chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 152789496 152789497 G A 16 GENIC homozygous 110058730 2 152794232 152794233 G T 23 GENIC homozygous 111268652 2 152794797 152794798 A G 24 GENIC possibly homozygous 111268654 2 152795694 152795695 T C 33 GENIC homozygous 111268656 2 152797104 152797105 G A 28 GENIC homozygous 111268658 2 152800016 152800017 G A 30 GENIC homozygous 111268660 2 152804988 152804989 A C 33 GENIC possibly homozygous 120150863 2 152804989 152804990 G T 33 GENIC possibly homozygous 120150864 2 152804990 152804991 A T 33 GENIC possibly homozygous 120150865 2 152805627 152805628 G C 28 GENIC homozygous 110058834 2 152806947 152806948 C T 15 GENIC homozygous 111268664 2 152807571 152807572 G A 34 GENIC homozygous 111268666 2 152808895 152808896 A T 19 GENIC homozygous 120150866 2 152811884 152811885 G A 26 GENIC homozygous 110058861 2 152814213 152814214 A C 22 GENIC homozygous 111268668 2 152815306 152815307 C T 18 GENIC homozygous 111268670 2 152815849 152815850 G T 15 GENIC homozygous 110058872 2 152816022 152816023 G C 17 GENIC homozygous 110058874 2 152816743 152816744 A G 19 GENIC homozygous 110058879 2 152818577 152818578 G T 20 GENIC homozygous 111268674 2 152819999 152820000 T A 29 GENIC possibly homozygous 111268676 2 152822049 152822050 G C 18 GENIC homozygous 110058909 2 152822698 152822699 A G 19 GENIC homozygous 111268682 2 152823831 152823832 T G 27 GENIC homozygous 111268684