chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5398846	5398847	C	T	24	GENIC	homozygous	45731719
20	5399469	5399471	AA	--	22	GENIC	possibly homozygous	45731720
20	5401013	5401014	T	C	21	GENIC	homozygous	45386585
20	5401119	5401120	A	G	30	GENIC	homozygous	45731721
20	5401289	5401290	A	G	28	GENIC	homozygous	45386589
20	5401514	5401515	T	C	21	GENIC	homozygous	45386591
20	5401677	5401691	TCTGCCACATGTAG	--------------	7	GENIC	homozygous	45731722
20	5401920	5401927	ATGCTAT	-------	19	GENIC	homozygous	45731723
20	5401931	5401932	T	A	13	GENIC	homozygous	45731724
20	5402251	5402252	G	T	21	GENIC	homozygous	45731725
20	5402565	5402566	C	CAA	4	GENIC	heterozygous	45386607
20	5402565	5402566	C	CAAA	4	GENIC	heterozygous	45955078
20	5403389	5403390	A	G	29	GENIC	homozygous	45386613