| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19432303-19432606 | Common:4; Rare:129 | ||||
| chr22:19433125-19433348 | Common:2; Rare:69 | ||||
| chr22:19447671-19447833 | Common:1; Rare:69 | ||||
| chr22:19854787-19854972 | Rare:63 | ||||
| chr22:19941722-19942124 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020892-20021145 | Common:1; Rare:83 | ||||
| chr22:20079936-20080305 | Common:1; Rare:122 | ||||
| chr22:20117169-20117592 | Common:3; Rare:136 | ||||
| chr22:20319991-20320158 | Common:2; Rare:55 | ||||
| chr22:20495771-20495919 | Common:1; Rare:55 | ||||
| chr22:20507518-20507622 | Rare:24 | ||||
| chr22:20858675-20859165 | Common:10; Rare:237; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20982196-20982353 | Common:2; Rare:36; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002251 | Common:4; Rare:59 | ||||
| chr22:21630012-21630262 | Common:2; Rare:77 |