| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36258386-36258622 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400837-36400968 | Common:3; Rare:61 | ||||
| chr9:36572735-36572948 | Common:1; Rare:67 | ||||
| chr9:37120365-37120652 | Common:3; Rare:105 | ||||
| chr9:37422576-37422774 | Common:2; Rare:100; Clinvar:1 | ||||
| chr9:37465189-37465548 | Common:3; Rare:115 | ||||
| chr9:37485731-37486000 | Common:1; Rare:94 | ||||
| chr9:37576211-37576516 | Common:1; Rare:83 | ||||
| chr9:37592434-37592705 | Common:3; Rare:93 | ||||
| chr9:37785015-37785167 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800690-37800794 | Common:1; Rare:31 | ||||
| chr9:37903980-37904251 | Common:2; Rare:81 | ||||
| chr9:37904354-37904476 | Rare:41 | ||||
| chr9:66900513-66900804 | Common:4; Rare:90 | ||||
| chr9:68356361-68356630 | Common:7; Rare:47 |