| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35103078-35103288 | Common:1; Rare:71 | ||||
| chr9:35489906-35490139 | Common:2; Rare:67 | ||||
| chr9:35657895-35658397 | Common:7; Rare:408; Clinvar:32; Clinvar (benign):13; Clinvar (pathogenic):37 | ||||
| chr9:35689783-35690184 | Common:4; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732073-35732320 | Common:1; Rare:66 | ||||
| chr9:35732371-35732676 | Common:2; Rare:77 | ||||
| chr9:35748999-35749336 | Common:2; Rare:124 | ||||
| chr9:35814983-35815292 | Rare:78 | ||||
| chr9:36190725-36190988 | Common:1; Rare:86 | ||||
| chr9:37485750-37485967 | Common:1; Rare:73 | ||||
| chr9:37592515-37592643 | Common:2; Rare:51 | ||||
| chr9:37904076-37904222 | Rare:49 | ||||
| chr9:68779884-68780079 | Common:2; Rare:70 | ||||
| chr9:69759924-69760139 | Common:3; Rare:96 | ||||
| chr9:70258845-70259069 | Common:3; Rare:106 |