| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20620919-20621039 | Common:1; Rare:38 | ||||
| chr9:25677376-25677708 | Common:4; Rare:141 | ||||
| chr9:32550811-32551103 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:34380783-34380900 | Common:1; Rare:41 | ||||
| chr9:35491665-35491876 | Rare:36 | ||||
| chr9:35491949-35492029 | Common:1; Rare:8 | ||||
| chr9:35657363-35657478 | Common:1; Rare:14 | ||||
| chr9:35657729-35657764 | Common:1; Rare:25; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35681907-35682042 | Rare:34 | ||||
| chr9:35686373-35686693 | Common:6; Rare:50 | ||||
| chr9:35698042-35698506 | Rare:104 | ||||
| chr9:35710559-35710888 | Rare:77 | ||||
| chr9:35710990-35711417 | Rare:106 | ||||
| chr9:35711750-35712125 | Common:2; Rare:94 | ||||
| chr9:35714659-35714877 | Rare:58 |