chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84506114	84506115	T	C	15	GENIC	homozygous	116069914
11	84506334	84506335	G	A	14	GENIC	homozygous	116069916
11	84506645	84506646	G	A	21	GENIC	homozygous	116069918
11	84506807	84506808	T	C	15	GENIC	homozygous	116069920
11	84507369	84507370	C	T	13	GENIC	homozygous	116069922
11	84508998	84508999	C	T	16	GENIC	homozygous	116069926
11	84509349	84509350	C	T	15	GENIC	homozygous	116069928
11	84510411	84510412	C	T	15	GENIC	homozygous	116069930
11	84510630	84510631	A	G	14	GENIC	homozygous	116069932
11	84510631	84510632	T	C	14	GENIC	homozygous	116069934
11	84510784	84510785	T	C	19	GENIC	homozygous	116069936
11	84511121	84511122	A	G	17	GENIC	homozygous	116069938
11	84511149	84511150	C	G	16	GENIC	homozygous	116069940
11	84511200	84511201	C	T	26	GENIC	homozygous	116069942
11	84511569	84511570	T	C	22	GENIC	homozygous	116069944
11	84511870	84511871	C	T	16	GENIC	homozygous	116069946
11	84511887	84511888	A	G	16	GENIC	homozygous	116069948
11	84511949	84511950	A	G	18	GENIC	homozygous	116069950
11	84512270	84512271	T	C	14	GENIC	homozygous	116069952
11	84512497	84512498	G	A	24	GENIC	homozygous	116069954
11	84513010	84513011	A	G	12	GENIC	homozygous	116069956
11	84513218	84513219	T	G	15	GENIC	homozygous	116069958
11	84513435	84513436	T	C	24	GENIC	homozygous	116069960
11	84513766	84513767	T	A	28	GENIC	homozygous	116069962
11	84513935	84513936	A	G	12	GENIC	homozygous	116069964
11	84514156	84514157	T	C	14	GENIC	homozygous	116069966