chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85959412459594125CA28GENIChomozygous53272590
85959453359594534CT35GENIChomozygous53272591
85959506159595062TC33GENIChomozygous52664068
85959524359595244TC41GENIChomozygous53272592
85959655959596560TC26GENIChomozygous53272594
85959699959597058TATTATAGGAAATAGATAATTTTACTTTTTCCTCTCCAGCTTGGATCAATTTTATTTAC-----------------------------------------------------------3GENIChomozygous53388679
85959610559596106GA23GENIChomozygous54149312
85959641359596414CT28GENIChomozygous54149314
85959682859596829TC9GENIChomozygous53388675
85959683059596831CCAGTT8GENIChomozygous53388676
85959683359596834TTAGAGCGC7GENIChomozygous53388677
85959683559596836TTGC5GENIChomozygous53388678
85959723759597238CT24GENIChomozygous53272595
85959725659597257GGTGTAA23GENIChomozygous53272597
85959736559597366CA16GENIChomozygous53272598
85959743059597431CCAA21GENICheterozygous52664080
85959743059597431CCA21GENICpossibly homozygous52664082
85959762759597628AG26GENIChomozygous54149316
85959764859597649AG26GENIChomozygous54149318
85959768759597688GA29GENIChomozygous53272601
85959778759597788GA23GENIChomozygous54149320
85959866859598669A-24GENIChomozygous52983292
85959927659599277CT38GENIChomozygous53272602
85959929159599292CT35GENIChomozygous53272603
85959974559599746GA35GENIChomozygous54149322
85960078959600790TC36GENIChomozygous54149324
85960240259602403TTA29GENIChomozygous53272604
85960261659602617TA28GENIChomozygous53272605
85960328159603282AG22GENIChomozygous52664084
85960398859603989TC28GENIChomozygous52664086
85960405559604056GA17GENIChomozygous53272606
85960441259604413GA24GENIChomozygous54149326
85960449459604495CA37GENIChomozygous53272607
85960509259605093T-18GENIChomozygous52664090
85960524059605241T-15GENICpossibly homozygous53364020
85960659959606600AAAAAC30GENIChomozygous52664096
85960672159606722GT41GENIChomozygous53272610
85960533359605334AAC12GENIChomozygous53122433
85960497659604977GGAAAAAAAA14GENICheterozygous53388680