chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	89384084	89384085	T	C	56	GENIC	homozygous	108884954
1	89384447	89384448	T	C	71	GENIC	homozygous	108884955
1	89386652	89386653	T	A	33	GENIC	homozygous	120503253
1	89386686	89386687	A	G	34	GENIC	homozygous	120483993
1	89386696	89386697	G	A	36	GENIC	homozygous	120483994
1	89387060	89387061	A	G	77	GENIC	homozygous	108884957
1	89390337	89390338	G	A	54	GENIC	homozygous	108884961
1	89391383	89391384	A	T	52	GENIC	homozygous	108884962
1	89392023	89392024	T	A	55	GENIC	homozygous	109308526
1	89392049	89392050	G	A	48	GENIC	homozygous	108884963
1	89392414	89392415	T	C	21	GENIC	homozygous	108884964
1	89392488	89392489	G	A	29	GENIC	homozygous	108884965
1	89392703	89392704	G	A	62	GENIC	homozygous	108884966
1	89393367	89393368	T	C	45	GENIC	homozygous	108884967
1	89393741	89393742	A	G	46	GENIC	homozygous	108884968
1	89395446	89395447	T	C	21	GENIC	homozygous	108884969
1	89395738	89395739	C	T	33	GENIC	homozygous	108884970
1	89396098	89396099	A	C	54	GENIC	homozygous	108884971
1	89397132	89397133	T	C	45	GENIC	homozygous	108884974
1	89397630	89397631	G	A	72	GENIC	homozygous	120560995
1	89398793	89398794	C	T	49	GENIC	possibly homozygous	108884975
1	89399002	89399003	T	A	30	GENIC	homozygous	108884976