| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132354955-132355232 | Common:4; Rare:92 | ||||
| chr9:132669969-132670057 | Common:1; Rare:41 | ||||
| chr9:132878291-132878402 | Common:1; Rare:40 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133336133-133336297 | Common:1; Rare:63 | ||||
| chr9:133348080-133348251 | Common:1; Rare:67 | ||||
| chr9:133356457-133356599 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr9:133375976-133376366 | Common:3; Rare:142 | ||||
| chr9:136410453-136410680 | Common:6; Rare:106 | ||||
| chr9:137086658-137086997 | Common:1; Rare:129; Clinvar:1 | ||||
| chr9:137188547-137188717 | Common:2; Rare:85 | ||||
| chr9:137205396-137205743 | Common:1; Rare:125 | ||||
| chr9:137618797-137619031 | Common:1; Rare:105 | ||||
| chrM:3168-3483 | |||||
| chrM:5576-5590 |