Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178725131-178725309 | Common:10; Rare:71 | ||||
chr1:179882168-179882860 | Common:1; Rare:242; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954464-179954817 | Common:3; Rare:87 | ||||
chr1:182589235-182589292 | Rare:12 | ||||
chr1:182839068-182839394 | Common:1; Rare:116 | ||||
chr1:183185902-183186339 | Common:5; Rare:95; Clinvar:5; Clinvar (benign):4 | ||||
chr1:183472261-183472515 | Common:2; Rare:91 | ||||
chr1:183635666-183636028 | Common:2; Rare:103 | ||||
chr1:184051607-184051782 | Common:3; Rare:67 | ||||
chr1:185156934-185157272 | Common:1; Rare:89 | ||||
chr1:185317161-185317464 | Common:1; Rare:88 | ||||
chr1:186375126-186375920 | Common:1; Rare:216 | ||||
chr1:193059280-193059665 | Rare:182 | ||||
chr1:193121674-193122179 | Common:3; Rare:172; Clinvar:5; Clinvar (benign):1 | ||||
chr1:200669914-200670126 | Common:4; Rare:54 |