| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92424443-92424530 | Rare:7 | ||||
| chr9:92482433-92482854 | Rare:54 | ||||
| chr9:92535964-92536186 | Common:1; Rare:33 | ||||
| chr9:92670024-92670338 | Common:1; Rare:93 | ||||
| chr9:92764761-92765028 | Common:2; Rare:96; Clinvar (benign):2 | ||||
| chr9:93451455-93451702 | Common:3; Rare:69 | ||||
| chr9:93452267-93452351 | Rare:15 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:94726572-94726727 | Rare:41 | ||||
| chr9:95003779-95004059 | Common:2; Rare:44 | ||||
| chr9:95004112-95004244 | Rare:39 | ||||
| chr9:95048333-95048558 | Common:1; Rare:46 | ||||
| chr9:95505871-95506195 | Common:1; Rare:111 | ||||
| chr9:95506560-95506674 | Rare:46; Clinvar:5; Clinvar (benign):6 | ||||
| chr9:95507360-95507517 | Rare:45 |