chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 46977813 46977814 C T 9 GENIC homozygous 971469482 X 46978965 46978966 G T 14 GENIC homozygous 971469483 X 46978977 46978978 G A 13 GENIC homozygous 971469484 X 46978978 46978979 A G 13 GENIC homozygous 971469485 X 46995399 46995400 A C 9 GENIC homozygous 971469486 X 47004296 47004297 G A 10 GENIC homozygous 971469487 X 47009839 47009840 A G 8 GENIC homozygous 971469488 X 47010768 47010769 G A 8 GENIC homozygous 971469489 X 47011337 47011338 C A 3 GENIC homozygous 971469490 X 47011466 47011467 A G 5 GENIC homozygous 971469491 X 47011814 47011815 C T 9 GENIC homozygous 971469492 X 47014863 47014864 A C 8 GENIC homozygous 971469493 X 47018763 47018764 C T 16 GENIC homozygous 971469494 X 47022045 47022046 G A 16 GENIC homozygous 971469495 X 47024308 47024309 A T 6 GENIC homozygous 971469496 X 47025892 47025893 T C 8 GENIC homozygous 971469497 X 47026357 47026358 C T 9 GENIC homozygous 971469498