| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132669939-132670040 | Common:1; Rare:49 | ||||
| chr9:132878272-132878408 | Common:1; Rare:52 | ||||
| chr9:133336133-133336330 | Common:1; Rare:79 | ||||
| chr9:133348080-133348258 | Common:1; Rare:74 | ||||
| chr9:133356458-133356607 | Common:1; Rare:69; Clinvar (benign):2 | ||||
| chr9:133376003-133376366 | Common:1; Rare:132 | ||||
| chr9:133479081-133479384 | Common:1; Rare:85 | ||||
| chr9:134641540-134641809 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chr9:136410330-136410695 | Common:7; Rare:158 | ||||
| chr9:136849652-136849760 | Common:1; Rare:41 | ||||
| chr9:137188547-137188717 | Common:2; Rare:85 | ||||
| chr9:137205473-137205714 | Common:1; Rare:75 | ||||
| chr9:137618797-137619038 | Common:1; Rare:109 | ||||
| chrM:3168-3376 | |||||
| chrM:5576-5753 |