chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72463912524639126T23GENICheterozygous131675311
72463959924639599A28GENICpossibly homozygous128443167
72464005124640052GA31GENIChomozygous118493969
72464466624644667G21GENIChomozygous128443172
72464321624643216C34GENIChomozygous128443169
72464455824644559G25GENIChomozygous128443171
72464216324642186CCGTCTCCTCATCTCTCTCTCTC5GENIChomozygous129936015
72464377724643778CT27GENIChomozygous115619111
72464135824641359AG19GENIChomozygous115619108
72464293624642937TC23GENIChomozygous115619109
72464460024644601AG23GENIChomozygous115619112
72464475424644754C31GENIChomozygous128443173
72464478424644784C28GENIChomozygous128443174
72464478924644790GA29GENIChomozygous115619113
72464482024644821TC37GENIChomozygous115619116
72464482924644830TC38GENIChomozygous115619117
72464482124644822GA37GENIChomozygous135115637
72464486924644870CT28GENIChomozygous115619119
72464712924647130TC21GENIChomozygous115619122
72464911624649117AC29GENIChomozygous118493971
72464913324649134CT34GENIChomozygous118493973
72464484024644841CT36GENIChomozygous135115638
72464484724644848T33GENIChomozygous135114632