Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:132347305-132347481 | Common:1; Rare:45 | ||||
chr2:150495996-150496333 | Common:2; Rare:42 | ||||
chr2:160270291-160270515 | Common:2; Rare:61 | ||||
chr2:170770762-170771096 | Common:2; Rare:58 | ||||
chr2:174788564-174788786 | Common:4; Rare:56 | ||||
chr2:176105214-176105496 | Common:1; Rare:49 | ||||
chr2:176637601-176637784 | Common:5; Rare:67 | ||||
chr2:178413888-178414000 | Common:1; Rare:33 | ||||
chr2:181123903-181123930 | Rare:4 | ||||
chr2:188994574-188994805 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr2:188996176-188996423 | Common:12; Rare:54; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr2:189004068-189004364 | Rare:89; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):19 | ||||
chr2:199459924-199460222 | Common:1; Rare:59 | ||||
chr2:207239362-207239687 | Rare:51 | ||||
chr2:207254286-207254294 | Rare:2 |