| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22583265-22583337 | Common:1; Rare:11 | ||||
| chr7:22589483-22589702 | Common:2; Rare:35 | ||||
| chr7:22703434-22703750 | Common:1; Rare:76 | ||||
| chr7:22704951-22705104 | Common:2; Rare:30 | ||||
| chr7:22707047-22707144 | Common:2; Rare:15 | ||||
| chr7:22707146-22707165 | Rare:6 | ||||
| chr7:22708754-22708958 | Common:3; Rare:61 | ||||
| chr7:22708982-22709258 | Common:1; Rare:53 | ||||
| chr7:22853854-22854160 | Common:5; Rare:69 | ||||
| chr7:22854480-22854574 | Rare:26 | ||||
| chr7:23471107-23471483 | Common:2; Rare:110 | ||||
| chr7:23490417-23490574 | Common:3; Rare:67 | ||||
| chr7:24820297-24820471 | Common:3; Rare:33 | ||||
| chr7:25856767-25856878 | Rare:29 | ||||
| chr7:26193249-26193696 | Rare:156; Clinvar (benign):2 |