chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,46991579,46991580,G,C,9,GENIC,heterozygous,893639819 X,46995349,46995350,C,T,8,GENIC,homozygous,893639820 X,46995424,46995425,G,T,7,GENIC,heterozygous,893639821 X,47008316,47008317,T,C,8,GENIC,homozygous,893639826 X,47009839,47009840,A,G,11,GENIC,homozygous,893639827 X,47012714,47012715,T,C,7,GENIC,homozygous,893639828 X,47014062,47014063,A,G,8,GENIC,homozygous,893639829 X,47014395,47014396,T,G,8,GENIC,homozygous,893639830 X,47018770,47018771,G,A,10,GENIC,homozygous,893639831 X,47020297,47020298,T,C,6,GENIC,homozygous,893639832 X,47021260,47021261,T,C,7,GENIC,homozygous,893639833 X,47021922,47021923,C,T,11,GENIC,homozygous,893639834 X,47022045,47022046,G,A,15,GENIC,homozygous,893639835 X,47022954,47022955,G,A,12,GENIC,homozygous,893639836 X,47023445,47023446,G,C,7,GENIC,homozygous,893639837 X,47023944,47023945,G,A,7,GENIC,homozygous,893639838 X,47025892,47025893,T,C,5,GENIC,homozygous,893639839