| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127451223-127451565 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr9:127569062-127569339 | Common:4; Rare:61 | ||||
| chr9:127612047-127612372 | Common:2; Rare:119; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127642195-127642470 | Common:1; Rare:48 | ||||
| chr9:127787951-127788286 | Common:2; Rare:108 | ||||
| chr9:127802719-127803047 | Common:3; Rare:89 | ||||
| chr9:127854490-127854541 | Rare:10; Clinvar:1 | ||||
| chr9:127854607-127854877 | Rare:56; Clinvar:5 | ||||
| chr9:127877626-127877767 | Rare:32 | ||||
| chr9:127897327-127897536 | Common:1; Rare:47 | ||||
| chr9:127899504-127899861 | Common:3; Rare:106 | ||||
| chr9:127905318-127905436 | Rare:22 | ||||
| chr9:127916989-127917265 | Common:1; Rare:81 | ||||
| chr9:127937817-127937895 | Common:1; Rare:27; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:128098289-128098551 | Common:1; Rare:56 |