chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47721302777213028CT11GENIChomozygous113350950
47721797977217980GA31GENIChomozygous112735709
47722388077223881TC27GENIChomozygous112735713
47722388177223882TC27GENIChomozygous112735715
47722788977227890AG37GENIChomozygous112735721
47722991177229912AT21GENIChomozygous113350952
47723058377230584GT29GENIChomozygous119434279
47723338077233381TG43GENIChomozygous113350954
47723793077237931AT27GENIChomozygous113350956
47724072377240724CT21GENIChomozygous113350958
47724514377245144TC30GENIChomozygous112735739
47724614277246143TC37GENIChomozygous112735743
47724833577248336TC21GENIChomozygous113350960
47725002377250024TA37GENIChomozygous119307310
47725002577250026AG35GENIChomozygous119307312
47725516277255163GA23GENIChomozygous112735753
47725521477255215CT20GENIChomozygous113350962
47725601077256011TA29GENIChomozygous113350964
47725628577256286GA32GENIChomozygous113350966
47726255477262555GA43GENIChomozygous113350968
47726429377264294GA18GENIChomozygous113350970
47726824977268250CT32GENIChomozygous112735775
47726857477268575CG22GENIChomozygous113350972
47727241777272418TG30GENIChomozygous112735792
47727348577273486AC33GENIChomozygous113350974
47727577277275773GA48GENIChomozygous112735794
47727942677279427AG49GENIChomozygous112735796
47728059377280594CT35GENIChomozygous113350976
47728145177281452AC23GENIChomozygous113350978
47725818677258187CA13GENICheterozygous119461955