chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5398406	5398407	C	T	33	GENIC	possibly homozygous	45386575
20	5398541	5398542	G	A	41	GENIC	homozygous	45386577
20	5399468	5399469	G	GAAAA	18	GENIC	homozygous	45386579
20	5399493	5399494	G	A	37	GENIC	homozygous	45386580
20	5399829	5399831	TG	--	14	GENIC	possibly homozygous	45386582
20	5401013	5401014	T	C	51	GENIC	homozygous	45386585
20	5401022	5401023	T	C	47	GENIC	homozygous	45386587
20	5401289	5401290	A	G	46	GENIC	homozygous	45386589
20	5401514	5401515	T	C	53	GENIC	homozygous	45386591
20	5401819	5401820	A	-	24	GENIC	possibly homozygous	45386593
20	5401929	5401931	TT	--	12	GENIC	homozygous	45386595
20	5402098	5402099	C	T	45	GENIC	homozygous	45386597
20	5402119	5402120	T	C	46	GENIC	homozygous	45386599
20	5402124	5402125	A	G	44	GENIC	possibly homozygous	45386601
20	5402202	5402203	G	A	48	GENIC	homozygous	45386603
20	5402269	5402270	G	A	45	GENIC	homozygous	45386605
20	5402565	5402566	C	CAA	8	GENIC	homozygous	45386607
20	5403058	5403059	C	T	41	GENIC	homozygous	45386609
20	5403066	5403067	C	G	48	GENIC	homozygous	45386611
20	5403389	5403390	A	G	33	GENIC	possibly homozygous	45386613
20	5403425	5403426	C	T	34	GENIC	homozygous	45386615