| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19291696-19291940 | Common:10; Rare:74 | ||||
| chr22:19432242-19432606 | Common:4; Rare:156 | ||||
| chr22:19447677-19447862 | Common:2; Rare:76 | ||||
| chr22:19854806-19855023 | Rare:84 | ||||
| chr22:19941736-19941881 | Rare:59; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:20079930-20080292 | Common:1; Rare:118 | ||||
| chr22:20117193-20117598 | Common:3; Rare:126 | ||||
| chr22:20319998-20320158 | Common:1; Rare:53 | ||||
| chr22:20495781-20495913 | Common:1; Rare:50 | ||||
| chr22:20917335-20917418 | Rare:24 | ||||
| chr22:20982168-20982358 | Common:2; Rare:51; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002087-21002250 | Common:4; Rare:59 | ||||
| chr22:21045758-21045966 | Rare:73 | ||||
| chr22:21642044-21642348 | Common:2; Rare:92 | ||||
| chr22:21952792-21952969 | Common:1; Rare:67 |