| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92528358-92528829 | Common:4; Rare:146; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590040-92590142 | Rare:41 | ||||
| chr7:93117862-93118123 | Common:1; Rare:40 | ||||
| chr7:93232189-93232407 | Common:2; Rare:46 | ||||
| chr7:93921966-93922129 | Common:4; Rare:40 | ||||
| chr7:94656114-94656367 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396334-95396480 | Common:2; Rare:67 | ||||
| chr7:95596181-95596230 | Rare:17 | ||||
| chr7:95596502-95596682 | Common:2; Rare:36 | ||||
| chr7:97117481-97117802 | Common:1; Rare:141 | ||||
| chr7:98106777-98106962 | Common:1; Rare:57 | ||||
| chr7:98107064-98107197 | Rare:30 | ||||
| chr7:98252114-98252378 | Common:1; Rare:58 | ||||
| chr7:98282101-98282383 | Common:1; Rare:95 | ||||
| chr7:99325801-99325997 | Common:1; Rare:77 |