chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 52572157 52572158 G A 61 GENIC homozygous 533886726 9 52572237 52572238 T C 48 GENIC homozygous 535160668 9 52572854 52572855 G T 38 GENIC homozygous 533886727 9 52572903 52572904 A G 43 GENIC homozygous 533886728 9 52572917 52572918 G T 45 GENIC homozygous 533886729 9 52573120 52573121 A G 44 GENIC homozygous 533886730 9 52573178 52573179 T C 46 GENIC homozygous 533886731 9 52573208 52573209 A T 47 GENIC homozygous 533886732 9 52573234 52573235 C A 38 GENIC homozygous 533886733 9 52573340 52573341 T A 49 GENIC homozygous 533886734 9 52573627 52573628 A G 43 GENIC homozygous 533886735 9 52573730 52573733 TAG --- 30 GENIC homozygous 695972684 9 52573789 52573790 T A 39 GENIC homozygous 533886736 9 52574192 52574193 A G 55 GENIC homozygous 533886737 9 52574475 52574476 G A 48 GENIC homozygous 535160669 9 52574489 52574490 C T 44 GENIC homozygous 533886738 9 52574696 52574697 T C 50 GENIC homozygous 533886739 9 52574737 52574738 T C 56 GENIC homozygous 533886740 9 52575120 52575121 G A 56 GENIC possibly homozygous 533886741 9 52575450 52575451 A G 38 GENIC homozygous 533886742 9 52575671 52575672 A G 21 GENIC homozygous 533886743 9 52576268 52576269 C A 36 GENIC possibly homozygous 535160670 9 52576280 52576281 T G 37 GENIC homozygous 533886744 9 52576321 52576322 G C 39 GENIC homozygous 533886745 9 52576513 52576514 C CT 33 GENIC homozygous 695972685 9 52576610 52576611 T C 39 GENIC homozygous 533886746 9 52576650 52576651 T A 37 GENIC homozygous 533886747 9 52576831 52576832 A G 39 GENIC homozygous 533886748 9 52577012 52577013 A T 55 GENIC homozygous 533886749 9 52577413 52577414 C T 61 GENIC homozygous 533886750 9 52577502 52577503 A T 50 GENIC homozygous 533886751 9 52577622 52577623 A G 49 GENIC homozygous 533886752 9 52577656 52577657 A G 52 GENIC homozygous 533886753