| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:5892411-5892750 | Common:1; Rare:86 | ||||
| chr9:5897373-5897653 | Rare:84 | ||||
| chr9:6015603-6015719 | Rare:50 | ||||
| chr9:6757100-6757424 | Common:3; Rare:89 | ||||
| chr9:6757550-6757679 | Common:1; Rare:52 | ||||
| chr9:6757865-6758182 | Common:6; Rare:126 | ||||
| chr9:7799538-7799623 | Common:1; Rare:30 | ||||
| chr9:12693133-12693235 | Rare:19 | ||||
| chr9:12693244-12693831 | Common:9; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:12696153-12696212 | Rare:9 | ||||
| chr9:12698299-12698314 | Rare:3 | ||||
| chr9:12701012-12701213 | Common:1; Rare:41 | ||||
| chr9:12701338-12701389 | Rare:13 | ||||
| chr9:12775830-12775887 | Common:3; Rare:41 | ||||
| chr9:13279345-13279380 | Rare:9 |