chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 46991579 46991580 G C 9 GENIC heterozygous 893639819 X 46995349 46995350 C T 8 GENIC homozygous 893639820 X 46995424 46995425 G T 7 GENIC heterozygous 893639821 X 47008316 47008317 T C 8 GENIC homozygous 893639826 X 47009839 47009840 A G 11 GENIC homozygous 893639827 X 47012714 47012715 T C 7 GENIC homozygous 893639828 X 47014062 47014063 A G 8 GENIC homozygous 893639829 X 47014395 47014396 T G 8 GENIC homozygous 893639830 X 47018770 47018771 G A 10 GENIC homozygous 893639831 X 47020297 47020298 T C 6 GENIC homozygous 893639832 X 47021260 47021261 T C 7 GENIC homozygous 893639833 X 47021922 47021923 C T 11 GENIC homozygous 893639834 X 47022045 47022046 G A 15 GENIC homozygous 893639835 X 47022954 47022955 G A 12 GENIC homozygous 893639836 X 47023445 47023446 G C 7 GENIC homozygous 893639837 X 47023944 47023945 G A 7 GENIC homozygous 893639838 X 47025892 47025893 T C 5 GENIC homozygous 893639839