chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71287977412879775AG4GENIChomozygous54711853
71288031812880319CT8GENIChomozygous54711855
71288048512880486TC10GENICpossibly homozygous54711857
71288080812880809TC20GENIChomozygous54711859
71288142112881422TG17GENIChomozygous54711861
71288192712881928GA7GENIChomozygous54711863
71288263512882636CG19GENIChomozygous54711865
71288327712883278TG5GENIChomozygous54711867
71288337112883372CG11GENICpossibly homozygous54711869
71288401112884012CCA6GENIChomozygous54711871
71288401212884013GGACA6GENIChomozygous54711875
71288402712884043CAGGCAGGCAGGCAGG----------------1GENIChomozygous54711877
71288406612884067GA4GENIChomozygous54711879
71288442212884423TC3GENIChomozygous54711881
71288446812884469CT8GENICpossibly homozygous54711883
71288462312884624TC19GENIChomozygous54711887
71288573612885737AG6GENIChomozygous54711897
71288635112886352CT19GENICpossibly homozygous54711899
71288652612886527TC13GENICpossibly homozygous53792013
71288713212887133GGAC10GENIChomozygous54711901
71288730712887308GGAAA2GENIChomozygous54181822
71288801012888011TC6GENIChomozygous53792021
71288917112889172AG20GENICpossibly homozygous53792037
71288936912889370GA13GENICpossibly homozygous54630986
71289022412890225TTGCCCACAGACCCC3GENIChomozygous53792047