chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 111673706 111673707 G A 11 GENIC homozygous 932660599 8 111675753 111675754 T A 13 GENIC homozygous 932660600 8 111676152 111676153 T C 13 GENIC homozygous 932660601 8 111676535 111676536 T C 10 GENIC homozygous 932660602 8 111676727 111676728 A C 6 GENIC homozygous 932660603 8 111677257 111677258 C T 11 GENIC homozygous 932660604 8 111677357 111677358 C T 8 GENIC homozygous 932660605 8 111677395 111677396 C T 12 GENIC homozygous 932660606 8 111677564 111677565 T C 9 GENIC homozygous 932660607 8 111677792 111677793 A G 17 GENIC homozygous 932660608 8 111678149 111678150 A G 18 GENIC homozygous 932660609 8 111678156 111678157 G C 17 GENIC homozygous 932660610 8 111678607 111678608 T C 6 GENIC homozygous 932660611 8 111679901 111679902 A C 9 GENIC homozygous 932660612 8 111680058 111680059 T C 10 GENIC homozygous 932660613 8 111681061 111681062 C T 10 GENIC homozygous 932660614 8 111681424 111681425 C T 12 GENIC homozygous 932660615 8 111682438 111682439 A G 4 GENIC homozygous 932660616 8 111682564 111682565 C G 10 GENIC homozygous 932660617 8 111683450 111683451 T C 17 GENIC homozygous 932660618 8 111684348 111684349 T G 9 GENIC homozygous 932660619 8 111684688 111684689 A G 7 GENIC homozygous 932660620 8 111684944 111684945 G A 6 GENIC homozygous 932660621 8 111685182 111685183 G A 12 GENIC possibly homozygous 932660622 8 111685759 111685760 G A 4 GENIC homozygous 932660623 8 111685985 111685986 A G 12 GENIC homozygous 932660624 8 111687071 111687072 C G 4 GENIC homozygous 932660625