| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36258354-36258599 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572785-36572902 | Rare:29 | ||||
| chr9:37422611-37422729 | Common:2; Rare:60 | ||||
| chr9:37753715-37753826 | Common:4; Rare:65 | ||||
| chr9:37785021-37785128 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37904076-37904417 | Common:3; Rare:110 | ||||
| chr9:38392541-38392749 | Common:2; Rare:64 | ||||
| chr9:65675845-65675957 | Rare:35 | ||||
| chr9:66900591-66900803 | Common:3; Rare:66 | ||||
| chr9:68356479-68356630 | Common:1; Rare:26 | ||||
| chr9:68779827-68780093 | Common:3; Rare:92 | ||||
| chr9:69759930-69760129 | Common:2; Rare:90 | ||||
| chr9:70258824-70259006 | Common:3; Rare:80 | ||||
| chr9:70413950-70414203 | Rare:51 | ||||
| chr9:71911222-71911510 | Common:3; Rare:85 |