chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170720291170720292CT32GENICheterozygous109166920
1170720634170720635GA16GENIChomozygous109166922
1170720813170720814CT28GENIChomozygous109166924
1170720929170720930CA37GENICpossibly homozygous109166926
1170720966170720967AG28GENIChomozygous109166928
1170721027170721028TC35GENICpossibly homozygous109166930
1170721105170721106TC36GENICheterozygous109166932
1170721136170721137TA23GENICheterozygous109166934
1170721170170721171AG18GENICheterozygous109166936
1170721264170721265CA31GENICheterozygous109166942
1170721961170721962CG31GENIChomozygous109166946
1170721996170721997TC31GENICpossibly homozygous109166948
1170722557170722558CT23GENICheterozygous109346570
1170722615170722616TC16GENIChomozygous109166950