chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
194829464048294641GA18GENIChomozygous46712012
194829520348295204CT28GENIChomozygous46712014
194829599448295995CT29GENIChomozygous46712015
194829619248296193CT30GENIChomozygous46150898
194829729148297292CT27GENIChomozygous46712017
194829759648297597AG19GENIChomozygous46150900
194829759948297600GA20GENIChomozygous46712019
194829904248299043TC17GENIChomozygous46150901
194830019748300198AG32GENIChomozygous46150904
194830266848302669GGAA29GENIChomozygous46150908
194830273448302735AG27GENICpossibly homozygous46712021
194830310348303104GA16GENIChomozygous46712023
194830359548303596GA21GENIChomozygous46150910
194830508548305086TTC23GENIChomozygous46150914
194830937448309375CT17GENIChomozygous46150920
194831173748311738TG20GENIChomozygous46150926
194831178648311787A-9GENIChomozygous46712025
194831212748312128GA20GENIChomozygous46150927
194831321248313213TG25GENIChomozygous46150930
194831458448314585GT15GENIChomozygous46150931
194831508648315087AT21GENIChomozygous46150932
194831509948315100AT19GENIChomozygous46150933
194831638048316381AAAGG4GENIChomozygous46150934
194831694848316949AG10GENIChomozygous46712027
194831726548317283ACACACACACACACACAC------------------10GENICheterozygous46150938
194831727548317283ACACACAC--------10GENICpossibly homozygous46712029
194831746848317469GA34GENIChomozygous46712030
194831774648317747TA28GENIChomozygous46712032
194831838548318386CG21GENICpossibly homozygous46712034
194831185148311852A-17GENIChomozygous46534296
194829925148299252AAATCCAGCCC2GENIChomozygous46565642
194831158748311588GGAAA16GENIChomozygous46565644
194831214648312148TT--20GENIChomozygous46565646
194830324448303245GGGTGT4GENICheterozygous46407698