| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131531182-131531332 | Common:9; Rare:69 | ||||
| chr9:132669937-132670051 | Common:1; Rare:54 | ||||
| chr9:132670253-132670511 | Rare:76 | ||||
| chr9:132878272-132878385 | Common:1; Rare:41 | ||||
| chr9:132878818-132878945 | Rare:21 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133336104-133336436 | Common:2; Rare:148 | ||||
| chr9:133348018-133348253 | Common:3; Rare:85 | ||||
| chr9:133356443-133356630 | Common:1; Rare:87; Clinvar (benign):2 | ||||
| chr9:133375965-133376375 | Common:4; Rare:149 | ||||
| chr9:133418040-133418094 | Common:1; Rare:7 | ||||
| chr9:133459939-133460044 | Common:1; Rare:46 | ||||
| chr9:136410609-136410671 | Rare:30 | ||||
| chr9:136741975-136742102 | Rare:37 | ||||
| chr9:136745824-136746216 | Common:1; Rare:112 |