| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19291707-19291915 | Common:9; Rare:64 | ||||
| chr22:19432303-19432595 | Common:4; Rare:122 | ||||
| chr22:19447452-19447656 | Common:1; Rare:90 | ||||
| chr22:19447667-19447836 | Common:1; Rare:75 | ||||
| chr22:19854806-19855061 | Common:1; Rare:96 | ||||
| chr22:19941640-19941878 | Rare:100; Clinvar:6; Clinvar (benign):7 | ||||
| chr22:20020911-20021141 | Common:1; Rare:73 | ||||
| chr22:20113461-20113638 | Rare:69 | ||||
| chr22:20116990-20117104 | Rare:25 | ||||
| chr22:20117154-20117571 | Common:3; Rare:135 | ||||
| chr22:20319989-20320178 | Common:2; Rare:65 | ||||
| chr22:20495783-20495993 | Common:2; Rare:80 | ||||
| chr22:20582939-20583178 | Rare:69 | ||||
| chr22:20858668-20859192 | Common:10; Rare:259; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20917170-20917484 | Rare:116 |