chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72463856824638569CT34GENIChomozygous118346061
72464321624643216C53GENIChomozygous128443169
72464329424643295TC58GENIChomozygous118346062
72464390224643902A47GENIChomozygous128443170
72464455424644555CT50GENIChomozygous126644293
72464455824644559G51GENIChomozygous128443171
72464466624644667G39GENIChomozygous128443172
72464475424644754C40GENIChomozygous128443173
72464477024644771CT39GENIChomozygous131688063
72464477124644772TA38GENIChomozygous131688064
72464477224644773GA38GENIChomozygous131688065
72464478424644784C37GENIChomozygous128443174
72463912524639126T40GENICheterozygous131675311
72464293624642937TC45GENIChomozygous115619109
72464460024644601AG41GENIChomozygous115619112
72464478924644790GA34GENIChomozygous115619113
72464239824642399GC1GENIChomozygous134946283
72464241924642420CT1GENIChomozygous134946284
72464241224642412T1GENIChomozygous134944340
72464241324642413CA1GENIChomozygous134944341
72464241624642416CACTCCTA1GENIChomozygous134944342
72464482024644821TC35GENIChomozygous115619116
72464482624644827AG34GENIChomozygous131688066
72464485824644859CT33GENIChomozygous131688067
72464486924644870CT37GENIChomozygous115619119
72464505524645056AG40GENIChomozygous118346063
72464712924647130TC48GENIChomozygous115619122
72464929724649298GT40GENIChomozygous118346064