chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4579874 4579875 A G 7 GENIC homozygous 109074755 20 4581986 4581987 G A 20 GENIC homozygous 109074761 20 4582119 4582120 C T 15 GENIC homozygous 109074763 20 4582721 4582722 T A 12 GENIC homozygous 109074765 20 4582830 4582831 G A 18 GENIC homozygous 109074767 20 4582956 4582957 G T 17 GENIC homozygous 109074769 20 4582995 4582996 G A 15 GENIC homozygous 109074771 20 4583257 4583258 C T 23 GENIC homozygous 109074773 20 4583468 4583469 C A 11 GENIC homozygous 109074775 20 4583562 4583563 G T 11 GENIC possibly homozygous 109074777 20 4586338 4586339 G A 7 GENIC homozygous 109074781 20 4586535 4586536 T A 10 GENIC homozygous 109074783 20 4586724 4586725 A G 4 GENIC homozygous 109074789 20 4586822 4586823 G A 7 GENIC homozygous 109296144 20 4587736 4587737 T G 13 GENIC homozygous 109296148 20 4588080 4588081 G A 15 GENIC homozygous 109329588 20 4588106 4588107 G A 22 GENIC homozygous 109329590 20 4589025 4589026 G A 14 GENIC homozygous 109074793 20 4589422 4589423 T C 5 GENIC homozygous 109074797 20 4591761 4591762 G A 13 GENIC homozygous 109329594