| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22500141-22500283 | Common:2; Rare:48 | ||||
| chr7:22822757-22822969 | Common:3; Rare:78 | ||||
| chr7:23014054-23014363 | Common:4; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105661-23105875 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23106506-23106661 | Common:1; Rare:24 | ||||
| chr7:23181708-23182117 | Common:2; Rare:143 | ||||
| chr7:23299177-23299433 | Common:2; Rare:130 | ||||
| chr7:23470316-23470773 | Common:1; Rare:120 | ||||
| chr7:23531958-23532130 | Common:2; Rare:70 | ||||
| chr7:23597219-23597485 | Common:1; Rare:86 | ||||
| chr7:23679943-23680230 | Common:5; Rare:87 | ||||
| chr7:24283507-24283721 | Common:2; Rare:41 | ||||
| chr7:24283959-24284278 | Rare:91 | ||||
| chr7:24285093-24285428 | Common:5; Rare:89; Clinvar (benign):1 | ||||
| chr7:24757395-24757494 | Common:2; Rare:30 |