chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47619202	47619203	C	T	51	GENIC	possibly homozygous	114548282
13	47619883	47619884	T	C	79	GENIC	homozygous	114548284
13	47620201	47620202	C	T	61	GENIC	homozygous	114548285
13	47620978	47620979	A	G	42	GENIC	homozygous	114548286
13	47621257	47621258	A	G	45	GENIC	homozygous	114548287
13	47622691	47622692	T	C	61	GENIC	possibly homozygous	114615029
13	47619832	47619834	AA		61	GENIC	homozygous	132171379
13	47621516	47621517	G	A	54	GENIC	homozygous	114615022
13	47622022	47622023	G	A	37	GENIC	homozygous	114615023
13	47622207	47622208	G	A	63	GENIC	possibly homozygous	114615024
13	47622361	47622362	G	C	69	GENIC	homozygous	114615025
13	47622566	47622567	G	A	50	GENIC	homozygous	114615026
13	47622586	47622587	C	T	50	GENIC	homozygous	114615027
13	47622677	47622678	C	T	58	GENIC	homozygous	114615028
13	47622716	47622717	T	C	63	GENIC	possibly homozygous	114615030
13	47622969	47622970	C	A	53	GENIC	homozygous	114615031
13	47623127	47623128	G	A	45	GENIC	homozygous	114615032
13	47623138	47623139	A	G	46	GENIC	homozygous	114615033
13	47623157	47623158	A	G	46	GENIC	homozygous	114615034
13	47623193	47623194	G	A	50	GENIC	homozygous	114615035
13	47623485	47623486	T	C	54	GENIC	possibly homozygous	114615036
13	47623605	47623606	C	T	59	GENIC	homozygous	114615037
13	47623698	47623699	T	C	41	GENIC	homozygous	114615038
13	47623765	47623766	G	A	38	GENIC	possibly homozygous	114615039