chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144161887144161888CT22GENIChomozygous114036701
5144163041144163042CT25GENIChomozygous114036702
5144163151144163152CA17GENIChomozygous114036703
5144163972144163973CT17GENIChomozygous114036704
5144166417144166418GT23GENIChomozygous114036705
5144167565144167566TC17GENIChomozygous114036706
5144169921144169922TC26GENIChomozygous114036707
5144169938144169939AG26GENIChomozygous114036708
5144171171144171172AG15GENIChomozygous114036709
5144171210144171211GC16GENIChomozygous114036710
5144162539144162539CCT25GENIChomozygous128249721
5144164535144164535CCAAGATG10GENIChomozygous128249722
5144170280144170281C17GENIChomozygous128249723
5144174150144174150A21GENIChomozygous128249724
5144174710144174711TC13GENIChomozygous114036711
5144174847144174847T12GENICpossibly homozygous128249725
5144175239144175240GT13GENIChomozygous114036712
5144175369144175370GA17GENIChomozygous114036713
5144175453144175454CT13GENIChomozygous114036714
5144177340144177341AG25GENIChomozygous114036715
5144177820144177821AG18GENIChomozygous114036716
5144173685144173686CA24GENIChomozygous118846232