| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92964171-92964325 | Rare:26 | ||||
| chr9:93134162-93134352 | Common:2; Rare:70 | ||||
| chr9:93451426-93451703 | Common:3; Rare:73 | ||||
| chr9:93452274-93452415 | Rare:26 | ||||
| chr9:93452468-93452692 | Common:2; Rare:75 | ||||
| chr9:93452893-93453180 | Common:1; Rare:60 | ||||
| chr9:93453527-93453687 | Rare:37 | ||||
| chr9:93576360-93576399 | Rare:11 | ||||
| chr9:94259286-94259345 | Common:1; Rare:19 | ||||
| chr9:94639480-94639618 | Common:1; Rare:36; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:94726547-94726741 | Rare:54 | ||||
| chr9:95004149-95004265 | Common:1; Rare:37 | ||||
| chr9:95004438-95004485 | Rare:10 | ||||
| chr9:95004676-95004706 | Rare:7 | ||||
| chr9:95317663-95317882 | Common:1; Rare:72; Clinvar:2 |