chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	30800512	30800513	A	G	4	GENIC	homozygous	45515412
20	30800518	30800519	A	AG	4	GENIC	homozygous	45515414
20	30800537	30800538	T	C	6	GENIC	homozygous	45515418
20	30800541	30800542	C	A	6	GENIC	homozygous	45515420
20	30800858	30800859	G	A	13	GENIC	homozygous	45515426
20	30800948	30800949	C	G	16	GENIC	homozygous	45515428
20	30800967	30800969	TG	--	14	GENIC	homozygous	45846535
20	30800969	30800970	G	GAC	12	GENIC	homozygous	45846536
20	30800974	30800975	G	A	13	GENIC	homozygous	45515430
20	30800977	30800978	T	A	12	GENIC	homozygous	45515432
20	30800979	30800980	T	A	13	GENIC	homozygous	45515434
20	30800981	30800982	T	A	12	GENIC	homozygous	45515436
20	30800983	30800984	T	C	13	GENIC	homozygous	45846537
20	30800984	30800985	G	T	13	GENIC	homozygous	45846538
20	30800987	30800988	T	G	13	GENIC	homozygous	45515438
20	30800991	30800992	T	A	13	GENIC	homozygous	45846539
20	30800992	30800993	G	A	13	GENIC	homozygous	45846540
20	30800993	30800994	T	G	13	GENIC	homozygous	45846541
20	30800997	30800998	T	A	14	GENIC	homozygous	45515440