chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4579874 4579875 A G 18 GENIC homozygous 109074755 20 4581497 4581498 C G 23 GENIC homozygous 109074759 20 4582119 4582120 C T 31 GENIC homozygous 109074763 20 4582624 4582625 C T 17 GENIC homozygous 109233527 20 4582721 4582722 T A 15 GENIC homozygous 109074765 20 4582830 4582831 G A 18 GENIC homozygous 109074767 20 4582956 4582957 G T 18 GENIC homozygous 109074769 20 4582995 4582996 G A 23 GENIC homozygous 109074771 20 4583257 4583258 C T 24 GENIC homozygous 109074773 20 4583562 4583563 G T 16 GENIC homozygous 109074777 20 4586338 4586339 G A 24 GENIC homozygous 109074781 20 4586535 4586536 T A 20 GENIC homozygous 109074783 20 4586724 4586725 A G 16 GENIC homozygous 109074789 20 4586822 4586823 G A 14 GENIC homozygous 109296144 20 4585946 4585947 A G 24 GENIC homozygous 109296142 20 4587736 4587737 T G 18 GENIC homozygous 109296148 20 4588080 4588081 G A 20 GENIC homozygous 109329588 20 4588106 4588107 G A 25 GENIC homozygous 109329590 20 4589025 4589026 G A 26 GENIC homozygous 109074793 20 4589422 4589423 T C 10 GENIC homozygous 109074797 20 4591221 4591222 C T 22 GENIC homozygous 109329592 20 4591761 4591762 G A 29 GENIC homozygous 109329594