| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22822676-22822901 | Common:2; Rare:94 | ||||
| chr7:23105673-23105865 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181777-23181861 | Rare:26 | ||||
| chr7:23181898-23182128 | Rare:97 | ||||
| chr7:23299193-23299378 | Common:2; Rare:93 | ||||
| chr7:23531916-23532085 | Common:2; Rare:72 | ||||
| chr7:24284177-24284273 | Rare:29 | ||||
| chr7:24980114-24980360 | Common:6; Rare:101 | ||||
| chr7:25125211-25125643 | Rare:178; Clinvar:3 | ||||
| chr7:26200541-26201008 | Common:2; Rare:226 | ||||
| chr7:26201082-26201288 | Common:1; Rare:91 | ||||
| chr7:26201412-26201555 | Rare:52 | ||||
| chr7:26201568-26201800 | Common:2; Rare:125 | ||||
| chr7:26864551-26864861 | Common:3; Rare:102 | ||||
| chr7:27095976-27096275 | Rare:78 |