chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97015464970154650T18GENIChomozygous128721728
97015473170154732G17GENIChomozygous128721729
97015475270154753AG17GENIChomozygous117373201
97015476370154763A17GENIChomozygous128721730
97015476970154769C19GENIChomozygous128721731
97015478770154788G17GENIChomozygous128721732
97015487770154877A11GENIChomozygous128721733
97015502170155021G4GENIChomozygous128721735
97015503670155037G4GENIChomozygous128721736
97015504370155044G4GENIChomozygous128721737
97015507570155076A7GENIChomozygous128721739
97015507870155078G7GENIChomozygous128721740
97015509670155097T8GENIChomozygous128721741
97015510470155105C8GENIChomozygous128721742
97015511770155119GC9GENIChomozygous128721743
97015513470155135G9GENIChomozygous128721744
97015514370155144T9GENIChomozygous128721745
97015515470155155C8GENIChomozygous128721746
97015518170155182AC13GENIChomozygous117735070
97015518270155183CT13GENIChomozygous117783381
97015519670155197G14GENIChomozygous128721747
97015519870155199T14GENIChomozygous128721748
97015520770155208G14GENIChomozygous128721749
97017923470179235G1GENIChomozygous128721750
97017967870179678T13GENIChomozygous128721751
97017969870179699CA13GENIChomozygous117584110
97017981670179841CTACTGATTGCAATATTAGCTGAGT8GENIChomozygous128721752
97018430370184304G6GENIChomozygous128721753
97018433870184338A3GENIChomozygous128721754
97024145670241457C19GENIChomozygous128721757
97026732870267328AGGTGGG15GENIChomozygous128721758
97026741370267413AT21GENIChomozygous128721759
97027231670272316T12GENICheterozygous133000423
97027352470273525CA10GENIChomozygous117557481
97027352870273529AG10GENIChomozygous117793699
97027354170273541T8GENIChomozygous128721760
97028373170283742GGAGCACTTAA14GENIChomozygous132134492
97028374670283747C14GENIChomozygous132134493