| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36258343-36258625 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572770-36572939 | Rare:48 | ||||
| chr9:37422615-37422783 | Common:2; Rare:84; Clinvar:1 | ||||
| chr9:37485787-37486002 | Rare:80 | ||||
| chr9:37785024-37785115 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37800707-37800822 | Rare:34 | ||||
| chr9:37904076-37904463 | Common:3; Rare:127 | ||||
| chr9:38620351-38620677 | Common:4; Rare:69 | ||||
| chr9:68356383-68356629 | Common:7; Rare:42 | ||||
| chr9:68779966-68780156 | Common:2; Rare:62 | ||||
| chr9:69173924-69174250 | Common:6; Rare:101 | ||||
| chr9:69759933-69760099 | Common:2; Rare:81 | ||||
| chr9:70258846-70259069 | Common:3; Rare:105 | ||||
| chr9:70414303-70414452 | Rare:28 | ||||
| chr9:71911191-71911523 | Common:3; Rare:98 |