chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71260634412606345GA63INTERGENIChomozygous780665782
71260641612606417TC42GENIChomozygous780665783
71260694712606948AT54GENIChomozygous780665784
71260695712606958GA51GENIChomozygous780665785
71260701712607018TG59GENICheterozygous780665786
71260702412607025CT59GENICheterozygous780665787
71260731612607317AG54GENIChomozygous780665788
71260735612607357GA55GENIChomozygous780665789
71260735712607358CA54GENIChomozygous780665790
71260742012607421CA42GENICpossibly homozygous780665791
71260785412607855TC54GENIChomozygous780665792
71260806112608062GC48GENIChomozygous780665793
71260844212608443GA71GENIChomozygous780665794
71260937412609375GT38GENIChomozygous780665795
71260939412609395CT35GENIChomozygous780665796
71260971312609714TC40INTERGENIChomozygous780665797