chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,113513374,113513375,A,T,8,GENIC,homozygous,801338539 X,113514458,113514459,G,T,12,GENIC,heterozygous,801338540 X,113514803,113514804,G,A,9,GENIC,homozygous,801338541 X,113516030,113516031,G,A,9,GENIC,homozygous,801338542