| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127424073-127424489 | Common:1; Rare:124 | ||||
| chr9:127451267-127451621 | Common:3; Rare:128; Clinvar (benign):1 | ||||
| chr9:127579032-127579305 | Common:4; Rare:58 | ||||
| chr9:127786363-127786522 | Rare:59 | ||||
| chr9:127802719-127803056 | Common:4; Rare:89 | ||||
| chr9:127854324-127854414 | Common:2; Rare:19; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:127854490-127854513 | Rare:4 | ||||
| chr9:127877627-127877771 | Rare:34 | ||||
| chr9:127897384-127897519 | Common:1; Rare:31 | ||||
| chr9:127916980-127917254 | Common:1; Rare:84 | ||||
| chr9:127937817-127937889 | Common:1; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:127980051-127980191 | Rare:58 | ||||
| chr9:128098266-128098544 | Common:1; Rare:57 | ||||
| chr9:128128108-128128322 | Common:8; Rare:91 | ||||
| chr9:128128433-128128517 | Common:2; Rare:44 |