| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93134191-93134352 | Common:2; Rare:61 | ||||
| chr9:93451462-93451703 | Common:3; Rare:69 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:95048333-95048660 | Common:1; Rare:72 | ||||
| chr9:95875453-95875699 | Common:1; Rare:81 | ||||
| chr9:95875961-95876056 | Common:5; Rare:48 | ||||
| chr9:96778057-96778156 | Rare:31 | ||||
| chr9:97633276-97633848 | Common:6; Rare:177 | ||||
| chr9:97666697-97666845 | Rare:32 | ||||
| chr9:97853004-97853221 | Common:1; Rare:63 | ||||
| chr9:97922487-97922580 | Common:2; Rare:46 | ||||
| chr9:98056528-98056783 | Common:1; Rare:87 | ||||
| chr9:98192623-98192855 | Common:6; Rare:63 | ||||
| chr9:98255593-98255830 | Common:3; Rare:69 | ||||
| chr9:99221554-99221709 | Rare:75; Clinvar:3; Clinvar (benign):4 |