| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24284811-24285315 | Common:6; Rare:123; Clinvar (benign):1 | ||||
| chr7:25125251-25125407 | Rare:62; Clinvar:3 | ||||
| chr7:26200573-26201008 | Common:2; Rare:211 | ||||
| chr7:26201300-26201442 | Rare:50 | ||||
| chr7:26201605-26201800 | Common:1; Rare:104 | ||||
| chr7:26864546-26864866 | Common:3; Rare:104 | ||||
| chr7:27095989-27096198 | Rare:62 | ||||
| chr7:27150948-27151091 | Common:1; Rare:41 | ||||
| chr7:27175196-27175508 | Common:1; Rare:58 | ||||
| chr7:27185185-27185554 | Common:1; Rare:121 | ||||
| chr7:27200155-27200483 | Rare:108 | ||||
| chr7:27662743-27663149 | Common:7; Rare:138 | ||||
| chr7:27740053-27740199 | Common:5; Rare:41 | ||||
| chr7:28180575-28180817 | Common:1; Rare:67 | ||||
| chr7:30026416-30026619 | Rare:60; Clinvar (benign):3; Clinvar (pathogenic):1 |