chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 3,181703622,181703623,T,C,21,GENIC,homozygous,606290215 3,181705045,181705046,T,TGTGC,23,GENIC,homozygous,733026723 3,181707382,181707383,T,-,15,GENIC,heterozygous,733026724 3,181707430,181707431,T,TGCTTGCTAG,6,GENIC,homozygous,733026725 3,181707434,181707435,A,AGCGC,7,GENIC,homozygous,733026726 3,181707436,181707437,G,C,7,GENIC,homozygous,608224021 3,181707438,181707439,A,AC,7,GENIC,homozygous,733026727 3,181707440,181707441,A,AC,6,GENIC,homozygous,733026728 3,181707442,181707443,G,GA,6,GENIC,homozygous,733026729 3,181707443,181707444,G,GCTAA,6,GENIC,homozygous,733026730 3,181708295,181708314,GTGGAAGCCTGCCTCTCCA,-------------------,7,GENIC,homozygous,733026731 3,181709097,181709098,C,G,25,GENIC,homozygous,606290216 3,181709215,181709217,CA,--,11,GENIC,homozygous,733026732