| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151059468-151059696 | Common:1; Rare:71 | ||||
| chr7:151232393-151232525 | Rare:43 | ||||
| chr7:151409023-151409284 | Common:1; Rare:65 | ||||
| chr7:151410394-151410504 | Common:1; Rare:13 | ||||
| chr7:151519146-151519493 | Common:2; Rare:89 | ||||
| chr7:151877087-151877487 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152025579-152025784 | Rare:83 | ||||
| chr7:152435674-152435731 | Common:1; Rare:14 | ||||
| chr7:155644339-155644856 | Common:6; Rare:166 | ||||
| chr7:156640535-156640737 | Common:3; Rare:100 | ||||
| chr7:156893171-156893382 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr7:157336749-157337138 | Common:3; Rare:182; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158704764-158704975 | Common:1; Rare:75 | ||||
| chr7:158827796-158828055 | Common:7; Rare:51 | ||||
| chr7:158856424-158856716 | Common:7; Rare:104 |