chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144162539144162539CCT14GENIChomozygous128249721
5144163972144163973CT12GENIChomozygous114036704
5144164535144164535CCAAGATG12GENIChomozygous128249722
5144166417144166418GT14GENIChomozygous114036705
5144167565144167566TC10GENIChomozygous114036706
5144169921144169922TC15GENIChomozygous114036707
5144169938144169939AG16GENIChomozygous114036708
5144171171144171172AG23GENIChomozygous114036709
5144172935144172936CT21GENIChomozygous114253959
5144164471144164472TA17GENIChomozygous114253947
5144164589144164590CT12GENIChomozygous114253949
5144164594144164595TG12GENIChomozygous114253951
5144167500144167501CG9GENIChomozygous114253953
5144169769144169770AT8GENIChomozygous114253955
5144172133144172134GA18GENIChomozygous114253957
5144173916144173917CT15GENIChomozygous114253961
5144174710144174711TC12GENIChomozygous114036711
5144174847144174847T14GENIChomozygous128249725
5144175239144175240GT7GENIChomozygous114036712
5144176574144176575CA15GENIChomozygous114152226
5144176990144176991GC14GENIChomozygous114152227