chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	65069038	65069042	TCTC	----	9	INTERGENIC	heterozygous	51202215
11	65069040	65069042	TC	--	9	INTERGENIC	heterozygous	51196598
11	65071683	65071685	CA	--	10	INTERGENIC	heterozygous	51186750
11	65076423	65076424	G	GTTTGGGGATTTAGCTCAGTGGTAGAGCGCTT	2	INTERGENIC	homozygous	51186751
11	65091713	65091715	AC	--	21	INTERGENIC	heterozygous	51196599
11	65093445	65093447	TG	--	9	INTERGENIC	heterozygous	51196600
11	65101931	65101933	AC	--	14	INTERGENIC	heterozygous	50882599
11	65127361	65127362	G	GAA	4	INTERGENIC	heterozygous	51186754
11	65133250	65133251	C	T	8	INTERGENIC	homozygous	51116160
11	65139649	65139651	AG	--	10	INTERGENIC	heterozygous	51019008
11	65150041	65150043	TG	--	12	INTERGENIC	heterozygous	51202219
11	65164420	65164422	GT	--	14	INTERGENIC	heterozygous	51186757
11	65165762	65165764	TG	--	5	INTERGENIC	heterozygous	51186759
11	65169312	65169314	AC	--	13	INTERGENIC	heterozygous	51186760
11	65175684	65175685	C	CAATA	2	INTERGENIC	heterozygous	50802505
11	65177337	65177338	A	-	16	INTERGENIC	heterozygous	50882608
11	65180366	65180367	T	-	12	INTERGENIC	heterozygous	51186761
11	65184692	65184693	T	-	7	INTERGENIC	heterozygous	51186762
11	65088354	65088358	AAGA	----	15	INTERGENIC	heterozygous	51257084
11	65132358	65132363	AGGAG	-----	10	INTERGENIC	homozygous	51257086
11	65101930	65101931	G	GAC	14	INTERGENIC	heterozygous	51243475
11	65203045	65203046	G	-	7	GENIC	heterozygous	51186764
11	65209063	65209064	A	G	20	GENIC	homozygous	50802522