Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:115641803-115642043 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
chr1:116373036-116373349 | Rare:105 | ||||
chr1:116570983-116571295 | Common:3; Rare:82 | ||||
chr1:116667672-116667923 | Common:2; Rare:89 | ||||
chr1:117060050-117060367 | Common:6; Rare:88 | ||||
chr1:117121707-117121981 | Common:1; Rare:83 | ||||
chr1:117929568-117929800 | Common:2; Rare:69 | ||||
chr1:119140625-119140785 | Common:1; Rare:54 | ||||
chr1:120176377-120176643 | Common:1; Rare:54 | ||||
chr1:145823922-145824267 | Rare:122 | ||||
chr1:145918693-145919005 | Common:2; Rare:62 | ||||
chr1:145927415-145927657 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145964537-145964731 | Rare:48 | ||||
chr1:147172420-147172804 | Common:1; Rare:100 | ||||
chr1:147242541-147242740 | Common:3; Rare:85 |