chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 100453740 100453741 G A 79 GENIC homozygous 117619632 9 100454305 100454306 G A 78 GENIC homozygous 117619634 9 100454306 100454307 T A 78 GENIC homozygous 117619636 9 100455072 100455073 A C 60 GENIC homozygous 117619638 9 100455134 100455135 C T 54 GENIC homozygous 117619640 9 100458959 100458960 G A 62 GENIC homozygous 117619642 9 100462506 100462507 T A 68 GENIC homozygous 117619644 9 100463061 100463062 A G 60 GENIC homozygous 117619646 9 100463918 100463919 C T 65 GENIC homozygous 117619648 9 100465199 100465200 A G 53 GENIC homozygous 117619650 9 100465789 100465790 A T 64 GENIC homozygous 117619652 9 100466014 100466015 C T 47 GENIC homozygous 117619654 9 100466497 100466498 A G 56 GENIC homozygous 117619656 9 100466730 100466731 T C 68 GENIC homozygous 117619658 9 100468820 100468821 C T 48 GENIC homozygous 117619660 9 100469094 100469095 T C 61 GENIC homozygous 117619662 9 100469095 100469096 G T 61 GENIC homozygous 117619664 9 100469135 100469136 C T 58 GENIC homozygous 117619666 9 100470261 100470262 T C 55 GENIC homozygous 117619668 9 100470916 100470917 G A 45 GENIC homozygous 117619670 9 100471616 100471617 C T 61 GENIC possibly homozygous 117619672 9 100471780 100471781 C T 46 GENIC homozygous 117619674 9 100474008 100474009 G A 56 GENIC homozygous 117619676 9 100475377 100475378 G A 47 GENIC homozygous 117400132 9 100476729 100476730 G A 88 GENIC homozygous 117619678 9 100476874 100476875 T A 46 GENIC homozygous 117619680 9 100477784 100477785 T C 59 GENIC homozygous 117619682 9 100478119 100478120 T C 59 GENIC homozygous 117619684 9 100478906 100478907 T C 57 GENIC homozygous 117619686 9 100479484 100479485 A G 71 GENIC homozygous 117619688 9 100457924 100457924 TGC 59 GENIC homozygous 128737392 9 100460269 100460269 TCCTTAGAACCGGCTTT 36 GENIC homozygous 128737393 9 100461545 100461599 CCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGC 34 GENIC homozygous 128737394