chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 20,13340354,13340355,C,CGT,7,GENIC,heterozygous,734978757 20,13340354,13340355,C,CGTGT,7,GENIC,heterozygous,734978758 20,13343283,13343284,C,CT,17,GENIC,heterozygous,734978759 20,13343283,13343284,C,CTT,17,GENIC,heterozygous,734978760 20,13348905,13348906,T,TC,5,GENIC,heterozygous,734978761 20,13357483,13357484,A,AC,9,GENIC,heterozygous,734978762 20,13358156,13358157,A,G,13,GENIC,homozygous,610718106 20,13360854,13360855,A,T,15,GENIC,homozygous,611383816 20,13361209,13361210,A,-,28,GENIC,homozygous,734978763 20,13363057,13363058,C,G,29,GENIC,homozygous,610718107 20,13370918,13370919,T,C,30,GENIC,homozygous,610718108 20,13373158,13373159,G,GGTGTGTGTGT,10,GENIC,homozygous,734978766 20,13374807,13374808,C,CA,3,GENIC,heterozygous,734978768 20,13378101,13378102,C,CG,23,GENIC,homozygous,734978770 20,13378877,13378878,C,CGT,14,GENIC,heterozygous,734978772 20,13378878,13378880,GT,--,14,GENIC,heterozygous,734978771