chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59587110	59587111	C	T	39	GENIC	possibly homozygous	51465833
10	59587678	59587679	C	T	49	GENIC	homozygous	51465834
10	59589767	59589768	T	C	46	GENIC	homozygous	51465835
10	59591293	59591300	GGCATTT	-------	38	GENIC	homozygous	51465836
10	59593907	59593908	T	C	62	GENIC	homozygous	51465837
10	59597105	59597106	G	GC	15	GENIC	homozygous	51465838
10	59599284	59599285	G	T	73	GENIC	homozygous	51465839
10	59599786	59599787	T	G	32	GENIC	heterozygous	51465840
10	59600128	59600129	G	-	39	GENIC	homozygous	51465841
10	59600682	59600683	G	GTTT	17	GENIC	heterozygous	51465842
10	59600682	59600683	G	GTT	17	GENIC	possibly homozygous	51465843
10	59604635	59604636	T	-	2	GENIC	homozygous	51465844
10	59604858	59604859	A	AGTGT	3	GENIC	homozygous	51465845
10	59606505	59606506	C	T	40	GENIC	homozygous	51465846
10	59607721	59607726	TTTTT	-----	13	GENIC	heterozygous	51465847
10	59607722	59607726	TTTT	----	13	GENIC	heterozygous	51465848