chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	58165032	58165033	C	A	22	GENIC	homozygous	136117516
2	58165418	58165419	A	T	48	GENIC	homozygous	136117517
2	58165438	58165439	T	C	48	GENIC	homozygous	136117518
2	58166002	58166003	C	G	64	GENIC	homozygous	136117519
2	58166900	58166901	A	C	35	GENIC	possibly homozygous	136117520
2	58167644	58167645	A		31	GENIC	homozygous	135909804
2	58167714	58167715	G	A	36	GENIC	homozygous	136117521
2	58169879	58169880	G	A	54	GENIC	homozygous	136117522
2	58170463	58170465	CA		35	GENIC	homozygous	135909805
2	58170763	58170764	C	T	27	GENIC	homozygous	136117523
2	58174022	58174023	G	A	36	GENIC	homozygous	136117524
2	58174845	58174846	T	C	53	GENIC	homozygous	136117525
2	58174929	58174930	T	A	57	GENIC	homozygous	136117526
2	58175132	58175133	C	T	51	GENIC	homozygous	136117527
2	58175799	58175800	C	T	49	GENIC	homozygous	136117528
2	58177430	58177448	GGTGTTGGATTTGCTTAG		52	GENIC	homozygous	135909806
2	58177863	58177864	G	A	52	GENIC	homozygous	136117529
2	58178015	58178016	C	T	45	GENIC	homozygous	136117530
2	58178132	58178133	T	C	50	GENIC	homozygous	136117531
2	58178222	58178229	GAGGCTC		53	GENIC	homozygous	135909807
2	58181621	58181622	C	T	47	GENIC	homozygous	136117532
2	58185350	58185351	A		47	GENIC	homozygous	135909808
2	58186922	58186923	T	C	58	GENIC	homozygous	136117533
2	58186965	58186966	T	C	55	GENIC	homozygous	136117534
2	58187710	58187710		TTAAA	52	GENIC	homozygous	135909809
2	58188349	58188350	G	A	57	GENIC	homozygous	136117535
2	58188821	58188822	T		44	GENIC	possibly homozygous	135909810