chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117418052117418053TC59GENIChomozygous112819096
4117418204117418205AT43GENIChomozygous112819098
4117418221117418222TC46GENICpossibly homozygous112819100
4117418449117418450CT54GENIChomozygous112819102
4117419910117419911TC63GENIChomozygous112819104
4117419917117419918CT62GENIChomozygous112819106
4117420419117420420TC47GENIChomozygous112819108
4117420728117420729AG44GENIChomozygous112819110
4117420916117420917TC53GENIChomozygous112819112
4117421019117421020TC49GENIChomozygous112819114
4117421062117421063CT38GENIChomozygous112819116
4117421960117421961GA33GENIChomozygous112819118
4117422251117422252GA35GENIChomozygous112819120
4117422386117422387AG41GENIChomozygous112819122