chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143066632143066633AG32GENIChomozygous659682876
4143067173143067174TA50GENIChomozygous659682877
4143067462143067463AG37GENIChomozygous659682878
4143067604143067605CT39GENIChomozygous659682879
4143067911143067912TC36GENIChomozygous659682880
4143068188143068191CGT---20GENIChomozygous762832992
4143068398143068399CT18GENIChomozygous659682881
4143068496143068497GA29GENIChomozygous659682882
4143068696143068697AG21GENICpossibly homozygous659682883
4143068742143068743AG34GENIChomozygous659682884
4143068974143068975T-5GENIChomozygous762832995
4143068982143068983TC8GENIChomozygous659682885
4143069523143069524AC20GENIChomozygous659682886
4143070410143070411CT42GENIChomozygous659682887
4143070429143070430TC41GENIChomozygous659682888
4143070847143070848AG46GENIChomozygous659682889
4143070907143070908GT23GENIChomozygous659682890
4143071028143071029CA15GENIChomozygous659682891
4143071303143071304GT26GENIChomozygous659682892
4143071608143071609GA16GENIChomozygous659682893
4143071742143071743AC17GENIChomozygous659682894