| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87876208-87876702 | Common:3; Rare:210 | ||||
| chr7:88220017-88220153 | Rare:66 | ||||
| chr7:90211633-90211905 | Common:4; Rare:84 | ||||
| chr7:90346603-90346736 | Common:3; Rare:58 | ||||
| chr7:91880677-91880825 | Common:2; Rare:40 | ||||
| chr7:92134405-92134849 | Common:5; Rare:124 | ||||
| chr7:92245890-92245979 | Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246099-92246459 | Common:3; Rare:132 | ||||
| chr7:92528383-92528816 | Common:3; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590042-92590142 | Rare:40 | ||||
| chr7:92836519-92836618 | Rare:22 | ||||
| chr7:93232180-93232412 | Common:2; Rare:50 | ||||
| chr7:93890737-93890947 | Common:2; Rare:49 | ||||
| chr7:94004310-94004478 | Rare:49 | ||||
| chr7:94656104-94656380 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 |