chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48555217185552172CG55GENICpossibly homozygous112761848
48555298085552981AG47GENIChomozygous112761850
48555391485553915CA48GENIChomozygous112761852
48555444485554445CT63GENIChomozygous112761854
48555462085554621TC54GENIChomozygous112761856
48555506285555063AG48GENIChomozygous112761858
48555659385556594GA44GENIChomozygous112761860
48555680485556805TC47GENIChomozygous112761862
48555742285557423GA55GENIChomozygous112761864
48555814785558148TA63GENIChomozygous112761866
48555828185558282CT51GENICpossibly homozygous112761868
48555889485558895TC36GENIChomozygous112761870
48555903285559033TC54GENIChomozygous112761872
48555905285559053TA57GENIChomozygous112761874
48556048685560487CA54GENIChomozygous112761876
48556067185560672GA51GENICpossibly homozygous112761878
48556079885560799GA55GENIChomozygous112761880
48556188385561884GA32GENIChomozygous112761882
48556215685562157CT36GENIChomozygous112761884
48556274085562741TC57GENIChomozygous112761886
48556342785563428CT37GENIChomozygous112761888
48556343185563432GA34GENIChomozygous112761890