| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23531786-23532136 | Common:3; Rare:137 | ||||
| chr7:23597231-23597452 | Common:1; Rare:74 | ||||
| chr7:23680115-23680265 | Common:5; Rare:57 | ||||
| chr7:24573277-24573492 | Common:1; Rare:77 | ||||
| chr7:24980152-24980389 | Common:6; Rare:97 | ||||
| chr7:25125212-25125443 | Rare:102; Clinvar:3 | ||||
| chr7:26152641-26152962 | Rare:98 | ||||
| chr7:26196557-26197036 | Common:2; Rare:170; Clinvar (benign):3 | ||||
| chr7:26197048-26197116 | Common:1; Rare:26 | ||||
| chr7:26197299-26197709 | Common:1; Rare:134; Clinvar (benign):2 | ||||
| chr7:26201317-26201966 | Common:4; Rare:287 | ||||
| chr7:26202058-26202221 | Rare:82 | ||||
| chr7:26202319-26202595 | Rare:114 | ||||
| chr7:26291759-26292038 | Common:2; Rare:89 | ||||
| chr7:26864574-26864875 | Common:3; Rare:97 |