| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87345443-87345701 | Common:4; Rare:85 | ||||
| chr7:87876208-87876688 | Common:3; Rare:203 | ||||
| chr7:90211632-90211905 | Common:4; Rare:84 | ||||
| chr7:90346585-90346744 | Common:4; Rare:68 | ||||
| chr7:90403349-90403553 | Common:1; Rare:53 | ||||
| chr7:90595940-90596016 | Common:5; Rare:30 | ||||
| chr7:91880655-91880826 | Common:2; Rare:49 | ||||
| chr7:91940735-91940998 | Common:4; Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134360-92134585 | Rare:71 | ||||
| chr7:92134709-92134853 | Common:3; Rare:37 | ||||
| chr7:92245843-92245974 | Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528421-92528816 | Common:3; Rare:126; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833906-92834085 | Rare:44 | ||||
| chr7:92836474-92836518 | Rare:7 | ||||
| chr7:93117954-93118123 | Rare:30 |