| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35814983-35815335 | Common:1; Rare:89 | ||||
| chr9:36190722-36190994 | Common:1; Rare:90 | ||||
| chr9:36258386-36258622 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572772-36572943 | Rare:48 | ||||
| chr9:37485762-37486000 | Rare:87 | ||||
| chr9:37785045-37785149 | Common:1; Rare:35; Clinvar (benign):2 | ||||
| chr9:37800707-37800808 | Rare:27 | ||||
| chr9:37904067-37904463 | Common:3; Rare:130 | ||||
| chr9:38392545-38392749 | Common:2; Rare:62 | ||||
| chr9:68779860-68780070 | Common:2; Rare:73 | ||||
| chr9:69759939-69760099 | Common:2; Rare:79 | ||||
| chr9:70258833-70259069 | Common:4; Rare:111 | ||||
| chr9:71911192-71911514 | Common:3; Rare:93 | ||||
| chr9:75088109-75088585 | Common:3; Rare:165 | ||||
| chr9:76394375-76394584 | Common:5; Rare:89 |