chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6169545	6169546	C	A	12	GENIC	possibly homozygous	64114779
20	6169613	6169614	C	T	9	GENIC	homozygous	63740719
20	6169844	6169845	G	T	18	GENIC	homozygous	63345679
20	6170283	6170284	C	T	15	GENIC	homozygous	63345681
20	6170338	6170339	A	G	9	GENIC	homozygous	63345682
20	6170358	6170359	A	G	11	GENIC	homozygous	63345684
20	6170872	6170873	T	G	24	GENIC	homozygous	63345689
20	6171049	6171050	G	A	19	GENIC	homozygous	63345691
20	6171269	6171270	A	G	27	GENIC	homozygous	63345692
20	6173005	6173006	A	G	22	GENIC	homozygous	63345694
20	6173007	6173008	T	A	22	GENIC	homozygous	63345696
20	6173038	6173039	T	C	24	GENIC	homozygous	63345698
20	6175623	6175624	T	A	26	GENIC	homozygous	63345699
20	6175766	6175767	T	G	35	GENIC	homozygous	63345701
20	6176093	6176094	T	C	20	GENIC	homozygous	63345704
20	6176264	6176265	T	C	25	GENIC	homozygous	63345706
20	6176337	6176338	G	A	22	GENIC	homozygous	63345708
20	6176468	6176469	C	A	30	GENIC	homozygous	63345710
20	6176504	6176505	T	A	29	GENIC	possibly homozygous	63345711
20	6177100	6177101	A	G	29	GENIC	homozygous	63345713