chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6633855	6633856	C	G	50	GENIC	possibly homozygous	130037576
20	6634144	6634148	GGGT		52	GENIC	homozygous	129980651
20	6635677	6635678	A	G	43	GENIC	homozygous	130037579
20	6635826	6635827	T	C	25	GENIC	homozygous	130037580
20	6636638	6636638		GACAT	28	GENIC	homozygous	129980653
20	6637902	6637903	T	C	43	GENIC	homozygous	143718342
20	6637919	6637920	T	C	38	GENIC	homozygous	130037582
20	6637982	6637983	T	C	31	GENIC	homozygous	130037583
20	6638319	6638320	A	G	39	GENIC	homozygous	130037585
20	6639099	6639103	AAAT		27	GENIC	homozygous	143710038
20	6639113	6639114	G	A	29	GENIC	homozygous	155133249
20	6639258	6639259	C	G	37	GENIC	homozygous	130037588
20	6639282	6639283	G	A	26	GENIC	homozygous	155133250
20	6640742	6640743	A		10	GENIC	homozygous	404039772
20	6639112	6639113	A		28	GENIC	heterozygous	404039769
20	6639112	6639113	A	G	28	GENIC	homozygous	404039770
20	6639113	6639114	G		29	GENIC	heterozygous	404039771
20	6640742	6640743	A	G	10	GENIC	heterozygous	404039773
20	6640744	6640745	A		10	GENIC	homozygous	404039774
20	6640744	6640745	A	G	10	GENIC	heterozygous	404039775
20	6640851	6640852	C	A	9	GENIC	heterozygous	147421937
20	6641035	6641035		TCC	32	GENIC	possibly homozygous	140483925
20	6641146	6641147	A	G	62	GENIC	homozygous	130037592
20	6641724	6641725	A	C	49	GENIC	homozygous	130037594
20	6641875	6641876	T	C	38	GENIC	homozygous	130037595
20	6642122	6642123	T	C	60	GENIC	homozygous	130037596
20	6642141	6642142	C	T	55	GENIC	homozygous	130037597