chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127145067127145068T23GENIChomozygous128645943
8127145084127145084A28GENIChomozygous128645944
8127145135127145135A36GENIChomozygous128645945
8127145142127145142GG36GENIChomozygous128645946
8127145144127145144C36GENIChomozygous128645947
8127145155127145155CC41GENIChomozygous128645948
8127145343127145343C43GENIChomozygous128645949
8127145400127145401AC27GENIChomozygous116715793
8127145412127145412G24GENIChomozygous128645950
8127145434127145434C16GENIChomozygous128645951
8127145441127145441C15GENIChomozygous128645952
8127145447127145448T12GENIChomozygous128645953
8127145504127145504C6GENIChomozygous128645955
8127145514127145514G8GENIChomozygous128645956
8127145526127145527GC10GENIChomozygous116715795
8127145617127145617A9GENIChomozygous128645960
8127145566127145566G6GENIChomozygous128645957
8127145577127145578T8GENIChomozygous128645958
8127145593127145593C9GENIChomozygous128645959
8127145635127145637CT10GENIChomozygous128645961
8127145920127145921CG27GENIChomozygous116715797
8127146001127146002A22GENIChomozygous128645962
8127146008127146008G22GENIChomozygous128645963
8127146013127146013G21GENIChomozygous128645964
8127146064127146065G7GENIChomozygous128645965
8127148479127148479T9GENIChomozygous128645966