| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92038998-92039048 | Common:1; Rare:9 | ||||
| chr9:92072889-92072965 | Common:1; Rare:15 | ||||
| chr9:92076154-92076286 | Common:1; Rare:21 | ||||
| chr9:92076362-92076624 | Common:1; Rare:40 | ||||
| chr9:92078223-92078378 | Rare:26 | ||||
| chr9:92253216-92253430 | Rare:45; Clinvar (pathogenic):1 | ||||
| chr9:92253540-92253712 | Rare:35 | ||||
| chr9:92255985-92256178 | Common:1; Rare:39 | ||||
| chr9:92289234-92289384 | Common:1; Rare:31 | ||||
| chr9:92320451-92320520 | Rare:11 | ||||
| chr9:92506432-92506584 | Rare:24 | ||||
| chr9:92630071-92630376 | Common:1; Rare:44 | ||||
| chr9:92669069-92669269 | Common:2; Rare:39 | ||||
| chr9:92708506-92708558 | Rare:11 | ||||
| chr9:92809150-92809316 | Rare:41 |