| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128275929-128276316 | Common:5; Rare:181 | ||||
| chr9:128322406-128322623 | Common:1; Rare:63 | ||||
| chr9:128322718-128322918 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128340440-128340806 | Common:3; Rare:117 | ||||
| chr9:128371110-128371423 | Common:1; Rare:106 | ||||
| chr9:128552408-128552607 | Rare:75; Clinvar:1 | ||||
| chr9:128630117-128630342 | Common:3; Rare:59; Clinvar (benign):3 | ||||
| chr9:128683342-128683429 | Common:1; Rare:13 | ||||
| chr9:128684955-128685069 | Rare:19 | ||||
| chr9:128724085-128724464 | Common:2; Rare:125 | ||||
| chr9:128771813-128772031 | Rare:57 | ||||
| chr9:128881901-128882202 | Common:2; Rare:98 | ||||
| chr9:128947567-128947734 | Common:1; Rare:78; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129080802-129081134 | Common:2; Rare:90 | ||||
| chr9:129098114-129098575 | Common:1; Rare:137 |