| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125241099-125241686 | Common:4; Rare:182 | ||||
| chr9:125261685-125261854 | Common:1; Rare:64 | ||||
| chr9:126804928-126805064 | Common:1; Rare:40 | ||||
| chr9:127122640-127122948 | Common:3; Rare:77 | ||||
| chr9:127245188-127245341 | Common:1; Rare:37 | ||||
| chr9:127424073-127424440 | Common:1; Rare:106 | ||||
| chr9:127449279-127449536 | Common:2; Rare:74 | ||||
| chr9:127451279-127451592 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr9:127612018-127612357 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127897406-127897536 | Common:1; Rare:35 | ||||
| chr9:127937794-127938029 | Common:2; Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:128098278-128098544 | Common:1; Rare:55 | ||||
| chr9:128160017-128160412 | Common:2; Rare:94 | ||||
| chr9:128190403-128190721 | Rare:85 | ||||
| chr9:128191494-128191657 | Rare:50 |