chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120486290120486291CT33GENIChomozygous115856434
7120486452120486453CT27GENIChomozygous115856436
7120487442120487443AG35GENIChomozygous115856438
7120487484120487485AG32GENIChomozygous115856440
7120488409120488410CT27GENIChomozygous115856442
7120488703120488704TC25GENIChomozygous115856444
7120488751120488752CA23GENICpossibly homozygous115856446
7120488861120488862TC28GENIChomozygous115856448
7120488011120488012TC20GENIChomozygous118259107
7120488007120488007C18GENIChomozygous128512251
7120489380120489384TGTA29GENIChomozygous128512252