chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6105596437105596438GC14GENIChomozygous54611729
6105596686105596687CT12GENICpossibly homozygous54611730
6105597552105597553GA16GENICpossibly homozygous54611731
6105599527105599528GA30GENIChomozygous54611732
6105599680105599681CT16GENIChomozygous54611733
6105599876105599877CA15GENIChomozygous54611734
6105600153105600154CT22GENICpossibly homozygous54611735
6105600855105600856GGA7GENIChomozygous54611736
6105601727105601728GA23GENIChomozygous54611737
6105602073105602074GC22GENIChomozygous54611738
6105603063105603064AT13GENICheterozygous54611739
6105603133105603134TC31GENIChomozygous54611740