chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47890606978906070TA25GENIChomozygous112739869
47890658478906585AG44GENIChomozygous112739871
47890664178906642AG32GENIChomozygous113353486
47890905178909052CA35GENIChomozygous112739877
47890914278909143CT33GENICpossibly homozygous113353488
47891073778910738TC29GENIChomozygous112739881
47891226178912262GT35GENIChomozygous113353490
47891629878916299GT26GENIChomozygous112739885
47891056678910567AG32GENIChomozygous113126098
47891550478915505CT42GENIChomozygous113126099
47891600378916004GA27GENIChomozygous113126100
47891685778916858AC17GENIChomozygous113126104
47891699278916993CT17GENIChomozygous113126105
47891856578918566TG34GENIChomozygous113126106
47891912078919121GA28GENIChomozygous113126107
47892118578921186AG39GENIChomozygous112739893
47892216378922164AG39GENIChomozygous113353492
47892216478922165AG42GENICpossibly homozygous113353494
47892261078922611TC33GENIChomozygous113126108
47892292578922926GA13GENICheterozygous113126109