chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,266258851,266258852,G,A,23,GENIC,homozygous,978060731 1,266258863,266258864,G,A,23,GENIC,homozygous,978060732 1,266262051,266262052,T,C,19,GENIC,homozygous,978060733 1,266262453,266262454,G,A,41,GENIC,homozygous,978060734 1,266264337,266264338,T,A,50,GENIC,homozygous,978060735 1,266265228,266265229,A,G,19,GENIC,homozygous,978060736 1,266266414,266266415,G,T,2,GENIC,homozygous,978060737 1,266266712,266266713,C,T,38,GENIC,homozygous,978060738 1,266267954,266267955,T,C,49,GENIC,homozygous,978060739 1,266268309,266268310,G,A,38,GENIC,homozygous,978060740 1,266270325,266270326,A,G,14,GENIC,homozygous,978060741