| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34048857-34048984 | Common:1; Rare:50 | ||||
| chr9:34126638-34126795 | Common:1; Rare:50 | ||||
| chr9:34329228-34329615 | Common:1; Rare:116 | ||||
| chr9:34612086-34612183 | Common:2; Rare:29 | ||||
| chr9:35657929-35658376 | Common:6; Rare:353; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):36 | ||||
| chr9:35732082-35732320 | Common:1; Rare:66 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35748978-35749369 | Common:2; Rare:145 | ||||
| chr9:35814984-35815272 | Rare:74 | ||||
| chr9:36190745-36190988 | Common:1; Rare:79 | ||||
| chr9:36258395-36258618 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37422557-37422753 | Common:2; Rare:98 | ||||
| chr9:37753678-37753816 | Common:6; Rare:73 | ||||
| chr9:37785043-37785141 | Common:1; Rare:34; Clinvar (benign):2 | ||||
| chr9:37904079-37904208 | Rare:40 |