| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50326975-50327185 | Common:3; Rare:70 | ||||
| chr22:50343224-50343402 | Common:2; Rare:73 | ||||
| chr22:50481400-50481552 | Rare:51 | ||||
| chr22:50525470-50525692 | Common:5; Rare:103; Clinvar:4; Clinvar (benign):3 | ||||
| chr22:50526417-50526775 | Common:3; Rare:168; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):7 | ||||
| chr22:50562886-50563043 | Common:3; Rare:46 | ||||
| chr22:50582358-50582462 | Rare:46 | ||||
| chr22:50582573-50582627 | Rare:23; Clinvar:1 | ||||
| chr22:50582774-50583125 | Common:7; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628066-50628313 | Common:9; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50674845-50674919 | Rare:24 | ||||
| chr22:50783598-50783821 | Common:2; Rare:73 | ||||
| chr3:2098649-2098951 | Common:4; Rare:120 | ||||
| chr3:3126810-3127067 | Common:4; Rare:106; Clinvar (benign):4 | ||||
| chr3:3799206-3799769 | Common:6; Rare:198 |