Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161215133-161215324 | Common:2; Rare:54 | ||||
chr1:161314265-161314412 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749749-161749837 | Rare:37 | ||||
chr1:161750220-161750447 | Rare:53 | ||||
chr1:161766147-161766393 | Common:3; Rare:80 | ||||
chr1:162023846-162024027 | Rare:68 | ||||
chr1:162497736-162497867 | Common:1; Rare:43 | ||||
chr1:162561375-162561700 | Common:3; Rare:122 | ||||
chr1:163069134-163069359 | Rare:58 | ||||
chr1:163321718-163322100 | Common:1; Rare:100 | ||||
chr1:165698380-165698786 | Common:5; Rare:154 | ||||
chr1:165768719-165769039 | Common:2; Rare:123; Clinvar:1 | ||||
chr1:166839236-166839534 | Rare:91 | ||||
chr1:167553496-167553658 | Rare:39 | ||||
chr1:167721795-167722236 | Common:4; Rare:103 |