chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59579142	59579143	T	C	18	GENIC	possibly homozygous	51465819
10	59579626	59579627	A	G	8	GENIC	homozygous	51465820
10	59579742	59579743	T	G	11	GENIC	homozygous	51465821
10	59580126	59580127	C	T	13	GENIC	homozygous	51465822
10	59581903	59581904	T	C	13	GENIC	heterozygous	51465823
10	59582156	59582157	A	G	18	GENIC	possibly homozygous	51465825
10	59582671	59582672	C	CA	6	GENIC	heterozygous	51465826
10	59583189	59583190	T	C	16	GENIC	possibly homozygous	51465827
10	59584465	59584466	T	C	8	GENIC	heterozygous	51465829
10	59584681	59584682	A	-	4	GENIC	homozygous	51465831
10	59584902	59584903	T	C	13	GENIC	homozygous	51465832
10	59587110	59587111	C	T	8	GENIC	possibly homozygous	51465833
10	59587678	59587679	C	T	10	GENIC	possibly homozygous	51465834
10	59589767	59589768	T	C	7	GENIC	possibly homozygous	51465835
10	59591293	59591300	GGCATTT	-------	10	GENIC	heterozygous	51465836
10	59593907	59593908	T	C	31	GENIC	homozygous	51465837
10	59595791	59595792	C	T	9	GENIC	heterozygous	51663687
10	59597105	59597106	G	GC	4	GENIC	heterozygous	51465838
10	59599284	59599285	G	T	26	GENIC	possibly homozygous	51465839
10	59600128	59600129	G	-	7	GENIC	possibly homozygous	51465841
10	59606505	59606506	C	T	24	GENIC	possibly homozygous	51465846
10	59612041	59612042	T	C	29	GENIC	possibly homozygous	51465850
10	59613097	59613098	T	C	28	GENIC	homozygous	51465853
10	59613284	59613285	A	G	24	GENIC	homozygous	51465854
10	59617487	59617488	A	T	1	GENIC	homozygous	52319594
10	59619162	59619163	G	GT	14	GENIC	possibly homozygous	51465860
10	59620287	59620288	G	-	7	GENIC	homozygous	51465863
10	59620423	59620424	G	GC	10	GENIC	homozygous	51465864
10	59620449	59620450	T	A	7	GENIC	homozygous	51465865
10	59623365	59623366	G	GA	10	GENIC	heterozygous	51465866
10	59626014	59626015	T	C	14	GENIC	possibly homozygous	51465868