chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71171269811712699GA53GENIChomozygous116003649
71171458811714589CT64GENICpossibly homozygous115568906
71171749011717491TC24GENIChomozygous115568908
71171817311718174GA60GENIChomozygous115568909
71171820011718201GC62GENIChomozygous115568910
71171824611718247GC70GENIChomozygous115568911
71171825711718258CT70GENICpossibly homozygous115568912
71171931511719316TC66GENICpossibly homozygous115568913
71172005411720055AT61GENIChomozygous115568914
71172008111720082GT62GENIChomozygous115568915
71172093911720940CT75GENICpossibly homozygous115568916
71172110911721110GA48GENICpossibly homozygous115568917
71172118511721186AG47GENIChomozygous115568918
71172141011721411GT54GENIChomozygous115568919
71172293211722933TG59GENICpossibly homozygous115568920
71172348511723486CA60GENICpossibly homozygous116003650
71172374911723750AG50GENIChomozygous115568921
71172405711724058CT62GENIChomozygous115568922
71172413711724138TC63GENIChomozygous115568923
71172426111724262TC77GENIChomozygous115568924