| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36258354-36258630 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400413-36400552 | Rare:39 | ||||
| chr9:36400948-36401238 | Common:2; Rare:99 | ||||
| chr9:36487170-36487276 | Rare:37 | ||||
| chr9:36572726-36572972 | Common:2; Rare:76 | ||||
| chr9:37120126-37120626 | Common:2; Rare:153 | ||||
| chr9:37120739-37120821 | Rare:27 | ||||
| chr9:37422617-37422753 | Common:2; Rare:71 | ||||
| chr9:37431679-37431882 | Common:1; Rare:36 | ||||
| chr9:37464916-37465167 | Common:2; Rare:78 | ||||
| chr9:37485861-37486088 | Common:2; Rare:86 | ||||
| chr9:37650754-37651079 | Common:2; Rare:100 | ||||
| chr9:37784711-37785149 | Common:1; Rare:190; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr9:37800702-37800837 | Rare:40 | ||||
| chr9:37801386-37801518 | Common:2; Rare:41 |