chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71182901211829013GT19GENIChomozygous53789461
71182902711829028CCG14GENIChomozygous53789462
71183272211832723AT7GENIChomozygous53789468
71183321511833216AAGAGGAC6GENIChomozygous53789469
71183391611833917CT15GENICpossibly homozygous53789470
71183456511834566TG18GENICpossibly homozygous53789471
71183505111835052TC11GENICheterozygous53789472
71183666911836670GA16GENICpossibly homozygous53789473
71183773511837736CT12GENIChomozygous53789474
71183949611839497AG14GENIChomozygous53789475
71184247411842475CT21GENICheterozygous53789476
71184295011842951AG7GENIChomozygous53789477
71184309111843092GA23GENIChomozygous53789481
71184363311843634CA15GENIChomozygous53789482
71184368111843682CT9GENICpossibly homozygous53789483
71184304711843073ATGCTGTCATGTCGTGATGTCATGTG--------------------------10GENICheterozygous54884904