chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97015464970154650T11GENIChomozygous128721728
97015473170154732G11GENIChomozygous128721729
97015475270154753AG10GENIChomozygous117373201
97015476370154763A11GENIChomozygous128721730
97015476970154769C11GENIChomozygous128721731
97015478770154788G12GENIChomozygous128721732
97015487770154877A2GENIChomozygous128721733
97015497370154974G6GENICheterozygous128721734
97015502170155021G5GENIChomozygous128721735
97015503670155037G6GENIChomozygous128721736
97015504370155044G6GENIChomozygous128721737
97015507570155076A12GENIChomozygous128721739
97015507870155078G13GENIChomozygous128721740
97015509670155097T16GENIChomozygous128721741
97015510470155105C17GENIChomozygous128721742
97015511770155119GC20GENIChomozygous128721743
97015513470155135G22GENIChomozygous128721744
97015514370155144T22GENIChomozygous128721745
97015515470155155C24GENIChomozygous128721746
97015518270155183CT22GENIChomozygous117783381
97015519670155197G24GENIChomozygous128721747
97015519870155199T24GENIChomozygous128721748
97015520770155208G26GENIChomozygous128721749
97017967870179678T7GENIChomozygous128721751
97017981670179841CTACTGATTGCAATATTAGCTGAGT6GENIChomozygous128721752
97018430370184304G2GENIChomozygous128721753
97018433870184338A2GENIChomozygous128721754
97024145670241457C14GENIChomozygous128721757
97026732870267328AGGTGGG25GENIChomozygous128721758
97026741370267413AT15GENIChomozygous128721759
97027352470273525CA9GENIChomozygous117557481
97027352870273529AG9GENIChomozygous117793699
97027354170273541T8GENIChomozygous128721760
97027090470270905TC2GENICheterozygous134342217
97015496070154965TATGG6GENICheterozygous134341464
97015518170155182AC22GENIChomozygous117735070
97017969870179699CA8GENIChomozygous117584110