chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	43017102	43017103	G	A	39	GENIC	homozygous	56850119
4	43017231	43017232	A	C	36	GENIC	homozygous	56850120
4	43017373	43017374	T	TTAAA	18	GENIC	homozygous	56850121
4	43017989	43017990	T	C	52	GENIC	homozygous	56850122
4	43018382	43018383	G	A	31	GENIC	homozygous	56850123
4	43018384	43018385	A	G	31	GENIC	homozygous	57300490
4	43019102	43019103	C	A	9	GENIC	homozygous	56850124
4	43019433	43019434	A	C	16	GENIC	homozygous	56850125
4	43019589	43019590	G	C	11	GENIC	homozygous	56850126
4	43019867	43019868	T	C	11	GENIC	homozygous	56850127
4	43019877	43019878	A	G	10	GENIC	homozygous	56850128
4	43020014	43020015	T	-	21	GENIC	possibly homozygous	56850129
4	43020493	43020494	C	T	38	GENIC	homozygous	56850130
4	43020678	43020679	G	GT	29	GENIC	homozygous	56850131
4	43020898	43020899	A	T	55	GENIC	homozygous	56850132
4	43021067	43021068	G	GTTTTGTTTTGTTTTTGT	19	GENIC	homozygous	56850135
4	43021378	43021379	C	T	18	GENIC	homozygous	56850137
4	43021535	43021536	G	A	31	GENIC	homozygous	56850138
4	43021579	43021580	G	T	40	GENIC	homozygous	56850139
4	43022032	43022033	T	C	21	GENIC	homozygous	56850140
4	43022065	43022066	T	C	23	GENIC	homozygous	56850141
4	43022074	43022075	C	CT	26	GENIC	homozygous	56850142