Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:115338224-115338349 | Rare:30 | ||||
chr1:115641811-115642032 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr1:115768506-115768965 | Common:8; Rare:98; Clinvar:10; Clinvar (benign):5 | ||||
chr1:116570970-116571148 | Common:1; Rare:53 | ||||
chr1:116667668-116667857 | Common:1; Rare:69 | ||||
chr1:116909580-116910125 | Common:3; Rare:150 | ||||
chr1:117060082-117060349 | Common:6; Rare:62 | ||||
chr1:117121705-117121997 | Common:1; Rare:93 | ||||
chr1:117929522-117929821 | Common:4; Rare:91 | ||||
chr1:119140640-119140782 | Common:1; Rare:44 | ||||
chr1:119648131-119648367 | Common:3; Rare:81 | ||||
chr1:120176377-120176616 | Common:1; Rare:52 | ||||
chr1:121184676-121185040 | Common:3; Rare:120 | ||||
chr1:145823869-145824265 | Rare:137 | ||||
chr1:145858996-145859115 | Rare:39 |