chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120486290120486291CT57GENIChomozygous115856434
7120486452120486453CT62GENIChomozygous115856436
7120486896120486897C54GENIChomozygous132866419
7120487382120487383CT48GENIChomozygous116303167
7120487442120487443AG57GENIChomozygous115856438
7120487484120487485AG65GENIChomozygous115856440
7120488409120488410CT54GENICpossibly homozygous115856442
7120488703120488704TC55GENIChomozygous115856444
7120488751120488752CA54GENICpossibly homozygous115856446
7120488861120488862TC51GENIChomozygous115856448
7120489879120489880AC25GENICheterozygous116303168
7120489954120489956CT43GENIChomozygous132866420
7120489997120489998GA64GENIChomozygous116303169
7120488011120488012TC43GENIChomozygous118259107
7120488007120488007C39GENIChomozygous128512251
7120489380120489384TGTA56GENIChomozygous128512252