| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125200426-125200590 | Common:1; Rare:61 | ||||
| chr9:125241080-125241637 | Common:3; Rare:175 | ||||
| chr9:125261680-125261848 | Common:1; Rare:64 | ||||
| chr9:127224385-127224659 | Common:1; Rare:75 | ||||
| chr9:127424064-127424450 | Common:1; Rare:116 | ||||
| chr9:127451251-127451533 | Common:2; Rare:122 | ||||
| chr9:127612047-127612338 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127771286-127771384 | Rare:30 | ||||
| chr9:127937824-127937906 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr9:128191440-128191651 | Rare:63 | ||||
| chr9:128191751-128191851 | Common:1; Rare:24 | ||||
| chr9:128275919-128276293 | Common:4; Rare:167 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322729-128322898 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128371224-128371404 | Rare:68 |