| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91940739-91940878 | Common:1; Rare:37 | ||||
| chr7:92134360-92134570 | Rare:63 | ||||
| chr7:92134721-92134852 | Common:3; Rare:32 | ||||
| chr7:92245865-92246296 | Common:6; Rare:116; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92477941-92478141 | Common:1; Rare:50 | ||||
| chr7:92528336-92528829 | Common:4; Rare:153; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833902-92834136 | Rare:55 | ||||
| chr7:92836398-92836529 | Rare:26 | ||||
| chr7:92836536-92836603 | Rare:16 | ||||
| chr7:93232169-93232417 | Common:2; Rare:57 | ||||
| chr7:93591198-93591590 | Common:4; Rare:127 | ||||
| chr7:93921710-93921901 | Common:1; Rare:40 | ||||
| chr7:93921933-93922119 | Common:4; Rare:47 | ||||
| chr7:94004300-94004496 | Rare:54 | ||||
| chr7:94656070-94656381 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):3 |