| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95505865-95506221 | Common:2; Rare:126 | ||||
| chr9:95506581-95506731 | Common:1; Rare:60; Clinvar:5; Clinvar (benign):5 | ||||
| chr9:95507378-95507763 | Rare:125 | ||||
| chr9:95875447-95875767 | Common:1; Rare:112 | ||||
| chr9:95875931-95876084 | Common:6; Rare:70; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96383584-96383783 | Common:3; Rare:62 | ||||
| chr9:96655251-96655431 | Common:1; Rare:55 | ||||
| chr9:96778038-96778163 | Rare:37 | ||||
| chr9:96854463-96854524 | Common:2; Rare:10 | ||||
| chr9:97411998-97412196 | Common:3; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:97501499-97501798 | Common:6; Rare:77 | ||||
| chr9:97633271-97633458 | Common:1; Rare:50 | ||||
| chr9:97633463-97633499 | Common:1; Rare:9 | ||||
| chr9:97633513-97633864 | Common:4; Rare:114 | ||||
| chr9:97666599-97666815 | Common:1; Rare:39 |