| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124940949-124941201 | Common:3; Rare:99 | ||||
| chr9:125189725-125189889 | Rare:94 | ||||
| chr9:125200420-125200626 | Common:2; Rare:84 | ||||
| chr9:125241275-125241701 | Common:4; Rare:136 | ||||
| chr9:125261643-125261854 | Common:2; Rare:77 | ||||
| chr9:125707109-125707381 | Common:2; Rare:89 | ||||
| chr9:126804891-126805070 | Common:3; Rare:58 | ||||
| chr9:126860576-126860720 | Common:2; Rare:46 | ||||
| chr9:127245172-127245389 | Common:3; Rare:55 | ||||
| chr9:127424253-127424440 | Common:1; Rare:61 | ||||
| chr9:127451049-127451207 | Common:1; Rare:52 | ||||
| chr9:127451267-127451584 | Common:3; Rare:125; Clinvar (benign):1 | ||||
| chr9:127612047-127612379 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127802716-127802927 | Common:2; Rare:43 | ||||
| chr9:127877662-127877799 | Rare:26 |