chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	75198089	75198090	C	T	32	INTERGENIC	possibly homozygous	66108846
13	75199932	75199933	T	C	26	INTERGENIC	homozygous	66108848
13	75200655	75200656	G	T	32	INTERGENIC	homozygous	66108850
13	75200972	75200973	C	T	9	INTERGENIC	homozygous	66108852
13	75201080	75201081	T	C	9	INTERGENIC	homozygous	66108854
13	75201289	75201290	T	C	32	INTERGENIC	homozygous	66108856
13	75201370	75201371	C	A	33	INTERGENIC	homozygous	66108858
13	75201853	75201854	G	A	32	INTERGENIC	homozygous	66108860
13	75201855	75201856	G	A	31	INTERGENIC	homozygous	66108862
13	75201954	75201955	G	A	27	INTERGENIC	homozygous	66108864
13	75202299	75202300	T	C	31	INTERGENIC	homozygous	66108866
13	75202442	75202443	T	C	39	INTERGENIC	homozygous	66108868
13	75202949	75202950	G	A	39	INTERGENIC	homozygous	66108870
13	75203739	75203740	A	T	31	INTERGENIC	homozygous	66108872
13	75206883	75206884	A	T	55	INTERGENIC	heterozygous	66426884
13	75205420	75205421	T	C	12	INTERGENIC	heterozygous	66426879
13	75206878	75206879	A	C	35	INTERGENIC	heterozygous	66426880
13	75206881	75206882	G	T	37	INTERGENIC	heterozygous	66426882
13	75206889	75206890	T	C	52	INTERGENIC	heterozygous	66426886
13	75210457	75210458	T	C	32	INTERGENIC	homozygous	66108874
13	75210822	75210823	C	T	24	INTERGENIC	homozygous	66108876
13	75210915	75210916	G	T	28	INTERGENIC	possibly homozygous	66108878
13	75210922	75210923	G	T	27	INTERGENIC	homozygous	66108880
13	75210925	75210926	C	T	26	INTERGENIC	homozygous	66108882
13	75210935	75210936	A	G	23	INTERGENIC	homozygous	66108884
13	75210976	75210977	T	C	25	INTERGENIC	homozygous	66108886
13	75211070	75211071	A	T	25	INTERGENIC	homozygous	66108888
13	75211071	75211072	G	C	26	INTERGENIC	homozygous	66108890
13	75225932	75225933	C	A	33	INTERGENIC	heterozygous	66108892