| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125189909-125190049 | Common:1; Rare:42 | ||||
| chr9:125200421-125200590 | Common:1; Rare:64 | ||||
| chr9:125241282-125241686 | Common:3; Rare:123 | ||||
| chr9:125484597-125484984 | Common:1; Rare:49 | ||||
| chr9:126804931-126805058 | Rare:37 | ||||
| chr9:126860593-126860705 | Common:2; Rare:38 | ||||
| chr9:127122640-127122961 | Common:3; Rare:82 | ||||
| chr9:127224366-127224652 | Rare:76 | ||||
| chr9:127245183-127245348 | Common:1; Rare:41 | ||||
| chr9:127424071-127424455 | Common:1; Rare:113 | ||||
| chr9:127449609-127449910 | Rare:78 | ||||
| chr9:127451261-127451562 | Common:3; Rare:124; Clinvar (benign):1 | ||||
| chr9:127612040-127612356 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127706901-127707028 | Rare:39 | ||||
| chr9:127787950-127788319 | Common:2; Rare:121 |