chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 159590044 159590045 C T 54 GENIC homozygous 794066688 5 159590355 159590356 A C 52 GENIC homozygous 794066689 5 159590356 159590357 G C 51 GENIC homozygous 794066690 5 159590377 159590378 G A 53 GENIC homozygous 794066691 5 159590516 159590517 A G 40 GENIC homozygous 794066692 5 159590543 159590544 T C 41 GENIC homozygous 794066693 5 159590567 159590568 T C 37 GENIC homozygous 794066694 5 159590810 159590811 G A 27 GENIC homozygous 794066695 5 159591041 159591042 C T 33 GENIC possibly homozygous 794066696 5 159591165 159591166 A G 49 GENIC homozygous 794066697 5 159591294 159591295 G A 52 GENIC homozygous 794066698 5 159591492 159591493 C T 39 GENIC homozygous 794066699 5 159591711 159591712 G A 44 GENIC homozygous 794066700 5 159591959 159591960 C T 32 GENIC homozygous 794066701 5 159592241 159592242 A G 34 GENIC homozygous 794066702 5 159592551 159592552 G A 35 GENIC homozygous 794066703 5 159592593 159592594 G A 31 GENIC possibly homozygous 794066704 5 159592713 159592714 C T 16 GENIC homozygous 794066705 5 159593011 159593012 T A 38 GENIC homozygous 794066706 5 159593229 159593230 A G 40 GENIC homozygous 794066707 5 159593316 159593317 A C 28 GENIC homozygous 794066708 5 159594481 159594482 G A 29 GENIC homozygous 794066709 5 159595521 159595522 G A 30 GENIC homozygous 794066710 5 159598268 159598269 G A 33 GENIC homozygous 794066711 5 159599504 159599505 T C 42 GENIC possibly homozygous 794066712 5 159600471 159600472 T C 53 GENIC possibly homozygous 794066713 5 159601143 159601144 C T 37 GENIC homozygous 794066714 5 159601217 159601218 A G 34 GENIC homozygous 794066715 5 159601274 159601275 A G 47 GENIC homozygous 794066716 5 159602018 159602019 C T 30 GENIC homozygous 794066717