Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58098216-58098474 | Common:8; Rare:95 | ||||
chr19:58183315-58183452 | Rare:47 | ||||
chr19:58278736-58278981 | Common:2; Rare:77 | ||||
chr19:58326875-58327043 | Common:1; Rare:38 | ||||
chr19:58499216-58499523 | Common:2; Rare:92; Clinvar:3 | ||||
chr19:58519770-58520022 | Rare:67 | ||||
chr2:677364-677518 | Common:1; Rare:59 | ||||
chr2:1654400-1654655 | Rare:68 | ||||
chr2:1744400-1744668 | Common:2; Rare:91 | ||||
chr2:3379625-3379771 | Common:2; Rare:59 | ||||
chr2:3519478-3519628 | Common:2; Rare:53 | ||||
chr2:3558251-3558695 | Common:6; Rare:163 | ||||
chr2:3575092-3575358 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423198-9423721 | Rare:150 | ||||
chr2:9474316-9474575 | Common:8; Rare:84 |