| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17774390-17774585 | Rare:68 | ||||
| chr22:17841957-17842155 | Rare:60 | ||||
| chr22:18077814-18078084 | Common:5; Rare:89; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:18149794-18150194 | Common:2; Rare:90 | ||||
| chr22:19122389-19122668 | Common:3; Rare:65 | ||||
| chr22:19291700-19291940 | Common:9; Rare:73 | ||||
| chr22:19431227-19431317 | Rare:28 | ||||
| chr22:19432303-19432616 | Common:4; Rare:131 | ||||
| chr22:19447664-19447729 | Rare:45 | ||||
| chr22:19479096-19479471 | Common:4; Rare:139 | ||||
| chr22:19479693-19479969 | Common:4; Rare:77 | ||||
| chr22:19524398-19524639 | Common:1; Rare:77 | ||||
| chr22:19854787-19855013 | Rare:83 | ||||
| chr22:19933469-19933620 | Common:4; Rare:32 | ||||
| chr22:19941762-19941886 | Rare:50; Clinvar:3 |