chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65851631158516312AC46GENICheterozygous54422739
65851688958516890TTC8GENIChomozygous54422742
65851736958517370TTG14GENIChomozygous54422745
65851826458518265T-22GENIChomozygous54422748
65851857358518574TTAA2GENIChomozygous54422751
65851858858518589C-5GENIChomozygous54422754
65851886958518870AT23GENICpossibly homozygous54422757
65851996258519963CT21GENIChomozygous54422760
65852014958520165TCTCTCTCTCTCTCTC----------------6GENIChomozygous54422763
65852020458520205CG19GENICheterozygous54422766
65852185958521860CCA9GENIChomozygous54422772
65852232058522321CG38GENIChomozygous54422775
65852352258523523CT33GENIChomozygous54422778
65852426658524267TTTCAA12GENIChomozygous54422781
65852426858524269GGC8GENIChomozygous54422784
65852426958524270TTTCA8GENIChomozygous54422787
65852504358525044GT23GENIChomozygous54422790
65852504658525047GA24GENIChomozygous54422793
65852627958526280TA36GENICpossibly homozygous54422796
65852628158526282TA36GENICpossibly homozygous54422799
65852696958526970TC22GENIChomozygous54422802
65852720058527201CT13GENIChomozygous54422805
65852860858528609TTAAA5GENIChomozygous54422808
65852875458528755GGA9GENIChomozygous54422811