chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 46978965 46978966 G T 12 GENIC homozygous 995703918 X 46978977 46978978 G A 10 GENIC homozygous 995703919 X 46978978 46978979 A G 10 GENIC homozygous 995703920 X 46985317 46985318 A C 16 GENIC possibly homozygous 995703921 X 46995349 46995350 C T 8 GENIC homozygous 995703922 X 47004354 47004355 C T 8 GENIC homozygous 995703923 X 47004609 47004610 T C 10 GENIC homozygous 995703924 X 47008316 47008317 T C 3 GENIC homozygous 995703925 X 47008767 47008768 A T 8 GENIC possibly homozygous 995703926 X 47009839 47009840 A G 18 GENIC possibly homozygous 995703927 X 47011337 47011338 C A 11 GENIC possibly homozygous 995703928 X 47011466 47011467 A G 9 GENIC possibly homozygous 995703929 X 47011554 47011555 C G 6 GENIC heterozygous 995703930 X 47011814 47011815 C T 10 GENIC homozygous 995703931 X 47011850 47011851 A T 13 GENIC homozygous 995703932 X 47012714 47012715 T C 22 GENIC possibly homozygous 995703933 X 47014062 47014063 A G 6 GENIC homozygous 995703934 X 47014395 47014396 T G 11 GENIC possibly homozygous 995703935 X 47014863 47014864 A C 9 GENIC homozygous 995703936 X 47014985 47014986 G C 11 GENIC homozygous 995703937 X 47016608 47016609 A G 6 GENIC homozygous 995703938 X 47016754 47016755 T A 13 GENIC homozygous 995703939 X 47018770 47018771 G A 6 GENIC homozygous 995703940 X 47020297 47020298 T C 4 GENIC homozygous 995703941 X 47020897 47020898 A T 10 GENIC homozygous 995703942 X 47021260 47021261 T C 7 GENIC homozygous 995703943 X 47021922 47021923 C T 12 GENIC possibly homozygous 995703944 X 47022045 47022046 G A 14 GENIC homozygous 995703945 X 47022954 47022955 G A 5 GENIC homozygous 995703946 X 47023445 47023446 G C 14 GENIC homozygous 995703947 X 47023944 47023945 G A 5 GENIC homozygous 995703948