chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 10617579 10617580 A C 73 GENIC homozygous 47609767 16 10617581 10617582 C A 73 GENIC homozygous 47609769 16 10617726 10617727 T A 61 GENIC homozygous 47271063 16 10617844 10617848 GTGA ---- 24 GENIC heterozygous 47271067 16 10617888 10617889 A ACAG 13 GENIC homozygous 47271069 16 10617893 10617894 T - 9 GENIC homozygous 47271073 16 10617897 10617898 C A 13 GENIC homozygous 47271075 16 10617898 10617899 C T 13 GENIC homozygous 47271077 16 10622524 10622526 TA -- 51 GENIC heterozygous 47271083 16 10628596 10628597 T TG 25 GENIC possibly homozygous 47609771 16 10631789 10631790 G A 68 GENIC homozygous 47271135 16 10633529 10633530 G GGTTTGT 13 GENIC homozygous 47271145 16 10634700 10634701 T TCTTC 10 GENIC homozygous 47609773 16 10634737 10634738 G C 27 GENIC heterozygous 47271149 16 10648584 10648588 CTGT ---- 23 GENIC homozygous 47271281 16 10652183 10652184 G A 37 GENIC homozygous 47609775