chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	39033444	39033445	T	G	59	GENIC	homozygous	111041978
17	39033855	39033856	A	G	47	GENIC	homozygous	111041980
17	39034328	39034329	G	T	42	GENIC	homozygous	111041982
17	39035422	39035423	T	C	53	GENIC	homozygous	111041984
17	39036893	39036894	G	A	37	GENIC	homozygous	111041986
17	39038700	39038701	T	C	67	GENIC	homozygous	111041988
17	39039398	39039399	T	C	35	GENIC	heterozygous	119284045
17	39039428	39039429	C	G	42	GENIC	heterozygous	119284047
17	39039945	39039946	A	G	44	GENIC	possibly homozygous	119284051
17	39040164	39040165	C	T	19	GENIC	heterozygous	119284053
17	39040280	39040281	C	G	48	GENIC	heterozygous	119284055
17	39040495	39040496	G	C	39	GENIC	possibly homozygous	119284057
17	39040740	39040741	A	C	49	GENIC	homozygous	111041990
17	39040917	39040918	A	G	55	GENIC	possibly homozygous	111201087
17	39041099	39041100	G	T	33	GENIC	homozygous	111041992
17	39042421	39042422	G	C	75	GENIC	heterozygous	119284059
17	39042543	39042544	T	A	79	GENIC	heterozygous	119338773
17	39042577	39042578	T	G	65	GENIC	heterozygous	119338775
17	39042663	39042664	T	C	50	GENIC	homozygous	119284061
17	39042999	39043000	C	T	60	GENIC	homozygous	111041994
17	39043027	39043028	T	C	50	GENIC	homozygous	111041996
17	39043812	39043813	T	A	41	GENIC	possibly homozygous	119284063