Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117367645-117367757 | Rare:20 | ||||
chr1:117929541-117929996 | Common:5; Rare:129 | ||||
chr1:119140628-119140771 | Common:1; Rare:46 | ||||
chr1:119647664-119647777 | Rare:19 | ||||
chr1:119648081-119648350 | Common:3; Rare:90 | ||||
chr1:120176343-120176614 | Common:1; Rare:57 | ||||
chr1:144461552-144461724 | Common:5; Rare:76 | ||||
chr1:145214850-145215000 | Rare:16 | ||||
chr1:145607831-145608075 | Common:2; Rare:74 | ||||
chr1:145823866-145824105 | Rare:93 | ||||
chr1:145824121-145824274 | Rare:46 | ||||
chr1:145918680-145919037 | Common:2; Rare:81 | ||||
chr1:145927130-145927286 | Common:1; Rare:27; Clinvar (benign):1 | ||||
chr1:145927364-145927690 | Common:1; Rare:87; Clinvar (pathogenic):1 | ||||
chr1:145957983-145958224 | Rare:57 |