| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36572767-36572939 | Rare:49 | ||||
| chr9:37034183-37034573 | Rare:98 | ||||
| chr9:37120384-37120626 | Common:2; Rare:87 | ||||
| chr9:37144818-37144886 | Rare:11 | ||||
| chr9:37283918-37284255 | Common:1; Rare:69 | ||||
| chr9:37327696-37327777 | Rare:20 | ||||
| chr9:37422570-37422734 | Common:2; Rare:83 | ||||
| chr9:37465226-37465620 | Common:3; Rare:125 | ||||
| chr9:37485727-37486017 | Common:3; Rare:104 | ||||
| chr9:37592516-37592649 | Common:2; Rare:52 | ||||
| chr9:37784899-37785109 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:37800676-37800801 | Common:1; Rare:37 | ||||
| chr9:37904067-37904462 | Common:3; Rare:130 | ||||
| chr9:66900574-66900804 | Common:3; Rare:73 | ||||
| chr9:68779960-68780070 | Common:1; Rare:30 |