| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:17298444-17298659 | Common:3; Rare:54 | ||||
| chr7:17940411-17940574 | Common:1; Rare:86 | ||||
| chr7:23105678-23105976 | Common:2; Rare:136; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23181757-23182096 | Common:2; Rare:126 | ||||
| chr7:24757424-24757552 | Common:1; Rare:41 | ||||
| chr7:25125275-25125643 | Rare:138; Clinvar:2 | ||||
| chr7:26200655-26200983 | Common:2; Rare:165 | ||||
| chr7:26201323-26201555 | Rare:82 | ||||
| chr7:26201619-26201800 | Common:1; Rare:97 | ||||
| chr7:27662773-27663215 | Common:8; Rare:157 | ||||
| chr7:27740061-27740199 | Common:5; Rare:36 | ||||
| chr7:30504780-30505046 | Common:1; Rare:84 | ||||
| chr7:30594722-30594935 | Common:3; Rare:98; Clinvar:6; Clinvar (benign):6 | ||||
| chr7:30771306-30771445 | Common:1; Rare:41 | ||||
| chr7:32070741-32071132 | Common:3; Rare:94 |