chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	43017102	43017103	G	A	25	GENIC	homozygous	56850119
4	43017231	43017232	A	C	13	GENIC	homozygous	56850120
4	43017373	43017374	T	TTAAA	11	GENIC	homozygous	56850121
4	43017989	43017990	T	C	12	GENIC	homozygous	56850122
4	43019102	43019103	C	A	8	GENIC	homozygous	56850124
4	43019433	43019434	A	C	6	GENIC	homozygous	56850125
4	43019589	43019590	G	C	11	GENIC	homozygous	56850126
4	43019867	43019868	T	C	7	GENIC	homozygous	56850127
4	43019877	43019878	A	G	7	GENIC	homozygous	56850128
4	43020014	43020015	T	-	10	GENIC	homozygous	56850129
4	43020493	43020494	C	T	19	GENIC	homozygous	56850130
4	43020678	43020679	G	GT	10	GENIC	homozygous	56850131
4	43020898	43020899	A	T	10	GENIC	homozygous	56850132
4	43021055	43021057	GG	--	11	GENIC	heterozygous	56850133
4	43021062	43021063	G	GT	12	GENIC	heterozygous	56850134
4	43021067	43021068	G	GTTTTGTTTTGTTTTTGT	13	GENIC	homozygous	56850135
4	43021073	43021074	T	-	14	GENIC	heterozygous	56850136
4	43021378	43021379	C	T	16	GENIC	homozygous	56850137
4	43021535	43021536	G	A	12	GENIC	homozygous	56850138
4	43021579	43021580	G	T	14	GENIC	homozygous	56850139
4	43022032	43022033	T	C	9	GENIC	possibly homozygous	56850140
4	43022065	43022066	T	C	10	GENIC	homozygous	56850141
4	43022074	43022075	C	CT	9	GENIC	homozygous	56850142