chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59587110	59587111	C	T	21	GENIC	homozygous	51465833
10	59587678	59587679	C	T	28	GENIC	homozygous	51465834
10	59591663	59591664	C	CTGTGTGTGTG	20	GENIC	heterozygous	52460892
10	59591663	59591664	C	CTCTCTCTCTGTGTGTGTGTGTG	20	GENIC	heterozygous	52460893
10	59593907	59593908	T	C	20	GENIC	homozygous	51465837
10	59594684	59594688	ACAC	----	13	GENIC	homozygous	52460894
10	59597105	59597106	G	GC	13	GENIC	homozygous	51465838
10	59599284	59599285	G	T	28	GENIC	homozygous	51465839
10	59600128	59600129	G	-	32	GENIC	homozygous	51465841
10	59600682	59600683	G	GTT	15	GENIC	homozygous	51465843
10	59604635	59604636	T	-	9	GENIC	homozygous	51465844
10	59604858	59604859	A	AGTGT	2	GENIC	heterozygous	51465845
10	59604858	59604859	A	AGT	2	GENIC	heterozygous	52460896
10	59606505	59606506	C	T	25	GENIC	homozygous	51465846
10	59607722	59607726	TTTT	----	9	GENIC	possibly homozygous	51465848