| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2617715-2617887 | Rare:44 | ||||
| chr7:4879636-4879651 | Common:1; Rare:5 | ||||
| chr7:5427808-5427885 | Rare:31 | ||||
| chr7:5693688-5693819 | Rare:20 | ||||
| chr7:5695459-5695482 | Rare:5 | ||||
| chr7:5695484-5695594 | Common:2; Rare:25 | ||||
| chr7:6016610-6016875 | Common:1; Rare:64 | ||||
| chr7:6729495-6729819 | Common:4; Rare:121 | ||||
| chr7:11194549-11194737 | Common:1; Rare:29 | ||||
| chr7:15688202-15688428 | Common:2; Rare:66 | ||||
| chr7:22854010-22854258 | Common:5; Rare:79 | ||||
| chr7:23490432-23490574 | Common:2; Rare:59 | ||||
| chr7:23680813-23680880 | Common:2; Rare:18 | ||||
| chr7:26193251-26193698 | Rare:156; Clinvar (benign):2 | ||||
| chr7:26197610-26197853 | Common:1; Rare:53; Clinvar (benign):2 |