| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50185683-50185946 | Common:4; Rare:109 | ||||
| chr22:50244949-50245080 | Common:2; Rare:49 | ||||
| chr22:50525538-50525694 | Common:3; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50532140-50532244 | Rare:24 | ||||
| chr22:50582365-50582584 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:50582784-50583121 | Common:7; Rare:105; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628056-50628256 | Common:8; Rare:89; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783592-50783859 | Common:2; Rare:87 | ||||
| chr3:197003-197324 | Common:3; Rare:113 | ||||
| chr3:2098651-2098947 | Common:4; Rare:117 | ||||
| chr3:3126784-3126984 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr3:4303247-4303422 | Common:2; Rare:70 | ||||
| chr3:4303526-4303637 | Common:1; Rare:38 | ||||
| chr3:4467225-4467313 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493176-4493498 | Rare:111; Clinvar:1; Clinvar (benign):1 |