| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92115366-92115513 | Common:1; Rare:44; Clinvar:1 | ||||
| chr9:92293638-92293849 | Common:3; Rare:71 | ||||
| chr9:92325299-92325984 | Common:9; Rare:183 | ||||
| chr9:92670032-92670314 | Common:1; Rare:85 | ||||
| chr9:92764771-92765139 | Common:2; Rare:115; Clinvar (benign):2 | ||||
| chr9:92877931-92878195 | Common:2; Rare:77 | ||||
| chr9:92947050-92947444 | Common:2; Rare:75 | ||||
| chr9:92947446-92947624 | Rare:26 | ||||
| chr9:93134224-93134357 | Common:2; Rare:48 | ||||
| chr9:93452292-93452355 | Rare:10 | ||||
| chr9:93453546-93453659 | Rare:23 | ||||
| chr9:94726544-94726727 | Common:1; Rare:50 | ||||
| chr9:95317653-95317827 | Common:1; Rare:56; Clinvar:2 | ||||
| chr9:95875453-95875703 | Common:1; Rare:82 | ||||
| chr9:95875944-95876058 | Common:6; Rare:55; Clinvar (pathogenic):1 |