| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43923568-43923746 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr22:43955275-43955578 | Common:3; Rare:92 | ||||
| chr22:44023697-44023935 | Common:1; Rare:43 | ||||
| chr22:45163684-45163948 | Common:4; Rare:90 | ||||
| chr22:46053793-46053873 | Rare:29 | ||||
| chr22:46250245-46250350 | Common:2; Rare:28 | ||||
| chr22:46267832-46268035 | Common:1; Rare:60 | ||||
| chr22:46296673-46296925 | Common:2; Rare:89 | ||||
| chr22:46762526-46762693 | Common:3; Rare:58 | ||||
| chr22:49918291-49918727 | Common:4; Rare:157; Clinvar (benign):3 | ||||
| chr22:50525532-50525815 | Common:6; Rare:155; Clinvar:6; Clinvar (benign):6 | ||||
| chr22:50526347-50526591 | Common:2; Rare:116; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr22:50582779-50583136 | Common:7; Rare:118; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628087-50628313 | Common:9; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783621-50783821 | Common:2; Rare:62 |