chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124761252347612524CCA20GENIChomozygous50223075
124761584747615848AAC16GENIChomozygous50223077
124761586047615865CTCCT-----18GENICheterozygous50223079
124761589947615903CTCT----11GENICheterozygous50223081
124761590147615903CT--11GENICheterozygous50223083
124761595647615957GGCA8GENICpossibly homozygous50223085
124761825747618258CG8GENICpossibly homozygous50223087
124761826447618265AG10GENICheterozygous50343200
124761826847618276GGTGAGCA--------10GENICheterozygous50223089
124761827247618276AGCA----10GENICheterozygous50223091
124762654647626547G-18GENIChomozygous50223093