chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75424008654240087TTG18GENIChomozygous54654733
75424053854240540TG--12GENIChomozygous54654735
75424066654240667TC10GENICheterozygous53926861
75424414354244144GA11GENIChomozygous54654737
75424450654244507TA20GENICpossibly homozygous53926864
75424507554245076CT5GENIChomozygous53926865
75424668554246686GA16GENICpossibly homozygous53926867
75424721254247213TC24GENIChomozygous53926868
75424759754247617AACATTCACGTTTCCAACTC--------------------3GENICheterozygous54654739
75424883754248838GA15GENIChomozygous53926870
75424946454249465AG9GENIChomozygous53926871
75425062854250629CT16GENICheterozygous54654741
75425118254251183GGA9GENIChomozygous54654743
75425202054252021AT1GENIChomozygous53926873
75425457454254575AG2GENIChomozygous54654745
75425526654255267CT13GENIChomozygous53926876
75425528554255286TC14GENIChomozygous53926877
75425592554255929CTTA----1GENIChomozygous54654747
75425685054256851TG13GENIChomozygous53926879
75425762554257626AT18GENICpossibly homozygous54654749
75425828654258287AG20GENIChomozygous54654751
75425891054258911AG17GENIChomozygous53926882
75425997054259971TG8GENICheterozygous53926886
75426147754261479GT--19GENIChomozygous53926888
75426238454262385TC20GENIChomozygous54654753
75426248254262483GA17GENICpossibly homozygous54654755