chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	89180275	89180276	T	C	43	GENIC	possibly homozygous	108884780
1	89180791	89180792	A	G	44	GENIC	homozygous	108884782
1	89184976	89184977	C	T	43	GENIC	homozygous	108884789
1	89185838	89185839	T	C	44	GENIC	homozygous	108884792
1	89185983	89185984	T	C	48	GENIC	homozygous	108884793
1	89187146	89187147	G	A	27	GENIC	homozygous	120483941
1	89180872	89180872		CCTGTACCTGATGTACCTGCAAGTTCCCTGTGCATCTG	37	GENIC	homozygous	131260003
1	89180876	89180876		CG	35	GENIC	homozygous	131260004
1	89181315	89181326	TTCTTTCTTTC		33	GENIC	possibly homozygous	131260005
1	89187145	89187145		T	27	GENIC	homozygous	131260006
1	89187085	89187086	T	A	25	GENIC	homozygous	120483939
1	89187095	89187096	G	A	24	GENIC	homozygous	120483940
1	89184981	89184982	C	T	44	GENIC	homozygous	120503177
1	89187500	89187501	G	A	38	GENIC	homozygous	108884797
1	89187746	89187747	C	T	34	GENIC	homozygous	109308026
1	89188130	89188130		GTGTGTGTGTGC	15	GENIC	homozygous	131260007
1	89188308	89188309	T	G	19	GENIC	homozygous	108884798
1	89188769	89188770	C	T	24	GENIC	possibly homozygous	108884799
1	89188887	89188887		AG	26	GENIC	homozygous	131260008
1	89189204	89189205	G	C	44	GENIC	homozygous	108884800
1	89189384	89189385	G	A	33	GENIC	homozygous	108884801
1	89189802	89189803	A	G	42	GENIC	homozygous	108884802
1	89189830	89189831	T	C	39	GENIC	homozygous	108884803
1	89190709	89190733	CTGCTGCAGCTGCCTCCGTCAGAC		28	GENIC	homozygous	131260009
1	89192088	89192088		TG	42	GENIC	possibly homozygous	131260010
1	89192190	89192191	T	C	28	GENIC	homozygous	109308036
1	89192477	89192478	T	A	44	GENIC	homozygous	108884806
1	89194255	89194256	C	G	48	GENIC	possibly homozygous	125397014
1	89192192	89192193	T	C	28	GENIC	homozygous	131593207
1	89188240	89188240		ATG	14	GENIC	homozygous	131576398
1	89188241	89188241		A	13	GENIC	homozygous	131576399
1	89189739	89189740	G	A	39	GENIC	homozygous	131276989