chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
669947896994790CT15GENIChomozygous54287762
669948166994817AAGTGTGTGTGTGT6GENIChomozygous55688649
669951966995197CG35GENIChomozygous54287764
669979636997964TC28GENIChomozygous54287765
669991546999155CT33GENIChomozygous54287767
670015387001539TTAC30GENIChomozygous54812628
670015807001582CT--17GENICheterozygous54812629
670015827001586CACA----13GENICheterozygous54287769
670016837001684TTAC33GENICpossibly homozygous54287771
670018827001883TA19GENIChomozygous54287772
670019687001969CT33GENIChomozygous54287773
670019907002000AGCGAGAGAG----------20GENICpossibly homozygous55647444
670042617004262CT42GENIChomozygous54287774
669963146996315CCTG2GENIChomozygous55863244
669980186998019CT25GENIChomozygous56243723
670006677000668CT26GENIChomozygous56243724
670018917001892CT13GENICheterozygous55024747
670059747005975AC24GENIChomozygous55063679
670062587006259CT34GENIChomozygous54287777
670064147006415GA28GENIChomozygous54287778
670065007006501CA33GENIChomozygous54287780
670073067007307AT21GENIChomozygous54287781
670080717008072TC34GENIChomozygous54287782