chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124790436047904361CT11GENIChomozygous986058858
124790442847904429AG6GENIChomozygous986058859
124790503947905040GC10GENIChomozygous986058860
124790505747905058CT11GENIChomozygous986058861
124790533247905333GA5GENIChomozygous986058862
124790592447905925TC13GENIChomozygous986058863
124790718647907187TC17GENIChomozygous986058864
124790723447907235CT15GENIChomozygous986058865
124790755047907551AG10GENIChomozygous986058866
124790807447908075GA10GENIChomozygous986058867
124790818247908183TC17GENIChomozygous986058868
124790853147908532CT13GENIChomozygous986058869
124790978347909784GT8GENIChomozygous986058870
124791088247910883GA10GENIChomozygous986058871
124791103247911033AG13GENIChomozygous986058872
124791118647911187CT9GENIChomozygous986058873
124791211047912111GA10GENIChomozygous986058874
124791214247912143AG10GENIChomozygous986058875
124791233847912339CT16GENIChomozygous986058876
124791237847912379CT14GENIChomozygous986058877
124791329847913299TC10GENIChomozygous986058878
124791396147913962CA7GENIChomozygous986058879
124791396447913965CA7GENIChomozygous986058880
124791409447914095GA7GENIChomozygous986058881
124791421247914213GA4GENIChomozygous986058882
124791539147915392TC18GENIChomozygous986058883
124791703447917035GA17GENIChomozygous986058884
124791720847917209TC17GENIChomozygous986058885
124791936847919369TC15GENIChomozygous986058886
124791985847919859AC13GENIChomozygous986058887