| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151187749-151187978 | Common:1; Rare:56 | ||||
| chr7:151227158-151227485 | Common:2; Rare:82 | ||||
| chr7:151232404-151232528 | Rare:40 | ||||
| chr7:151519913-151520213 | Common:1; Rare:83 | ||||
| chr7:151632569-151632596 | Rare:12 | ||||
| chr7:151736282-151736624 | Common:6; Rare:54 | ||||
| chr7:151877113-151877518 | Common:3; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152435669-152435731 | Common:1; Rare:16 | ||||
| chr7:152435785-152435790 | Rare:1 | ||||
| chr7:152676101-152676286 | Common:2; Rare:72; Clinvar (benign):6 | ||||
| chr7:155644377-155644804 | Common:4; Rare:139 | ||||
| chr7:156640548-156640694 | Common:2; Rare:77 | ||||
| chr7:157336770-157337101 | Common:3; Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704733-158704955 | Common:1; Rare:77 | ||||
| chr7:158856423-158856749 | Common:7; Rare:115 |