chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76348034063480341TG14GENIChomozygous141984763
76348045263480453CT14GENIChomozygous141984764
76348059563480595G22GENIChomozygous141917882
76348083263480833TC29GENIChomozygous141984765
76348099063480990A23GENIChomozygous141917883
76348122063481221GA24GENIChomozygous141984766
76348131263481313CT16GENIChomozygous141984767
76348153163481550TGGGAGTAAGAACTCGGAG23GENIChomozygous141917884
76348184063481841TC25GENIChomozygous141984768
76348269163482692CT25GENIChomozygous141984769
76348396463483965AG28GENIChomozygous141984770
76348422863484229TC24GENIChomozygous141984771
76348568763485688GA29GENIChomozygous141984772
76348668363486684CT35GENIChomozygous141984773
76348732163487322TC27GENIChomozygous141984774
76348760463487605AG25GENIChomozygous141984775
76348762763487628AG25GENIChomozygous141984776
76348790963487910AG30GENIChomozygous141984777
76348875063488751CT31GENIChomozygous141984778
76348907763489078CT25GENIChomozygous141984779
76348910463489105TC27GENIChomozygous141984780
76349095163490952CT8GENIChomozygous141984781
76349185163491852AC5GENIChomozygous141984782
76349196763491968T14GENICpossibly homozygous141917888
76348644963486449TTTTG16GENIChomozygous141917885
76348976863489768ACA16GENICpossibly homozygous141917886
76349086963490869G15GENIChomozygous141917887
76349121263491213GC12GENIChomozygous138104548
76348629263486292T21GENICheterozygous143348134
76349462263494623TC27GENIChomozygous141984785
76349291963492920CG21GENIChomozygous141984783
76349408863494089AG46GENIChomozygous138104550
76349410363494104AG45GENIChomozygous141984784
76349470363494704AG25GENIChomozygous141984786
76349518663495216CCCCCTCCCTCCACCTGCCCATCAACCTTT2GENIChomozygous144781065
76349566063495661CT6GENIChomozygous138104551
76349600263496003AG16GENIChomozygous138104552
76349698563496986TC13GENIChomozygous138104554