| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133054405-133054714 | Rare:93 | ||||
| chr9:133348039-133348246 | Common:2; Rare:77 | ||||
| chr9:133356452-133356618 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr9:133376003-133376340 | Common:1; Rare:124 | ||||
| chr9:133459946-133460044 | Common:1; Rare:44 | ||||
| chr9:136354650-136355009 | Common:2; Rare:104 | ||||
| chr9:136410612-136410680 | Rare:34 | ||||
| chr9:136741974-136742184 | Rare:58 | ||||
| chr9:136745841-136745978 | Rare:48 | ||||
| chr9:136745990-136746216 | Common:1; Rare:52 | ||||
| chr9:136849355-136849874 | Common:3; Rare:208 | ||||
| chr9:136977362-136977692 | Common:1; Rare:80 | ||||
| chr9:136981725-136981937 | Rare:44 | ||||
| chr9:137086661-137086997 | Common:1; Rare:128; Clinvar:1 |