chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4578221 4578222 C T 6 GENIC homozygous 109233522 20 4581789 4581790 C T 10 GENIC homozygous 109233526 20 4582624 4582625 C T 8 GENIC homozygous 109233527 20 4582830 4582831 G A 15 GENIC homozygous 109074767 20 4582909 4582910 T A 16 GENIC homozygous 109233528 20 4582956 4582957 G T 17 GENIC possibly homozygous 109074769 20 4582995 4582996 G A 15 GENIC homozygous 109074771 20 4583048 4583049 C T 11 GENIC homozygous 109233529 20 4583257 4583258 C T 10 GENIC homozygous 109074773 20 4583260 4583261 T C 11 GENIC homozygous 109233530 20 4583562 4583563 G T 12 GENIC homozygous 109074777 20 4584880 4584881 C T 10 GENIC homozygous 109296140 20 4582288 4582289 C T 11 GENIC homozygous 109296134 20 4582400 4582401 G A 10 GENIC homozygous 109296136 20 4583599 4583600 G A 12 GENIC homozygous 109296138 20 4585946 4585947 A G 14 GENIC homozygous 109296142 20 4586338 4586339 G A 18 GENIC homozygous 109074781 20 4586535 4586536 T A 18 GENIC homozygous 109074783 20 4586724 4586725 A G 15 GENIC homozygous 109074789 20 4586822 4586823 G A 12 GENIC homozygous 109296144 20 4586877 4586878 C T 10 GENIC homozygous 109296146 20 4587736 4587737 T G 5 GENIC homozygous 109296148 20 4588747 4588748 C T 29 GENIC possibly homozygous 109296150 20 4589025 4589026 G A 28 GENIC homozygous 109074793 20 4589366 4589367 C T 18 GENIC homozygous 109296152 20 4589422 4589423 T C 12 GENIC homozygous 109074797 20 4590244 4590245 G A 12 GENIC homozygous 109296154 20 4592461 4592462 G T 20 GENIC homozygous 109296156