chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120486290120486291CT47GENIChomozygous115856434
7120486452120486453CT57GENIChomozygous115856436
7120487442120487443AG73GENIChomozygous115856438
7120487484120487485AG69GENIChomozygous115856440
7120488409120488410CT37GENIChomozygous115856442
7120488703120488704TC54GENIChomozygous115856444
7120488751120488752CA48GENICpossibly homozygous115856446
7120488861120488862TC51GENIChomozygous115856448
7120488011120488012TC47GENIChomozygous118259107
7120489380120489384TGTA40GENIChomozygous128512252
7120488007120488007C45GENIChomozygous128512251