chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144162539144162539CCT56GENIChomozygous128249721
5144163972144163973CT34GENIChomozygous114036704
5144164471144164472TA27GENIChomozygous114253947
5144164535144164535CCAAGATG29GENIChomozygous128249722
5144164589144164590CT41GENIChomozygous114253949
5144164594144164595TG42GENIChomozygous114253951
5144166417144166418GT63GENIChomozygous114036705
5144167500144167501CG43GENIChomozygous114253953
5144167565144167566TC34GENIChomozygous114036706
5144169769144169770AT50GENIChomozygous114253955
5144169921144169922TC52GENIChomozygous114036707
5144169938144169939AG53GENIChomozygous114036708
5144171171144171172AG53GENIChomozygous114036709
5144172133144172134GA51GENIChomozygous114253957
5144172935144172936CT46GENIChomozygous114253959
5144173916144173917CT39GENIChomozygous114253961
5144174710144174711TC18GENIChomozygous114036711
5144174847144174847T43GENICpossibly homozygous128249725
5144175239144175240GT58GENIChomozygous114036712
5144176574144176575CA46GENIChomozygous114152226
5144176990144176991GC74GENIChomozygous114152227