| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87345437-87345712 | Common:5; Rare:87 | ||||
| chr7:87876219-87876685 | Common:3; Rare:198 | ||||
| chr7:90346605-90346736 | Common:2; Rare:58 | ||||
| chr7:91880677-91880801 | Common:1; Rare:33 | ||||
| chr7:91940735-91940878 | Common:1; Rare:38 | ||||
| chr7:92134418-92134556 | Rare:39 | ||||
| chr7:92134711-92134880 | Common:3; Rare:50 | ||||
| chr7:92245890-92245974 | Rare:25; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528421-92528808 | Common:3; Rare:121; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93117916-93118104 | Rare:29 | ||||
| chr7:93232189-93232407 | Common:2; Rare:46 | ||||
| chr7:93890751-93890983 | Common:2; Rare:53 | ||||
| chr7:93921775-93922130 | Common:5; Rare:81 | ||||
| chr7:94656114-94656372 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95434884-95435097 | Common:1; Rare:90; Clinvar (benign):1 |