chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,105298659,105298660,A,C,2,GENIC,homozygous,1002274416 X,105302163,105302164,C,A,5,GENIC,homozygous,1002274417 X,105302184,105302185,T,C,4,GENIC,homozygous,1002274418 X,105302210,105302211,C,A,2,GENIC,homozygous,1002274419