chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146924200146924201AG23GENIChomozygous112873747
4146924555146924556GA13GENIChomozygous113394374
4146924822146924823CT11GENIChomozygous113394376
4146926799146926800TC20GENIChomozygous113180091
4146927088146927089AG21GENIChomozygous112873749
4146928922146928923AG8GENIChomozygous112873750
4146929263146929264CT18GENIChomozygous113394378
4146930568146930569TC16GENIChomozygous112873752
4146932544146932545TC14GENIChomozygous112873754
4146932641146932642CT7GENIChomozygous112873755
4146933680146933681TC13GENIChomozygous112873756
4146933975146933976CT28GENIChomozygous113394380
4146934115146934116TG13GENIChomozygous112873757
4146936175146936176TC11GENIChomozygous113394384
4146936379146936380TC15GENIChomozygous113394390
4146936262146936263AG20GENIChomozygous113394386
4146936346146936347AG9GENIChomozygous113394388
4146936461146936462TC23GENIChomozygous113394392
4146940904146940905CT22GENIChomozygous113394394
4146942146146942147TC5GENICheterozygous113562817
4146944735146944736GC15GENIChomozygous113394396
4146944814146944815TC23GENIChomozygous113180102
4146944835146944836CT27GENIChomozygous113394398
4146946058146946059TC11GENIChomozygous113180105
4146946272146946273AG14GENIChomozygous113180106
4146946408146946409CT16GENIChomozygous112873771
4146946448146946449CG10GENIChomozygous113394400
4146946875146946876CT19GENIChomozygous113180108
4146946988146946989GA10GENIChomozygous113394402
4146947778146947779TC15GENIChomozygous113180109
4146948636146948637GA18GENIChomozygous113394404
4146948720146948721GA18GENIChomozygous113180110
4146951278146951279TC18GENIChomozygous112873774
4146951604146951605TC24GENIChomozygous112873775
4146952428146952429GA19GENIChomozygous112873777
4146952686146952687AG13GENIChomozygous112873778
4146952707146952708CT17GENIChomozygous112873779
4146936816146936817CA4GENIChomozygous113059245
4146947078146947079AG10GENIChomozygous126101964