chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 8,62170191,62170192,G,GTTTGT,29,GENIC,homozygous,719911269 8,62172226,62172227,T,TGGG,5,GENIC,homozygous,719911270 8,62172241,62172242,G,GCCTAGCAAGC,1,GENIC,homozygous,719911271