| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128275277-128275465 | Rare:38 | ||||
| chr9:128275903-128276312 | Common:5; Rare:181 | ||||
| chr9:128322410-128322646 | Common:1; Rare:66 | ||||
| chr9:128322729-128322924 | Common:3; Rare:91; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128371193-128371431 | Rare:91 | ||||
| chr9:128455911-128456547 | Common:3; Rare:197 | ||||
| chr9:128456783-128457033 | Common:1; Rare:66 | ||||
| chr9:128504583-128504822 | Rare:110; Clinvar:6 | ||||
| chr9:128552398-128552693 | Rare:113; Clinvar:6; Clinvar (benign):3 | ||||
| chr9:128608757-128608977 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):8 | ||||
| chr9:128630096-128630374 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:128656662-128656801 | Common:1; Rare:64; Clinvar (pathogenic):1 | ||||
| chr9:128683544-128683890 | Rare:76 | ||||
| chr9:128689407-128689643 | Rare:84 | ||||
| chr9:128724065-128724483 | Common:4; Rare:142 |