chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,131067242,131067246,TCTG,,1,GENIC,homozygous,140597278 X,131131865,131131866,G,,9,GENIC,homozygous,140597279 X,131140104,131140105,T,C,5,GENIC,homozygous,140703181