chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	17869630	17869631	A	G	65	GENIC	homozygous	117270953
9	17869834	17869835	A	G	49	GENIC	homozygous	117270954
9	17869911	17869912	T	C	45	GENIC	homozygous	117270955
9	17870016	17870017	G	T	59	GENIC	homozygous	117270956
9	17870286	17870287	C	T	40	GENIC	homozygous	117270957
9	17871216	17871217	C	T	47	GENIC	homozygous	117270958
9	17871409	17871410	A	T	43	GENIC	homozygous	117270959
9	17871530	17871531	T	A	76	GENIC	possibly homozygous	117270960
9	17871762	17871763	G	A	37	GENIC	homozygous	117270961
9	17874849	17874850	T	C	55	GENIC	homozygous	117270962
9	17876811	17876812	A	T	37	GENIC	possibly homozygous	117270963
9	17877037	17877038	T	C	46	GENIC	homozygous	117270964
9	17877907	17877908	A	G	33	GENIC	possibly homozygous	117270965
9	17878115	17878116	G	A	35	GENIC	homozygous	117270966
9	17879067	17879068	T	C	41	GENIC	homozygous	117270967
9	17879812	17879813	C	T	52	GENIC	homozygous	117270968
9	17879955	17879956	T	A	51	GENIC	homozygous	117270969
9	17880083	17880084	C	G	50	GENIC	homozygous	117270970
9	17880358	17880359	A	C	46	GENIC	homozygous	117270971
9	17880524	17880525	G	C	36	GENIC	homozygous	117270972