chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	92596881	92596882	A	AG	14	GENIC	homozygous	49859696
13	92596940	92596941	G	A	22	GENIC	possibly homozygous	49859697
13	92597011	92597012	G	A	10	GENIC	heterozygous	49859698
13	92597038	92597039	A	G	16	GENIC	possibly homozygous	49859699
13	92597103	92597104	C	A	8	GENIC	homozygous	49962818
13	92597104	92597105	A	G	9	GENIC	homozygous	50497370
13	92597116	92597117	A	C	13	GENIC	homozygous	49859700
13	92599969	92599970	G	A	11	GENIC	homozygous	51223702
13	92601948	92601949	T	C	13	GENIC	homozygous	49962831
13	92609071	92609073	TG	--	8	GENIC	homozygous	49962846
13	92609437	92609438	T	C	7	GENIC	homozygous	49962849
13	92611415	92611416	A	G	33	GENIC	heterozygous	49859707
13	92628084	92628085	C	A	7	GENIC	homozygous	49859713
13	92629614	92629615	C	T	11	GENIC	homozygous	49962906
13	92629615	92629616	T	A	12	GENIC	homozygous	50497376