chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9537822	9537823	C	CTGTG	34	GENIC	possibly homozygous	45841798
20	9539675	9539677	AG	--	9	GENIC	homozygous	45680169
20	9539700	9539701	A	AAAG	5	GENIC	heterozygous	45924512
20	9547025	9547026	T	C	60	GENIC	homozygous	45423816
20	9560483	9560484	A	AG	11	GENIC	possibly homozygous	45863622
20	9555534	9555535	G	-	7	GENIC	homozygous	45974517
20	9558372	9558373	G	A	29	GENIC	homozygous	45974518
20	9562329	9562330	T	-	14	GENIC	heterozygous	45863625
20	9562986	9562993	GGGGGGG	-------	25	GENIC	homozygous	45900338
20	9562992	9562993	G	GCAACCAA	21	GENIC	homozygous	45900339
20	9564346	9564347	T	TA	49	GENIC	homozygous	45423898
20	9564663	9564664	C	T	16	GENIC	homozygous	45974524
20	9565099	9565100	A	C	75	GENIC	homozygous	45680204
20	9565100	9565101	A	T	75	GENIC	homozygous	45680205
20	9565337	9565338	C	T	58	GENIC	homozygous	45680209
20	9565703	9565704	C	T	48	GENIC	homozygous	45974525
20	9565805	9565811	ACACAC	------	5	GENIC	heterozygous	45900340
20	9581879	9581880	T	-	5	GENIC	heterozygous	45423977
20	9582218	9582219	C	T	57	GENIC	homozygous	45680232
20	9592253	9592255	AA	--	6	GENIC	heterozygous	45680250
20	9592423	9592424	T	TA	5	GENIC	heterozygous	45680252
20	9592771	9592773	GT	--	10	GENIC	heterozygous	45900346