| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:148814685-148815034 | Common:1; Rare:68; Clinvar:1 | ||||
| chr7:148820924-148821242 | Common:4; Rare:44 | ||||
| chr7:149486441-149486756 | Rare:48 | ||||
| chr7:149611500-149611808 | Rare:62 | ||||
| chr7:149839620-149839914 | Common:3; Rare:44 | ||||
| chr7:149840036-149840085 | Rare:10 | ||||
| chr7:151053915-151054285 | Rare:90; Clinvar (benign):1 | ||||
| chr7:151055290-151055549 | Common:3; Rare:56 | ||||
| chr7:151700049-151700269 | Common:3; Rare:53 | ||||
| chr7:154928314-154928547 | Common:4; Rare:58 | ||||
| chr7:154944278-154944366 | Common:1; Rare:11 | ||||
| chr7:156950568-156950651 | Common:1; Rare:26 | ||||
| chr7:157569024-157569098 | Common:2; Rare:25 | ||||
| chr7:158818601-158818831 | Rare:40 | ||||
| chr7:158828254-158828319 | Common:1; Rare:16 |