chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71244078312440784TC71GENIChomozygous115569960
71244439012444391AC55GENIChomozygous115569961
71244879512448796CA64GENIChomozygous115569963
71244889412448895GA68GENIChomozygous115569964
71244957912449580GA41GENIChomozygous115569966
71245195612451957GA44GENIChomozygous115569967
71245200712452008GA40GENIChomozygous115569968
71245200812452009GA40GENIChomozygous115569969
71245227812452279AG44GENIChomozygous115569970
71245255412452555AG49GENIChomozygous115569971
71245421712454218CG53GENICpossibly homozygous115569972
71245466512454666CT56GENIChomozygous115569974
71245514412455145CT60GENIChomozygous115569975
71245525412455255CG55GENIChomozygous115569977
71245555812455559AG46GENIChomozygous115569984
71245556912455570CT43GENIChomozygous115569985
71245449312454494GA60GENIChomozygous116274599
71245547412455474GG31GENIChomozygous131673822
71244378212443785CCT49GENIChomozygous128435765
71245544912455449G17GENICheterozygous132981760
71245547312455473A32GENIChomozygous131673821
71245556612455567CA45GENIChomozygous131683060
71245587012455871GA67GENIChomozygous116274603
71245617212456175GTC58GENIChomozygous131673823
71245680012456801G50GENIChomozygous131673824