chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6138616130138616131TC13GENICheterozygous54756825
6138616247138616248CT6GENIChomozygous54756827
6138616262138616263GT8GENICpossibly homozygous54756829
6138616277138616278AG11GENIChomozygous54756830
6138616391138616392TC23GENICpossibly homozygous54756832
6138616519138616520CA15GENICpossibly homozygous54756834
6138616557138616558CT13GENIChomozygous54756835
6138616674138616675TA1GENIChomozygous54756837
6138616710138616711CT10GENIChomozygous54756839
6138616839138616840AC20GENIChomozygous54756841
6138616979138616980GA8GENICheterozygous54756845
6138617329138617330AG19GENIChomozygous54756847
6138617754138617760GTGGAA------2GENIChomozygous54756849
6138617766138617767AG4GENIChomozygous54756851
6138618110138618111GA4GENICheterozygous54756857
6138621659138621660TA17GENIChomozygous54756861