| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122931482-122931674 | Common:3; Rare:34 | ||||
| chr9:124861908-124862121 | Rare:92 | ||||
| chr9:124940957-124941156 | Common:3; Rare:70 | ||||
| chr9:125189725-125189889 | Rare:94 | ||||
| chr9:125200434-125200571 | Common:1; Rare:47 | ||||
| chr9:125241175-125241658 | Common:3; Rare:142 | ||||
| chr9:125261685-125261848 | Common:1; Rare:62 | ||||
| chr9:127424075-127424499 | Common:1; Rare:125 | ||||
| chr9:127451267-127451565 | Common:3; Rare:123; Clinvar (benign):1 | ||||
| chr9:127802719-127803047 | Common:3; Rare:89 | ||||
| chr9:127804378-127804663 | Common:3; Rare:81 | ||||
| chr9:127854608-127854882 | Rare:58; Clinvar:5 | ||||
| chr9:127899518-127899811 | Common:2; Rare:94 | ||||
| chr9:127937832-127938132 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128098297-128098549 | Common:1; Rare:53 |