chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71103313711033138TC36GENIChomozygous154425236
71103317811033179AG41GENIChomozygous138004095
71103439811034399GC55GENICpossibly homozygous138004096
71103448711034488TG54GENICpossibly homozygous138004097
71103522311035224CT64GENIChomozygous138004098
71103530411035305GA65GENIChomozygous138004099
71103535811035359TG56GENIChomozygous138004100
71103558111035582AG62GENIChomozygous138004101
71103587811035879CT75GENIChomozygous138004102
71103600311036004CT67GENIChomozygous138004103
71103644811036449TC63GENIChomozygous138004104
71103713111037132CT46GENIChomozygous138004105
71103728411037285GA64GENIChomozygous138004106
71103842311038424CT57GENIChomozygous138004107
71103872911038730AG74GENIChomozygous138004108
71103875211038753GC73GENIChomozygous138004109
71103621811036220CA54GENIChomozygous137935421
71103439411034398ATTA54GENICpossibly homozygous137935419
71103586911035870A74GENIChomozygous137935420