GGAGGAGGAGGAGCUGA 17 3569 BCL11A-3085 + GGGGGCUGGGAGGGAGG 17 3570 BCL11A-3086 + CUGGGAGGGAGGAGGGG 17 3571 BCL11A-3087 CGAGGAAGAGGAAGAAG 17 3572 BCL11A-3088 GGACGAGGAGGAAGAGG 17 3573 BCL11A-3089 GGAAGAAGAGGAGGAAG 17 3574 BCL11A-3090 GGAAGAGGAAGAAGAGG 17 3575 BCL11A-3091 AGAAGAGGAGGAAGAGG 17 3576 BCL11A-3092 AGAGGAGGAAGAGGAGG 17 3577 BCL11A-3093 GGAGGAAGAGGAGGAGG 17 3578 BCL11A-3094 + GUCUAUGCGGUCCGACUCGC 20 3579 BCL11A-3095 + UCGUCGGACUUGACCGUCAU 20 3580 BCL11A-3096 + CGUCGGACUUGACCGUCAUG 20 3581 BCL11A-3097 AUGACGGUCAAGUCCGACGA 20 3582 BCL11A-3098 GAGUCGGACCGCAUAGACGA 20 3583 BCL11A-3099 + CGGGCCCGGACCACUAAUAU 20 3584 BCL11A-3100 + GUCGUCGGACUUGACCGUCA 20 3585 BCL11A-3101 + CUCUGGGUACUACGCCGAAU 20 3586 BCL11A-3102 + CUGGGUACUACGCCGAAUGG 20 3587 BCL11A-3103 + CCGGGCCCGGACCACUAAUA 20 3588 BCL11A-3104 CCGCGGGUUGGUAUCCCUUC 20 3589 BCL11A-3105 + UCUGGGUACUACGCCGAAUG 20 3590 BCL11A-3106 + GGAUACCAACCCGCGGGGUC 20 3591 BCL11A-3107 ACGCCCCAUAUUAGUGGUCC 20 3592 BCL11A-3108 CACUUGCGACGAAGACUCGG 20 3593 BCL11A-3109 + UCUCUGGGUACUACGCCGAA 20 3594 BCL11A-3110 UAAGCGCAUCAAGCUCGAGA 20 3595 BCL11A-3111 UGCGACGAAGACUCGGUGGC 20 3596 BCL11A-3112 + CGCGCUUAUGCUUCUCGCCC 20 3597 BCL11A-3113 + UGAAGGGAUACCAACCCGCG 20 3598 BCL11A-3114 + GGGCCCGGACCACUAAUAUG 20 3599 BCL11A-3115 + CGUGUUGGGCAUCGCGGCCG 20 3600 BCL11A-3116 + UCCGUGUUGGGCAUCGCGGC 20 3601 BCL11A-3117 + GUCGGACUUGACCGUCAUGG 20 3602 BCL11A-3118 + GCGCAAACUCCCGUUCUCCG 20 3603 BCL11A-3119 + CUCCGAGGAGUGCUCCGACG 20 3604 BCL11A-3120 + CACGGACUUGAGCGCGCUGC 20 3605 BCL11A-3121 CACGCCCCAUAUUAGUGGUC 20 3606 BCL11A-3122 + GAUACCAACCCGCGGGGUCA 20 3607 BCL11A-3123 CAGCGCGCUCAAGUCCGUGG 20 3608 BCL11A-3124 + GGGUGCACGCGUGGUCGCAC 20 3609 BCL11A-3125 GAAGCAUAAGCGCGGCCACC 20 3610 BCL11A-3126 GUGCGACCACGCGUGCACCC 20 3611 BCL11A-3127 + GAGUACACGUUCUCCGUGUU 20 3612 BCL11A-3128 + GUCUCGGUGGUGGACUAAAC 20 3613 BCL11A-3129 + CCGUUCUCCGGGAUCAGGUU 20 3614 BCL11A-3130 + CGAGUACACGUUCUCCGUGU 20 3615 BCL11A-3131 CGGAGAACGUGUACUCGCAG 20 3616 BCL11A-3132 GGGAGCACGCCCCAUAUUAG 20 3617 BCL11A-3133 CCAUAUUAGUGGUCCGGGCC 20 3618 BCL11A-3134 + GCCGCAGAACUCGCAUGACU 20 3619 BCL11A-3135 + CGCCCCGCGAGCUGUUCUCG 20 3620 BCL11A-3136 GCAGUGGCUCGCCGGCUACG 20 3621 BCL11A-3137 CAUAUUAGUGGUCCGGGCCC 20 3622 BCL11A-3138 + CUGAAGGGAUACCAACCCGC 20 3623 BCL11A-3139 + AUACCAACCCGCGGGGUCAG 20 3624 BCL11A-3140 CAGCAGCGCGCUCAAGUCCG 20 3625 BCL11A-3141 + CGUCCCCGUUCUCCGGGAUC 20 3626 BCL11A-3142 CACCACGAGAACAGCUCGCG 20 3627 BCL11A-3143 GCGGUUGAAUCCAAUGGCUA 20 3628 BCL11A-3144 GGACACUUGCGACGAAGACU 20 3629 BCL11A-3145 + GUGUUGGGCAUCGCGGCCGG 20 3630 BCL11A-3146 + CUUCGUCGCAAGUGUCCCUG 20 3631 BCL11A-3147 + CCCCAGGCGCUCUAUGCGGU 20 3632 BCL11A-3148 + CCGUGUUGGGCAUCGCGGCC 20 3633 BCL11A-3149 + CGUUCUCCGGGAUCAGGUUG 20 3634 BCL11A-3150 + GCCUCUCUCGAUACUGAUCC 20 3635 BCL11A-3151 + UCGCAUGACUUGGACUUGAC 20 3636 BCL11A-3152 AUCACCCGAGUGCCUUUGAC 20 3637 BCL11A-3153 UAAGCGCGGCCACCUGGCCG 20 3638 BCL11A-3154 GCACAAAUCGUCCCCCAUGA 20 3639 BCL11A-3155 CGCCCUGCCCGACGUCAUGC 20 3640 BCL11A-3156 CAACCUGAUCCCGGAGAACG 20 3641 BCL11A-3157 CGGAGCACUCCUCGGAGAAC 20 3642 BCL11A-3158 AGACUCGGUGGCCGGCGAGU 20 3643 BCL11A-3159 + GGCGGUGGAGAGACCGUCGU 20 3644 BCL11A-3160 GUGUACUCGCAGUGGCUCGC 20 3645 BCL11A-3161 UCGGAGCACUCCUCGGAGAA 20 3646 BCL11A-3162 CCCGGCCGCGAUGCCCAACA 20 3647 BCL11A-3163 + CCCGUUCUCCGGGAUCAGGU 20 3648 BCL11A-3164 + UCGGUGGUGGACUAAACAGG 20 3649 BCL11A-3165 + CCUGAAGGGAUACCAACCCG 20 3650 BCL11A-3166 + GUCGUUCUCGCUCUUGAACU 20 3651 BCL11A-3167 CCCCACCGCAUAGAGCGCCU 20 3652 BCL11A-3168 + GUCGCUGGUGCCGGGUUCCG 20 3653 BCL11A-3169 CGAGAACAGCUCGCGGGGCG 20 3654 BCL11A-3170 + CGCAUGACUUGGACUUGACC 20 3655 BCL11A-3171 CCCACCGCAUAGAGCGCCUG 20 3656 BCL11A-3172 + AAGUCGCUGGUGCCGGGUUC 20 3657 BCL11A-3173 + CGAGGAGUGCUCCGACGAGG 20 3658 BCL11A-3174 UCCCCGGGCGAGUCGGCCUC 20 3659 BCL11A-3175 CUCCCCGGGCGAGUCGGCCU 20 3660 BCL11A-3176 + CAUGACUUGGACUUGACCGG 20 3661 BCL11A-3177 AGCUCGCGGGGCGCGGUCGU 20 3662 BCL11A-3178 + UGCUCCGACGAGGAGGCAAA 20 3663 BCL11A-3179 + CUUUUUGGACAGGCCCCCCG 20 3664 BCL11A-3180 CUACGGCUUCGGGCUGAGCC 20 3665 BCL11A-3181 CCCCGGGCGAGUCGGCCUCG 20 3666 BCL11A-3182 + UAACAGUGCCAUCGUCUAUG 20 3667 BCL11A-3183 CUCCUCGUCGGAGCACUCCU 20 3668 BCL11A-3184 CCCGGCACCAGCGACUUGGU 20 3669 BCL11A-3185 GCGCUUCUCCACACCGCCCG 20 3670 BCL11A-3186 + CUCGGUGGUGGACUAAACAG 20 3671 BCL11A-3187 CCCCCACCGCAUAGAGCGCC 20 3672 BCL11A-3188 GAUCCCGGAGAACGGGGACG 20 3673 BCL11A-3189 + CCAGGCGCUCUAUGCGGUGG 20 3674 BCL11A-3190 UUAGUGGUCCGGGCCCGGGC 20 3675 BCL11A-3191 + CCCAGGCGCUCUAUGCGGUG 20 3676 BCL11A-3192 CGGCUGCUCCCCGGGCGAGU 20 3677 BCL11A-3193 UCGCCGGCUACGCGGCCUCC 20 3678 BCL11A-3194 AUCGAGAGAGGCUUCCGGCC 20 3679 BCL11A-3195 + GGGUCCAAGUGAUGUCUCGG 20 3680 BCL11A-3196 AUCGCCUUUUGCCUCCUCGU 20 3681 BCL11A-3197 AUCUCGGGGCGCAGCGGCAC 20 3682 BCL11A-3198 + CGGUGGUGGACUAAACAGGG 20 3683 BCL11A-3199 GAUGGCACUGUUAAUGGCCG 20 3684 BCL11A-3200 + UGCCCUGCAUGACGUCGGGC 20 3685 BCL11A-3201 + UCUCGGUGGUGGACUAAACA 20 3686 BCL11A-3202 AGAGGGUGGACUACGGCUUC 20 3687 BCL11A-3203 + CCCCGAGGCCGACUCGCCCG 20 3688 BCL11A-3204 GAUCUCGGGGCGCAGCGGCA 20 3689 BCL11A-3205 ACGGAAGUCCCCUGACCCCG 20 3690 BCL11A-3206 + ACUCGCCCGGGGAGCAGCCG 20 3691 BCL11A-3207 UUGCGCUUCUCCACACCGCC 20 3692 BCL11A-3208 GGAACCCGGCACCAGCGACU 20 3693 BCL11A-3209 + GCAUGACUUGGACUUGACCG 20 3694 BCL11A-3210 UAAUGGCCGCGGCUGCUCCC 20 3695 BCL11A-3211 CCGGGCGAGUCGGCCUCGGG 20 3696 BCL11A-3212 + GUCAAAGGCACUCGGGUGAU 20 3697 BCL11A-3213 GGUGCUGCGGUUGAAUCCAA 20 3698 BCL11A-3214 CUGGGCGAGAAGCAUAAGCG 20 3699 BCL11A-3215 + ACUUGGACUUGACCGGGGGC 20 3700 BCL11A-3216 + CCCCCCGAGGCCGACUCGCC 20 3701 BCL11A-3217 CCACCGCAUAGAGCGCCUGG 20 3702 BCL11A-3218 + AGUCGCUGGUGCCGGGUUCC 20 3703 BCL11A-3219 + UCGCACAGGUUGCACUUGUA 20 3704 BCL11A-3220 + GCCCUGCAUGACGUCGGGCA 20 3705 BCL11A-3221 + CCGCCCCCAGGCGCUCUAUG 20 3706 BCL11A-3222 GCCCUGCCCGACGUCAUGCA 20 3707 BCL11A-3223 + GUCGCACAGGUUGCACUUGU 20 3708 BCL11A-3224 AGGUAGCAAGCCGCCCUUCC 20 3709 BCL11A-3225 CCAACCUGAUCCCGGAGAAC 20 3710 BCL11A-3226 + AGGAAGGGCGGCUUGCUACC 20 3711 BCL11A-3227 GAAGGAGUUCGACCUGCCCC 20 3712 BCL11A-3228 + CUUGGACUUGACCGGGGGCU 20 3713 BCL11A-3229 GAGAGGGUGGACUACGGCUU 20 3714 BCL11A-3230 UCCAAGUCAUGCGAGUUCUG 20 3715 BCL11A-3231 ACCCGGCACCAGCGACUUGG 20 3716 BCL11A-3232 + CCCCCAGGCGCUCUAUGCGG 20 3717 BCL11A-3233 + GCGUCUGCCCUCUUUUGAGC 20 3718 BCL11A-3234 GCCCGACGUCAUGCAGGGCA 20 3719 BCL11A-3235 + GAGCUUGAUGCGCUUAGAGA 20 3720 BCL11A-3236 CAGCUCGCGGGGCGCGGUCG 20 3721 BCL11A-3237 + CGUGGUGGCGCGCCGCCUCC 20 3722 BCL11A-3238 UCACCCGAGUGCCUUUGACA 20 3723 BCL11A-3239 GAACGACCCCAACCUGAUCC 20 3724 BCL11A-3240 + CAACCGCAGCACCCUGUCAA 20 3725 BCL11A-3241 + UCCAAGUGAUGUCUCGGUGG 20 3726 BCL11A-3242 + GUUCUCCGUGUUGGGCAUCG 20 3727 BCL11A-3243 CGGAAGUCCCCUGACCCCGC 20 3728 BCL11A-3244 + UAUGCUUCUCGCCCAGGACC 20 3729 BCL11A-3245 AGCUGGACGGAGGGAUCUCG 20 3730 BCL11A-3246 + GGCUGCGCCGGUGCACCACC 20 3731 BCL11A-3247 GUUGGUAUCCCUUCAGGACU 20 3732 BCL11A-3248 AUAGACGAUGGCACUGUUAA 20 3733 BCL11A-3249 CUCCCGCCAUGGAUUUCUCU 20 3734 BCL11A-3250 ACCAGGAUCAGUAUCGAGAG 20 3735 BCL11A-3251 AGUCCCCUGACCCCGCGGGU 20 3736 BCL11A-3252 + GUCUGGAGUCUCCGAAGCUA 20 3737 BCL11A-3253 GCCGGCCCAGCCCUAUGCAA 20 3738 BCL11A-3254 GAUGUGUGGCAGUUUUCGGA 20 3739 BCL11A-3255 + CUAGAGAAAUCCAUGGCGGG 20 3740 BCL11A-3256 + GGCGCUGCCCACCAAGUCGC 20 3741 BCL11A-3257 CCCGGGCGAGUCGGCCUCGG 20 3742 BCL11A-3258 ACACCGCCCGGGGAGCUGGA 20 3743 BCL11A-3259 + CAGUAACCUUUGCAUAGGGC 20 3744 BCL11A-3260 UCAGUAUCGAGAGAGGCUUC 20 3745 BCL11A-3261 + GCAUGACGUCGGGCAGGGCG 20 3746 BCL11A-3262 CCGCAUAGAGCGCCUGGGGG 20 3747 BCL11A-3263 + CCCCCGAGGCCGACUCGCCC 20 3748 BCL11A-3264 + AGGGCGGCUUGCUACCUGGC 20 3749 BCL11A-3265 + GCACCCUGUCAAAGGCACUC 20 3750 BCL11A-3266 + CUGAUCCUGGUAUUCUUAGC 20 3751 BCL11A-3267 + CAUGUGGCGCUUCAGCUUGC 20 3752 BCL11A-3268 + CCCACCAAGUCGCUGGUGCC 20 3753 BCL11A-3269 + GGAGGCAAAAGGCGAUUGUC 20 3754 BCL11A-3270 CCCAACCUGAUCCCGGAGAA 20 3755 BCL11A-3271 + GAGUCUCCGAAGCUAAGGAA 20 3756 BCL11A-3272 GGCUAUGGAGCCUCCCGCCA 20 3757 BCL11A-3273 + CGUCUGCCCUCUUUUGAGCU 20 3758 BCL11A-3274 CGCCCGGGGAGCUGGACGGA 20 3759 BCL11A-3275 + AGUAACCUUUGCAUAGGGCU 20 3760 BCL11A-3276 UCCACCACCGAGACAUCACU 20 3761 BCL11A-3277 + GGUUGCAGUAACCUUUGCAU 20 3762 BCL11A-3278 + GCAAUAUGAAUCCCAUGGAG 20 3763 BCL11A-3279 + ACCAUGCCCUGCAUGACGUC 20 3764 BCL11A-3280 + GGCCUCGCUGAAGUGCUGCA 20 3765 BCL11A-3281 AGAGCAACCUGGUGGUGCAC 20 3766 BCL11A-3282 + GCCCACCAAGUCGCUGGUGC 20 3767 BCL11A-3283 + UGUCAAAGGCACUCGGGUGA 20 3768 BCL11A-3284 + AGCUUGAUGCGCUUAGAGAA 20 3769 BCL11A-3285 + AGGGGGGGCGUCGCCAGGAA 20 3770 BCL11A-3286 + GUGGAAAGCGCCCUUCUGCC 20 3771 BCL11A-3287 + UGGGGGUCCAAGUGAUGUCU 20 3772 BCL11A-3288 CUCCAUGCAGCACUUCAGCG 20 3773 BCL11A-3289 + GCGCUUCAGCUUGCUGGCCU 20 3774 BCL11A-3290 CUUCAGCGAGGCCUUCCACC 20 3775 BCL11A-3291 + GGAGUCUCCGAAGCUAAGGA 20 3776 BCL11A-3292 + CACUCGGGUGAUGGGUGGCC 20 3777 BCL11A-3293 UGCGCUUCUCCACACCGCCC 20 3778 BCL11A-3294 + GGUGGUGGACUAAACAGGGG 20 3779 BCL11A-3295 CGAGGCCUUCCACCAGGUCC 20 3780 BCL11A-3296 AAUGGCCGCGGCUGCUCCCC 20 3781 BCL11A-3297 + GUUGUACAUGUGUAGCUGCU 20 3782 BCL11A-3298 GUUCUUCACACACCCCCAUU 20 3783 BCL11A-3299 CGCAGCGGCACGGGAAGUGG 20 3784 BCL11A-3300 + GCGGGAGGCUCCAUAGCCAU 20 3785 BCL11A-3301 GGUGCACCGGCGCAGCCACA 20 3786 BCL11A-3302 CUCCACACCGCCCGGGGAGC 20 3787 BCL11A-3303 + AAAGCGCCCUUCUGCCAGGC 20 3788 BCL11A-3304 + ACUCGGGUGAUGGGUGGCCA 20 3789 BCL11A-3305 + CUGCCUGGAGGCCGCGUAGC 20 3790 BCL11A-3306 + GUCCAGCUCCCCGGGCGGUG 20 3791 BCL11A-3307 GAGCUGGACGGAGGGAUCUC 20 3792 BCL11A-3308 UCUAGCCCACCGCUGUCCCC 20 3793 BCL11A-3309 + AGUUGUACAUGUGUAGCUGC 20 3794 BCL11A-3310 + AUUCUGCACCUAGUCCUGAA 20 3795 BCL11A-3311 CCACCACGAGAACAGCUCGC 20 3796 BCL11A-3312 + CUCCUAGAGAAAUCCAUGGC 20 3797 BCL11A-3313 UUUAACCUGCUAAGAAUACC 20 3798 BCL11A-3314 + GGACUAAACAGGGGGGGAGU 20 3799 BCL11A-3315 GGCCACCUGGCCGAGGCCGA 20 3800 BCL11A-3316 + GGCUUGCUACCUGGCUGGAA 20 3801 BCL11A-3317 + CAUUCUGCACCUAGUCCUGA 20 3802 BCL11A-3318 + UGCUGGCCUGGGUGCACGCG 20 3803 BCL11A-3319 + UGUGGCCCUCGGCCUCGGCC 20 3804 BCL11A-3320 CCGCCCGGGGAGCUGGACGG 20 3805 BCL11A-3321 UGGCCGAGGCCGAGGGCCAC 20 3806 BCL11A-3322 + UGGGCAUCGCGGCCGGGGGC 20 3807 BCL11A-3323 + UCUCCUAGAGAAAUCCAUGG 20 3808 BCL11A-3324 + GGGCCAUCUCUUCCGCCCCC 20 3809 BCL11A-3325 + GUUGCAGUAACCUUUGCAUA 20 3810 BCL11A-3326 + AAAGGCACUCGGGUGAUGGG 20 3811 BCL11A-3327 + GAAGGGAUCUUUGAGCUGCC 20 3812 BCL11A-3328 + GCCACACAUCUUGAGCUCUC 20 3813 BCL11A-3329 GGAGGGAUCUCGGGGCGCAG 20 3814 BCL11A-3330 CCCGGAGAACGGGGACGAGG 20 3815 BCL11A-3331 + UGCAUAGGGCUGGGCCGGCC 20 3816 BCL11A-3332 CGGGGCGCGGUCGUGGGCGU 20 3817 BCL11A-3333 + GAGGGGGGGCGUCGCCAGGA 20 3818 BCL11A-3334 ACCGCCAGCUCCCCGGAACC 20 3819 BCL11A-3335 + GGUAUUCUUAGCAGGUUAAA 20 3820 BCL11A-3336 AGGCUUCCGGCCUGGCAGAA 20 3821 BCL11A-3337 + GAUCCCUCCGUCCAGCUCCC 20 3822 BCL11A-3338 + UGGUAUUCUUAGCAGGUUAA 20 3823 BCL11A-3339 AUCUACUUAGAAAGCGAACA 20 3824 BCL11A-3340 CGGCCACCUGGCCGAGGCCG 20 3825 BCL11A-3341 CAACACGCACAGAACACUCA 20 3826 BCL11A-3342 + GCCGGCCUGGGGACAGCGGU 20 3827 BCL11A-3343 GCCACCACGAGAACAGCUCG 20 3828 BCL11A-3344 + GUAUUCUUAGCAGGUUAAAG 20 3829 BCL11A-3345 CUCUAGGAGACUUAGAGAGC 20 3830 BCL11A-3346 AACAGCCAUUCACCAGUGCA 20 3831 BCL11A-3347 + UUGCAAGAGAAACCAUGCAC 20 3832 BCL11A-3348 + GACUUGACCGGGGGCUGGGA 20 3833 BCL11A-3349 + ACCUUUGCAUAGGGCUGGGC 20 3834 BCL11A-3350 + UCUUUUGAGCUGGGCCUGCC 20 3835 BCL11A-3351 GAGGCCUUCCACCAGGUCCU 20 3836 BCL11A-3352 + CUUUUGAGCUGGGCCUGCCC 20 3837 BCL11A-3353 + GGGAUCUUUGAGCUGCCUGG 20 3838 BCL11A-3354 GGGCAGGCCCAGCUCAAAAG 20 3839 BCL11A-3355 + AGCACCCUGUCAAAGGCACU 20 3840 BCL11A-3356 + UGGACUAAACAGGGGGGGAG 20 3841 BCL11A-3357 + GCUCUUGAACUUGGCCACCA 20 3842 BCL11A-3358 + GAAUCCCAUGGAGAGGUGGC 20 3843 BCL11A-3359 GUGCACCGGCGCAGCCACAC 20 3844 BCL11A-3360 AAAGAUCCCUUCCUUAGCUU 20 3845 BCL11A-3361 + UGUCUGCAAUAUGAAUCCCA 20 3846 BCL11A-3362 GGCAGGCCCAGCUCAAAAGA 20 3847 BCL11A-3363 + CCUCCGUCCAGCUCCCCGGG 20 3848 BCL11A-3364 CUGUCCAAAAAGCUGCUGCU 20 3849 BCL11A-3365 + GCUUGAUGCGCUUAGAGAAG 20 3850 BCL11A-3366 CGGCUUCGGGCUGAGCCUGG 20 3851 BCL11A-3367 + CACCAUGCCCUGCAUGACGU 20 3852 BCL11A-3368 UCAAGAUGUGUGGCAGUUUU 20 3853 BCL11A-3369 GUUCAAAUUUCAGAGCAACC 20 3854 BCL11A-3370 + GAGAAGGGGCUCAGCGAGCU 20 3855 BCL11A-3371 GCAGCGGCACGGGAAGUGGA 20 3856 BCL11A-3372 + AAGUCUCCUAGAGAAAUCCA 20 3857 BCL11A-3373 + GGUGCCGGGUUCCGGGGAGC 20 3858 BCL11A-3374 CCUGUCCAAAAAGCUGCUGC 20 3859 BCL11A-3375 + AUAUGAAUCCCAUGGAGAGG 20 3860 BCL11A-3376 GGGCGCAGCGGCACGGGAAG 20 3861 BCL11A-3377 GGCCGAGGCCGAGGGCCACA 20 3862 BCL11A-3378 + GCAAGUGUCCCUGUGGCCCU 20 3863 BCL11A-3379 + GGACUUGACCGGGGGCUGGG 20 3864 BCL11A-3380 + GCUUCUCGCCCAGGACCUGG 20 3865 BCL11A-3381 GCGCCUGGGGGCGGAAGAGA 20 3866 BCL11A-3382 + GUCCCUGUGGCCCUCGGCCU 20 3867 BCL11A-3383 + AUCCCUCCGUCCAGCUCCCC 20 3868 BCL11A-3384 GUGCCUUUGACAGGGUGCUG 20 3869 BCL11A-3385 CCCAGAGAGCUCAAGAUGUG 20 3870 BCL11A-3386 + GGCCCUCGGCCUCGGCCAGG 20 3871 BCL11A-3387 GAGAGCGAGAGGGUGGACUA 20 3872 BCL11A-3388 + GGGGGCGUCGCCAGGAAGGG 20 3873 BCL11A-3389 + AGAGAAGGGGCUCAGCGAGC 20 3874 BCL11A-3390 + CCACACAUCUUGAGCUCUCU 20 3875 BCL11A-3391 + GCUGCCCAGCAGCAGCUUUU 20 3876 BCL11A-3392 GGAGCUGGACGGAGGGAUCU 20 3877 BCL11A-3393 GGGGGCGGAAGAGAUGGCCC 20 3878 BCL11A-3394 AGGAGACUUAGAGAGCUGGC 20 3879 BCL11A-3395 GAGGCUUCCGGCCUGGCAGA 20 3880 BCL11A-3396 + AAUCCCAUGGAGAGGUGGCU 20 3881 BCL11A-3397 + UGUGCAUGUGCGUCUUCAUG 20 3882 BCL11A-3398 + CUCGCCCAGGACCUGGUGGA 20 3883 BCL11A-3399 + UCCUCCUCGUCCCCGUUCUC 20 3884 BCL11A-3400 + AGAAACCAUGCACUGGUGAA 20 3885 BCL11A-3401 CUUCGGGCUGAGCCUGGAGG 20 3886 BCL11A-3402 + GCCGGGUUCCGGGGAGCUGG 20 3887 BCL11A-3403 + AGAAGGGGCUCAGCGAGCUG 20 3888 BCL11A-3404 + CUAAACAGGGGGGGAGUGGG 20 3889 BCL11A-3405 CAAAUUUCAGAGCAACCUGG 20 3890 BCL11A-3406 + GAGGGAGGGGGGGCGUCGCC 20 3891 BCL11A-3407 + CCUCCUCGUCCCCGUUCUCC 20 3892 BCL11A-3408 + CCAGCAGCAGCUUUUUGGAC 20 3893 BCL11A-3409 GCCCACCGCUGUCCCCAGGC 20 3894 BCL11A-3410 GGAGACUUAGAGAGCUGGCA 20 3895 BCL11A-3411 AGGAGCUGACGGAGAGCGAG 20 3896 BCL11A-3412 + GAGGGGCGGAUUGCAGAGGA 20 3897 BCL11A-3413 + CAUAGGGCUGGGCCGGCCUG 20 3898 BCL11A-3414 + GGCGGAUUGCAGAGGAGGGA 20 3899 BCL11A-3415 + GGAGGGGCGGAUUGCAGAGG 20 3900 BCL11A-3416 UUACUGCAACCAUUCCAGCC 20 3901 BCL11A-3417 + GCAUAGGGCUGGGCCGGCCU 20 3902 BCL11A-3418 + GGGCGGAUUGCAGAGGAGGG 20 3903 BCL11A-3419 + GGGUUCCGGGGAGCUGGCGG 20 3904 BCL11A-3420 + UCUCGCCCGUGUGGCUGCGC 20 3905 BCL11A-3421 CUUCCCAGCCACCUCUCCAU 20 3906 BCL11A-3422 GCUGACGGAGAGCGAGAGGG 20 3907 BCL11A-3423 + GCGGAUUGCAGAGGAGGGAG 20 3908 BCL11A-3424 GGAGCUGACGGAGAGCGAGA 20 3909 BCL11A-3425 UCUCUCCACCGCCAGCUCCC 20 3910 BCL11A-3426 + UUGACCGGGGGCUGGGAGGG 20 3911 BCL11A-3427 + CGGAUUGCAGAGGAGGGAGG 20 3912 BCL11A-3428 GCGGGGCGCGGUCGUGGGCG 20 3913 BCL11A-3429 + GAGCUGGGCCUGCCCGGGCC 20 3914 BCL11A-3430 + CUGGGCCGGCCUGGGGACAG 20 3915 BCL11A-3431 + UGUAGGGCUUCUCGCCCGUG 20 3916 BCL11A-3432 + CCAUGGAGAGGUGGCUGGGA 20 3917 BCL11A-3433 + GGAGGAGGGGCGGAUUGCAG 20 3918 BCL11A-3434 CCUUCCCAGCCACCUCUCCA 20 3919 BCL11A-3435 + CCCGCGAGCUGUUCUCGUGG 20 3920 BCL11A-3436 + GAUUGCAGAGGAGGGAGGGG 20 3921 BCL11A-3437 + GGCCGGCCUGGGGACAGCGG 20 3922 BCL11A-3438 + GGAUUGCAGAGGAGGGAGGG 20 3923 BCL11A-3439 + ACCGGGGGCUGGGAGGGAGG 20 3924 BCL11A-3440 + CCGGGGGCUGGGAGGGAGGA 20 3925 BCL11A-3441 GAACGGGGACGAGGAGGAAG 20 3926 BCL11A-3442 CCCUCCUCCCUCCCAGCCCC 20 3927 BCL11A-3443 + CGGGGGCUGGGAGGGAGGAG 20 3928 BCL11A-3444 + GGCGCUUCAGCUUGCUGGCC 20 3929 BCL11A-3445 CGGGGACGAGGAGGAAGAGG 20 3930 BCL11A-3446 AGAGGAGGAGGAGGAGCUGA 20 3931 BCL11A-3447 + GGGCUGGGAGGGAGGAGGGG 20 3932 BCL11A-3448 AGAGGAGGACGACGAGGAAG 20 3933 BCL11A-3449 CGACGAGGAAGAGGAAGAAG 20 3934 BCL11A-3450 GGAGGAAGAGGAGGACGACG 20 3935 BCL11A-3451 CGAGGAAGAGGAAGAAGAGG 20 3936 BCL11A-3452 GGAAGAAGAGGAGGAAGAGG 20 3937 BCL11A-3453 AGAGGAAGAAGAGGAGGAAG 20 3938 BCL11A-3454 AGAAGAGGAGGAAGAGGAGG 20 3939 BCL11A-3455 AGAGGAGGAAGAGGAGGAGG 20 3940

Table 5A provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to first tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon, good orthogonality, start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. aureus Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. aureus Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. aureus Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 5A Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO BCL11A-3456 GAACCAGACCACGGCCCGUU 20 3941 BCL11A-3457 + GACCUGGAUGCCAACCUCCA 20 3942 BCL11A-3458 + GAUUAGAGCUCCAUGUG 17 3943 BCL11A-3459 GAUUGUUUAUCAACGUCAUC 20 3944 BCL11A-3460 + GCACUCAUCCCAGGCGU 17 3945 BCL11A-3461 + GGGGAUUAGAGCUCCAUGUG 20 3946 BCL11A-3462 GUGCAGAAUAUGCCCCG 17 3947

Table 5B provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to second tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon, good orthogonality, and do not start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. aureus Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. aureus Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. aureus Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL43A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL3A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 5B 2nd Tier Target SEQ DNA Site ID gRNA Name Strand Targeting Domain Length NO BCL11A-3463 AACCAGACCACGGCCCG 17 3948 BCL11A-3464 + AAUUCCCGUUUGCUUAAGUG 20 3949 BCL11A-3465 ACCAGACCACGGCCCGU 17 3950 BCL11A-3466 AUGAACCAGACCACGGCCCG 20 3951 BCL11A-3467 + AUUCCCGUUUGCUUAAGUGC 20 3952 BCL11A-3468 CCAGACCACGGCCCGUU 17 3953 BCL11A-3469 + CCCGUUUGCUUAAGUGC 17 3954 BCL11A-3470 + CCUGGAUGCCAACCUCC 17 3955 BCL11A-3471 + CUGGAUGCCAACCUCCA 17 3956 BCL11A-3472 + UCAUCCUCUGGCGUGAC 17 3957 BCL11A-3473 + UCCCGUUUGCUUAAGUG 17 3958 BCL11A-3474 + UCGUCAUCCUCUGGCGUGAC 20 3959 BCL11A-3475 + UCUGCACUCAUCCCAGGCGU 20 3960 BCL11A-3476 + UCUGGUUCAUCAUCUGU 17 3961 BCL11A-3477 UGAACCAGACCACGGCCCGU 20 3962 BCL11A-3478 + UGACCUGGAUGCCAACCUCC 20 3963 BCL11A-3479 UGAGUGCAGAAUAUGCCCCG 20 3964 BCL11A-3480 + UGCACUCAUCCCAGGCG 17 3965 BCL11A-3481 + UGGUCUGGUUCAUCAUCUGU 20 3966 BCL11A-3482 UGUUUAUCAACGUCAUC 17 3967 BCL11A-3483 UGUUUAUCAACGUCAUCUAG 20 3968 BCL11A-3484 UUAUCAACGUCAUCUAG 17 3969 BCL11A-3485 + UUCUGCACUCAUCCCAGGCG 20 3970 BCL11A-3486 UUGUUUAUCAACGUCAUCUA 20 3971 BCL11A-3487 UUUAUCAACGUCAUCUA 17 3972

Table 5C provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to third tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon and start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. aureus Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. aureus Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. aureus Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 5C 3rd Tier Target SEQ gRNA DNA Targeting Site  ID Name Strand Domain Length NO BCL11A-3488 GAAAAAAGCAUCCAAUCCCG 20 3973 BCL11A-3489 + GAGAGGCCCCUCCAGUG 17 3974 BCL11A-3490 + GAGCUCCAUGUGCAGAACGA 20 3975 BCL11A-3491 GAGGAAUUUGCCCCAAA 17 3976 BCL11A-3492 + GAGGAGAGGCCCCUCCAGUG 20 3977 BCL11A-3493 + GAGGAGGUCAUGAUCCCCUU 20 3978 BCL11A-3494 + GAGGUCAUGAUCCCCUU 17 3979 BCL11A-3495 GCAUCCAGGUCACGCCA 17 3980 BCL11A-3496 GCCACCUUCCCCUUCACCAA 20 3981 BCL11A-3497 GCCAGAUGAACUUCCCA 17 3982 BCL11A-3498 GCCAGAUGAACUUCCCAUUG 20 3983 BCL11A-3499 GCCCGUUGGGAGCUCCAGAA 20 3984 BCL11A-3500 GCCUCUGCUUAGAAAAAGCU 20 3985 BCL11A-3501 + GCUCCAUGUGCAGAACG 17 3986 BCL11A-3502 GCUCUAAUCCCCACGCC 17 3987 BCL11A-3503 GGACAUUCUUAUUUUUA 17 3988 BCL11A-3504 GGAGCUCUAAUCCCCACGCC 20 3989 BCL11A-3505 GGAUCAUGACCUCCUCACCU 20 3990 BCL11A-3506 + GGAUGCCAACCUCCACGGGA 20 3991 BCL11A-3507 + GGCACUGCCCACAGGUG 17 3992 BCL11A-3508 GGCCCGUUGGGAGCUCCAGA 20 3993 BCL11A-3509 GGGGGACAUUCUUAUUUUUA 20 3994 BCL11A-3510 GGUUGGCAUCCAGGUCACGC 20 3995 BCL11A-3511 + GGUUUGCCUUGCUUGCG 17 3996 BCL11A-3512 + GUGCAGAACGAGGGGAG 17 3997 BCL11A-3513 GUGCCAGAUGAACUUCCCAU 20 3998

Table 5D provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to forth tier parameters. The targeting domains bind within first 500 bp of coding sequence downstream of start codon and do not start with G. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. aureus Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. aureus Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. aureus Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL4A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 5D Target SEQ 4th Tier DNA Targeting Site ID gRNA Name Strand Domain Length NO BCL11A-3514 AAAAAGCAUCCAAUCCC 17 3999 BCL11A-3515 + AAAAAUAAGAAUGUCCCCCA 20 4000 BCL11A-3516 AAAAGCAUCCAAUCCCG 17 4001 BCL11A-3517 + AAAAUAAGAAUGUCCCCCAA 20 4002 BCL11A-3518 AAACCCCAGCACUUAAGCAA 20 4003 BCL11A-3519 + AAAUAAGAAUGUCCCCCAAU 20 4004 BCL11A-3520 AACCCCAGCACUUAAGCAAA 20 4005 BCL11A-3521 + AAUAAGAAUGUCCCCCA 17 4006 BCL11A-3522 ACCCCAGCACUUAAGCAAAC 20 4007 BCL11A-3523 ACCUUCCCCUUCACCAA 17 4008 BCL11A-3524 + AGAGCUCCAUGUGCAGA 17 4009 BCL11A-3525 + AGAGCUCCAUGUGCAGAACG 20 4010 BCL11A-3526 AGAUGAACUUCCCAUUG 17 4011 BCL11A-3527 AGCCAUUCUUACAGAUG 17 4012 BCL11A-3528 + AGCUCCAUGUGCAGAAC 17 4013 BCL11A-3529 + AGCUCCAUGUGCAGAACGAG 20 4014 BCL11A-3530 AGCUCUAAUCCCCACGC 17 4015 BCL11A-3531 AGGAAUUUGCCCCAAAC 17 4016 BCL11A-3532 + AGGAGGUCAUGAUCCCCUUC 20 4017 BCL11A-3533 + AGGUCAUGAUCCCCUUC 17 4018 BCL11A-3534 AGUGCCAGAUGAACUUCCCA 20 4019 BCL11A-3535 + AUAAGAAUGUCCCCCAA 17 4020 BCL11A-3536 + AUCCCAGGCGUGGGGAU 17 4021 BCL11A-3537 + AUCCCCUUCUGGAGCUCCCA 20 4022 BCL11A-3538 + AUCUGGCACUGCCCACAGGU 20 4023 BCL11A-3539 AUGCAAUGGCAGCCUCUGCU 20 4024 BCL11A-3540 + AUGUGCAGAACGAGGGG 17 4025 BCL11A-3541 + AUUAGAGCUCCAUGUGCAGA 20 4026 BCL11A-3542 + AUUCUGCACUCAUCCCAGGC 20 4027 BCL11A-3543 AUUUUUAUCGAGCACAA 17 4028 BCL11A-3544 CAAUGGCAGCCUCUGCU 17 4029 BCL11A-3545 CACGCCUGGGAUGAGUG 17 4030 BCL11A-3546 CAGAUGAACUUCCCAUU 17 4031 BCL11A-3547 + CAUCUCGAUUGGUGAAG 17 4032 BCL11A-3548 + CAUGUGCAGAACGAGGG 17 4033 BCL11A-3549 + CAUGUGCAGAACGAGGGGAG 20 4034 BCL11A-3550 + CCACAGCUUUUUCUAAG 17 4035 BCL11A-3551 CCACGGCCCGUUGGGAGCUC 20 4036 BCL11A-3552 CCAGAUGAACUUCCCAU 17 4037 BCL11A-3553 CCAGCACUUAAGCAAAC 17 4038 BCL11A-3554 CCCAGCACUUAAGCAAA 17 4039 BCL11A-3555 CCCCACGCCUGGGAUGAGUG 20 4040 BCL11A-3556 CCCCAGCACUUAAGCAA 17 4041 BCL11A-3557 CCCCUUCACCAAUCGAG 17 4042 BCL11A-3558 CCCGUUGGGAGCUCCAG 17 4043 BCL11A-3559 + CCCUUCUGGAGCUCCCA 17 4044 BCL11A-3560 CCGUUGGGAGCUCCAGA 17 4045 BCL11A-3561 CCUGUGGGCAGUGCCAG 17 4046 BCL11A-3562 CGGCCCGUUGGGAGCUC 17 4047 BCL11A-3563 CGGCCCGUUGGGAGCUCCAG 20 4048 BCL11A-3564 CGUUGGGAGCUCCAGAA 17 4049 BCL11A-3565 + CGUUUGUGCUCGAUAAAAAU 20 4050 BCL11A-3566 CUAGAGGAAUUUGCCCCAAA 20 4051 BCL11A-3567 + CUCAUCCCAGGCGUGGGGAU 20 4052 BCL11A-3568 + CUCCAUGUGCAGAACGA 17 4053 BCL11A-3569 + CUCCAUGUGCAGAACGAGGG 20 4054 BCL11A-3570 CUCCCCUCGUUCUGCAC 17 4055 BCL11A-3571 CUCCUCCCCUCGUUCUGCAC 20 4056 BCL11A-3572 CUCUAAUCCCCACGCCUGGG 20 4057 BCL11A-3573 + CUGCACUCAUCCCAGGC 17 4058 BCL11A-3574 CUUAUUUUUAUCGAGCACAA 20 4059 BCL11A-3575 CUUCCCCUUCACCAAUCGAG 20 4060 BCL11A-3576 + UAAGAAUGUCCCCCAAU 17 4061 BCL11A-3577 UAAUCCCCACGCCUGGG 17 4062 BCL11A-3578 + UAGAGCUCCAUGUGCAGAAC 20 4063 BCL11A-3579 UAGAGGAAUUUGCCCCAAAC 20 4064 BCL11A-3580 + UAUCCACAGCUUUUUCUAAG 20 4065 BCL11A-3581 UCACCUGUGGGCAGUGCCAG 20 4066 BCL11A-3582 + UCAUCUCGAUUGGUGAA 17 4067 BCL11A-3583 + UCAUCUGGCACUGCCCACAG 20 4068 BCL11A-3584 + UCAUCUGUAAGAAUGGCUUC 20 4069 BCL11A-3585 UCAUGACCUCCUCACCU 17 4070 BCL11A-3586 + UCCAUGUGCAGAACGAG 17 4071 BCL11A-3587 + UCCAUGUGCAGAACGAGGGG 20 4072 BCL11A-3588 UCCCCUCGUUCUGCACA 17 4073 BCL11A-3589 UCCUCCCCUCGUUCUGCACA 20 4074 BCL11A-3590 UCUGCUUAGAAAAAGCU 17 4075 BCL11A-3591 + UCUGGCACUGCCCACAG 17 4076 BCL11A-3592 + UCUGGCACUGCCCACAGGUG 20 4077 BCL11A-3593 + UCUGUAAGAAUGGCUUC 17 4078 BCL11A-3594 UGAAAAAAGCAUCCAAUCCC 20 4079 BCL11A-3595 UGAAGCCAUUCUUACAGAUG 20 4080 BCL11A-3596 + UGCCAACCUCCACGGGA 17 4081 BCL11A-3597 UGCCAGAUGAACUUCCCAUU 20 4082 BCL11A-3598 + UGCUUUUUUCAUCUCGAUUG 20 4083 BCL11A-3599 UGGAGCUCUAAUCCCCACGC 20 4084 BCL11A-3600 + UGGCACUGCCCACAGGU 17 4085 BCL11A-3601 UGGCAUCCAGGUCACGC 17 4086 BCL11A-3602 + UGGGGUUUGCCUUGCUUGCG 20 4087 BCL11A-3603 UUAUUUUUAUCGAGCACAAA 20 4088 BCL11A-3604 + UUCAUCUCGAUUGGUGA 17 4089 BCL11A-3605 UUGGCAUCCAGGUCACGCCA 20 4090 BCL11A-3606 + UUGUGCUCGAUAAAAAU 17 4091 BCL11A-3607 + UUUCAUCUCGAUUGGUG 17 4092 BCL11A-3608 + UUUCAUCUCGAUUGGUGAAG 20 4093 BCL11A-3609 + UUUUCAUCUCGAUUGGUGAA 20 4094 BCL11A-3610 UUUUUAUCGAGCACAAA 17 4095 BCL11A-3611 + UUUUUCAUCUCGAUUGGUGA 20 4096 BCL11A-3612 + UUUUUUCAUCUCGAUUG 17 4097 BCL11A-3613 + UUUUUUCAUCUCGAUUGGUG 20 4098

Table 5E provides exemplary targeting domains for knocking out the BCL11A gene by targeting the early coding sequence the BCL11A gene selected according to fifth tier parameters. The targeting domains target outside the first 500 bp of coding sequence downstream of start codon. It is contemplated herein that the targeting domain hybridizes to the target domain through complementary base pairing. Any of the targeting domains in the table can be used with a S. aureus Cas9 molecule that generates a double strand break (Cas9 nuclease) or a single-strand break (Cas9 nickase). In an embodiment, dual targeting is used to create two double strand breaks to remove the enhancer region in the BCL11A gene, e.g., the first gRNA is used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second gRNA is used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

Any of the targeting domains in the table can be used with a S. aureus Cas9 (nickase) molecule to generate a single strand break. In an embodiment, dual targeting is used to create two nicks on opposite DNA strands by using S. aureus Cas9 nickases with two targeting domains that are complementary to opposite DNA strands, e.g., a gRNA comprising any minus strand targeting domain may be paired any gRNA comprising a plus strand targeting domain provided that the two gRNAs are oriented on the DNA such that PAMs face outward and the distance between the 5′ ends of the gRNAs is 0-50 bp.

In an embodiment, four gRNAs (e.g., two pairs) are used to target four Cas9 nickases to create four nicks to remove the enhancer region in the BCL11A gene, e.g., the first pair of gRNAs are used to target upstream (i.e., 5′) of the enhancer region in the BCL11A gene and the second pair of gRNAs are used to target downstream (i.e., 3′) of the enhancer region in the BCL11A gene.

TABLE 5E Target SEQ 5th Tier DNA Targeting Site ID gRNA Name Strand Domain Length NO BCL11A-3614 + UCGUCGGACUUGACCGUCAU 20 4099 BCL11A-3615 + GUCGUCGGACUUGACCGUCA 20 4100 BCL11A-3616 + CGUCGUCGGACUUGACCGUC 20 4101 BCL11A-3617 + CGUCGGACUUGACCGUCAUG 20 4102 BCL11A-3618 CCCAUAUUAGUGGUCCGGGC 20 4103 BCL11A-3619 + GCGGUCCGACUCGCCGGCCA 20 4104 BCL11A-3620 + CUCCGAGGAGUGCUCCGACG 20 4105 BCL11A-3621 CCCCCAUUCGGCGUAGUACC 20 4106 BCL11A-3622 + UCUCCGAGGAGUGCUCCGAC 20 4107 BCL11A-3623 CCCGCGGGUUGGUAUCCCUU 20 4108 BCL11A-3624 + GCGAGUACACGUUCUCCGUG 20 4109 BCL11A-3625 CCCAUUCGGCGUAGUACCCA 20 4110 BCL11A-3626 + CUCCGUGUUGGGCAUCGCGG 20 4111 BCL11A-3627 + CCGCGCUUAUGCUUCUCGCC 20 4112 BCL11A-3628 CGACGAAGACUCGGUGGCCG 20 4113 BCL11A-3629 ACCCCCACCGCAUAGAGCGC 20 4114 BCL11A-3630 + ACUACGCCGAAUGGGGGUGU 20 4115 BCL11A-3631 + CCGGGCCCGGACCACUAAUA 20 4116 BCL11A-3632 + CGCGUAGCCGGCGAGCCACU 20 4117 BCL11A-3633 UCGGAGCACUCCUCGGAGAA 20 4118 BCL11A-3634 CGGAGCACUCCUCGGAGAAC 20 4119 BCL11A-3635 + UCUCUGGGUACUACGCCGAA 20 4120 BCL11A-3636 + UGCCGCAGAACUCGCAUGAC 20 4121 BCL11A-3637 + GAUACCAACCCGCGGGGUCA 20 4122 BCL11A-3638 + GGAUACCAACCCGCGGGGUC 20 4123 BCL11A-3639 + GGGAUACCAACCCGCGGGGU 20 4124 BCL11A-3640 CCCCCACCGCAUAGAGCGCC 20 4125 BCL11A-3641 + GGUUGGGGUCGUUCUCGCUC 20 4126 BCL11A-3642 GCACGCCCCAUAUUAGUGGU 20 4127 BCL11A-3643 UAAGCGCAUCAAGCUCGAGA 20 4128 BCL11A-3644 + GUUCUCCGAGGAGUGCUCCG 20 4129 BCL11A-3645 + UCUCGAGCUUGAUGCGCUUA 20 4130 BCL11A-3646 CUAAGCGCAUCAAGCUCGAG 20 4131 BCL11A-3647 GUCGGAGCACUCCUCGGAGA 20 4132 BCL11A-3648 UGGCCGCGGCUGCUCCCCGG 20 4133 BCL11A-3649 CCCCACCGCAUAGAGCGCCU 20 4134 BCL11A-3650 + CCUGAAGGGAUACCAACCCG 20 4135 BCL11A-3651 GCGCUUCUCCACACCGCCCG 20 4136 BCL11A-3652 GCGCCCUGCCCGACGUCAUG 20 4137 BCL11A-3653 AACCCGGCACCAGCGACUUG 20 4138 BCL11A-3654 + CUCUGGGUACUACGCCGAAU 20 4139 BCL11A-3655 + CCCGUUCUCCGGGAUCAGGU 20 4140 BCL11A-3656 GAACGACCCCAACCUGAUCC 20 4141 BCL11A-3657 + ACGCCGAAUGGGGGUGUGUG 20 4142 BCL11A-3658 + GUCGCUGGUGCCGGGUUCCG 20 4143 BCL11A-3659 CCCCGGGCGAGUCGGCCUCG 20 4144 BCL11A-3660 + CGGUGCACCACCAGGUUGCU 20 4145 BCL11A-3661 GUCCACCACCGAGACAUCAC 20 4146 BCL11A-3662 UUAAUGGCCGCGGCUGCUCC 20 4147 BCL11A-3663 + CUCUCUGGGUACUACGCCGA 20 4148 BCL11A-3664 + GCGCAAACUCCCGUUCUCCG 20 4149 BCL11A-3665 + CCCGGGCCCGGACCACUAAU 20 4150 BCL11A-3666 + GCCCCCAGGCGCUCUAUGCG 20 4151 BCL11A-3667 AUCGCCUUUUGCCUCCUCGU 20 4152 BCL11A-3668 CCUCGUCGGAGCACUCCUCG 20 4153 BCL11A-3669 + GAGCUUGAUGCGCUUAGAGA 20 4154 BCL11A-3670 + CCCCGUUCUCCGGGAUCAGG 20 4155 BCL11A-3671 CGGCCGCGAUGCCCAACACG 20 4156 BCL11A-3672 + GCCCCCCGAGGCCGACUCGC 20 4157 BCL11A-3673 CCCGGCCGCGAUGCCCAACA 20 4158 BCL11A-3674 CUCCUCGUCGGAGCACUCCU 20 4159 BCL11A-3675 + GUCUCGGUGGUGGACUAAAC 20 4160 BCL11A-3676 + CCCCAGGCGCUCUAUGCGGU 20 4161 BCL11A-3677 + GGUCGCACAGGUUGCACUUG 20 4162 BCL11A-3678 + AGUCGCUGGUGCCGGGUUCC 20 4163 BCL11A-3679 CCCGGUCAAGUCCAAGUCAU 20 4164 BCL11A-3680 AGAACGACCCCAACCUGAUC 20 4165 BCL11A-3681 + UCCGUGUUGGGCAUCGCGGC 20 4166 BCL11A-3682 CCUCCUCGUCGGAGCACUCC 20 4167 BCL11A-3683 UCACUUGGACCCCCACCGCA 20 4168 BCL11A-3684 CCCAACCUGAUCCCGGAGAA 20 4169 BCL11A-3685 ACUACGGCUUCGGGCUGAGC 20 4170 BCL11A-3686 UUUGCGCUUCUCCACACCGC 20 4171 BCL11A-3687 + AAGUCGCUGGUGCCGGGUUC 20 4172 BCL11A-3688 CCCCAACCUGAUCCCGGAGA 20 4173 BCL11A-3689 AAGACUCGGUGGCCGGCGAG 20 4174 BCL11A-3690 GCGCGGCCACCUGGCCGAGG 20 4175 BCL11A-3691 AAUCGCCUUUUGCCUCCUCG 20 4176 BCL11A-3692 ACGACCCCAACCUGAUCCCG 20 4177 BCL11A-3693 GAUCCCGGAGAACGGGGACG 20 4178 BCL11A-3694 + GGGGCAGGUCGAACUCCUUC 20 4179 BCL11A-3695 UGGCUAUGGAGCCUCCCGCC 20 4180 BCL11A-3696 + CCCCCAGGCGCUCUAUGCGG 20 4181 BCL11A-3697 GCGGUUGAAUCCAAUGGCUA 20 4182 BCL11A-3698 CUACGGCUUCGGGCUGAGCC 20 4183 BCL11A-3699 ACAGCUCGCGGGGCGCGGUC 20 4184 BCL11A-3700 CCCCCCUGUUUAGUCCACCA 20 4185 BCL11A-3701 + CGCAUGACUUGGACUUGACC 20 4186 BCL11A-3702 CACGGAAGUCCCCUGACCCC 20 4187 BCL11A-3703 CCUCCCGCCAUGGAUUUCUC 20 4188 BCL11A-3704 + UCUCGGUGGUGGACUAAACA 20 4189 BCL11A-3705 + UGAACUUGGCCACCACGGAC 20 4190 BCL11A-3706 CUUCUCUAAGCGCAUCAAGC 20 4191 BCL11A-3707 + AGCGCAAACUCCCGUUCUCC 20 4192 BCL11A-3708 + UCGGUGGUGGACUAAACAGG 20 4193 BCL11A-3709 CGCCACCACGAGAACAGCUC 20 4194 BCL11A-3710 CUCCCGCCAUGGAUUUCUCU 20 4195 BCL11A-3711 + CGAGCUUGAUGCGCUUAGAG 20 4196 BCL11A-3712 + AUGCCCUGCAUGACGUCGGG 20 4197 BCL11A-3713 UCUCUAAGCGCAUCAAGCUC 20 4198 BCL11A-3714 + GUCCAAGUGAUGUCUCGGUG 20 4199 BCL11A-3715 + CCCCCGAGGCCGACUCGCCC 20 4200 BCL11A-3716 + CCCCGAGGCCGACUCGCCCG 20 4201 BCL11A-3717 + GAAAUUUGAACGUCUUGCCG 20 4202 BCL11A-3718 + GUCGCUGCGUCUGCCCUCUU 20 4203 BCL11A-3719 UGGAGGCGGCGCGCCACCAC 20 4204 BCL11A-3720 + CUUCUCGAGCUUGAUGCGCU 20 4205 BCL11A-3721 + GAAGCGCAAACUCCCGUUCU 20 4206 BCL11A-3722 GAGAGAGGCUUCCGGCCUGG 20 4207 BCL11A-3723 UCCCCGGGCGAGUCGGCCUC 20 4208 BCL11A-3724 + CAAGUCGCUGGUGCCGGGUU 20 4209 BCL11A-3725 CAUAGAGCGCCUGGGGGCGG 20 4210 BCL11A-3726 + CUCGGUGGUGGACUAAACAG 20 4211 BCL11A-3727 + CCCCCCGAGGCCGACUCGCC 20 4212 BCL11A-3728 GGUUUCUCUUGCAACACGCA 20 4213 BCL11A-3729 + ACUUGGACUUGACCGGGGGC 20 4214 BCL11A-3730 UGAUCCCGGAGAACGGGGAC 20 4215 BCL11A-3731 + UGUCUGGAGUCUCCGAAGCU 20 4216 BCL11A-3732 AUGGAUUUCUCUAGGAGACU 20 4217 BCL11A-3733 UGCGGUUGAAUCCAAUGGCU 20 4218 BCL11A-3734 CUCCCCGGGCGAGUCGGCCU 20 4219 BCL11A-3735 CCUGAUCCCGGAGAACGGGG 20 4220 BCL11A-3736 + UGUCUCGGUGGUGGACUAAA 20 4221 BCL11A-3737 + CGGUGGUGGACUAAACAGGG 20 4222 BCL11A-3738 + UGCCCACCAAGUCGCUGGUG 20 4223 BCL11A-3739 CGUGGUGGCCAAGUUCAAGA 20 4224 BCL11A-3740 CAUCACCCGAGUGCCUUUGA 20 4225 BCL11A-3741 GCGGCAAGACGUUCAAAUUU 20 4226 BCL11A-3742 + AAGGGCUCUCGAGCUUCCAU 20 4227 BCL11A-3743 + GUCUGGAGUCUCCGAAGCUA 20 4228 BCL11A-3744 CCCCGGCCGCGAUGCCCAAC 20 4229 BCL11A-3745 + CUGUCAAAGGCACUCGGGUG 20 4230 BCL11A-3746 + CUUGGACUUGACCGGGGGCU 20 4231 BCL11A-3747 + GACUUGGACUUGACCGGGGG 20 4232 BCL11A-3748 + UGCGUCUGCCCUCUUUUGAG 20 4233 BCL11A-3749 + GGAGGCAAAAGGCGAUUGUC 20 4234 BCL11A-3750 GCAACACGCACAGAACACUC 20 4235 BCL11A-3751 + GCAGUAACCUUUGCAUAGGG 20 4236 BCL11A-3752 UGGUGCACCGGCGCAGCCAC 20 4237 BCL11A-3753 UGGUGGCCAAGUUCAAGAGC 20 4238 BCL11A-3754 GCAUAAGCGCGGCCACCUGG 20 4239 BCL11A-3755 + UUGCAUAGGGCUGGGCCGGC 20 4240 BCL11A-3756 CCAACCUGAUCCCGGAGAAC 20 4241 BCL11A-3757 AGAUGUGUGGCAGUUUUCGG 20 4242 BCL11A-3758 CAGUUUUCGGAUGGAAGCUC 20 4243 BCL11A-3759 GCUCCCCGGGCGAGUCGGCC 20 4244 BCL11A-3760 GGGUGGACUACGGCUUCGGG 20 4245 BCL11A-3761 UAUCCCUUCAGGACUAGGUG 20 4246 BCL11A-3762 AUCUCGGGGCGCAGCGGCAC 20 4247 BCL11A-3763 + CGCUCUUGAACUUGGCCACC 20 4248 BCL11A-3764 GCACCGGCGCAGCCACACGG 20 4249 BCL11A-3765 + GCUUCUCGCCCAGGACCUGG 20 4250 BCL11A-3766 UCCCGGAGAACGGGGACGAG 20 4251 BCL11A-3767 + CAGCACCCUGUCAAAGGCAC 20 4252 BCL11A-3768 + CAUUCUGCACCUAGUCCUGA 20 4253 BCL11A-3769 CUUUAACCUGCUAAGAAUAC 20 4254 BCL11A-3770 GUCUCUCCACCGCCAGCUCC 20 4255 BCL11A-3771 UCUCUCCACCGCCAGCUCCC 20 4256 BCL11A-3772 + UGCUUCUCGCCCAGGACCUG 20 4257 BCL11A-3773 + GCGCCGCCUCCAGGCUCAGC 20 4258 BCL11A-3774 + AGAUCCCUCCGUCCAGCUCC 20 4259 BCL11A-3775 CGAGAGGGUGGACUACGGCU 20 4260 BCL11A-3776 + CGUCCAGCUCCCCGGGCGGU 20 4261 BCL11A-3777 + CCAGCUCUCUAAGUCUCCUA 20 4262 BCL11A-3778 + UCGCAUGACUUGGACUUGAC 20 4263 BCL11A-3779 + GCACCAUGCCCUGCAUGACG 20 4264 BCL11A-3780 + AAGGCGAUUGUCUGGAGUCU 20 4265 BCL11A-3781 + GCCUGGAGGCCGCGUAGCCG 20 4266 BCL11A-3782 GCGGCCACCUGGCCGAGGCC 20 4267 BCL11A-3783 AGAAUACCAGGAUCAGUAUC 20 4268 BCL11A-3784 GAUGUGUGGCAGUUUUCGGA 20 4269 BCL11A-3785 UCUCCACACCGCCCGGGGAG 20 4270 BCL11A-3786 CCUGGAGGCGGCGCGCCACC 20 4271 BCL11A-3787 + CUGGUAUUCUUAGCAGGUUA 20 4272 BCL11A-3788 + UAGAGAAGGGGCUCAGCGAG 20 4273 BCL11A-3789 + GAGUGUUCUGUGCGUGUUGC 20 4274 BCL11A-3790 AAUAACCCCUUUAACCUGCU 20 4275 BCL11A-3791 + AAAGCGCCCUUCUGCCAGGC 20 4276 BCL11A-3792 + GUCCAGCUCCCCGGGCGGUG 20 4277 BCL11A-3793 + AAGGGCGGCUUGCUACCUGG 20 4278 BCL11A-3794 + GAAAGCGCCCUUCUGCCAGG 20 4279 BCL11A-3795 + AGGGCGGCUUGCUACCUGGC 20 4280 BCL11A-3796 CGCGGGGCGCGGUCGUGGGC 20 4281 BCL11A-3797 GCGAGGCCUUCCACCAGGUC 20 4282 BCL11A-3798 + ACUUCCCGUGCCGCUGCGCC 20 4283 BCL11A-3799 GCACAGAACACUCAUGGAUU 20 4284 BCL11A-3800 + CCAGCUCCCCGGGCGGUGUG 20 4285 BCL11A-3801 ACCGCCCGGGGAGCUGGACG 20 4286 BCL11A-3802 + UGGUUGCAGUAACCUUUGCA 20 4287 BCL11A-3803 AGGAGACUUAGAGAGCUGGC 20 4288 BCL11A-3804 ACCGGCGCAGCCACACGGGC 20 4289 BCL11A-3805 + ACAUUCUGCACCUAGUCCUG 20 4290 BCL11A-3806 + GUGUUCUGUGCGUGUUGCAA 20 4291 BCL11A-3807 UGGCCCUGGCCACCCAUCAC 20 4292 BCL11A-3808 + UGCAUAGGGCUGGGCCGGCC 20 4293 BCL11A-3809 AAUACCAGGAUCAGUAUCGA 20 4294 BCL11A-3810 + UCCUGAAGGGAUACCAACCC 20 4295