chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	101057856	101057857	T	G	39	GENIC	heterozygous	61484001
1	101057864	101057865	G	C	42	GENIC	heterozygous	60779710
1	101057942	101057943	C	G	49	GENIC	heterozygous	60779711
1	101057964	101057965	A	AC	43	GENIC	heterozygous	60779712
1	101058033	101058034	A	T	50	GENIC	heterozygous	60779713
1	101058043	101058044	G	A	48	GENIC	heterozygous	60779714
1	101058078	101058079	A	-	32	GENIC	heterozygous	60779715
1	101058536	101058538	AC	--	8	GENIC	homozygous	60779717
1	101058689	101058690	A	AAG	12	GENIC	heterozygous	61484006
1	101058689	101058690	A	AAGAG	12	GENIC	heterozygous	61484007
1	101058927	101058928	C	A	26	GENIC	heterozygous	60779718
1	101058981	101058982	C	A	23	GENIC	heterozygous	61892423
1	101059460	101059461	A	T	40	GENIC	heterozygous	61484008
1	101059489	101059490	C	T	45	GENIC	heterozygous	61484009
1	101063603	101063604	C	T	52	GENIC	heterozygous	61892424
1	101063606	101063607	C	T	53	GENIC	heterozygous	60779719
1	101063627	101063628	A	G	54	GENIC	heterozygous	60779720
1	101063642	101063643	G	T	50	GENIC	heterozygous	60779721