chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
88002383580023836TTA1GENIChomozygous52677840
88002424080024246TTTTTG------4GENICheterozygous53850777
88002945980029460GA18GENIChomozygous53130575
88003058280030583C-5GENIChomozygous53130577
88003084980030850CT19GENICpossibly homozygous53130579
88003121780031218AG25GENIChomozygous53130581
88003134680031347GC14GENICheterozygous53130583
88003155380031554CT16GENICpossibly homozygous53130585
88003185180031852GA7GENIChomozygous53130587
88003297680032977AG35GENIChomozygous53130588
88003399680033997CA20GENIChomozygous53130590
88003422880034229AG24GENIChomozygous53130592
88003463280034633AC13GENIChomozygous53130594
88003568980035690GA17GENIChomozygous53130596
88003620480036206TG--1GENIChomozygous53130605
88003625280036253CT6GENICheterozygous53130607
88003627680036278TG--4GENICheterozygous53130609
88003631280036332TGTGTGTATGTGTGTGTGTC--------------------2GENIChomozygous53130611
88003757080037571GA17GENICheterozygous53130615
88003939780039398AG8GENIChomozygous53130617
88003950880039509CT21GENIChomozygous53130619
88004040680040407TC22GENIChomozygous53130621
88004084580040846AG17GENICpossibly homozygous53130623
88004148380041484AG15GENIChomozygous53130643
88004276080042761AAT4GENIChomozygous53130649
88004316680043167AG12GENICheterozygous53130651
88004340780043408CT4GENICheterozygous53130653
88004398180043982TG22GENICpossibly homozygous53130655
88004400780044008CG19GENIChomozygous53130657
88004411880044126CTCCCTCC--------2GENIChomozygous53130659
88004430580044306GGC5GENIChomozygous53130661
88004549580045496CT24GENIChomozygous53130662
88004598480045985CT22GENICheterozygous53130664
88004733980047340AG16GENIChomozygous53130668
88004762180047622AG1GENIChomozygous53130670
88004762780047628TC3GENIChomozygous53130672
88004873880048739TC20GENICpossibly homozygous53130674
88004882680048827GA21GENICpossibly homozygous53130676
88004887980048880CT14GENIChomozygous53130677
88005009280050093CT11GENICheterozygous53130685
88005047180050472TC15GENIChomozygous53130689