| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93452294-93452391 | Rare:15 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:94259290-94259343 | Rare:17 | ||||
| chr9:94726570-94726732 | Rare:44 | ||||
| chr9:95004124-95004264 | Common:1; Rare:43 | ||||
| chr9:95505860-95506223 | Common:2; Rare:129 | ||||
| chr9:95506574-95506709 | Common:1; Rare:57; Clinvar:5; Clinvar (benign):5 | ||||
| chr9:95875449-95875731 | Common:1; Rare:100 | ||||
| chr9:95875961-95876037 | Common:4; Rare:37 | ||||
| chr9:96655284-96655408 | Rare:35 | ||||
| chr9:96778054-96778163 | Rare:33 | ||||
| chr9:97633271-97633458 | Common:1; Rare:50 | ||||
| chr9:97633552-97633848 | Common:3; Rare:93 | ||||
| chr9:97697304-97697618 | Common:1; Rare:122; Clinvar:5 | ||||
| chr9:97922453-97922571 | Common:3; Rare:62 |