| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:112450322-112450526 | Common:1; Rare:75 | ||||
| chr7:112939705-112940118 | Common:4; Rare:137 | ||||
| chr7:114086191-114086545 | Common:2; Rare:130 | ||||
| chr7:114087429-114087705 | Common:2; Rare:73 | ||||
| chr7:116210459-116210749 | Common:2; Rare:75 | ||||
| chr7:116222676-116222979 | Common:2; Rare:47 | ||||
| chr7:116499435-116499866 | Common:3; Rare:146 | ||||
| chr7:116499926-116500086 | Common:1; Rare:40 | ||||
| chr7:116524522-116525105 | Rare:153 | ||||
| chr7:116525119-116526059 | Common:9; Rare:243 | ||||
| chr7:116526284-116526683 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:116953254-116953542 | Common:2; Rare:73 | ||||
| chr7:118183965-118184251 | Common:2; Rare:107 | ||||
| chr7:120950603-120950816 | Common:2; Rare:64 | ||||
| chr7:122144159-122144369 | Rare:43 |