chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 10,56269482,56269483,T,C,18,GENIC,possibly homozygous,563439950 10,56270594,56270595,A,G,14,GENIC,possibly homozygous,563439951 10,56271790,56271791,C,T,21,GENIC,homozygous,563439952 10,56272337,56272338,C,CCT,9,GENIC,homozygous,707721752