chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225310431225310432AG9GENIChomozygous108556816
1225310670225310671AC5GENIChomozygous108556817
1225312287225312288TC22GENIChomozygous108556825
1225314404225314405CT18GENIChomozygous108556836
1225316586225316587AG11GENIChomozygous108996930
1225318529225318530TC19GENIChomozygous108556859
1225320534225320535TC13GENIChomozygous120595472
1225322378225322379CG14GENIChomozygous120595474
1225322458225322459TC6GENIChomozygous108556864
1225322564225322565GT13GENIChomozygous120595476
1225325979225325980AG18GENIChomozygous108556866
1225326060225326061TC10GENIChomozygous108556867
1225326063225326064GA7GENIChomozygous108556868
1225326247225326248CT6GENIChomozygous108556870
1225326300225326301GT7GENIChomozygous125312969
1225326450225326451AT5GENIChomozygous108556872
1225326941225326942AT11GENIChomozygous108556874
1225327170225327171GA9GENICheterozygous108556875
1225328128225328129CT23GENIChomozygous108556878
1225328508225328509TC7GENIChomozygous108556880
1225328708225328709GA31GENIChomozygous108556881
1225328848225328849CT7GENIChomozygous108556882
1225328851225328852CT7GENIChomozygous108556883
1225328860225328861TC8GENIChomozygous108556884
1225329419225329420CT7GENIChomozygous108556886