| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151075758-151076142 | Common:6; Rare:98; Clinvar:1 | ||||
| chr7:151080760-151080974 | Rare:69 | ||||
| chr7:151227166-151227436 | Common:1; Rare:72 | ||||
| chr7:151232382-151232675 | Common:1; Rare:94 | ||||
| chr7:151876601-151876753 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:151876903-151877059 | Rare:27; Clinvar:3 | ||||
| chr7:151877095-151877663 | Common:4; Rare:148; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152435674-152435730 | Common:1; Rare:13 | ||||
| chr7:152435843-152436278 | Rare:145 | ||||
| chr7:152676122-152676276 | Common:2; Rare:56; Clinvar (benign):2 | ||||
| chr7:155644172-155644751 | Common:4; Rare:190 | ||||
| chr7:155644754-155644897 | Common:4; Rare:37 | ||||
| chr7:156640529-156640791 | Common:3; Rare:127 | ||||
| chr7:156893163-156893424 | Common:4; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:157009325-157009434 | Common:1; Rare:27 |