| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37422617-37422759 | Common:2; Rare:74 | ||||
| chr9:37592516-37592645 | Common:2; Rare:51 | ||||
| chr9:37753685-37753829 | Common:6; Rare:85 | ||||
| chr9:37785041-37785132 | Common:1; Rare:35; Clinvar (benign):2 | ||||
| chr9:37800707-37800794 | Rare:25 | ||||
| chr9:37904076-37904462 | Common:3; Rare:127 | ||||
| chr9:66900479-66900813 | Common:4; Rare:102 | ||||
| chr9:68779915-68780100 | Common:3; Rare:72 | ||||
| chr9:69759921-69760123 | Common:2; Rare:91 | ||||
| chr9:70044073-70044169 | Rare:21 | ||||
| chr9:70258824-70259069 | Common:4; Rare:117 | ||||
| chr9:71911235-71911508 | Common:3; Rare:80 | ||||
| chr9:75088120-75088586 | Common:3; Rare:165 | ||||
| chr9:76394283-76394558 | Common:7; Rare:88 | ||||
| chr9:78296890-78297213 | Common:2; Rare:94; Clinvar (benign):1 |