| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35103064-35103297 | Common:1; Rare:88 | ||||
| chr9:35538813-35539021 | Common:2; Rare:49 | ||||
| chr9:35657865-35658392 | Common:8; Rare:435; Clinvar:38; Clinvar (benign):14; Clinvar (pathogenic):40 | ||||
| chr9:35732029-35732349 | Common:2; Rare:85 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35748989-35749378 | Common:2; Rare:145 | ||||
| chr9:35812133-35812283 | Rare:59 | ||||
| chr9:35814983-35815299 | Rare:81 | ||||
| chr9:35829072-35829269 | Common:1; Rare:52 | ||||
| chr9:36190780-36190973 | Rare:69 | ||||
| chr9:36258374-36258599 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572750-36572902 | Common:1; Rare:48 | ||||
| chr9:37422615-37422735 | Common:2; Rare:64 | ||||
| chr9:37576238-37576399 | Rare:45 | ||||
| chr9:37592455-37592667 | Common:2; Rare:75 |