chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47619542	47619543	C	T	33	GENIC	homozygous	114760286
13	47619883	47619884	T	C	15	GENIC	homozygous	114548284
13	47620978	47620979	A	G	23	GENIC	possibly homozygous	114548286
13	47621257	47621258	A	G	24	GENIC	homozygous	114548287
13	47621516	47621517	G	A	21	GENIC	possibly homozygous	114615022
13	47622207	47622208	G	A	26	GENIC	homozygous	114615024
13	47622361	47622362	G	C	18	GENIC	homozygous	114615025
13	47622566	47622567	G	A	21	GENIC	possibly homozygous	114615026
13	47622586	47622587	C	T	22	GENIC	possibly homozygous	114615027
13	47622677	47622678	C	T	15	GENIC	homozygous	114615028
13	47622691	47622692	T	C	16	GENIC	homozygous	114615029
13	47622716	47622717	T	C	20	GENIC	possibly homozygous	114615030
13	47622969	47622970	C	A	22	GENIC	possibly homozygous	114615031
13	47623138	47623139	A	G	28	GENIC	homozygous	114615033
13	47623157	47623158	A	G	27	GENIC	homozygous	114615034
13	47623193	47623194	G	A	35	GENIC	homozygous	114615035
13	47623262	47623263	C	T	22	GENIC	homozygous	114760288
13	47623485	47623486	T	C	22	GENIC	possibly homozygous	114615036
13	47623605	47623606	C	T	25	GENIC	possibly homozygous	114615037
13	47623698	47623699	T	C	14	GENIC	possibly homozygous	114615038
13	47623765	47623766	G	A	40	GENIC	possibly homozygous	114615039