chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	22453697	22453698	G	A	59	GENIC	homozygous	109396140
20	22454417	22454418	A	G	62	GENIC	homozygous	109138992
20	22454748	22454748		T	52	GENIC	possibly homozygous	129671800
20	22454858	22454858		C	45	GENIC	homozygous	133342952
20	22456250	22456251	C	T	53	GENIC	homozygous	109396142
20	22455196	22455197	C	T	58	GENIC	homozygous	109138996
20	22455729	22455730	G	A	62	GENIC	homozygous	109138998
20	22455792	22455793	T	C	73	GENIC	homozygous	109396141
20	22455996	22455997	G	C	59	GENIC	homozygous	109139000
20	22454866	22454867	T	C	46	GENIC	homozygous	133349433
20	22457005	22457006	T	A	61	GENIC	homozygous	109396143
20	22457259	22457260	A	G	70	GENIC	homozygous	109396144
20	22457780	22457781	T	C	81	GENIC	homozygous	109139008
20	22458090	22458091	T	C	55	GENIC	homozygous	109396145
20	22458209	22458210	C	A	57	GENIC	homozygous	109396146
20	22458566	22458567	C		54	GENIC	homozygous	133342953
20	22459288	22459288		AT	44	GENIC	possibly homozygous	133342954
20	22459585	22459586	A	G	43	GENIC	homozygous	109139010
20	22459652	22459653	A	G	45	GENIC	homozygous	109139012
20	22460341	22460342	G	A	41	GENIC	homozygous	109139016