| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34048853-34049003 | Common:2; Rare:62 | ||||
| chr9:34049354-34049589 | Common:1; Rare:72 | ||||
| chr9:34126020-34126420 | Rare:117 | ||||
| chr9:34126617-34126977 | Common:1; Rare:98 | ||||
| chr9:34178795-34179070 | Common:1; Rare:69 | ||||
| chr9:34328732-34328832 | Common:2; Rare:15 | ||||
| chr9:34329181-34329667 | Common:1; Rare:151 | ||||
| chr9:34376982-34377204 | Common:1; Rare:49 | ||||
| chr9:34457264-34457454 | Rare:35 | ||||
| chr9:34458515-34458892 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:34589560-34589980 | Common:1; Rare:118 | ||||
| chr9:34612073-34612302 | Common:8; Rare:80 | ||||
| chr9:34620463-34620635 | Common:1; Rare:41 | ||||
| chr9:34637732-34638140 | Common:3; Rare:104 | ||||
| chr9:34646475-34646730 | Common:1; Rare:75; Clinvar:2; Clinvar (pathogenic):2 |