| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46534269-46534543 | Rare:91 | ||||
| chr22:46534670-46534983 | Common:1; Rare:98 | ||||
| chr22:46626226-46626412 | Common:1; Rare:47 | ||||
| chr22:46762447-46762701 | Common:3; Rare:96 | ||||
| chr22:49918378-49918690 | Common:2; Rare:116; Clinvar (benign):1 | ||||
| chr22:50185725-50185953 | Common:4; Rare:95 | ||||
| chr22:50244629-50244671 | Rare:12 | ||||
| chr22:50244954-50245070 | Common:2; Rare:45 | ||||
| chr22:50278437-50278747 | Common:1; Rare:97 | ||||
| chr22:50281938-50282235 | Common:2; Rare:104 | ||||
| chr22:50283337-50283584 | Rare:85 | ||||
| chr22:50447600-50447784 | Rare:52 | ||||
| chr22:50454639-50455018 | Common:1; Rare:152; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50525509-50525681 | Common:4; Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50580028-50580328 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |