| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128340433-128340752 | Common:2; Rare:97 | ||||
| chr9:128371181-128371442 | Rare:105 | ||||
| chr9:128455948-128456203 | Common:1; Rare:82 | ||||
| chr9:128504605-128504852 | Rare:108; Clinvar:6 | ||||
| chr9:128552394-128552676 | Rare:108; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:128656646-128657051 | Common:2; Rare:123; Clinvar (pathogenic):1 | ||||
| chr9:128683594-128683898 | Rare:67 | ||||
| chr9:128684429-128684587 | Rare:31 | ||||
| chr9:128684932-128685154 | Rare:36 | ||||
| chr9:128692653-128692999 | Common:1; Rare:67 | ||||
| chr9:128702526-128702822 | Rare:68 | ||||
| chr9:128724064-128724487 | Common:4; Rare:145 | ||||
| chr9:128771904-128772008 | Rare:21 | ||||
| chr9:128772484-128772487 | |||||
| chr9:128787144-128787335 | Common:3; Rare:63 |