chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7215915	7215916	G	A	34	GENIC	possibly homozygous	45409885
20	7215936	7215937	T	G	31	GENIC	homozygous	45409886
20	7215973	7215974	G	C	31	GENIC	homozygous	45409887
20	7216152	7216158	AAAAAA	------	9	GENIC	homozygous	45409888
20	7216168	7216171	AAA	---	16	GENIC	possibly homozygous	45409889
20	7216172	7216174	AA	--	16	GENIC	heterozygous	45409890
20	7216417	7216418	C	T	32	GENIC	homozygous	45409891
20	7216453	7216454	G	GGAAT	21	GENIC	homozygous	45409892
20	7216481	7216482	A	T	31	GENIC	homozygous	45409893
20	7216602	7216603	G	A	43	GENIC	homozygous	45409894
20	7216853	7216854	T	G	29	GENIC	homozygous	45409895
20	7216904	7216905	T	A	36	GENIC	homozygous	45409896
20	7217038	7217039	G	C	30	GENIC	homozygous	45409897
20	7217192	7217193	A	C	17	GENIC	homozygous	45409898
20	7217451	7217452	A	C	36	GENIC	homozygous	45409899
20	7217474	7217475	C	T	34	GENIC	homozygous	45756162
20	7217649	7217650	A	G	33	GENIC	homozygous	45409900
20	7218715	7218716	C	T	36	GENIC	homozygous	45409901
20	7218835	7218836	A	G	29	GENIC	possibly homozygous	45409902
20	7218945	7218946	A	G	39	GENIC	homozygous	45409903
20	7218958	7218959	A	G	41	GENIC	homozygous	45409904
20	7219023	7219024	T	C	28	GENIC	homozygous	45409905
20	7219832	7219833	G	T	35	GENIC	possibly homozygous	45409906