chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154832973848329739AG12GENIChomozygous112502721
154833058748330588TC16GENIChomozygous112502723
154833103148331032GA19GENIChomozygous112502725
154833281248332812TGCATGT3GENIChomozygous129253787
154833282248332823G3GENIChomozygous129253788
154833283048332830A2GENIChomozygous129253789
154833366148333662CT23GENIChomozygous112502727
154833373848333739CG22GENIChomozygous112502730
154833619248336193AG20GENIChomozygous112502732
154833625848336258C22GENIChomozygous129253790
154833900248339002TT16GENIChomozygous129253791
154833918248339183AC20GENIChomozygous112502734
154833930248339303GA11GENIChomozygous112502736
154833940948339410GA2GENIChomozygous112502738
154834289748342898GA22GENICpossibly homozygous112502740
154834434448344345GA7GENIChomozygous112502742
154834501548345016AG23GENIChomozygous112502744
154834842048348421A19GENIChomozygous129253792
154834855748348558AG8GENIChomozygous112502746
154835134048351341C18GENIChomozygous129253793
154835135348351353C22GENIChomozygous129253794
154835670048356701AG12GENIChomozygous112502756
154835300948353010AG13GENIChomozygous112502748
154835386348353864GA14GENIChomozygous112502750
154835504448355045GA13GENIChomozygous112502752
154835669948356700CG12GENIChomozygous112502754
154835358248353583GA17GENIChomozygous112809018
154835753248357532T13GENIChomozygous129253795
154835925648359257CT13GENIChomozygous112502758
154836000948360010CT20GENIChomozygous112502760
154836482648364827TA15GENIChomozygous112502762
154836640548366406GC19GENIChomozygous112502766
154836784448367845TC16GENIChomozygous112502768
154836816648368167GA17GENIChomozygous112502770
154837018848370189T12GENICheterozygous129253796
154837037048370370T11GENIChomozygous129253797
154837600348376004TC15GENIChomozygous112502772
154837634648376346TCTCT15GENIChomozygous129253798
154837734848377349CA11GENIChomozygous125777443