| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128530470-128530572 | Rare:26 | ||||
| chr7:128828239-128828351 | Common:1; Rare:17 | ||||
| chr7:128858009-128858494 | Common:2; Rare:125; Clinvar:10; Clinvar (benign):14 | ||||
| chr7:129443774-129443927 | Rare:21 | ||||
| chr7:131106344-131106519 | Common:1; Rare:34 | ||||
| chr7:131107028-131107277 | Common:2; Rare:44 | ||||
| chr7:131107956-131108196 | Common:1; Rare:38 | ||||
| chr7:139614163-139614298 | Rare:31 | ||||
| chr7:139648708-139648751 | Rare:16 | ||||
| chr7:139775800-139776036 | Common:1; Rare:41 | ||||
| chr7:141367020-141367158 | Common:8; Rare:19 | ||||
| chr7:143267827-143268121 | Common:2; Rare:43 | ||||
| chr7:143836672-143836881 | Common:1; Rare:11 | ||||
| chr7:148987246-148987493 | Common:8; Rare:83 | ||||
| chr7:150631605-150631758 | Common:4; Rare:29 |