| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95317681-95317852 | Common:1; Rare:52; Clinvar:1 | ||||
| chr9:95875449-95875708 | Common:1; Rare:88 | ||||
| chr9:95875961-95876041 | Common:4; Rare:40 | ||||
| chr9:96566797-96566849 | Rare:19 | ||||
| chr9:96655278-96655424 | Rare:43 | ||||
| chr9:96778046-96778156 | Rare:36 | ||||
| chr9:97039079-97039298 | Common:1; Rare:88 | ||||
| chr9:97501513-97501802 | Common:6; Rare:71 | ||||
| chr9:97633267-97633848 | Common:6; Rare:177 | ||||
| chr9:97697217-97697468 | Common:2; Rare:138; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922471-97922580 | Common:3; Rare:55 | ||||
| chr9:98056528-98056777 | Common:1; Rare:83 | ||||
| chr9:98192618-98192820 | Common:5; Rare:57 | ||||
| chr9:98943779-98943944 | Common:3; Rare:54 | ||||
| chr9:99221906-99222365 | Common:2; Rare:182; Clinvar:3; Clinvar (benign):2 |