chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,113513374,113513375,A,T,8,GENIC,homozygous,971498581 X,113514458,113514459,G,T,9,GENIC,heterozygous,971498582 X,113514803,113514804,G,A,9,GENIC,homozygous,971498583 X,113516030,113516031,G,A,9,GENIC,homozygous,971498584