chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189901293189901294AT37GENICpossibly homozygous110805149
2189901598189901599CT37GENIChomozygous110172193
2189901605189901606TC38GENIChomozygous110172195
2189901611189901612CA37GENIChomozygous110172197
2189901666189901667TC38GENICpossibly homozygous110172199
2189903318189903319CT42GENIChomozygous110172214