| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93591186-93591729 | Common:6; Rare:194 | ||||
| chr7:94004303-94004427 | Rare:44 | ||||
| chr7:94509701-94510126 | Rare:142 | ||||
| chr7:94656088-94656387 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94907531-94907693 | Common:1; Rare:38 | ||||
| chr7:95434947-95435077 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr7:95596610-95596699 | Common:1; Rare:15 | ||||
| chr7:96321964-96322190 | Rare:102; Clinvar:4 | ||||
| chr7:96709720-96709923 | Common:1; Rare:67 | ||||
| chr7:97005385-97005603 | Common:1; Rare:63 | ||||
| chr7:97006115-97006178 | Common:1; Rare:42 | ||||
| chr7:97006369-97006476 | Common:1; Rare:30 | ||||
| chr7:97024676-97024768 | Rare:18 | ||||
| chr7:97117442-97117802 | Common:2; Rare:158 | ||||
| chr7:97872365-97872621 | Common:2; Rare:81 |