| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128160018-128160477 | Common:2; Rare:109 | ||||
| chr9:128191439-128191647 | Rare:63 | ||||
| chr9:128191717-128191804 | Common:1; Rare:19 | ||||
| chr9:128191806-128191840 | Rare:7 | ||||
| chr9:128275911-128276307 | Common:5; Rare:173 | ||||
| chr9:128322404-128322629 | Common:1; Rare:64 | ||||
| chr9:128322729-128322924 | Common:3; Rare:91; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128340433-128340711 | Common:2; Rare:88 | ||||
| chr9:128371193-128371401 | Rare:78 | ||||
| chr9:128504630-128504814 | Rare:84; Clinvar:6 | ||||
| chr9:128552398-128552616 | Rare:83; Clinvar:1 | ||||
| chr9:128656629-128657002 | Common:2; Rare:127; Clinvar (pathogenic):1 | ||||
| chr9:128684959-128685069 | Rare:19 | ||||
| chr9:128689534-128689650 | Rare:46 | ||||
| chr9:128724081-128724472 | Common:3; Rare:128 |