| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133348039-133348258 | Common:2; Rare:86 | ||||
| chr9:133356436-133356607 | Common:1; Rare:79; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375947-133376372 | Common:4; Rare:149 | ||||
| chr9:133418040-133418296 | Common:4; Rare:51 | ||||
| chr9:136410609-136410671 | Rare:30 | ||||
| chr9:136662809-136663024 | Common:2; Rare:49 | ||||
| chr9:136745794-136745958 | Rare:59 | ||||
| chr9:136746004-136746221 | Common:1; Rare:52 | ||||
| chr9:136977362-136977692 | Common:1; Rare:80 | ||||
| chr9:136979957-136980283 | Rare:131 | ||||
| chr9:137086658-137087081 | Common:1; Rare:171; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137111717-137111974 | Common:3; Rare:119 | ||||
| chr9:137188547-137188744 | Common:2; Rare:98 | ||||
| chr9:137205502-137205735 | Common:1; Rare:80 |