Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116399267-116399543 | Rare:45 | ||||
chr1:116909719-116909923 | Common:1; Rare:55 | ||||
chr1:117929591-117929800 | Common:1; Rare:57 | ||||
chr1:119140634-119140779 | Common:1; Rare:48 | ||||
chr1:119768838-119769060 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr1:121184906-121185091 | Rare:63 | ||||
chr1:121185478-121185803 | Rare:14 | ||||
chr1:145823937-145824238 | Rare:106 | ||||
chr1:145858992-145859173 | Rare:51 | ||||
chr1:145918667-145919022 | Common:2; Rare:86; Clinvar:1 | ||||
chr1:145927364-145927634 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964749 | Rare:44 | ||||
chr1:145994874-145995360 | Rare:209 | ||||
chr1:145995809-145996790 | Common:3; Rare:362 | ||||
chr1:147172420-147172785 | Common:1; Rare:94 |