Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161159369-161159507 | Common:1; Rare:36 | ||||
chr1:161166268-161166511 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199020-161199320 | Rare:45 | ||||
chr1:161225818-161226069 | Common:9; Rare:35 | ||||
chr1:161314265-161314412 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367864-161367905 | Rare:10 | ||||
chr1:161749749-161749833 | Rare:35 | ||||
chr1:161766202-161766363 | Common:3; Rare:54 | ||||
chr1:162497761-162497818 | Common:1; Rare:20 | ||||
chr1:162561340-162561682 | Common:3; Rare:129 | ||||
chr1:162790516-162790781 | Common:4; Rare:76 | ||||
chr1:163321705-163322117 | Common:1; Rare:108 | ||||
chr1:165698464-165698708 | Common:3; Rare:112 | ||||
chr1:165768757-165769030 | Common:2; Rare:108 | ||||
chr1:166165813-166165905 | Rare:26 |