| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26857252-26857527 | Common:3; Rare:58 | ||||
| chr9:27002393-27002483 | Rare:21 | ||||
| chr9:29212988-29213219 | Common:1; Rare:42 | ||||
| chr9:29214025-29214332 | Common:3; Rare:85 | ||||
| chr9:29450773-29450960 | Common:3; Rare:67 | ||||
| chr9:32168317-32168411 | Common:1; Rare:17 | ||||
| chr9:32344572-32344837 | Common:6; Rare:48 | ||||
| chr9:32550837-32551195 | Common:1; Rare:142; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33511122-33511215 | Rare:28 | ||||
| chr9:33677419-33677449 | Common:1; Rare:12 | ||||
| chr9:33818119-33818393 | Common:2; Rare:72 | ||||
| chr9:34193786-34193963 | Common:1; Rare:28 | ||||
| chr9:34996729-34997044 | Common:1; Rare:66 | ||||
| chr9:35156331-35156350 | Rare:1 | ||||
| chr9:35604023-35604189 | Common:3; Rare:45 |