chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2239069800239069801GA19GENIChomozygous111182530
2239070632239070633TC20GENIChomozygous110329109
2239071980239071981CA26GENIChomozygous110329115
2239074707239074708CT34GENICpossibly homozygous110329121
2239074867239074868GA17GENIChomozygous110329123
2239074997239074998TA21GENIChomozygous110329125
2239075263239075264TC24GENIChomozygous110329127
2239075317239075318TG21GENIChomozygous110329129
2239075776239075777CA14GENIChomozygous110329131
2239076303239076304AT27GENIChomozygous110329133
2239076658239076659TC28GENIChomozygous110329135
2239076793239076794AC26GENIChomozygous110329137
2239077030239077031GA20GENICpossibly homozygous111182532
2239077984239077985CT26GENICpossibly homozygous110329139