| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18077819-18078042 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19291637-19291921 | Common:12; Rare:99 | ||||
| chr22:19432289-19432614 | Common:4; Rare:139 | ||||
| chr22:19447465-19447733 | Common:1; Rare:137 | ||||
| chr22:19478880-19479067 | Common:1; Rare:58 | ||||
| chr22:19479081-19479471 | Common:4; Rare:142 | ||||
| chr22:19524398-19524639 | Common:1; Rare:77 | ||||
| chr22:19525360-19525667 | Common:1; Rare:66 | ||||
| chr22:19854795-19854979 | Rare:63 | ||||
| chr22:19941721-19941891 | Rare:73; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20117185-20117571 | Common:3; Rare:121 | ||||
| chr22:20319994-20320160 | Common:2; Rare:54 | ||||
| chr22:20495768-20495932 | Common:2; Rare:59 | ||||
| chr22:20858704-20859129 | Common:9; Rare:212; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20982183-20982358 | Common:2; Rare:43; Clinvar (benign):2; Clinvar (pathogenic):1 |