| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:25677393-25677673 | Common:3; Rare:112 | ||||
| chr9:27534153-27534370 | Rare:33 | ||||
| chr9:32405271-32405513 | Common:1; Rare:41 | ||||
| chr9:32418978-32419122 | Rare:38 | ||||
| chr9:32448752-32449040 | Common:5; Rare:98 | ||||
| chr9:32457498-32457759 | Common:3; Rare:54 | ||||
| chr9:32550829-32551156 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33130542-33130744 | Common:2; Rare:46 | ||||
| chr9:33185053-33185252 | Rare:40 | ||||
| chr9:33466071-33466342 | Common:2; Rare:88 | ||||
| chr9:33818698-33818944 | Common:1; Rare:48 | ||||
| chr9:33847388-33847651 | Common:2; Rare:43 | ||||
| chr9:33916830-33917048 | Rare:58 | ||||
| chr9:33922831-33922980 | Rare:45 | ||||
| chr9:33927897-33928127 | Common:2; Rare:72 |