chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1695990716959908G-19GENICpossibly homozygous45098658
X1696017016960171G-14GENIChomozygous45098659
X1696018216960183TA20GENIChomozygous45098660
X1697459816974599T-10GENICheterozygous45098661
X1698081116980812AG15GENIChomozygous45098662