| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219178142-219178450 | Common:6; Rare:132 | ||||
| chr2:219206670-219206916 | Rare:90 | ||||
| chr2:219229336-219229419 | Rare:28 | ||||
| chr2:219229553-219229891 | Common:2; Rare:107 | ||||
| chr2:219245407-219245511 | Rare:26 | ||||
| chr2:219253859-219254067 | Common:2; Rare:67 | ||||
| chr2:219279203-219279523 | Common:2; Rare:100 | ||||
| chr2:219418394-219419043 | Common:5; Rare:219; Clinvar:40; Clinvar (benign):22; Clinvar (pathogenic):3 | ||||
| chr2:219419887-219420172 | Common:2; Rare:66; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:219420215-219420656 | Common:4; Rare:130; Clinvar:18; Clinvar (benign):18; Clinvar (pathogenic):2 | ||||
| chr2:219434542-219434870 | Common:2; Rare:61 | ||||
| chr2:219441905-219442062 | Rare:37 | ||||
| chr2:219460451-219460795 | Common:4; Rare:84 | ||||
| chr2:219498663-219498925 | Common:2; Rare:55 | ||||
| chr2:219543802-219544083 | Common:3; Rare:87 |