| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22822766-22822964 | Common:3; Rare:74 | ||||
| chr7:23105661-23105865 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181832-23182092 | Common:2; Rare:105 | ||||
| chr7:23299186-23299361 | Common:2; Rare:80 | ||||
| chr7:23470276-23470558 | Rare:87 | ||||
| chr7:23531948-23532092 | Common:1; Rare:58 | ||||
| chr7:24757406-24757623 | Common:1; Rare:64 | ||||
| chr7:24980092-24980441 | Common:8; Rare:140 | ||||
| chr7:24981886-24982080 | Common:1; Rare:30 | ||||
| chr7:25125275-25125636 | Rare:137; Clinvar:2 | ||||
| chr7:26200640-26201311 | Common:3; Rare:312 | ||||
| chr7:26201412-26201821 | Common:2; Rare:193 | ||||
| chr7:26864426-26864868 | Common:3; Rare:133 | ||||
| chr7:27095976-27096233 | Rare:73 | ||||
| chr7:27113676-27113954 | Common:1; Rare:61 |