chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7000594	7000595	A	G	6	GENIC	homozygous	46071919
20	7000711	7000712	T	C	11	GENIC	heterozygous	46071921
20	7000723	7000724	T	A	12	GENIC	heterozygous	46071923
20	7000766	7000767	T	C	15	GENIC	heterozygous	46071926
20	7000789	7000790	T	G	10	GENIC	homozygous	46071928
20	7000794	7000795	A	G	12	GENIC	homozygous	46071930
20	7000821	7000822	G	T	12	GENIC	homozygous	46044359
20	7000828	7000829	G	A	16	GENIC	homozygous	46044361
20	7000850	7000851	C	T	21	GENIC	heterozygous	46044365
20	7000875	7000876	C	G	27	GENIC	heterozygous	45676475
20	7000899	7000900	T	A	27	GENIC	heterozygous	46044367
20	7000911	7000912	A	G	27	GENIC	heterozygous	45676476
20	7000916	7000917	C	T	28	GENIC	heterozygous	45408093
20	7000921	7000922	G	A	28	GENIC	heterozygous	46044369
20	7000928	7000929	C	A	21	GENIC	heterozygous	45676477
20	7000931	7000932	A	G	21	GENIC	homozygous	45408094
20	7000941	7000942	T	G	22	GENIC	heterozygous	45736072
20	7000953	7000954	G	T	17	GENIC	heterozygous	45408097
20	7000954	7000955	C	G	17	GENIC	heterozygous	45408098
20	7000972	7000973	C	G	15	GENIC	heterozygous	45408100
20	7000989	7000990	C	T	15	GENIC	heterozygous	45408101
20	7001009	7001010	A	G	19	GENIC	heterozygous	46044371
20	7001015	7001016	C	T	16	GENIC	homozygous	45408104
20	7001039	7001040	A	G	21	GENIC	homozygous	45408106
20	7001110	7001111	T	A	35	GENIC	homozygous	45408110