| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122264735-122264919 | Common:2; Rare:52 | ||||
| chr9:122913288-122913388 | Common:1; Rare:19 | ||||
| chr9:122931501-122931680 | Common:3; Rare:33 | ||||
| chr9:124415390-124415627 | Common:1; Rare:89 | ||||
| chr9:124861903-124862116 | Rare:91 | ||||
| chr9:124940969-124941265 | Common:3; Rare:108 | ||||
| chr9:125200440-125200590 | Common:1; Rare:57 | ||||
| chr9:125241317-125241679 | Common:3; Rare:106 | ||||
| chr9:125261728-125261841 | Common:1; Rare:40 | ||||
| chr9:127424253-127424406 | Rare:53 | ||||
| chr9:127451280-127451580 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr9:127877671-127877771 | Rare:18 | ||||
| chr9:127937816-127937889 | Common:1; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:128160024-128160413 | Common:2; Rare:93 | ||||
| chr9:128275919-128276293 | Common:4; Rare:167 |