chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4118241097118241098AT28GENIChomozygous112821720
4118242641118242642AG16GENIChomozygous112821722
4118243711118243712CT9GENIChomozygous112821724
4118244850118244851AG41GENICpossibly homozygous112821726
4118245852118245853AG28GENIChomozygous112821728
4118246729118246730AG27GENIChomozygous112821730
4118253725118253726GA38GENICpossibly homozygous112821732
4118255057118255058GC21GENIChomozygous112821734
4118256600118256601TC29GENICpossibly homozygous112821736
4118259196118259197TG30GENIChomozygous112821738
4118267193118267194TG37GENIChomozygous112821740