chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144162539144162539CCT39GENIChomozygous128249721
5144163972144163973CT56GENIChomozygous114036704
5144164535144164535CCAAGATG35GENIChomozygous128249722
5144166417144166418GT45GENIChomozygous114036705
5144167500144167501CG45GENIChomozygous114253953
5144164471144164472TA34GENIChomozygous114253947
5144164589144164590CT40GENIChomozygous114253949
5144164594144164595TG40GENIChomozygous114253951
5144167565144167566TC45GENIChomozygous114036706
5144169769144169770AT37GENIChomozygous114253955
5144169921144169922TC62GENIChomozygous114036707
5144169938144169939AG61GENIChomozygous114036708
5144171171144171172AG50GENIChomozygous114036709
5144172133144172134GA53GENICpossibly homozygous114253957
5144172935144172936CT60GENIChomozygous114253959
5144173916144173917CT35GENIChomozygous114253961
5144174710144174711TC12GENIChomozygous114036711
5144174847144174847T23GENIChomozygous128249725
5144175239144175240GT27GENIChomozygous114036712
5144176574144176575CA41GENICpossibly homozygous114152226
5144176990144176991GC69GENIChomozygous114152227