| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35814983-35815235 | Rare:70 | ||||
| chr9:36190737-36190978 | Common:1; Rare:81 | ||||
| chr9:36258424-36258622 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572835-36572948 | Rare:32 | ||||
| chr9:37120363-37120614 | Common:2; Rare:93 | ||||
| chr9:37485732-37485988 | Common:1; Rare:91 | ||||
| chr9:37592516-37592645 | Common:2; Rare:51 | ||||
| chr9:37785004-37785126 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800707-37800837 | Rare:40 | ||||
| chr9:37904095-37904219 | Rare:37 | ||||
| chr9:65675723-65675957 | Rare:54 | ||||
| chr9:68779960-68780070 | Common:1; Rare:30 | ||||
| chr9:69759924-69760124 | Common:2; Rare:92 | ||||
| chr9:70258833-70259069 | Common:4; Rare:111 | ||||
| chr9:71121401-71121606 | Common:4; Rare:42 |