| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151083451-151083549 | Common:1; Rare:19 | ||||
| chr7:151174709-151174987 | Common:2; Rare:73 | ||||
| chr7:151205450-151205625 | Rare:31 | ||||
| chr7:151227138-151227378 | Common:1; Rare:69 | ||||
| chr7:151232366-151232531 | Common:1; Rare:58 | ||||
| chr7:151341578-151341864 | Common:4; Rare:91 | ||||
| chr7:151519893-151520021 | Rare:30 | ||||
| chr7:151736469-151736638 | Rare:31 | ||||
| chr7:151877089-151877139 | Rare:10; Clinvar:1 | ||||
| chr7:151956304-151956463 | Common:2; Rare:28 | ||||
| chr7:152025558-152025791 | Common:1; Rare:93 | ||||
| chr7:152311871-152312178 | Rare:81 | ||||
| chr7:152435669-152435732 | Common:1; Rare:17 | ||||
| chr7:152676096-152676295 | Common:2; Rare:84; Clinvar (benign):6 | ||||
| chr7:152759623-152759863 | Common:4; Rare:93 |