chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 13,50186436,50186437,C,T,14,GENIC,homozygous,126065960 13,50186912,50186913,C,T,13,GENIC,heterozygous,126065961 13,50189177,50189178,T,C,22,GENIC,homozygous,126065962 13,50189353,50189354,C,T,4,GENIC,homozygous,126065963 13,50190936,50190937,C,T,22,GENIC,homozygous,126065964