chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104997208104997209CA15GENICheterozygous118070897
10104997230104997231CT17GENICheterozygous118070898
10104997231104997232AG18GENICheterozygous118070899
10104997248104997249AC21GENICheterozygous118070900
10104997372104997373GC31GENICpossibly homozygous118070901
10104997473104997474CG6GENIChomozygous118076414
10104997496104997497GC4GENIChomozygous131102815
10104997562104997563CT5GENIChomozygous118070902
10104997618104997619TC10GENIChomozygous131102816
10104997642104997643GT16GENIChomozygous131102817
10104997697104997698TG17GENICpossibly homozygous131102818
10104997781104997782AT7GENIChomozygous131102819
10104997785104997785CC6GENIChomozygous131098775
10104997787104997789AA5GENIChomozygous131098776
10104997789104997790GC5GENIChomozygous131102820
10104997793104997794CT4GENIChomozygous131102821
10104997806104997807GA2GENIChomozygous131906924
10104997812104997813AT1GENIChomozygous131906925
10104997814104997815GA1GENIChomozygous131906926
10104997815104997816TA1GENIChomozygous131906927
10104997883104997884CA3GENIChomozygous131102822
10104997888104997889CT4GENIChomozygous131102823
10104997889104997890CG5GENIChomozygous131102824
10104997912104997913AG11GENIChomozygous131102825
10104997943104997944GA16GENIChomozygous118070903
10104997950104997951CT17GENIChomozygous118070904
10104997957104997958GA21GENIChomozygous118070905
10104997968104997969GA23GENIChomozygous131102826
10104997969104997970AT25GENIChomozygous131102827
10104997980104997981CT28GENIChomozygous118070906
10104997990104997991CG31GENIChomozygous118070907
10104997998104997999AT35GENIChomozygous118070908
10104998127104998128GT25GENIChomozygous118070912
10104998094104998095AG28GENIChomozygous118070909
10104998120104998121TG24GENIChomozygous118070910
10104998123104998124AG23GENIChomozygous118070911
10104998173104998174TC29GENIChomozygous118070913
10104998177104998178TG33GENIChomozygous118070914
10104998194104998195AG33GENIChomozygous118070915
10104998202104998204GT33GENIChomozygous131098777
10104998216104998217AT36GENIChomozygous118070916
10104998268104998269CT42GENIChomozygous118070917
10104998339104998340TG30GENIChomozygous118070918
10104998359104998360AT25GENIChomozygous118070919
10104998436104998437AG24GENIChomozygous118070920
10104998444104998445GC25GENIChomozygous118070921
10104998475104998476AG28GENIChomozygous118070922
10104998478104998479TA28GENIChomozygous118070923
10104998483104998484AT28GENIChomozygous118070924
10104998657104998658CT43GENIChomozygous118070925
10104998668104998669CA47GENICpossibly homozygous118070926
10104998707104998707GGTTCTTGG43GENIChomozygous131098778
10104998718104998719TC34GENIChomozygous118070927
10104998755104998756AG35GENIChomozygous118070928
10104998760104998761GA36GENIChomozygous118070929
10104999028104999028TCT48GENIChomozygous131098779
10104999084104999087CTT30GENIChomozygous131098780
10104999121104999122AT27GENIChomozygous118070930
10104999197104999198GC24GENIChomozygous118070931
10104999341104999342CT34GENIChomozygous118070932
10104999480104999481AG42GENIChomozygous118070933
10104999489104999490AG44GENIChomozygous118070934
10104999505104999506CT40GENIChomozygous118070935
10104999630104999631GA34GENIChomozygous118070936
10104999786104999787AG36GENIChomozygous118070937
10104999881104999882TG35GENIChomozygous118070938
10104999918104999919CA35GENIChomozygous118070939
10104999930104999931GC36GENIChomozygous118070940
10104999934104999935GA37GENIChomozygous118070941
10104998800104998801GA33GENIChomozygous116961668
10104998788104998789CT34GENIChomozygous116961666