chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75093032350930324TC26GENIChomozygous53918512
75093136150931362CT47GENICpossibly homozygous53918513
75093176650931767CT29GENICheterozygous55354595
75093179250931793AG44GENICheterozygous53918515
75093198450931985AG35GENIChomozygous53918516
75093328950933290TC28GENIChomozygous53918521
75093355350933554G-8GENIChomozygous53918522
75093393350933934TC28GENIChomozygous53918527
75093540650935409AAG---6GENICheterozygous53918532
75093683650936837C-15GENICheterozygous55058351
75093733450937335GT45GENICpossibly homozygous53918535
75093773950937740GC18GENIChomozygous53918536
75093774050937741GT18GENIChomozygous53918537
75093774550937746GGC17GENIChomozygous53918538
75093778950937790GA14GENIChomozygous53918539
75093784050937841TG11GENICpossibly homozygous53918540
75093784450937845A-11GENICpossibly homozygous53918541
75093789950937903TAAT----6GENIChomozygous53918542
75093819050938191CT15GENIChomozygous53918543
75093862650938627GT18GENIChomozygous53918544
75094110250941103GC29GENIChomozygous53918545