chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4816862	4816863	C		59	GENIC	possibly homozygous	129979676
20	4817135	4817138	CTT		61	GENIC	homozygous	129979677
20	4817729	4817730	G	A	60	GENIC	homozygous	143716918
20	4818709	4818710	G	A	65	GENIC	homozygous	143716919
20	4819241	4819242	T	C	60	GENIC	homozygous	130032844
20	4817763	4817764	A	G	68	GENIC	homozygous	130032841
20	4819177	4819178	T	G	64	GENIC	homozygous	130032843
20	4819253	4819254	C	A	61	GENIC	homozygous	130032845
20	4819860	4819861	G	A	47	GENIC	homozygous	130032846
20	4820019	4820020	T	C	55	GENIC	homozygous	130032848
20	4820059	4820060	C	T	51	GENIC	homozygous	143716920
20	4820140	4820141	G	A	60	GENIC	homozygous	143716921
20	4820350	4820351	A	G	70	GENIC	homozygous	130032849
20	4820401	4820402	A	G	84	GENIC	homozygous	130032850
20	4820448	4820449	C	T	82	GENIC	homozygous	143716922
20	4821313	4821314	G	A	60	GENIC	homozygous	130032851
20	4821372	4821373	G	T	54	GENIC	homozygous	130032852
20	4821379	4821380	C	T	50	GENIC	homozygous	130032853
20	4822320	4822321	A	G	64	GENIC	homozygous	130032854
20	4822860	4822861	G	A	58	GENIC	homozygous	130032855
20	4823142	4823143	G		55	GENIC	homozygous	129979679
20	4819338	4819344	CCCCCA		33	GENIC	possibly homozygous	143709681
20	4821450	4821450		G	56	GENIC	homozygous	143709682
20	4821539	4821542	GCT		57	GENIC	homozygous	143709683