| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124940969-124941184 | Common:3; Rare:76 | ||||
| chr9:125189725-125190039 | Common:1; Rare:142 | ||||
| chr9:125200421-125200590 | Common:1; Rare:64 | ||||
| chr9:125241270-125241698 | Common:3; Rare:136 | ||||
| chr9:125261716-125261848 | Common:1; Rare:47 | ||||
| chr9:125707152-125707364 | Common:2; Rare:69 | ||||
| chr9:126804874-126805060 | Common:1; Rare:58 | ||||
| chr9:127122602-127122989 | Common:3; Rare:107 | ||||
| chr9:127424106-127424440 | Common:1; Rare:92 | ||||
| chr9:127451272-127451533 | Common:2; Rare:113 | ||||
| chr9:127578998-127579150 | Common:3; Rare:22 | ||||
| chr9:127877662-127877755 | Rare:18 | ||||
| chr9:127897406-127897546 | Common:1; Rare:37 | ||||
| chr9:127916987-127917292 | Common:1; Rare:89 | ||||
| chr9:127937820-127937946 | Common:1; Rare:33; Clinvar:3; Clinvar (benign):1 |