chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143356406433564065CT8GENIChomozygous890608903
143356407233564073GA10GENIChomozygous890608904
143356473933564740CA16GENIChomozygous890608905
143356569033565691TC24GENIChomozygous890608906
143356577833565779CG12GENIChomozygous890608907
143356581233565813GT21GENIChomozygous890608908
143356627533566276GA15GENIChomozygous890608909
143356761233567613TC21GENIChomozygous890608910
143356781533567816CT11GENIChomozygous890608911
143356817633568177CT22GENIChomozygous890608912
143356822133568222TC23GENIChomozygous890608913
143357017833570179TC8GENIChomozygous890608914
143357083233570833AT19GENIChomozygous890608915
143357108833571089AT11GENIChomozygous890608916
143357125933571260CT14GENIChomozygous890608917
143357130533571306CT12GENIChomozygous890608918
143357136733571368TC9GENIChomozygous890608919
143357172433571725TC6GENIChomozygous890608920
143357190133571902TC16GENIChomozygous890608921
143357190233571903GA17GENIChomozygous890608922
143357236333572364AG18GENIChomozygous890608923
143357284633572847GA15GENIChomozygous890608924
143357304933573050GA19GENIChomozygous890608925
143357331833573319TG19GENICheterozygous890608926
143357378933573790CT18GENIChomozygous890608927
143357381233573813AG24GENIChomozygous890608928
143357389733573898GA10GENIChomozygous890608929
143357409933574100AG12GENIChomozygous890608930
143357435933574360AG19GENIChomozygous890608931
143357451133574512TC24GENIChomozygous890608932
143357464533574646AG11GENIChomozygous890608933
143357492433574925CT5GENICheterozygous890608934
143357563433575635CT19GENIChomozygous890608935
143357607033576071AG13GENIChomozygous890608936
143357650133576502CG7GENIChomozygous890608937
143357888533578886CG18GENIChomozygous890608938
143357911333579114AG11GENIChomozygous890608939
143357951133579512CT22GENIChomozygous890608940
143357954333579544CA18GENIChomozygous890608941
143358002833580029AG13GENIChomozygous890608942