chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 51517615 51517616 C T 22 GENIC homozygous 801450648 1 51518070 51518071 T C 32 GENIC homozygous 801450649 1 51518299 51518300 T G 28 GENIC possibly homozygous 801450650 1 51518491 51518492 T G 28 GENIC homozygous 801450651 1 51518579 51518580 C G 34 GENIC homozygous 801450652 1 51519293 51519294 T C 21 GENIC homozygous 801450653 1 51520529 51520530 G C 40 GENIC homozygous 801450654 1 51520540 51520541 A G 40 GENIC homozygous 801450655 1 51520582 51520583 T C 30 GENIC homozygous 801450656 1 51521636 51521637 C A 12 GENIC homozygous 801450657 1 51521880 51521881 C A 19 GENIC homozygous 801450658 1 51523441 51523442 G C 27 GENIC homozygous 801450659 1 51523455 51523456 T C 28 GENIC homozygous 801450660 1 51526033 51526034 T C 26 GENIC homozygous 801450661