| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127568952-127569374 | Common:12; Rare:195 | ||||
| chr9:127578978-127579340 | Common:9; Rare:128 | ||||
| chr9:127611990-127612332 | Common:2; Rare:246; Clinvar:8; Clinvar (benign):3 | ||||
| chr9:127734940-127735180 | Common:1; Rare:60 | ||||
| chr9:127735273-127735378 | Common:1; Rare:31 | ||||
| chr9:127771270-127771750 | Common:1; Rare:158 | ||||
| chr9:127785084-127785224 | Rare:37 | ||||
| chr9:127785425-127785758 | Common:2; Rare:183 | ||||
| chr9:127785924-127786172 | Common:2; Rare:212; Clinvar:2 | ||||
| chr9:127802567-127803054 | Common:4; Rare:125 | ||||
| chr9:127803130-127803347 | Common:1; Rare:54 | ||||
| chr9:127803786-127804072 | Common:4; Rare:73 | ||||
| chr9:127804048-127804549 | Common:2; Rare:118 | ||||
| chr9:127877640-127877809 | Rare:64 | ||||
| chr9:127899514-127899739 | Rare:82 |