| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128552398-128552607 | Rare:77; Clinvar:1 | ||||
| chr9:128656644-128656990 | Common:2; Rare:116; Clinvar (pathogenic):1 | ||||
| chr9:128683117-128683434 | Common:5; Rare:44 | ||||
| chr9:128683679-128683893 | Rare:54 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 | ||||
| chr9:128881929-128882226 | Common:2; Rare:104 | ||||
| chr9:128921976-128922331 | Common:1; Rare:79 | ||||
| chr9:128947573-128947732 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129036365-129036666 | Common:2; Rare:83 | ||||
| chr9:129098250-129098575 | Rare:89 | ||||
| chr9:129110642-129111029 | Common:5; Rare:119 | ||||
| chr9:129803056-129803236 | Common:2; Rare:68 | ||||
| chr9:129824102-129824299 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:129835210-129835481 | Common:2; Rare:111 | ||||
| chr9:130043118-130043291 | Common:2; Rare:58 |