chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	50666672	50666673	A	G	20	INTERGENIC	possibly homozygous	56215575
5	50668240	50668241	T	C	21	INTERGENIC	possibly homozygous	56215577
5	50668685	50668686	G	A	27	INTERGENIC	possibly homozygous	56215581
5	50669807	50669808	C	T	17	INTERGENIC	homozygous	56215583
5	50670601	50670602	A	AT	15	INTERGENIC	heterozygous	55368381
5	50670602	50670603	T	-	15	INTERGENIC	possibly homozygous	56215585
5	50670842	50670843	T	C	13	INTERGENIC	homozygous	55368383
5	50672928	50672929	T	C	22	INTERGENIC	homozygous	55368388
5	50673493	50673494	G	GTT	2	INTERGENIC	heterozygous	55368397
5	50675721	50675722	C	T	14	INTERGENIC	homozygous	56215586
5	50676131	50676132	T	A	11	INTERGENIC	possibly homozygous	56215588
5	50677394	50677395	T	-	7	INTERGENIC	homozygous	56215590
5	50677638	50677639	C	T	19	INTERGENIC	possibly homozygous	56215592
5	50677769	50677770	C	-	6	INTERGENIC	homozygous	55368425
5	50677793	50677794	T	C	16	INTERGENIC	homozygous	56215593
5	50678434	50678435	T	G	12	INTERGENIC	homozygous	55368428
5	50678944	50678945	T	C	17	INTERGENIC	possibly homozygous	55368431
5	50679855	50679856	T	G	17	INTERGENIC	homozygous	55368444
5	50683221	50683222	T	G	18	INTERGENIC	homozygous	55368460
5	50683423	50683424	T	-	18	INTERGENIC	possibly homozygous	56215597
5	50684768	50684769	G	A	19	INTERGENIC	homozygous	56215599
5	50685075	50685076	T	C	17	INTERGENIC	possibly homozygous	56215601
5	50691508	50691509	G	A	19	INTERGENIC	heterozygous	55368488
5	50691509	50691510	A	G	19	INTERGENIC	heterozygous	55368489
5	50677773	50677774	G	A	7	INTERGENIC	homozygous	55876912