chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	80845906	80845907	A	G	16	GENIC	homozygous	111635872
3	80851385	80851386	T	C	15	GENIC	homozygous	111635873
3	80852917	80852918	G	A	22	GENIC	homozygous	111635874
3	80853285	80853286	A	C	15	GENIC	homozygous	111635875
3	80858604	80858605	T	C	21	GENIC	homozygous	111635876
3	80860414	80860415	G	T	21	GENIC	homozygous	111635877
3	80861192	80861193	C	A	12	GENIC	homozygous	111635878
3	80861743	80861744	G	T	10	GENIC	homozygous	111635879
3	80861881	80861882	A	C	5	GENIC	homozygous	111635880
3	80864543	80864544	C	T	11	GENIC	homozygous	111635882
3	80866609	80866610	G	A	16	GENIC	homozygous	111635883
3	80870611	80870612	T	C	10	GENIC	homozygous	111635884
3	80872848	80872849	A	G	12	GENIC	homozygous	111635885
3	80873683	80873684	G	C	5	GENIC	homozygous	111635886
3	80875346	80875347	G	T	12	GENIC	homozygous	111635887
3	80851063	80851064	C		14	GENIC	homozygous	127901022
3	80853509	80853513	CGCG		9	GENIC	homozygous	127901023
3	80857954	80857954		AT	5	GENIC	homozygous	127901024
3	80857972	80857976	ATAT		6	GENIC	homozygous	127901025
3	80876256	80876261	CCTGT		10	GENIC	homozygous	127901026
3	80877616	80877625	AAACAAACA		11	GENIC	homozygous	127901027
3	80877702	80877702		GTGTGG	12	GENIC	homozygous	127901028
3	80879939	80879940	A	G	18	GENIC	homozygous	111635888
3	80879942	80879943	C	T	18	GENIC	homozygous	111635889
3	80880632	80880633	G	C	16	GENIC	homozygous	111635890
3	80881248	80881259	ACCTCCAGGCA		12	GENIC	homozygous	127901029
3	80882748	80882748		T	22	GENIC	homozygous	127901030
3	80883192	80883193	C	T	12	GENIC	homozygous	111635891
3	80883349	80883350	T	C	17	GENIC	homozygous	111635892
3	80884462	80884463	C	T	17	GENIC	homozygous	111635893
3	80885765	80885766	G	T	10	GENIC	homozygous	111635894
3	80885967	80885968	C	A	12	GENIC	homozygous	111635895
3	80886102	80886103	G	C	17	GENIC	possibly homozygous	111635896
3	80886142	80886143	A	G	13	GENIC	homozygous	111635897