chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	36148461	36148462	T	C	35	GENIC	homozygous	114313949
13	36149890	36149891	C	T	48	GENIC	homozygous	114313950
13	36151009	36151010	T	C	29	GENIC	homozygous	114313951
13	36151595	36151596	A	G	29	GENIC	possibly homozygous	114313952
13	36152181	36152182	C	T	20	GENIC	homozygous	118446745
13	36152185	36152186	G	T	19	GENIC	homozygous	118446746
13	36152248	36152249	G	A	27	GENIC	homozygous	118446747
13	36152269	36152270	T	G	24	GENIC	homozygous	118446748
13	36152320	36152321	A	T	32	GENIC	homozygous	118446749
13	36152388	36152389	A	T	25	GENIC	homozygous	114313954
13	36152681	36152682	C	T	59	GENIC	homozygous	114313955
13	36153366	36153367	A	G	40	GENIC	homozygous	114313956
13	36154854	36154855	G	T	53	GENIC	possibly homozygous	114313957
13	36155503	36155504	G	T	52	GENIC	homozygous	114313958
13	36152340	36152341	C	G	45	GENIC	homozygous	114752602
13	36154973	36154974	G	A	58	GENIC	possibly homozygous	114752604
13	36152350	36152351	C	A	44	GENIC	homozygous	115099214