chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195605508756055088TA19GENIChomozygous109737736
195605518456055185TC25GENIChomozygous109737738
195605549356055494GA29GENIChomozygous109737740
195605549456055495AC29GENIChomozygous109737742
195605549656055497CT30GENIChomozygous109737744
195605549856055499AG30GENIChomozygous109737746
195605559556055596GT24GENIChomozygous109737748
195605638456056385AG25GENIChomozygous109737750
195605697856056979CA28GENIChomozygous109737752
195605752656057527GA19GENIChomozygous109737754
195605852656058527GC27GENIChomozygous109737756
195605930256059303TC37GENIChomozygous109737758
195606056656060567AT33GENIChomozygous109737760
195606059856060599AG32GENIChomozygous109737762
195606076556060766TC20GENIChomozygous109737764
195606098756060988TG10GENIChomozygous109825772
195606138056061381TG13GENIChomozygous109737766
195606217256062173GA26GENIChomozygous109737768
195606302956063030CT16GENICpossibly homozygous109737770
195606633356066334TC30GENIChomozygous109737772
195606737256067373CT17GENIChomozygous109737774
195606743756067438CA15GENIChomozygous109737776