chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	130622937	130622938	T	TGGG	4	GENIC	homozygous	57675484
3	130624447	130624448	A	G	29	GENIC	homozygous	57675489
3	130625837	130625838	G	A	31	GENIC	homozygous	57675491
3	130627458	130627459	G	GGA	4	GENIC	heterozygous	58695904
3	130628078	130628079	G	A	21	GENIC	homozygous	57675493
3	130628320	130628321	G	A	21	GENIC	homozygous	57675496
3	130628703	130628704	C	CT	8	GENIC	homozygous	57675501
3	130628756	130628757	C	T	17	GENIC	homozygous	57675503
3	130628958	130628959	A	G	31	GENIC	homozygous	57675505
3	130629430	130629431	T	C	43	GENIC	homozygous	57675508
3	130630313	130630316	TTA	---	10	GENIC	heterozygous	57675510
3	130630314	130630316	TA	--	8	GENIC	heterozygous	57675513
3	130630672	130630673	A	G	32	GENIC	homozygous	57675515
3	130631056	130631057	G	A	17	GENIC	homozygous	57675517
3	130632053	130632054	T	C	35	GENIC	homozygous	57675519
3	130632109	130632110	G	A	25	GENIC	homozygous	57675521
3	130632212	130632213	A	G	22	GENIC	homozygous	57675523
3	130633317	130633318	C	T	18	GENIC	homozygous	57675526
3	130633845	130633846	C	T	24	GENIC	homozygous	57675529
3	130634641	130634649	GTGTGTGT	--------	5	GENIC	homozygous	58695905
3	130635567	130635568	T	TTG	13	GENIC	possibly homozygous	57675535