| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20858256-20858577 | Common:3; Rare:83 | ||||
| chr22:20858748-20859089 | Common:4; Rare:169; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:20917118-20917508 | Rare:135 | ||||
| chr22:20979230-20979490 | Common:4; Rare:105 | ||||
| chr22:20981914-20982064 | Rare:65 | ||||
| chr22:20982133-20982368 | Common:2; Rare:65; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:21001724-21001900 | Common:2; Rare:69 | ||||
| chr22:21002002-21002250 | Common:5; Rare:98 | ||||
| chr22:21045736-21045994 | Common:1; Rare:90 | ||||
| chr22:21567719-21568119 | Common:2; Rare:158 | ||||
| chr22:21629975-21630178 | Common:2; Rare:83 | ||||
| chr22:21642009-21642327 | Common:2; Rare:95 | ||||
| chr22:21651870-21652239 | Common:2; Rare:76 | ||||
| chr22:21665928-21666052 | Rare:33 | ||||
| chr22:21666234-21666340 | Rare:24 |