chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17569352575693526GT49GENIChomozygous109501865
17569508675695087GC48GENIChomozygous109501866
17569521375695214CA40GENIChomozygous109501867
17569527675695277AG35GENIChomozygous109501868
17569596375695964AG52GENIChomozygous109501869
17569604175696042TC39GENICpossibly homozygous109501870
17569607275696073TC42GENICpossibly homozygous109501871
17569610475696105TC59GENICheterozygous109501872
17569659975696600CG44GENIChomozygous109501873
17569715275697153AT28GENICpossibly homozygous109501874
17569750275697503GA45GENIChomozygous109501875
17569783175697832TC39GENIChomozygous109501876
17569816175698162CG43GENIChomozygous109501877
17569862975698630TC36GENIChomozygous109501878
17570142975701430TG50GENIChomozygous109501879
17570250075702501TG35GENIChomozygous109501880
17570380575703806CT25GENIChomozygous109501881
17570396175703962GA64GENIChomozygous109501882
17570499475704995TC52GENIChomozygous109501883
17570583675705837TC40GENIChomozygous109501884