| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:10973660-10973919 | Rare:116 | ||||
| chr7:13988875-13989006 | Common:1; Rare:26 | ||||
| chr7:16645696-16646208 | Common:3; Rare:183 | ||||
| chr7:17298444-17298659 | Common:3; Rare:54 | ||||
| chr7:17940454-17940595 | Common:2; Rare:59 | ||||
| chr7:20331733-20331788 | Common:1; Rare:18 | ||||
| chr7:22822766-22822964 | Common:3; Rare:74 | ||||
| chr7:23014047-23014373 | Common:5; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105682-23105841 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181840-23182083 | Common:2; Rare:98 | ||||
| chr7:23470362-23470557 | Rare:58 | ||||
| chr7:24757397-24757622 | Common:2; Rare:66 | ||||
| chr7:24980161-24980452 | Common:9; Rare:119 | ||||
| chr7:25125275-25125643 | Rare:138; Clinvar:2 | ||||
| chr7:26201417-26201815 | Common:2; Rare:187 |