| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94374290-94374367 | Rare:25 | ||||
| chr9:94726544-94726759 | Common:1; Rare:59 | ||||
| chr9:95317193-95317324 | Common:3; Rare:43 | ||||
| chr9:95317655-95317852 | Common:1; Rare:64; Clinvar:2 | ||||
| chr9:95509145-95509460 | Rare:78 | ||||
| chr9:95516736-95517064 | Common:2; Rare:98; Clinvar (pathogenic):1 | ||||
| chr9:95517066-95517091 | Common:1; Rare:3 | ||||
| chr9:95875396-95875805 | Common:1; Rare:138 | ||||
| chr9:95875870-95876083 | Common:6; Rare:80; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96778032-96778187 | Rare:48 | ||||
| chr9:97013687-97013865 | Common:2; Rare:46 | ||||
| chr9:97633080-97633865 | Common:6; Rare:248 | ||||
| chr9:97697209-97697429 | Common:1; Rare:127; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922112-97922327 | Common:1; Rare:83 | ||||
| chr9:97922471-97922609 | Common:3; Rare:64 |