chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 6,59211512,59211513,T,C,27,GENIC,heterozygous,927717019 6,59221447,59221448,A,AT,53,GENIC,heterozygous,927766970 6,59221448,59221449,C,T,40,GENIC,heterozygous,927717020 6,59221456,59221457,C,A,37,GENIC,heterozygous,927717021 6,59224250,59224251,C,T,9,GENIC,heterozygous,927717022 6,59225831,59225832,A,ATTC,15,GENIC,heterozygous,927766971 6,59225856,59225857,T,C,15,GENIC,heterozygous,927717023 6,59225922,59225923,C,T,10,GENIC,heterozygous,927717024 6,59236674,59236675,C,T,16,GENIC,heterozygous,927717025 6,59236679,59236680,C,T,16,GENIC,heterozygous,927717026 6,59236787,59236788,T,C,28,GENIC,heterozygous,927717027 6,59236895,59236896,C,CTTAAGTATCCT,14,GENIC,heterozygous,927766972 6,59242208,59242210,GA,--,13,GENIC,heterozygous,927766973 6,59244957,59244958,C,T,9,GENIC,heterozygous,927717028 6,59246714,59246715,A,G,14,GENIC,heterozygous,927717029 6,59268322,59268323,G,A,11,GENIC,heterozygous,927717030 6,59268324,59268325,T,A,11,GENIC,heterozygous,927717031 6,59268326,59268327,A,T,11,GENIC,heterozygous,927717032 6,59268330,59268342,GCGTGTGTCAAT,------------,11,GENIC,heterozygous,927766974