| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95018484-95018671 | Rare:27 | ||||
| chr9:95127450-95127472 | Rare:4 | ||||
| chr9:95127490-95127513 | Rare:6 | ||||
| chr9:95317233-95317510 | Common:6; Rare:90 | ||||
| chr9:95317653-95317799 | Common:1; Rare:50; Clinvar:2 | ||||
| chr9:95505837-95506244 | Common:2; Rare:148 | ||||
| chr9:95506653-95506851 | Common:2; Rare:59 | ||||
| chr9:95507397-95507623 | Rare:70 | ||||
| chr9:95509140-95509354 | Rare:61 | ||||
| chr9:95516842-95517140 | Common:4; Rare:71 | ||||
| chr9:95875441-95875740 | Common:1; Rare:110 | ||||
| chr9:95875961-95876084 | Common:5; Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96254866-96255180 | Common:1; Rare:69; Clinvar (pathogenic):4 | ||||
| chr9:96383501-96383783 | Common:3; Rare:93 | ||||
| chr9:96418377-96418638 | Common:2; Rare:70 |