chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4957217	4957218	C	T	53	GENIC	homozygous	143717325
20	4957539	4957540	C	T	42	GENIC	homozygous	143717326
20	4957828	4957829	A		13	GENIC	heterozygous	129980008
20	4958586	4958587	G	A	59	GENIC	homozygous	143717327
20	4958780	4958781	A	T	58	GENIC	homozygous	130034891
20	4959168	4959169	C	T	43	GENIC	homozygous	130034892
20	4959482	4959483	A	G	40	GENIC	homozygous	130034895
20	4959523	4959524	A	C	26	GENIC	homozygous	130034896
20	4961469	4961469		A	49	GENIC	homozygous	129980012
20	4961508	4961509	G	A	36	GENIC	homozygous	143717329
20	4961516	4961516		TC	31	GENIC	homozygous	129980013
20	4962079	4962080	G	A	62	GENIC	homozygous	130034900
20	4962582	4962582		A	41	GENIC	homozygous	129980014
20	4962875	4962876	C	T	53	GENIC	homozygous	130034901
20	4962884	4962885	T	C	52	GENIC	homozygous	143717330
20	4963978	4963979	T	C	55	GENIC	possibly homozygous	130034903
20	4964153	4964154	G	T	52	GENIC	homozygous	130034904
20	4964189	4964190	G	A	54	GENIC	homozygous	130034905
20	4964290	4964291	C	A	64	GENIC	homozygous	143717331
20	4964512	4964513	A	G	54	GENIC	homozygous	143717332
20	4964726	4964727	G	C	50	GENIC	possibly homozygous	143717333
20	4964729	4964730	C	T	51	GENIC	possibly homozygous	143717334
20	4964767	4964768	C	A	47	GENIC	homozygous	143717335
20	4964856	4964857	G	T	60	GENIC	homozygous	143717336
20	4965832	4965833	A	G	67	GENIC	homozygous	130034906
20	4959198	4959198		GT	39	GENIC	homozygous	143709764
20	4959270	4959271	A	G	41	GENIC	homozygous	403865995
20	4959270	4959271	A		41	GENIC	heterozygous	403865996