| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50327320-50327670 | Common:4; Rare:124 | ||||
| chr22:50343156-50343447 | Common:6; Rare:274 | ||||
| chr22:50474955-50475285 | Common:13; Rare:178 | ||||
| chr22:50481397-50481716 | Common:2; Rare:175 | ||||
| chr22:50481630-50482040 | Common:7; Rare:243 | ||||
| chr22:50507501-50508450 | Common:13; Rare:644 | ||||
| chr22:50525107-50525507 | Common:5; Rare:151; Clinvar (benign):1 | ||||
| chr22:50525470-50525873 | Common:20; Rare:496; Clinvar:17; Clinvar (benign):20; Clinvar (pathogenic):1 | ||||
| chr22:50526338-50526463 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50526417-50526529 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr22:50532005-50532405 | Common:3; Rare:156 | ||||
| chr22:50562886-50563144 | Common:9; Rare:156 | ||||
| chr22:50582239-50582662 | Common:2; Rare:241; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr22:50582587-50583266 | Common:29; Rare:550; Clinvar:9; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr22:50600207-50601019 | Common:3; Rare:407 |