chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 123617040 123617041 G A 46 GENIC homozygous 115863746 7 123617071 123617072 G A 41 GENIC homozygous 115863750 7 123617353 123617354 G A 49 GENIC homozygous 115863756 7 123617398 123617399 C T 41 GENIC homozygous 115863758 7 123617960 123617961 T G 57 GENIC homozygous 115863760 7 123618397 123618398 T C 68 GENIC homozygous 115863762 7 123618448 123618449 G T 56 GENIC homozygous 115863764 7 123618480 123618481 G T 50 GENIC homozygous 115863766 7 123618527 123618528 A G 48 GENIC homozygous 115863768 7 123618547 123618548 C A 45 GENIC homozygous 115863770 7 123618552 123618553 C A 45 GENIC homozygous 115863772 7 123618618 123618619 C T 47 GENIC homozygous 115863774 7 123618698 123618699 T G 52 GENIC homozygous 115863776 7 123618998 123618999 A G 20 GENIC homozygous 115863778 7 123619006 123619007 T C 16 GENIC homozygous 115863780 7 123619019 123619020 G T 16 GENIC homozygous 115863782 7 123619023 123619024 G C 14 GENIC homozygous 128562680 7 123619530 123619531 G A 53 GENIC possibly homozygous 115863784 7 123620686 123620687 T G 52 GENIC homozygous 115863788