| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:12210966-12211395 | Common:4; Rare:163 | ||||
| chr7:16645712-16646205 | Common:3; Rare:175 | ||||
| chr7:17298444-17298730 | Common:3; Rare:76 | ||||
| chr7:17299136-17299236 | Rare:30 | ||||
| chr7:17940419-17940584 | Common:1; Rare:82 | ||||
| chr7:20217375-20217577 | Common:1; Rare:46 | ||||
| chr7:23105673-23105861 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181921-23182107 | Rare:79 | ||||
| chr7:24980147-24980414 | Common:8; Rare:111 | ||||
| chr7:25125175-25125640 | Rare:183; Clinvar:3 | ||||
| chr7:26200573-26201013 | Common:2; Rare:214 | ||||
| chr7:26201056-26201533 | Common:1; Rare:190 | ||||
| chr7:26201619-26201821 | Common:1; Rare:105 | ||||
| chr7:26292927-26293073 | Rare:27 | ||||
| chr7:26864562-26864849 | Common:3; Rare:89 |