Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113904771-113905442 | Common:7; Rare:192; Clinvar (benign):2 | ||||
chr1:114581527-114581818 | Common:1; Rare:129 | ||||
chr1:114670004-114670255 | Common:1; Rare:77 | ||||
chr1:114716658-114716866 | Common:1; Rare:84; Clinvar:4; Clinvar (benign):3 | ||||
chr1:114757925-114758139 | Common:3; Rare:68 | ||||
chr1:114780539-114780798 | Common:1; Rare:101 | ||||
chr1:115089455-115089612 | Common:2; Rare:59 | ||||
chr1:115338194-115338370 | Rare:44 | ||||
chr1:116373086-116373411 | Rare:109 | ||||
chr1:116389175-116389687 | Common:2; Rare:98 | ||||
chr1:116399255-116399541 | Rare:48 | ||||
chr1:116570961-116571197 | Common:2; Rare:69 | ||||
chr1:116754351-116754476 | Rare:35 | ||||
chr1:117060203-117060353 | Common:2; Rare:41 | ||||
chr1:117929546-117929821 | Common:4; Rare:84 |