chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	20587532	20587533	C		47	GENIC	homozygous	129670002
20	20587536	20587536		GACTG	47	GENIC	homozygous	129670003
20	20589894	20589896	GT		10	GENIC	homozygous	129670005
20	20589966	20589966		T	38	GENIC	homozygous	129670006
20	20589990	20589990		G	38	GENIC	homozygous	129670007
20	20590023	20590023		G	31	GENIC	homozygous	129670008
20	20590030	20590030		T	33	GENIC	homozygous	129670009
20	20590040	20590041	G		32	GENIC	homozygous	129670010
20	20590052	20590053	G	T	31	GENIC	homozygous	124648598
20	20590053	20590054	T	G	31	GENIC	homozygous	109528785
20	20590058	20590058		G	30	GENIC	homozygous	129670011
20	20590117	20590117		G	28	GENIC	homozygous	129670015
20	20590067	20590067		TG	32	GENIC	homozygous	129670012
20	20590101	20590101		T	25	GENIC	homozygous	129670013
20	20590107	20590107		G	29	GENIC	homozygous	129670014
20	20590128	20590130	TG		34	GENIC	homozygous	129670016
20	20590147	20590148	G		34	GENIC	homozygous	129670017
20	20590179	20590179		C	40	GENIC	homozygous	129670018