| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128626112-128626408 | Common:2; Rare:68; Clinvar (benign):2 | ||||
| chr9:128632356-128632717 | Common:1; Rare:125; Clinvar:2; Clinvar (benign):11 | ||||
| chr9:128656629-128657002 | Common:2; Rare:127; Clinvar (pathogenic):1 | ||||
| chr9:128683141-128683951 | Common:6; Rare:161 | ||||
| chr9:128692492-128692760 | Common:3; Rare:60 | ||||
| chr9:128724081-128724467 | Common:2; Rare:128 | ||||
| chr9:128771836-128771965 | Rare:36 | ||||
| chr9:128787056-128787341 | Common:4; Rare:86 | ||||
| chr9:128881880-128882234 | Common:2; Rare:115 | ||||
| chr9:128882545-128882660 | Common:1; Rare:21 | ||||
| chr9:128921938-128922331 | Common:1; Rare:86 | ||||
| chr9:128947549-128947735 | Common:1; Rare:89; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:129081102-129081134 | Rare:11 | ||||
| chr9:129110635-129111029 | Common:5; Rare:122 | ||||
| chr9:129111240-129111609 | Common:3; Rare:104 |