chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,104468622,104468623,G,C,16,GENIC,homozygous,108307831 X,104468626,104468627,C,T,16,GENIC,homozygous,108307833 X,104469275,104469276,C,T,12,GENIC,homozygous,108307835 X,104469317,104469318,G,C,8,GENIC,homozygous,108452260 X,104487145,104487146,A,T,9,GENIC,homozygous,108506642