Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26432090-26432418 | Common:5; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695941-26696028 | Rare:34 | ||||
chr1:28505823-28506084 | Common:3; Rare:114 | ||||
chr1:28643065-28643161 | Rare:32 | ||||
chr1:29122733-29122864 | Common:1; Rare:36 | ||||
chr1:31296665-31297075 | Common:6; Rare:149 | ||||
chr1:31703400-31703594 | Common:1; Rare:36 | ||||
chr1:31937771-31937993 | Common:1; Rare:60 | ||||
chr1:32650929-32651247 | Common:2; Rare:111 | ||||
chr1:32817258-32817679 | Rare:114; Clinvar:5 | ||||
chr1:35193119-35193432 | Common:2; Rare:102 | ||||
chr1:35557373-35557442 | Rare:14 | ||||
chr1:35557636-35557851 | Common:2; Rare:86 | ||||
chr1:37474395-37474581 | Common:1; Rare:74 | ||||
chr1:37808184-37808653 | Common:1; Rare:108 |