| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151089233-151089705 | Common:2; Rare:115 | ||||
| chr7:151227152-151227435 | Common:1; Rare:78 | ||||
| chr7:151232390-151232525 | Rare:44 | ||||
| chr7:151277123-151277252 | Rare:38 | ||||
| chr7:151519893-151520208 | Common:1; Rare:88 | ||||
| chr7:151736251-151736621 | Common:6; Rare:67 | ||||
| chr7:151877155-151877535 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:152025558-152025807 | Common:1; Rare:98 | ||||
| chr7:152676073-152676316 | Common:2; Rare:109; Clinvar (benign):12 | ||||
| chr7:152759642-152759829 | Common:4; Rare:75 | ||||
| chr7:155002917-155003014 | Common:1; Rare:34 | ||||
| chr7:155644146-155644916 | Common:8; Rare:250 | ||||
| chr7:156640554-156640692 | Common:2; Rare:73 | ||||
| chr7:157336770-157337128 | Common:3; Rare:169; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704732-158705135 | Common:1; Rare:134 |