| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125200292-125200590 | Common:1; Rare:102 | ||||
| chr9:125261679-125261848 | Common:1; Rare:64 | ||||
| chr9:126804881-126805049 | Rare:51 | ||||
| chr9:127449615-127449796 | Rare:42 | ||||
| chr9:127451280-127451520 | Common:2; Rare:106 | ||||
| chr9:127877671-127877767 | Rare:16 | ||||
| chr9:127899562-127899752 | Common:1; Rare:70 | ||||
| chr9:128275919-128276288 | Common:4; Rare:165 | ||||
| chr9:128322410-128322861 | Common:4; Rare:134; Clinvar (benign):5 | ||||
| chr9:128371213-128371383 | Rare:57 | ||||
| chr9:128504605-128504798 | Rare:90; Clinvar:5 | ||||
| chr9:128552401-128552612 | Rare:81; Clinvar:1 | ||||
| chr9:128656662-128657002 | Common:1; Rare:112; Clinvar (pathogenic):1 | ||||
| chr9:128724089-128724467 | Common:2; Rare:125 | ||||
| chr9:128947598-128947739 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):2 |