chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47289816372898164CT17GENIChomozygous112711895
47289831672898317CT19GENIChomozygous113116780
47289874772898748CT25GENIChomozygous112711897
47289899772898998GA25GENIChomozygous112711899
47289911772899118TC24GENIChomozygous112711901
47289928272899283AG21GENIChomozygous112711903
47290012072900121GA25GENIChomozygous113116781
47290047472900475GA22GENIChomozygous113116783
47290121272901213GA24GENIChomozygous112711911
47290199572901996CA20GENIChomozygous113116784
47290200372902004AG20GENIChomozygous112711913
47290346472903465TC26GENIChomozygous112711917
47290384372903844CT23GENIChomozygous113116786
47290384672903847CT23GENIChomozygous113116787
47290437472904375TG22GENIChomozygous113116789
47290442772904428GC19GENIChomozygous119306809
47290469172904692GC25GENIChomozygous112711921
47290500372905004TC20GENIChomozygous113116790
47290502972905030GC21GENIChomozygous112711923
47290590172905902AG25GENIChomozygous112711925
47290605572906056AT22GENIChomozygous112711927
47290620572906206GA28GENIChomozygous112711929
47290647272906473AG24GENIChomozygous112711931
47290683772906838TA19GENIChomozygous112711935
47290756672907567GT23GENIChomozygous112711937
47290802172908022CG17GENIChomozygous112711939
47290803172908032CG18GENIChomozygous112711941
47290856972908570TA17GENIChomozygous112711943
47290888772908888GA27GENIChomozygous112711945
47290901872909019GA32GENIChomozygous113116791
47290926872909269AG33GENIChomozygous112711947
47290929772909298GA33GENIChomozygous112711949
47290959872909599CG18GENIChomozygous112711951
47290974472909745TC24GENIChomozygous112711953
47291059972910600TA29GENIChomozygous112711955
47291083472910835TC26GENIChomozygous112711959
47291087972910880GA24GENIChomozygous112711961
47291142772911428GA34GENIChomozygous112711963