chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4579874 4579875 A G 25 GENIC homozygous 109074755 20 4580274 4580275 G A 51 GENIC possibly homozygous 109074757 20 4581497 4581498 C G 12 GENIC homozygous 109074759 20 4581986 4581987 G A 30 GENIC homozygous 109074761 20 4582119 4582120 C T 36 GENIC homozygous 109074763 20 4582624 4582625 C T 36 GENIC homozygous 109233527 20 4582721 4582722 T A 38 GENIC homozygous 109074765 20 4582830 4582831 G A 44 GENIC homozygous 109074767 20 4582956 4582957 G T 25 GENIC homozygous 109074769 20 4582995 4582996 G A 26 GENIC homozygous 109074771 20 4583257 4583258 C T 42 GENIC homozygous 109074773 20 4583468 4583469 C A 43 GENIC homozygous 109074775 20 4583562 4583563 G T 40 GENIC homozygous 109074777 20 4585946 4585947 A G 31 GENIC homozygous 109296142 20 4586338 4586339 G A 16 GENIC homozygous 109074781 20 4586535 4586536 T A 40 GENIC homozygous 109074783 20 4586724 4586725 A G 21 GENIC homozygous 109074789 20 4586822 4586823 G A 37 GENIC homozygous 109296144 20 4587736 4587737 T G 38 GENIC homozygous 109296148 20 4588080 4588081 G A 35 GENIC possibly homozygous 109329588 20 4588106 4588107 G A 28 GENIC homozygous 109329590 20 4589025 4589026 G A 42 GENIC homozygous 109074793 20 4589422 4589423 T C 32 GENIC possibly homozygous 109074797 20 4591221 4591222 C T 45 GENIC homozygous 109329592 20 4591761 4591762 G A 37 GENIC homozygous 109329594