chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 104609611 104609612 G A 55 GENIC homozygous 139614763 14 104609835 104609836 A G 66 GENIC homozygous 139614764 14 104611865 104611869 AATT 19 GENIC homozygous 140913741 14 104613029 104613030 C T 47 GENIC homozygous 139614765 14 104613624 104613625 A C 49 GENIC homozygous 139614766 14 104614642 104614643 T C 62 GENIC homozygous 139614767 14 104614732 104614733 C T 58 GENIC homozygous 139614768 14 104614749 104614750 G A 55 GENIC homozygous 139614769 14 104614843 104614844 T A 46 GENIC homozygous 139614770 14 104615287 104615288 G C 35 GENIC homozygous 139614771 14 104615317 104615318 C T 27 GENIC homozygous 139614772 14 104615370 104615371 A T 6 GENIC heterozygous 403368772 14 104615368 104615369 A 5 GENIC homozygous 403368769 14 104615368 104615369 A T 5 GENIC heterozygous 403368770 14 104615370 104615371 A 6 GENIC heterozygous 403368771 14 104615372 104615373 A 5 GENIC heterozygous 403368773 14 104615372 104615373 A T 5 GENIC heterozygous 403368774 14 104615374 104615375 A 8 GENIC heterozygous 403368775 14 104615374 104615375 A T 8 GENIC heterozygous 403368776 14 104615376 104615377 A T 8 GENIC heterozygous 139614773 14 104615697 104615698 G A 46 GENIC homozygous 139614774 14 104615851 104615852 G A 37 GENIC homozygous 139614775 14 104616059 104616060 C A 49 GENIC homozygous 139614776 14 104616089 104616090 A T 40 GENIC homozygous 139614777 14 104617345 104617346 A G 43 GENIC homozygous 139614778 14 104617594 104617595 A G 46 GENIC homozygous 139614779 14 104618073 104618074 G A 53 GENIC homozygous 139614780 14 104618759 104618760 T A 60 GENIC homozygous 139614781