chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	40230215	40230215		C	36	GENIC	possibly homozygous	140022404
17	40230341	40230342	T	G	46	GENIC	homozygous	140114950
17	40232587	40232588	T	C	47	GENIC	homozygous	140114951
17	40233544	40233545	T	C	50	GENIC	homozygous	140114952
17	40234231	40234232	A	T	53	GENIC	homozygous	140114953
17	40234338	40234339	A	G	59	GENIC	homozygous	140114954
17	40234888	40234889	C	G	52	GENIC	homozygous	140114955
17	40235528	40235528		AAAC	42	GENIC	homozygous	140022405
17	40236699	40236700	C	A	41	GENIC	homozygous	140114956
17	40236763	40236764	T	C	38	GENIC	homozygous	140114957
17	40236953	40236954	T	C	57	GENIC	homozygous	140114958
17	40237914	40237915	A		42	GENIC	possibly homozygous	140022406
17	40237935	40237936	A	G	47	GENIC	homozygous	140114959
17	40238444	40238445	C		10	GENIC	homozygous	140022407
17	40239085	40239086	A	G	44	GENIC	homozygous	140114960
17	40239641	40239642	G	C	66	GENIC	homozygous	140114961