| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128322729-128322922 | Common:3; Rare:91; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128371220-128371383 | Rare:55 | ||||
| chr9:128552408-128552607 | Rare:75; Clinvar:1 | ||||
| chr9:128624841-128625158 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:128724089-128724453 | Common:2; Rare:118 | ||||
| chr9:128771860-128771966 | Rare:26 | ||||
| chr9:128881929-128882206 | Common:2; Rare:95 | ||||
| chr9:128921976-128922330 | Common:1; Rare:79 | ||||
| chr9:128947588-128947722 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129111264-129111432 | Common:2; Rare:62 | ||||
| chr9:129835185-129835481 | Common:2; Rare:121 | ||||
| chr9:130042964-130043293 | Common:2; Rare:94 | ||||
| chr9:130053860-130053929 | Common:1; Rare:23 | ||||
| chr9:130579456-130579683 | Common:6; Rare:98 | ||||
| chr9:131096383-131096545 | Common:3; Rare:42 |