| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91880662-91880822 | Common:2; Rare:44 | ||||
| chr7:91940827-91941040 | Common:3; Rare:71; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134303-92134603 | Rare:97 | ||||
| chr7:92134789-92134899 | Common:1; Rare:37 | ||||
| chr7:92245837-92246016 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:92528370-92528816 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833906-92834074 | Rare:43 | ||||
| chr7:93117944-93118156 | Rare:34 | ||||
| chr7:93232201-93232389 | Common:2; Rare:34 | ||||
| chr7:93890718-93890949 | Common:3; Rare:54 | ||||
| chr7:93921612-93922182 | Common:7; Rare:133 | ||||
| chr7:94004310-94004587 | Rare:73 | ||||
| chr7:94394674-94394919 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr7:94395048-94395096 | Rare:15; Clinvar (benign):2 | ||||
| chr7:94425779-94426043 | Rare:82; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 |