chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832057478320575AG23GENIChomozygous789292940
47832062078320621AC19GENIChomozygous789292941
47832063878320639CA14GENIChomozygous789292942
47832081578320816GA14GENIChomozygous789292943
47832140078321401TC26GENIChomozygous789292944
47832144778321448TA28GENIChomozygous789292945
47832274678322747CA26GENIChomozygous789292946
47832291378322914TA21GENIChomozygous789292947
47832291878322919CA22GENICpossibly homozygous789292948
47832306478323065CT28GENIChomozygous789292949
47832315378323154GA26GENIChomozygous789292950
47832367778323678GA20GENIChomozygous789292951
47832382878323829TC20GENIChomozygous789292952
47832399678323997GA15GENIChomozygous789292953
47832419778324198CT30GENIChomozygous789292954
47832429778324298CT26GENIChomozygous789292955
47832433978324340GT19GENIChomozygous789292956
47832469278324693TA28GENIChomozygous789292957
47832473778324738GC22GENIChomozygous789292958
47832505378325054AG25GENIChomozygous789292959
47832524978325250CT13GENIChomozygous789292960
47832595578325956AG29GENIChomozygous789292961
47832653078326531AG29GENIChomozygous789292962
47832659078326591AG22GENIChomozygous789292963
47832682978326830TC26GENIChomozygous789292964
47832691478326915AG29GENIChomozygous789292965
47832703778327038TC23GENICpossibly homozygous789292966