Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117929568-117929790 | Common:1; Rare:67 | ||||
chr1:119140640-119140767 | Rare:38 | ||||
chr1:119648114-119648364 | Common:3; Rare:85 | ||||
chr1:120176378-120176614 | Common:1; Rare:52 | ||||
chr1:145607875-145608025 | Common:2; Rare:39 | ||||
chr1:145823869-145824280 | Rare:142 | ||||
chr1:145918680-145919013 | Common:2; Rare:74 | ||||
chr1:145927374-145927628 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958223 | Rare:53 | ||||
chr1:145964567-145964742 | Rare:45 | ||||
chr1:145994141-145994205 | Rare:26 | ||||
chr1:145995142-145995477 | Rare:131 | ||||
chr1:145996412-145996885 | Common:2; Rare:175 | ||||
chr1:147172419-147172823 | Common:1; Rare:103 | ||||
chr1:149886641-149887004 | Common:2; Rare:135 |