| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128191748-128191861 | Common:1; Rare:29 | ||||
| chr9:128275903-128276327 | Common:5; Rare:191 | ||||
| chr9:128322357-128322649 | Common:1; Rare:96 | ||||
| chr9:128322739-128322928 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128371181-128371414 | Rare:92 | ||||
| chr9:128455987-128456183 | Common:1; Rare:67 | ||||
| chr9:128504581-128504793 | Rare:98; Clinvar:5 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128656662-128656845 | Common:1; Rare:78; Clinvar (pathogenic):1 | ||||
| chr9:128683635-128683902 | Rare:67 | ||||
| chr9:128723996-128724467 | Common:2; Rare:175 | ||||
| chr9:128771871-128771980 | Rare:27 | ||||
| chr9:128881901-128882202 | Common:2; Rare:98 | ||||
| chr9:128921966-128922324 | Common:1; Rare:78 | ||||
| chr9:128947537-128947721 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):1 |