| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94374286-94374580 | Common:2; Rare:99 | ||||
| chr9:94639469-94639726 | Common:2; Rare:63; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:94726568-94726734 | Rare:45 | ||||
| chr9:95317681-95317870 | Common:1; Rare:57; Clinvar:1 | ||||
| chr9:95875459-95875731 | Common:1; Rare:97 | ||||
| chr9:95875965-95876066 | Common:5; Rare:50; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96566820-96566920 | Common:1; Rare:33 | ||||
| chr9:96654868-96654938 | Rare:19 | ||||
| chr9:96655284-96655408 | Rare:35 | ||||
| chr9:96778036-96778176 | Rare:41 | ||||
| chr9:97013687-97013840 | Common:2; Rare:38 | ||||
| chr9:97039137-97039350 | Common:1; Rare:78 | ||||
| chr9:97501512-97501738 | Common:6; Rare:58 | ||||
| chr9:97633080-97633892 | Common:7; Rare:255 | ||||
| chr9:97697282-97697618 | Common:2; Rare:137; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 |