| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107283002-107283600 | Common:3; Rare:172 | ||||
| chr9:107488434-107488591 | Common:1; Rare:48 | ||||
| chr9:107488665-107488778 | Rare:36 | ||||
| chr9:107489767-107490046 | Common:4; Rare:118 | ||||
| chr9:107490366-107490570 | Common:1; Rare:47 | ||||
| chr9:108933951-108933979 | Common:1; Rare:11; Clinvar:3 | ||||
| chr9:108934065-108934504 | Common:7; Rare:176; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109119490-109119569 | Common:1; Rare:33 | ||||
| chr9:109498227-109498464 | Rare:74 | ||||
| chr9:110207467-110207707 | Rare:81 | ||||
| chr9:110256410-110256671 | Common:2; Rare:95 | ||||
| chr9:110579558-110579633 | Common:1; Rare:19 | ||||
| chr9:111038190-111038356 | Common:2; Rare:51 | ||||
| chr9:111599337-111599360 | Rare:8 | ||||
| chr9:111599367-111599754 | Common:3; Rare:91 |