chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
478897527889753AT21GENIChomozygous793465719
478907827890783CT37GENIChomozygous793465720
478926637892664CT34GENICpossibly homozygous793465721
478940247894025CT43GENIChomozygous793465722
478944117894412TC48GENICpossibly homozygous793465723
478959197895920TC32GENIChomozygous793465724
478963117896312GT27GENIChomozygous793465725
478972327897233GT22GENICpossibly homozygous793465726
478972607897261CT27GENICheterozygous793465727
478976207897621GA33GENICpossibly homozygous793465728
478977517897752CT43GENIChomozygous793465729
478980487898049CA30GENIChomozygous793465730
479001317900132AC38GENICpossibly homozygous793465731
479003627900363CT38GENIChomozygous793465732
479010837901084TC44GENIChomozygous793465733
479035067903507AG33GENIChomozygous793465734
479037627903763AG50GENIChomozygous793465735
479041107904111AC58GENIChomozygous793465736
479044517904452TC40GENICpossibly homozygous793465737
479055167905517GA30GENIChomozygous793465738
479057847905785GT10GENIChomozygous793465739
479062957906296AG49GENIChomozygous793465740
479064167906417AG53GENIChomozygous793465741
479066697906670GA46GENIChomozygous793465742
479085977908598AG48GENIChomozygous793465743
479090717909072CT26GENIChomozygous793465744
479107217910722AG46GENIChomozygous793465745
479116437911644TA29GENIChomozygous793465746
479119817911982GA17GENICheterozygous793465747
479128227912823GA44GENIChomozygous793465748
479131467913147CT32GENIChomozygous793465749
479138737913874CA34GENIChomozygous793465750
479152747915275TC38GENIChomozygous793465751
479155017915502TC45GENIChomozygous793465752
479159467915947GA24GENIChomozygous793465753
479161797916180CA32GENIChomozygous793465754
479165827916583GA40GENIChomozygous793465755
479166077916608CT44GENIChomozygous793465756
479167827916783CT50GENIChomozygous793465757
479168837916884TG41GENIChomozygous793465758
479171127917113GA28GENIChomozygous793465759
479180257918026GA32GENIChomozygous793465760
479182997918300AG43GENIChomozygous793465761
479190627919063GT27GENICpossibly homozygous793465762
479191317919132AG29GENICheterozygous793465763
479205527920553GA37GENIChomozygous793465764
479223737922374AC4GENIChomozygous793465765
479226517922652AC17GENIChomozygous793465766
479229287922929GC35GENIChomozygous793465767
479229297922930GA36GENIChomozygous793465768
479233997923400AG41GENICpossibly homozygous793465769
479234417923442AG36GENIChomozygous793465770
479266697926670CT39GENIChomozygous793465771
479270117927012GA45GENIChomozygous793465772
479278807927881TC27GENIChomozygous793465773
479279827927983AT29GENIChomozygous793465774
479284357928436GA35GENIChomozygous793465775
479287497928750TG30GENIChomozygous793465776
479292767929277TC31GENIChomozygous793465777
479304437930444CT39GENIChomozygous793465778