| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127449610-127449863 | Rare:64 | ||||
| chr9:127451269-127451557 | Common:3; Rare:121; Clinvar (benign):1 | ||||
| chr9:127612016-127612356 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127787951-127788286 | Common:2; Rare:108 | ||||
| chr9:127802748-127803032 | Common:3; Rare:78 | ||||
| chr9:127899518-127899808 | Common:2; Rare:94 | ||||
| chr9:127905318-127905422 | Rare:21 | ||||
| chr9:127916980-127917125 | Common:1; Rare:44 | ||||
| chr9:127979960-127980360 | Rare:120 | ||||
| chr9:128098291-128098544 | Common:1; Rare:53 | ||||
| chr9:128100848-128101137 | Common:2; Rare:50 | ||||
| chr9:128149319-128149472 | Rare:28 | ||||
| chr9:128159996-128160383 | Common:3; Rare:94 | ||||
| chr9:128191515-128191657 | Rare:39 | ||||
| chr9:128191687-128191777 | Rare:24 |