chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186141796861417969CG18GENIChomozygous46483766
186141817861418179CG29GENIChomozygous46483767
186141848161418482CG32GENIChomozygous46483768
186141893961418940TC27GENIChomozygous46483769
186141942861419429CT21GENIChomozygous46483770
186141953561419536TTTGTGTGTGTGTGTGTG8GENIChomozygous46898467
186141995761419958TTA20GENICpossibly homozygous46483773
186142013361420134TC23GENIChomozygous46483774
186142015261420153AG29GENIChomozygous46483775
186142020861420211TTT---13GENICheterozygous46898468
186142020961420211TT--13GENICheterozygous46887637
186142066461420665GC22GENICpossibly homozygous46483776