| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124450109-124450469 | Common:2; Rare:78 | ||||
| chr9:124597801-124597980 | Rare:31 | ||||
| chr9:125238639-125239130 | Common:1; Rare:122 | ||||
| chr9:125746532-125746732 | Common:1; Rare:73 | ||||
| chr9:126077500-126077509 | Rare:2 | ||||
| chr9:127448414-127448629 | Rare:89 | ||||
| chr9:127795774-127795894 | Rare:15 | ||||
| chr9:128229024-128229167 | Common:1; Rare:21 | ||||
| chr9:128258490-128258675 | Common:2; Rare:52 | ||||
| chr9:128576930-128577216 | Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:128584429-128584842 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:128684429-128684559 | Rare:26 | ||||
| chr9:128693658-128693977 | Rare:79; Clinvar:1 | ||||
| chr9:128703215-128703364 | Rare:45 | ||||
| chr9:128733490-128733724 | Rare:46 |