| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92764512-92764841 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):5 | ||||
| chr9:93134213-93134595 | Common:2; Rare:108 | ||||
| chr9:93267500-93267815 | Common:1; Rare:50 | ||||
| chr9:93451472-93451702 | Common:3; Rare:67 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:95048358-95048660 | Common:1; Rare:71 | ||||
| chr9:95875459-95875723 | Common:1; Rare:95 | ||||
| chr9:95875944-95876058 | Common:6; Rare:55; Clinvar (pathogenic):1 | ||||
| chr9:96655300-96655408 | Rare:28 | ||||
| chr9:96778040-96778156 | Rare:37 | ||||
| chr9:97633271-97633856 | Common:6; Rare:183 | ||||
| chr9:97666649-97666805 | Common:1; Rare:26 | ||||
| chr9:97922179-97922320 | Common:1; Rare:50 | ||||
| chr9:97922439-97922574 | Common:3; Rare:75 | ||||
| chr9:98056486-98056777 | Common:1; Rare:94 |