chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205047215205047216GT4GENIChomozygous61063956
1205047451205047452AAG13GENIChomozygous61063957
1205048085205048086CCTT15GENIChomozygous61585399
1205050460205050461TTG11GENIChomozygous61063965
1205050495205050496GGTGTGTGTGTGT1GENIChomozygous62192381
1205052758205052759AG17GENIChomozygous61063971
1205057339205057340CA1GENIChomozygous61063975
1205057360205057361CA5GENICheterozygous62095802
1205057600205057602AA--12GENICpossibly homozygous61063977
1205057601205057602A-12GENICheterozygous61063978
1205057931205057932AAT7GENICpossibly homozygous61063980
1205059523205059524A-2GENICheterozygous62192383
1205059748205059749AG16GENIChomozygous61063985
1205060090205060092TT--6GENIChomozygous62192385
1205060101205060102TG9GENIChomozygous62192387
1205060163205060164TC18GENIChomozygous61063989
1205060169205060170AC18GENIChomozygous61063990
1205060408205060409TTTG1GENIChomozygous62192389
1205060411205060412CCTTG1GENIChomozygous62192391
1205060412205060413CCTAGG1GENIChomozygous62192393
1205060420205060424CGTG----1GENIChomozygous62192395
1205060426205060427TTCTACCAC1GENIChomozygous62192397
1205060429205060430AAGCTAAATCC2GENIChomozygous62192398
1205062431205062432GGA10GENIChomozygous61585401
1205063150205063151TG28GENIChomozygous61063993
1205066432205066433GGCACACA3GENIChomozygous62192400
1205067677205067691TTTTTTTTTTTTTT--------------3GENIChomozygous61585403
1205070008205070009AATGTGTGTGTGTGTGTG4GENIChomozygous62192402
1205070415205070416AG16GENIChomozygous61064003
1205072732205072733CCTT9GENICpossibly homozygous61585405
1205073081205073082TTGACAGGCGAGTGG22GENIChomozygous61064007
1205073360205073361CCGT4GENICheterozygous62192404
1205073360205073361CCGTGT4GENICheterozygous62192406