chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47890606978906070TA11GENIChomozygous112739869
47890658478906585AG15GENIChomozygous112739871
47890689478906895TA22GENIChomozygous119390733
47890905178909052CA18GENIChomozygous112739877
47891056678910567AG24GENIChomozygous113126098
47891073778910738TC20GENIChomozygous112739881
47891550478915505CT18GENIChomozygous113126099
47891557878915584ACACCC16GENIChomozygous131354291
47891600378916004GA18GENIChomozygous113126100
47891629878916299GT24GENIChomozygous112739885
47891630578916306TA23GENIChomozygous113126101
47891685778916858AC20GENIChomozygous113126104
47891699278916993CT19GENIChomozygous113126105
47891788278917883T15GENIChomozygous128052371
47891527078915271C16GENIChomozygous128052369
47891856578918566TG19GENIChomozygous113126106
47891912078919121GA33GENIChomozygous113126107
47891992178919921AAAG27GENIChomozygous131354292
47892118578921186AG16GENIChomozygous112739893
47892198278921983AT24GENIChomozygous112739899
47892216278922162CGGA27GENIChomozygous131354293
47892233478922335CT17GENIChomozygous119517372
47892240878922409A14GENIChomozygous128052373
47892261078922611TC15GENIChomozygous113126108
47892292578922926GA5GENIChomozygous113126109
47892293878922939A3GENIChomozygous128052374