| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131531164-131531350 | Common:9; Rare:85 | ||||
| chr9:132669939-132670051 | Common:1; Rare:53 | ||||
| chr9:132878282-132878385 | Common:1; Rare:36 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133163910-133164006 | Common:2; Rare:24 | ||||
| chr9:133348039-133348276 | Common:2; Rare:99 | ||||
| chr9:133356481-133356630 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr9:133375965-133376340 | Common:3; Rare:138 | ||||
| chr9:134641547-134641802 | Common:2; Rare:80 | ||||
| chr9:136410615-136410678 | Rare:29 | ||||
| chr9:136849620-136849787 | Common:1; Rare:60 | ||||
| chr9:136849958-136850060 | Rare:45 | ||||
| chr9:136977215-136977549 | Rare:64 | ||||
| chr9:136996553-136996861 | Common:2; Rare:89 | ||||
| chr9:137086648-137087146 | Common:2; Rare:206; Clinvar:6; Clinvar (benign):1 |