chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59587110	59587111	C	T	27	GENIC	homozygous	51465833
10	59587678	59587679	C	T	39	GENIC	homozygous	51465834
10	59589767	59589768	T	C	29	GENIC	homozygous	51465835
10	59591293	59591300	GGCATTT	-------	28	GENIC	homozygous	51465836
10	59591663	59591664	C	CTGTGTGTGTG	6	GENIC	heterozygous	52460892
10	59591663	59591664	C	CTCTCTCTCTGTGTGTGTGTGTG	6	GENIC	heterozygous	52460893
10	59593907	59593908	T	C	31	GENIC	homozygous	51465837
10	59597105	59597106	G	GC	14	GENIC	homozygous	51465838
10	59599284	59599285	G	T	21	GENIC	homozygous	51465839
10	59600128	59600129	G	-	28	GENIC	homozygous	51465841
10	59600682	59600683	G	GTT	8	GENIC	homozygous	51465843
10	59602077	59602079	CA	--	2	GENIC	heterozygous	52460895
10	59604635	59604636	T	-	14	GENIC	possibly homozygous	51465844
10	59606505	59606506	C	T	32	GENIC	homozygous	51465846
10	59607721	59607726	TTTTT	-----	10	GENIC	heterozygous	51465847
10	59607722	59607726	TTTT	----	10	GENIC	heterozygous	51465848