Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119140546-119140887 | Common:1; Rare:108; Clinvar (pathogenic):1 | ||||
chr1:119141088-119141251 | Rare:31 | ||||
chr1:119648066-119648622 | Common:5; Rare:164 | ||||
chr1:119711760-119712004 | Common:2; Rare:73; Clinvar:4; Clinvar (benign):2 | ||||
chr1:120069349-120069491 | Common:7; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
chr1:120176142-120176215 | Common:1; Rare:13 | ||||
chr1:120176244-120176291 | Rare:7 | ||||
chr1:120176314-120176671 | Common:1; Rare:66 | ||||
chr1:120723770-120724021 | Rare:10 | ||||
chr1:120914104-120914308 | Rare:27 | ||||
chr1:121183921-121184020 | Rare:26 | ||||
chr1:121184780-121185091 | Common:1; Rare:105 | ||||
chr1:143905657-143905802 | Common:1; Rare:69 | ||||
chr1:144461208-144461465 | Common:2; Rare:104 | ||||
chr1:144461558-144461693 | Common:5; Rare:61 |