| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91940735-91941138 | Common:4; Rare:127; Clinvar:5; Clinvar (benign):3 | ||||
| chr7:92134407-92134592 | Rare:58 | ||||
| chr7:92245865-92245986 | Rare:36; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528394-92528839 | Common:4; Rare:149; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833815-92834126 | Rare:68 | ||||
| chr7:92836365-92836614 | Rare:51 | ||||
| chr7:93921640-93921829 | Common:2; Rare:33 | ||||
| chr7:93921919-93922063 | Common:2; Rare:32 | ||||
| chr7:94004310-94004566 | Rare:71 | ||||
| chr7:95434913-95435049 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr7:96322043-96322145 | Rare:53; Clinvar:3 | ||||
| chr7:98252133-98252364 | Common:1; Rare:52 | ||||
| chr7:99325805-99325963 | Common:1; Rare:61 | ||||
| chr7:99408549-99408667 | Common:2; Rare:38 | ||||
| chr7:99408789-99409092 | Common:1; Rare:90 |