chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47890606978906070TA24GENIChomozygous112739869
47890658478906585AG27GENIChomozygous112739871
47890905178909052CA31GENIChomozygous112739877
47891073778910738TC26GENIChomozygous112739881
47890689478906895TA19GENIChomozygous119390733
47891056678910567AG26GENIChomozygous113126098
47891550478915505CT21GENIChomozygous113126099
47891600378916004GA23GENIChomozygous113126100
47891629878916299GT15GENIChomozygous112739885
47891630578916306TA15GENIChomozygous113126101
47891685778916858AC17GENIChomozygous113126104
47891699278916993CT29GENIChomozygous113126105
47891856578918566TG26GENIChomozygous113126106
47891912078919121GA27GENIChomozygous113126107
47892118578921186AG20GENIChomozygous112739893
47892198278921983AT20GENIChomozygous112739899
47892261078922611TC23GENIChomozygous113126108
47892292578922926GA8GENIChomozygous113126109
47892296178922961AAAAAAAC6GENIChomozygous133729759
47891557878915584ACACCC19GENIChomozygous131354291
47891992178919921AAAG20GENIChomozygous131354292
47892216278922162CGGA19GENIChomozygous131354293
47891527078915271C25GENIChomozygous128052369
47891788278917883T13GENIChomozygous128052371
47892240878922409A19GENIChomozygous128052373
47892293878922939A7GENIChomozygous128052374