chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	41739933	41739934	A	G	15	GENIC	homozygous	114541096
13	41740554	41740555	T	C	25	GENIC	homozygous	114329878
13	41741000	41741001	T	C	15	GENIC	homozygous	114329880
13	41742308	41742309	G	A	21	GENIC	homozygous	114329882
13	41743203	41743204	A	G	18	GENIC	homozygous	114329884
13	41743594	41743595	C	T	21	GENIC	possibly homozygous	114329886
13	41747233	41747234	C	T	20	GENIC	homozygous	114329888
13	41747305	41747306	T	C	20	GENIC	homozygous	114329890
13	41747761	41747762	C	T	27	GENIC	homozygous	114329892
13	41748428	41748429	C	A	19	GENIC	homozygous	114329894
13	41749680	41749681	G	A	20	GENIC	homozygous	114329896
13	41749887	41749888	C	T	18	GENIC	homozygous	114821367
13	41750028	41750029	T	C	21	GENIC	homozygous	114329898
13	41751906	41751907	A	C	19	GENIC	homozygous	114329900
13	41755431	41755432	T	A	29	GENIC	homozygous	114329904
13	41758730	41758731	C	T	21	GENIC	homozygous	114329906
13	41758850	41758851	G	A	20	GENIC	homozygous	114329908
13	41758911	41758912	G	C	11	GENIC	homozygous	114329910