chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64069445240694453AT21GENIChomozygous961113852
64069477540694776CG27GENIChomozygous961113853
64069512140695122TC29GENIChomozygous961113854
64069516440695165AG32GENIChomozygous961113855
64069517140695172TC28GENIChomozygous961113856
64069636240696363AG19GENIChomozygous961113857
64069911140699112AG24GENIChomozygous961113858
64070400540704006TA25GENIChomozygous961113859
64070423540704236AC29GENIChomozygous961113860
64070564240705643GA30GENIChomozygous961113861
64070572540705726GA35GENIChomozygous961113862
64070649440706495CA25GENIChomozygous961113863
64070653040706531CT29GENIChomozygous961113864
64070716540707166CT21GENIChomozygous961113865
64070747540707476GT21GENIChomozygous961113866
64070749640707497TG21GENIChomozygous961113867
64070799540707996GA21GENIChomozygous961113868
64070879140708792AG31GENIChomozygous961113869
64070914340709144TA26GENIChomozygous961113870
64070915340709154TG28GENIChomozygous961113871
64070943240709433TC20GENIChomozygous961113872
64070947140709472TA21GENIChomozygous961113873
64070985340709854TA29GENIChomozygous961113874
64070985440709855GC30GENIChomozygous961113875
64070988040709881GA30GENIChomozygous961113876
64071041340710414TC23GENIChomozygous961113877
64071066740710668GA19GENIChomozygous961113878
64071068040710681GA18GENIChomozygous961113879
64071076740710768CT19GENIChomozygous961113880
64071079940710800AG16GENIChomozygous961113881
64071154840711549GA35GENIChomozygous961113882
64071250040712501TA23GENIChomozygous961113883
64071331540713316TC30GENIChomozygous961113884
64071333840713339GA26GENIChomozygous961113885