chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116716619	116716620	T	G	21	GENIC	homozygous	116669949
8	116718327	116718328	A	C	23	GENIC	homozygous	116669953
8	116718387	116718388	A	T	17	GENIC	homozygous	116669955
8	116718756	116718757	T	C	9	GENIC	homozygous	116669957
8	116718927	116718928	A	T	19	GENIC	homozygous	116669959
8	116719284	116719285	A	G	9	GENIC	homozygous	116669961
8	116719444	116719445	G	A	20	GENIC	homozygous	116669963
8	116719639	116719640	G	A	23	GENIC	homozygous	116669965
8	116719949	116719950	A	G	16	GENIC	homozygous	116669967
8	116721097	116721098	G	A	9	GENIC	homozygous	116669969
8	116721572	116721573	A	G	10	GENIC	homozygous	116669971
8	116721971	116721972	G	A	16	GENIC	homozygous	116669973
8	116722153	116722154	C	T	6	GENIC	homozygous	116669975
8	116723146	116723147	G	T	19	GENIC	homozygous	116669977
8	116723187	116723188	C	T	17	GENIC	homozygous	116669979
8	116724337	116724338	A	G	26	GENIC	homozygous	116669983
8	116724974	116724975	T	C	15	GENIC	homozygous	116669985
8	116725236	116725237	C	T	25	GENIC	homozygous	116669987
8	116725326	116725327	A	G	17	GENIC	homozygous	116669989
8	116728564	116728565	G	A	17	GENIC	homozygous	116669993
8	116729082	116729083	C	T	21	GENIC	homozygous	116669995