chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,15066401,15066402,G,A,7,GENIC,homozygous,880797435 X,15076799,15076800,A,G,11,GENIC,heterozygous,880797436 X,15087981,15087982,T,C,4,GENIC,homozygous,880797437 X,15088527,15088528,G,A,6,GENIC,homozygous,880797438