| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124861890-124862141 | Common:1; Rare:107 | ||||
| chr9:124862310-124862426 | Common:1; Rare:24 | ||||
| chr9:124940961-124941224 | Common:3; Rare:100 | ||||
| chr9:125189724-125190028 | Common:1; Rare:139 | ||||
| chr9:125200418-125200590 | Common:1; Rare:67 | ||||
| chr9:125241312-125241693 | Common:3; Rare:121 | ||||
| chr9:125261691-125261854 | Common:1; Rare:64 | ||||
| chr9:125707147-125707371 | Common:2; Rare:74 | ||||
| chr9:126804851-126805064 | Common:2; Rare:67 | ||||
| chr9:126860576-126860673 | Common:2; Rare:28 | ||||
| chr9:127122626-127122868 | Common:3; Rare:61 | ||||
| chr9:127424111-127424450 | Common:1; Rare:95 | ||||
| chr9:127451272-127451560 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr9:127802719-127802927 | Common:2; Rare:43 | ||||
| chr9:127877657-127877767 | Rare:21 |