chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145146563145146564TC33GENIChomozygous944304818
7145147728145147729CA22GENIChomozygous944304819
7145148101145148102AG30GENIChomozygous944304820
7145148126145148127AG40GENIChomozygous944304821
7145148400145148401TC30GENIChomozygous944304822
7145149929145149930GA29GENIChomozygous944304823
7145149955145149956TC35GENIChomozygous944304824
7145150310145150311CA29GENIChomozygous944304825
7145150986145150987TC30GENIChomozygous944304826
7145151136145151137TC31GENIChomozygous944304827
7145151185145151186TC18GENIChomozygous944304828
7145151315145151316GC23GENIChomozygous944304829
7145151424145151425GC29GENIChomozygous944304830
7145152460145152461TC34GENIChomozygous944304831
7145152860145152861GC21GENIChomozygous944304832
7145153663145153664AG17GENIChomozygous944304833