chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6169613	6169614	C	T	9	GENIC	homozygous	63740719
20	6169844	6169845	G	T	17	GENIC	homozygous	63345679
20	6170283	6170284	C	T	12	GENIC	homozygous	63345681
20	6170338	6170339	A	G	5	GENIC	heterozygous	63345682
20	6170358	6170359	A	G	4	GENIC	homozygous	63345684
20	6171269	6171270	A	G	25	GENIC	homozygous	63345692
20	6173005	6173006	A	G	22	GENIC	homozygous	63345694
20	6173007	6173008	T	A	22	GENIC	homozygous	63345696
20	6173085	6173086	C	T	25	GENIC	homozygous	63575010
20	6170120	6170121	T	C	30	GENIC	homozygous	63574990
20	6170162	6170163	A	G	23	GENIC	homozygous	63574992
20	6170274	6170275	G	A	17	GENIC	homozygous	63574994
20	6170573	6170574	T	A	19	GENIC	heterozygous	63574998
20	6170611	6170612	T	C	11	GENIC	possibly homozygous	63575000
20	6170618	6170619	T	C	13	GENIC	possibly homozygous	63575002
20	6171320	6171321	G	A	22	GENIC	homozygous	63575004
20	6171949	6171950	T	G	19	GENIC	homozygous	63575006
20	6172005	6172006	T	C	27	GENIC	homozygous	63575008
20	6175005	6175006	T	C	21	GENIC	homozygous	63575012
20	6175684	6175685	T	C	38	GENIC	homozygous	63575014
20	6175821	6175822	C	T	29	GENIC	homozygous	63575016
20	6176093	6176094	T	C	22	GENIC	homozygous	63345704
20	6176264	6176265	T	C	35	GENIC	homozygous	63345706