| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18110622-18110857 | Rare:62 | ||||
| chr22:19122389-19122667 | Common:3; Rare:65 | ||||
| chr22:19291674-19291947 | Common:10; Rare:87 | ||||
| chr22:19432303-19432616 | Common:4; Rare:131 | ||||
| chr22:19447677-19447926 | Common:2; Rare:103 | ||||
| chr22:19524408-19524665 | Rare:78 | ||||
| chr22:19854795-19854972 | Rare:61 | ||||
| chr22:19941770-19941891 | Rare:50; Clinvar:2 | ||||
| chr22:20020864-20021141 | Common:1; Rare:90 | ||||
| chr22:20079929-20080253 | Common:1; Rare:106 | ||||
| chr22:20117193-20117571 | Common:3; Rare:117 | ||||
| chr22:20319989-20320158 | Common:2; Rare:57 | ||||
| chr22:20495781-20495925 | Common:2; Rare:55 | ||||
| chr22:20507454-20507643 | Rare:58 | ||||
| chr22:20858690-20859100 | Common:6; Rare:203; Clinvar:3; Clinvar (benign):3 |