Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20896897-20897129 | Common:1; Rare:33 | ||||
chr1:21694296-21694577 | Common:3; Rare:42 | ||||
chr1:22025016-22025127 | Rare:22 | ||||
chr1:22025188-22025575 | Common:8; Rare:98 | ||||
chr1:23192893-23193199 | Common:6; Rare:71 | ||||
chr1:23217463-23217582 | Rare:29 | ||||
chr1:23554843-23555169 | Common:1; Rare:120 | ||||
chr1:23695764-23696151 | Common:1; Rare:84; Clinvar (benign):1 | ||||
chr1:24646417-24646701 | Common:3; Rare:63 | ||||
chr1:25808770-25809112 | Common:2; Rare:101; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr1:26457666-26457752 | Common:1; Rare:12 | ||||
chr1:26697445-26697526 | Rare:24 | ||||
chr1:26714984-26715161 | Rare:35 | ||||
chr1:26863986-26864327 | Rare:51 | ||||
chr1:26864367-26864458 | Rare:18 |