| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22220146-22220359 | Common:2; Rare:35 | ||||
| chr7:22726986-22727226 | Common:2; Rare:33 | ||||
| chr7:22727269-22727461 | Rare:71 | ||||
| chr7:23013997-23014356 | Common:4; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:23105682-23105841 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181779-23182096 | Common:2; Rare:121 | ||||
| chr7:23470333-23470550 | Rare:68 | ||||
| chr7:23531932-23532092 | Common:2; Rare:66 | ||||
| chr7:24980101-24980389 | Common:6; Rare:119 | ||||
| chr7:25125235-25125633 | Rare:160; Clinvar:3 | ||||
| chr7:26200655-26201290 | Common:3; Rare:299 | ||||
| chr7:26201411-26201805 | Common:2; Rare:187 | ||||
| chr7:26864562-26864832 | Common:3; Rare:84 | ||||
| chr7:27095982-27096290 | Rare:80 | ||||
| chr7:27156232-27156366 | Common:1; Rare:51 |