chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 52562980 52562981 C T 20 GENIC homozygous 115356626 12 52563287 52563288 A G 6 GENIC homozygous 115356627 12 52564237 52564238 T C 13 GENIC homozygous 115356628 12 52564271 52564272 G A 11 GENIC homozygous 115356629 12 52564584 52564585 C T 12 GENIC homozygous 115356630 12 52565118 52565119 G A 25 GENIC homozygous 115356631 12 52565418 52565419 A T 20 GENIC homozygous 115404587 12 52565448 52565449 T C 15 GENIC homozygous 115404589 12 52566435 52566436 A G 13 GENIC homozygous 115356632 12 52566984 52566985 A T 9 GENIC homozygous 115356633 12 52568272 52568273 A G 19 GENIC homozygous 115356634 12 52568677 52568678 G T 19 GENIC homozygous 115356635 12 52569100 52569101 T A 17 GENIC homozygous 115356636 12 52570576 52570577 G A 18 GENIC homozygous 115356637 12 52571042 52571043 T A 24 GENIC homozygous 115356638 12 52571368 52571369 T C 24 GENIC homozygous 115356639 12 52571613 52571614 A G 18 GENIC homozygous 115356640 12 52573929 52573930 G C 20 GENIC homozygous 115356641 12 52574639 52574640 A G 19 GENIC homozygous 115356642 12 52575060 52575061 T C 26 GENIC homozygous 115356643 12 52576060 52576061 T G 30 GENIC homozygous 115356645 12 52576542 52576543 T C 12 GENIC homozygous 115404597 12 52576770 52576771 C A 21 GENIC homozygous 115356646 12 52577111 52577112 A G 28 GENIC homozygous 115356647 12 52577767 52577768 T C 32 GENIC homozygous 115356648 12 52577874 52577875 A G 16 GENIC homozygous 115356649 12 52578856 52578857 C T 20 GENIC homozygous 115404599 12 52579711 52579712 G C 13 GENIC homozygous 115356650 12 52584342 52584343 C T 20 GENIC homozygous 115356652 12 52587413 52587414 A C 19 GENIC homozygous 115356653 12 52590523 52590524 T C 19 GENIC homozygous 115356654 12 52594242 52594243 T G 14 GENIC homozygous 115356655 12 52595237 52595238 A G 18 GENIC homozygous 115356656