chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105533940455339405GC9GENICpossibly homozygous579383771
105534032855340329TC23GENIChomozygous579383772
105534060455340605CT10GENICheterozygous579383773
105534071955340720CT12GENIChomozygous579383774
105534082655340827GGA4GENICheterozygous716989628
105534205455342055CCTT1GENIChomozygous716989632
105534297455342976TC--9GENIChomozygous716989633
105534417855344179GGGATT10GENIChomozygous716989634
105534449755344498CT20GENIChomozygous579383775
105534470855344709AG9GENIChomozygous579383776
105534471955344720CT12GENIChomozygous579383777
105534507855345079TTTGGGTTTCTC3GENIChomozygous716989635
105534538355345384TC4GENIChomozygous579383778
105534731455347315TA12GENICpossibly homozygous579383779
105534909755349098CT24GENICpossibly homozygous581235651
105535074555350746GGACACAC1GENIChomozygous716989636
105535100455351005TTC10GENIChomozygous716989639
105535174455351745CT28GENIChomozygous579383780
105535251255352513GA13GENIChomozygous579383781
105535501655355017CT18GENICpossibly homozygous581235652
105535545755355458CT20GENICpossibly homozygous579383782
105535574655355747CT14GENIChomozygous581235653
105535601955356020TC14GENICpossibly homozygous579383783
105535612655356127GA18GENICpossibly homozygous581235654
105535806955358070GA28GENIChomozygous579383784
105535966955359670CT26GENICpossibly homozygous579383785