chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47289798672897987GT9GENIChomozygous112711893
47289816372898164CT10GENIChomozygous112711895
47289874772898748CT16GENIChomozygous112711897
47289899772898998GA10GENIChomozygous112711899
47289911772899118TC9GENIChomozygous112711901
47289928272899283AG13GENIChomozygous112711903
47289955472899555TG15GENIChomozygous112711905
47290118072901181CT19GENIChomozygous112711909
47290121272901213GA17GENIChomozygous112711911
47290200372902004AG25GENIChomozygous112711913
47290346472903465TC14GENIChomozygous112711917
47290417072904171TC25GENIChomozygous112711919
47290469172904692GC21GENIChomozygous112711921
47290502972905030GC27GENIChomozygous112711923
47290590172905902AG15GENIChomozygous112711925
47290605572906056AT13GENICpossibly homozygous112711927
47290620572906206GA13GENIChomozygous112711929
47290647272906473AG14GENIChomozygous112711931
47290683772906838TA8GENIChomozygous112711935
47290756672907567GT11GENIChomozygous112711937
47290802172908022CG12GENIChomozygous112711939
47290803172908032CG13GENIChomozygous112711941
47290856972908570TA13GENIChomozygous112711943
47290888772908888GA15GENIChomozygous112711945
47290926872909269AG13GENIChomozygous112711947
47290929772909298GA17GENIChomozygous112711949
47290959872909599CG16GENIChomozygous112711951
47290974472909745TC24GENIChomozygous112711953
47291018472910185CG11GENIChomozygous113237777
47290011672900117CT21GENIChomozygous113237773
47290206572902066AG27GENIChomozygous113237774
47290444672904447AC16GENIChomozygous113237775
47290793072907931GA14GENIChomozygous113237776
47291059972910600TA15GENIChomozygous112711955
47291083472910835TC17GENIChomozygous112711959
47291087972910880GA15GENIChomozygous112711961
47291142772911428GA22GENIChomozygous112711963