chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46273435862734359GGACACACACAC2GENIChomozygous58443874
46273606862736069CT27GENIChomozygous56919119
46273774462737745CT28GENIChomozygous56919120
46273779562737796AAT29GENICheterozygous56919121
46273779562737796AATT29GENICheterozygous57330820
46273795162737975TGTGTGTGTGTGTGTGTGTGTGTG------------------------14GENIChomozygous58280527
46273909462739097CAG---29GENIChomozygous56919125
46273940962739410T-18GENIChomozygous57835647
46273952962739530AG24GENIChomozygous56919126
46274022662740227TTC17GENICpossibly homozygous56919128
46274048562740486TC19GENIChomozygous56919129
46274083562740836A-15GENIChomozygous56919130
46274296562742966CT18GENIChomozygous56919131
46274705962747060CT28GENIChomozygous56919132
46274797962747980AAT27GENICpossibly homozygous56919133
46274877162748772CT28GENIChomozygous56919134
46274978362749784A-20GENIChomozygous56919135
46275007962750089CACACACACA----------1GENIChomozygous56919136
46275287362752874TC23GENIChomozygous56919138
46275322862753229CA25GENIChomozygous56919139
46275355462753555CG28GENIChomozygous56919140
46275424662754247CA14GENIChomozygous56919141
46275523162755232TTA26GENIChomozygous56919142
46275537762755378G-21GENIChomozygous56919143
46275707962757080TA36GENIChomozygous56919144
46275806862758069TTG31GENIChomozygous56919145
46275845162758458AACTGCA-------24GENIChomozygous56919146