chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84506114	84506115	T	C	65	GENIC	homozygous	116069914
11	84506227	84506228	G	A	59	GENIC	homozygous	116207837
11	84506334	84506335	G	A	59	GENIC	homozygous	116069916
11	84506477	84506478	T		60	GENIC	homozygous	132157948
11	84506645	84506646	G	A	56	GENIC	homozygous	116069918
11	84506807	84506808	T	C	56	GENIC	homozygous	116069920
11	84507369	84507370	C	T	42	GENIC	homozygous	116069922
11	84509933	84510056	AAGAACACAGTTGTGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCAGTCCCCAGCTCCGAAAAAAAGAACAAAAAAAAAAAAAAAAAAAAAA		17	GENIC	heterozygous	132157949
11	84510411	84510412	C	T	61	GENIC	homozygous	116069930
11	84508412	84508413	C	T	33	GENIC	homozygous	116069924
11	84508998	84508999	C	T	38	GENIC	homozygous	116069926
11	84509349	84509350	C	T	53	GENIC	homozygous	116069928
11	84510630	84510631	A	G	60	GENIC	homozygous	116069932
11	84510631	84510632	T	C	59	GENIC	homozygous	116069934
11	84510784	84510785	T	C	55	GENIC	homozygous	116069936
11	84511121	84511122	A	G	62	GENIC	homozygous	116069938
11	84511149	84511150	C	G	58	GENIC	homozygous	116069940
11	84511200	84511201	C	T	64	GENIC	homozygous	116069942
11	84511569	84511570	T	C	67	GENIC	homozygous	116069944
11	84511870	84511871	C	T	43	GENIC	homozygous	116069946
11	84511887	84511888	A	G	44	GENIC	homozygous	116069948
11	84511949	84511950	A	G	55	GENIC	homozygous	116069950
11	84512075	84512075		TTG	12	GENIC	heterozygous	132417608
11	84512076	84512076		TG	13	GENIC	heterozygous	132157950
11	84512270	84512271	T	C	43	GENIC	homozygous	116069952
11	84512497	84512498	G	A	55	GENIC	homozygous	116069954
11	84513010	84513011	A	G	52	GENIC	homozygous	116069956
11	84513218	84513219	T	G	74	GENIC	homozygous	116069958
11	84513435	84513436	T	C	48	GENIC	homozygous	116069960
11	84513766	84513767	T	A	68	GENIC	homozygous	116069962
11	84513807	84513807		G	57	GENIC	possibly homozygous	132157951
11	84513935	84513936	A	G	47	GENIC	homozygous	116069964
11	84514156	84514157	T	C	58	GENIC	homozygous	116069966