chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 35175534 35175535 G T 6 GENIC homozygous 801268719 X 35175653 35175654 T G 5 GENIC homozygous 801268720 X 35177318 35177319 T G 25 GENIC heterozygous 801268721 X 35177341 35177342 T G 33 GENIC heterozygous 801268722 X 35187282 35187283 T C 15 GENIC homozygous 801268723 X 35187292 35187293 C T 17 GENIC homozygous 801268724 X 35187385 35187386 C T 18 GENIC homozygous 801268725 X 35187398 35187399 C T 14 GENIC homozygous 801268726 X 35187399 35187400 C T 14 GENIC homozygous 801268727 X 35189723 35189724 A G 22 GENIC possibly homozygous 801268728 X 35191919 35191920 C A 93 GENIC heterozygous 801268729 X 35191946 35191947 A T 88 GENIC heterozygous 801268730 X 35191993 35191994 T G 88 GENIC heterozygous 801268731 X 35192014 35192015 C G 77 GENIC heterozygous 801268732 X 35192041 35192042 G A 85 GENIC heterozygous 801268733 X 35192054 35192055 A G 83 GENIC heterozygous 801268734