chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144162539144162539CCT22GENIChomozygous128249721
5144163972144163973CT19GENIChomozygous114036704
5144164471144164472TA16GENIChomozygous114253947
5144164535144164535CCAAGATG11GENIChomozygous128249722
5144164589144164590CT15GENIChomozygous114253949
5144164594144164595TG15GENIChomozygous114253951
5144166417144166418GT15GENIChomozygous114036705
5144167500144167501CG8GENIChomozygous114253953
5144167565144167566TC10GENIChomozygous114036706
5144169769144169770AT23GENIChomozygous114253955
5144169921144169922TC17GENIChomozygous114036707
5144169938144169939AG21GENIChomozygous114036708
5144171171144171172AG13GENIChomozygous114036709
5144172133144172134GA14GENIChomozygous114253957
5144172935144172936CT14GENIChomozygous114253959
5144173916144173917CT18GENIChomozygous114253961
5144174710144174711TC9GENIChomozygous114036711
5144174847144174847T18GENICpossibly homozygous128249725
5144175239144175240GT10GENIChomozygous114036712
5144176574144176575CA22GENIChomozygous114152226
5144176990144176991GC22GENIChomozygous114152227