chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 46978965 46978966 G T 13 GENIC homozygous 977726259 X 46978977 46978978 G A 12 GENIC homozygous 977726260 X 46978978 46978979 A G 12 GENIC homozygous 977726261 X 46985317 46985318 A C 15 GENIC homozygous 977726262 X 47004354 47004355 C T 13 GENIC homozygous 977726263 X 47008767 47008768 A T 7 GENIC homozygous 977726264 X 47009839 47009840 A G 25 GENIC homozygous 977726265 X 47011337 47011338 C A 16 GENIC possibly homozygous 977726266 X 47011466 47011467 A G 16 GENIC homozygous 977726267 X 47011554 47011555 C G 26 GENIC homozygous 977726268 X 47011814 47011815 C T 18 GENIC homozygous 977726269 X 47011850 47011851 A T 14 GENIC homozygous 977726270 X 47012714 47012715 T C 15 GENIC homozygous 977726271 X 47014062 47014063 A G 11 GENIC homozygous 977726272 X 47014395 47014396 T G 17 GENIC homozygous 977726273 X 47014863 47014864 A C 8 GENIC homozygous 977726274 X 47014985 47014986 G C 5 GENIC homozygous 977726275 X 47016754 47016755 T A 5 GENIC homozygous 977726276 X 47018770 47018771 G A 10 GENIC homozygous 977726277 X 47020297 47020298 T C 5 GENIC homozygous 977726278 X 47020897 47020898 A T 11 GENIC homozygous 977726279 X 47021260 47021261 T C 15 GENIC homozygous 977726280 X 47021922 47021923 C T 12 GENIC homozygous 977726281 X 47022045 47022046 G A 10 GENIC homozygous 977726282 X 47022954 47022955 G A 13 GENIC homozygous 977726283 X 47023445 47023446 G C 13 GENIC homozygous 977726284 X 47023944 47023945 G A 10 GENIC homozygous 977726285 X 47025892 47025893 T C 12 GENIC homozygous 977726286