| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92245886-92245966 | Rare:25; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528397-92528816 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92836333-92836518 | Rare:39 | ||||
| chr7:93232223-93232417 | Common:2; Rare:41 | ||||
| chr7:93890741-93890949 | Common:2; Rare:48 | ||||
| chr7:94394689-94395123 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:94425743-94426050 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94427005-94427295 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:94656053-94656434 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:95596554-95596713 | Common:2; Rare:32 | ||||
| chr7:99325806-99325979 | Common:1; Rare:65 | ||||
| chr7:99408555-99408667 | Common:2; Rare:36 | ||||
| chr7:99408811-99409032 | Common:1; Rare:69 | ||||
| chr7:99438727-99438977 | Common:1; Rare:77 | ||||
| chr7:99466142-99466232 | Rare:34 |