| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90346573-90346747 | Common:4; Rare:77 | ||||
| chr7:90595883-90596046 | Common:6; Rare:66 | ||||
| chr7:91880658-91880812 | Common:1; Rare:45 | ||||
| chr7:91940831-91941142 | Common:3; Rare:104; Clinvar:6; Clinvar (benign):3 | ||||
| chr7:92133914-92134112 | Common:1; Rare:31 | ||||
| chr7:92134157-92134227 | Rare:21 | ||||
| chr7:92134413-92134550 | Rare:37 | ||||
| chr7:92134728-92135042 | Common:3; Rare:75 | ||||
| chr7:92245495-92245706 | Rare:59; Clinvar (benign):1 | ||||
| chr7:92245825-92246011 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:92246029-92246483 | Common:4; Rare:155; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:92447440-92447502 | Common:2; Rare:27 | ||||
| chr7:92528368-92528896 | Common:5; Rare:166; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590336-92590594 | Rare:75 | ||||
| chr7:92833830-92834067 | Rare:54 |