chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	85211266	85211267	C	T	25	GENIC	homozygous	61886310
1	85211369	85211370	T	TG	30	GENIC	homozygous	61886311
1	85211838	85211839	G	GAA	13	GENIC	homozygous	61886312
1	85212028	85212029	G	C	34	GENIC	homozygous	61454163
1	85212149	85212150	C	T	30	GENIC	homozygous	61454164
1	85212328	85212329	A	C	52	GENIC	homozygous	61454165
1	85213769	85213770	T	C	12	GENIC	homozygous	61454170
1	85213779	85213780	G	T	13	GENIC	homozygous	61454171
1	85214209	85214210	T	C	34	GENIC	homozygous	61454172
1	85214478	85214479	T	C	43	GENIC	homozygous	61454173
1	85214553	85214554	A	G	32	GENIC	homozygous	61454174
1	85214726	85214727	T	C	32	GENIC	homozygous	61454175
1	85215697	85215698	A	C	37	GENIC	homozygous	61454177
1	85216209	85216210	T	C	45	GENIC	homozygous	61454178
1	85216721	85216722	C	G	28	GENIC	homozygous	61454179
1	85217105	85217106	C	T	16	GENIC	homozygous	61886313
1	85217902	85217903	A	AAT	3	GENIC	homozygous	61454180
1	85218013	85218014	C	T	29	GENIC	homozygous	61886314
1	85219349	85219350	C	A	19	GENIC	homozygous	61454183