chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	176510009	176510010	T	C	45	GENIC	homozygous	112963990
4	176510250	176510250		G	34	GENIC	homozygous	128107904
4	176510303	176510304	A	G	37	GENIC	homozygous	112963992
4	176510956	176510957	T	C	46	GENIC	homozygous	112963994
4	176511450	176511454	AAAT		43	GENIC	homozygous	128107905
4	176512622	176512623	A	T	53	GENIC	homozygous	112963996
4	176513229	176513237	TCTATCTA		28	GENIC	homozygous	128107906
4	176513335	176513336	G	T	50	GENIC	homozygous	112963998
4	176513369	176513370	A	G	55	GENIC	homozygous	112964000
4	176513809	176513810	A	G	52	GENIC	homozygous	112964002
4	176513899	176513900	T	C	57	GENIC	homozygous	112964004
4	176514199	176514200	A	T	30	GENIC	homozygous	112964006
4	176514517	176514517		C	59	GENIC	homozygous	128107907
4	176514642	176514643	A	C	53	GENIC	homozygous	112964008
4	176514745	176514746	G	A	49	GENIC	homozygous	112964010
4	176514776	176514777	T	A	55	GENIC	homozygous	112964012
4	176516152	176516153	G		50	GENIC	homozygous	128107908
4	176517892	176517893	A	G	53	GENIC	homozygous	112964014