chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71260634412606345GA18GENIChomozygous958277142
71260641612606417TC18GENIChomozygous958277143
71260694712606948AT22GENIChomozygous958277144
71260695712606958GA21GENIChomozygous958277145
71260701712607018TG19GENIChomozygous958277146
71260702412607025CT22GENIChomozygous958277147
71260731612607317AG17GENIChomozygous958277148
71260735612607357GA16GENIChomozygous958277149
71260735712607358CA16GENIChomozygous958277150
71260742012607421CA23GENICpossibly homozygous958277151
71260785412607855TC34GENIChomozygous958277152
71260806112608062GC35GENIChomozygous958277153
71260844212608443GA26GENIChomozygous958277154
71260937412609375GT23GENICpossibly homozygous958277155
71260939412609395CT27GENIChomozygous958277156
71260971312609714TC18GENIChomozygous958277157