| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35615811-35615972 | Common:1; Rare:27 | ||||
| chr9:35769955-35769976 | Rare:6 | ||||
| chr9:35791473-35791591 | Rare:27 | ||||
| chr9:35845878-35846030 | Common:2; Rare:53 | ||||
| chr9:35846354-35846467 | Rare:54 | ||||
| chr9:35971297-35971322 | Rare:6 | ||||
| chr9:36198724-36199045 | Common:4; Rare:94 | ||||
| chr9:36415530-36415668 | Rare:33 | ||||
| chr9:36472637-36472895 | Common:2; Rare:51 | ||||
| chr9:36953713-36953976 | Common:3; Rare:44 | ||||
| chr9:37079796-37080055 | Common:4; Rare:83 | ||||
| chr9:37087308-37087549 | Common:1; Rare:45 | ||||
| chr9:37506218-37506387 | Rare:30 | ||||
| chr9:40992021-40992307 | Common:7; Rare:21 | ||||
| chr9:69234488-69234596 | Common:2; Rare:36; Clinvar (pathogenic):1 |