chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	4474837	4474838	C	G	49	GENIC	homozygous	113118797
15	4475110	4475111	C	T	52	GENIC	homozygous	113118799
15	4475786	4475787	C	T	42	GENIC	homozygous	113118801
15	4476629	4476630	A	G	58	GENIC	homozygous	112786509
15	4476705	4476706	C	T	45	GENIC	homozygous	113118803
15	4476747	4476748	C	T	44	GENIC	homozygous	113118805
15	4476758	4476759	A	G	46	GENIC	homozygous	112786513
15	4476939	4476941	AG		43	GENIC	homozygous	134614629
15	4476942	4476943	G		43	GENIC	homozygous	134614630
15	4477257	4477258	T	G	45	GENIC	homozygous	112786519
15	4477374	4477375	A	G	45	GENIC	homozygous	112786521
15	4477430	4477431	C	T	51	GENIC	homozygous	113118808
15	4477590	4477591	G	A	59	GENIC	homozygous	112786523
15	4477956	4477957	C	T	51	GENIC	homozygous	113118810
15	4478018	4478019	C	T	43	GENIC	homozygous	113118812
15	4478043	4478044	G	A	43	GENIC	homozygous	112786525
15	4478497	4478498	G	A	11	GENIC	homozygous	134619095
15	4478548	4478548		GA	20	GENIC	heterozygous	134614631
15	4478550	4478550		GA	14	GENIC	heterozygous	134242963
15	4478552	4478556	AGGA		20	GENIC	heterozygous	134614632
15	4478866	4478867	C	T	43	GENIC	homozygous	113118814
15	4479545	4479546	G	A	51	GENIC	homozygous	112786529
15	4479638	4479639	C	G	44	GENIC	homozygous	112786531
15	4479661	4479662	C	A	45	GENIC	possibly homozygous	113118816