chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3995774	3995775	A	G	21	INTERGENIC	homozygous	45374464
20	3996374	3996375	G	A	32	GENIC	homozygous	45374465
20	3996471	3996472	T	G	33	GENIC	homozygous	45374466
20	3996647	3996648	C	T	19	GENIC	homozygous	45374467
20	3996651	3996652	G	A	19	GENIC	homozygous	45374468
20	3996859	3996860	G	GCA	31	GENIC	possibly homozygous	45730054
20	3997166	3997167	G	GTGTA	13	GENIC	homozygous	45772923
20	3997871	3997874	GGA	---	11	GENIC	heterozygous	45374470
20	3997872	3997874	GA	--	11	GENIC	heterozygous	45374471
20	3998002	3998003	A	-	19	GENIC	homozygous	45620594
20	3998760	3998761	A	G	28	GENIC	homozygous	45374475
20	3999950	3999951	T	TA	21	GENIC	heterozygous	45730058
20	4003516	4003517	C	CACAGACAG	14	GENIC	homozygous	45861841
20	4005569	4005579	ACACACACAC	----------	11	GENIC	homozygous	45374492
20	4006512	4006515	AAA	---	2	GENIC	heterozygous	45374496
20	4008958	4008960	GT	--	2	GENIC	heterozygous	45838325
20	4008973	4008974	G	A	2	GENIC	homozygous	45818336