| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50343176-50343383 | Common:4; Rare:169 | ||||
| chr22:50474980-50475202 | Common:8; Rare:152 | ||||
| chr22:50481422-50481602 | Rare:117 | ||||
| chr22:50486529-50487400 | Common:8; Rare:262 | ||||
| chr22:50507440-50508411 | Common:20; Rare:728 | ||||
| chr22:50525490-50525800 | Common:9; Rare:262; Clinvar:9; Clinvar (benign):8 | ||||
| chr22:50526421-50526527 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr22:50532494-50532693 | Common:2; Rare:50 | ||||
| chr22:50582220-50582740 | Common:3; Rare:391; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):4 | ||||
| chr22:50582778-50583176 | Common:18; Rare:279; Clinvar:4; Clinvar (benign):6 | ||||
| chr22:50600470-50600812 | Rare:153 | ||||
| chr22:50628038-50628326 | Common:18; Rare:234; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:50674822-50674947 | Rare:42 | ||||
| chr22:50783597-50783821 | Common:4; Rare:147 | ||||
| chr3:3126737-3127078 | Common:10; Rare:244; Clinvar (benign):8 |