| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:88991318-88991475 | Common:1; Rare:41 | ||||
| chr9:89310955-89311225 | Common:3; Rare:87 | ||||
| chr9:89318405-89318550 | Common:4; Rare:72 | ||||
| chr9:92115354-92115494 | Common:1; Rare:43; Clinvar:1 | ||||
| chr9:92293581-92293943 | Common:6; Rare:116 | ||||
| chr9:92325316-92325991 | Common:9; Rare:184 | ||||
| chr9:93134228-93134352 | Common:2; Rare:45 | ||||
| chr9:94259306-94259325 | Rare:5 | ||||
| chr9:95875453-95875708 | Common:1; Rare:86 | ||||
| chr9:95875961-95876078 | Common:5; Rare:59; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:97633316-97633632 | Common:3; Rare:99 | ||||
| chr9:97633726-97633848 | Common:2; Rare:38 | ||||
| chr9:97983147-97983577 | Common:2; Rare:162 | ||||
| chr9:98056400-98056777 | Common:5; Rare:112 | ||||
| chr9:99221898-99222355 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):3 |