| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:123033453-123033672 | Rare:35 | ||||
| chr9:124861903-124862163 | Common:1; Rare:113 | ||||
| chr9:124940949-124941178 | Common:3; Rare:82 | ||||
| chr9:125189714-125190050 | Common:1; Rare:146 | ||||
| chr9:125200440-125200606 | Common:1; Rare:64 | ||||
| chr9:125241161-125241686 | Common:4; Rare:161 | ||||
| chr9:125261679-125261890 | Common:2; Rare:82 | ||||
| chr9:126804951-126805070 | Common:3; Rare:38 | ||||
| chr9:126860576-126860673 | Common:2; Rare:28 | ||||
| chr9:127245188-127245341 | Common:1; Rare:37 | ||||
| chr9:127424073-127424499 | Common:1; Rare:126 | ||||
| chr9:127451257-127451592 | Common:3; Rare:132; Clinvar (benign):1 | ||||
| chr9:127611984-127612323 | Common:1; Rare:128; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127778664-127778873 | Common:1; Rare:36 | ||||
| chr9:127786373-127786464 | Rare:30 |