chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 170364466 170364467 A G 12 GENIC homozygous 112203732 3 170365980 170365981 A G 17 GENIC homozygous 111834356 3 170366006 170366007 T A 14 GENIC homozygous 111834358 3 170366683 170366684 T C 18 GENIC homozygous 112203737 3 170366984 170366985 G T 21 GENIC homozygous 112203739 3 170367592 170367593 A G 19 GENIC homozygous 112203741 3 170368090 170368091 A G 18 GENIC homozygous 112203743 3 170368318 170368319 A G 20 GENIC homozygous 112203745 3 170368339 170368340 G A 20 GENIC homozygous 112203747 3 170369149 170369150 T C 26 GENIC homozygous 111834368 3 170370128 170370129 G A 19 GENIC homozygous 112203749 3 170370978 170370979 A G 9 GENIC homozygous 112203751 3 170371347 170371348 A G 9 GENIC homozygous 111834378 3 170371396 170371397 T C 10 GENIC homozygous 111834380 3 170372875 170372876 C A 7 GENIC homozygous 112203753 3 170373273 170373274 A G 16 GENIC homozygous 111834384 3 170375409 170375410 T C 15 GENIC homozygous 111834390 3 170376620 170376621 G A 20 GENIC homozygous 112203757 3 170377194 170377195 A C 10 GENIC homozygous 112203761 3 170377560 170377561 T C 13 GENIC homozygous 112203763 3 170377719 170377720 A G 12 GENIC homozygous 111834394 3 170379686 170379687 C T 15 GENIC homozygous 112203767 3 170379834 170379835 G A 6 GENIC homozygous 111834398 3 170380008 170380009 T C 17 GENIC homozygous 112203769