| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37650754-37651070 | Common:2; Rare:98 | ||||
| chr9:37753788-37753829 | Common:3; Rare:34 | ||||
| chr9:37784896-37785149 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:37800655-37800816 | Common:2; Rare:48 | ||||
| chr9:37904067-37904476 | Common:3; Rare:133 | ||||
| chr9:66900558-66900804 | Common:3; Rare:78 | ||||
| chr9:68779960-68780091 | Common:1; Rare:42 | ||||
| chr9:69759919-69760107 | Common:2; Rare:88 | ||||
| chr9:70258820-70259069 | Common:4; Rare:119 | ||||
| chr9:71121375-71121666 | Common:5; Rare:67 | ||||
| chr9:71911216-71911510 | Common:3; Rare:86 | ||||
| chr9:72577230-72577336 | Rare:14 | ||||
| chr9:74497123-74497427 | Common:3; Rare:66 | ||||
| chr9:74497529-74497625 | Rare:24 | ||||
| chr9:74952207-74952423 | Rare:68 |