| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151410009-151410198 | Rare:59 | ||||
| chr7:151410527-151410778 | Common:3; Rare:46 | ||||
| chr7:151518511-151519183 | Common:3; Rare:188 | ||||
| chr7:151519730-151520330 | Common:3; Rare:176 | ||||
| chr7:151632081-151632373 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):6 | ||||
| chr7:151736360-151736760 | Common:6; Rare:61 | ||||
| chr7:151814201-151815003 | Common:6; Rare:262 | ||||
| chr7:151875883-151877649 | Common:16; Rare:711; Clinvar:33; Clinvar (benign):19 | ||||
| chr7:152025586-152025809 | Rare:86 | ||||
| chr7:152435860-152436290 | Rare:144 | ||||
| chr7:152436500-152436880 | Rare:128 | ||||
| chr7:152676053-152676326 | Common:2; Rare:120; Clinvar:1; Clinvar (benign):13 | ||||
| chr7:152759581-152759840 | Common:4; Rare:97 | ||||
| chr7:155002726-155002907 | Common:2; Rare:81 | ||||
| chr7:155003056-155003579 | Common:10; Rare:182 |