chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	89384033	89384034	G	T	20	GENIC	homozygous	120503250
1	89384084	89384085	T	C	16	GENIC	homozygous	108884954
1	89384447	89384448	T	C	18	GENIC	homozygous	108884955
1	89385543	89385544	A	G	28	GENIC	homozygous	120503251
1	89385546	89385547	C	T	27	GENIC	homozygous	120503252
1	89385819	89385821	AA		3	GENIC	homozygous	131984944
1	89385822	89385822		GGC	3	GENIC	homozygous	131984945
1	89386078	89386079	C	T	13	GENIC	homozygous	125397039
1	89386098	89386098		GTGTGTGTGTGTGTGTGTGTGT	7	GENIC	homozygous	131984946
1	89386101	89386102	A	T	7	GENIC	homozygous	125397040
1	89386286	89386286		TTA	17	GENIC	homozygous	131984947
1	89386652	89386653	T	A	17	GENIC	homozygous	120503253
1	89386686	89386687	A	G	21	GENIC	homozygous	120483993
1	89386696	89386697	G	A	19	GENIC	homozygous	120483994
1	89387060	89387061	A	G	20	GENIC	homozygous	108884957
1	89387811	89387811		G	17	GENIC	homozygous	131984948
1	89389471	89389472	T	C	15	GENIC	homozygous	120503254
1	89391383	89391384	A	T	21	GENIC	homozygous	108884962
1	89392019	89392019		A	19	GENIC	homozygous	131260066
1	89392023	89392024	T	A	19	GENIC	homozygous	109308526
1	89393367	89393368	T	C	12	GENIC	homozygous	108884967
1	89393741	89393742	A	G	11	GENIC	homozygous	108884968
1	89394637	89394638	G	A	16	GENIC	homozygous	120503255
1	89395446	89395447	T	C	16	GENIC	homozygous	108884969
1	89396098	89396099	A	C	6	GENIC	homozygous	108884971
1	89396699	89396700	G	T	15	GENIC	homozygous	108884972
1	89396745	89396746	T	C	20	GENIC	homozygous	108884973
1	89397132	89397133	T	C	25	GENIC	homozygous	108884974
1	89398793	89398794	C	T	17	GENIC	homozygous	108884975
1	89399002	89399003	T	A	17	GENIC	homozygous	108884976