chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 110903046 110903047 A T 5 GENIC homozygous 936914764 X 110903049 110903050 T A 6 GENIC homozygous 936914765 X 110903511 110903512 G C 10 GENIC homozygous 936914766 X 110906891 110906892 C T 21 GENIC homozygous 936914767 X 110906892 110906893 C T 21 GENIC homozygous 936914768 X 110911116 110911117 C A 5 GENIC homozygous 936914769 X 110926714 110926715 A G 14 GENIC homozygous 936914770 X 110927167 110927168 T G 10 GENIC homozygous 936914771 X 110929848 110929849 C A 14 GENIC homozygous 936914772 X 110945603 110945604 A G 11 GENIC homozygous 936914773 X 110953989 110953990 C T 6 GENIC homozygous 936914774 X 110957382 110957383 T A 15 GENIC homozygous 936914775 X 110957386 110957387 A T 15 GENIC homozygous 936914776 X 110961229 110961230 G A 8 GENIC homozygous 936914777 X 110969270 110969271 G A 17 GENIC homozygous 936914778 X 110978913 110978914 T A 11 GENIC homozygous 936914779