| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50580028-50580293 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:50582404-50582425 | Rare:8 | ||||
| chr22:50582777-50583145 | Common:7; Rare:127; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628073-50628280 | Common:9; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783550-50783898 | Common:2; Rare:114 | ||||
| chr3:197260-197332 | Rare:23 | ||||
| chr3:2098568-2098970 | Common:4; Rare:161 | ||||
| chr3:3126773-3126990 | Common:4; Rare:95; Clinvar (benign):2 | ||||
| chr3:3128875-3129136 | Common:2; Rare:78; Clinvar (benign):4 | ||||
| chr3:4303252-4303415 | Common:1; Rare:64 | ||||
| chr3:4493151-4493532 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4795031-4795107 | Rare:23 | ||||
| chr3:4813068-4813211 | Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:4814165-4814559 | Common:5; Rare:110; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:4979154-4979726 | Common:4; Rare:135 |