| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122913268-122913421 | Common:3; Rare:33 | ||||
| chr9:122940830-122941065 | Common:2; Rare:94 | ||||
| chr9:124861875-124862134 | Common:1; Rare:113 | ||||
| chr9:124940969-124941168 | Common:3; Rare:67 | ||||
| chr9:125189725-125190039 | Common:1; Rare:142 | ||||
| chr9:125200287-125200590 | Common:1; Rare:102 | ||||
| chr9:125241374-125241686 | Common:2; Rare:85 | ||||
| chr9:125261729-125261848 | Common:1; Rare:41 | ||||
| chr9:125707160-125707364 | Common:2; Rare:64 | ||||
| chr9:126804919-126805060 | Common:1; Rare:46 | ||||
| chr9:127424270-127424429 | Common:1; Rare:49 | ||||
| chr9:127449279-127449612 | Common:2; Rare:96 | ||||
| chr9:127451267-127451557 | Common:3; Rare:121; Clinvar (benign):1 | ||||
| chr9:127579032-127579278 | Common:4; Rare:54 | ||||
| chr9:127877656-127877767 | Rare:22 |