chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195617930856179309CT4GENIChomozygous109978894
195617990056179901TG16GENIChomozygous109737996
195618028756180288GA24GENIChomozygous109738002
195618154256181543AC19GENIChomozygous109738018
195618285156182852TC17GENIChomozygous109738036
195618338156183382GA25GENIChomozygous109978896
195618357156183572GA15GENIChomozygous109978898
195618402556184026TC10GENIChomozygous109738048
195618521056185211TC23GENIChomozygous109738054
195618541456185415AG32GENIChomozygous109738062
195618786056187861TG20GENIChomozygous109738074
195618823056188231CT6GENIChomozygous109978904
195618841356188414GA27GENIChomozygous109738084
195618942756189428TG20GENIChomozygous109978906
195618960856189609AG11GENIChomozygous109738090
195619362256193623GT7GENIChomozygous109978908
195619592356195924GA11GENIChomozygous109738116
195619626356196264CT19GENIChomozygous109978910
195619637756196378TC13GENIChomozygous109738118
195619710956197110TA18GENIChomozygous109738122
195619795656197957GA18GENIChomozygous109738126
195619900756199008AG15GENIChomozygous109738132
195619938656199387TC13GENIChomozygous109738134
195620098656200987GC22GENIChomozygous109738136
195620137756201378AG22GENIChomozygous109738138
195620152256201523AG17GENIChomozygous109738140
195620676556206766AG9GENIChomozygous109738144
195620846656208467CT25GENIChomozygous109978919
195620861256208613TC12GENIChomozygous109738150
195620900356209004AG17GENIChomozygous109738154
195621041856210419AG15GENIChomozygous109738158
195621125656211257AG14GENIChomozygous109738160
195621156156211562TC13GENIChomozygous109738162
195620059456200595GT29GENIChomozygous110087572