Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48810999-48811135 | Rare:45 | ||||
chr19:48872193-48872449 | Common:2; Rare:83 | ||||
chr19:48954621-48954925 | Common:1; Rare:105 | ||||
chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr19:48993281-48993481 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
chr19:48993553-48993909 | Common:5; Rare:93 | ||||
chr19:49085550-49085629 | Rare:25 | ||||
chr19:49114059-49114416 | Common:4; Rare:92 | ||||
chr19:49155394-49155534 | Rare:27 | ||||
chr19:49335362-49335490 | Common:1; Rare:32 | ||||
chr19:49335596-49335642 | Common:1; Rare:13 | ||||
chr19:49362375-49362473 | Rare:27 | ||||
chr19:49453094-49453311 | Common:1; Rare:69 | ||||
chr19:49526950-49527199 | Rare:37 | ||||
chr19:49527555-49527869 | Common:1; Rare:75 |