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. 2020 Sep 9;3(11):e202000757. doi: 10.26508/lsa.202000757

Table 1.

Number of hg38 genome matches, considering 0–3 mismatches, using two different methods (A, Aho–Corasick; B, Bowtie).

Target CRISPR site No. of mismatches
Gene Spacer range Spacer sequence PAM 0 1 2 3
A0 B0 A1 B1 A2 B2 A3 B3
CFTR chr7:117559575-94:+ ATTAAAGAAAATATCATCTT TGG 1 1 7 7 145 143 2,304 2,277
chr7:117559606-25:− TCTGTATCTATATTCATCAT AGG 1 1 7 7 125 124 1701 1,672
HBB chr11:5227003-22:− CATGGTGCATCTGACTCCTG AGG 2 2 0 0 14 13 210 208
chr11:5226984-7003:+ GTAACGGCAGACTTCTCCTC AGG 1 1 0 0 7 7 83 82
HEXA chr15:72346551-70:+ TGTAGAAATCCTTCCAGTCA GGG 1 1 0 0 25 25 295 292
chr15:72346558-77:+ ATCCTTCCAGTCAGGGCCAT AGG 1 1 0 0 6 6 201 199
PRNP chr20:4699568-87:+ AGCAGCTGGGGCAGTGGTGG GGG 1 1 2 2 95 88 904 891
chr20:4699569-88:+ GCAGCTGGGGCAGTGGTGGG GGG 1 1 12 12 98 93 1,043 1,024
chr20:4699575-94:+ GGGGCAGTGGTGGGGGGCCT TGG 1 1 2 2 55 54 857 826
chr20:4699578-97:+ GCAGTGGTGGGGGGCCTTGG CGG 1 1 0 0 32 31 417 412