chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47890606978906070TA37GENIChomozygous112739869
47890658478906585AG16GENIChomozygous112739871
47890905178909052CA23GENICpossibly homozygous112739877
47891073778910738TC22GENIChomozygous112739881
47891629878916299GT20GENIChomozygous112739885
47891630578916306TA21GENIChomozygous113126101
47891056678910567AG20GENIChomozygous113126098
47891550478915505CT27GENIChomozygous113126099
47891600378916004GA17GENIChomozygous113126100
47891654378916544TC36GENIChomozygous113126102
47891682778916828TG21GENIChomozygous113126103
47891685778916858AC21GENIChomozygous113126104
47891699278916993CT28GENIChomozygous113126105
47891856578918566TG22GENIChomozygous113126106
47891912078919121GA24GENIChomozygous113126107
47892118578921186AG20GENIChomozygous112739893
47892198278921983AT18GENIChomozygous112739899
47892261078922611TC18GENIChomozygous113126108
47892292578922926GA10GENIChomozygous113126109
47892327478923275GA32GENIChomozygous113126110