chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	176102336	176102337	T	G	50	GENIC	homozygous	111841336
3	176102360	176102361	G	A	55	GENIC	homozygous	133126218
3	176102604	176102605	A	G	78	GENIC	homozygous	119747757
3	176103729	176103729		CACTCA	57	GENIC	homozygous	127965213
3	176103943	176103944	G	A	65	GENIC	possibly homozygous	119747759
3	176104030	176104031	T	C	63	GENIC	homozygous	112218578
3	176105054	176105055	G	A	79	GENIC	homozygous	119747761
3	176105681	176105682	A	G	77	GENIC	homozygous	112218583
3	176108922	176108923	A	T	66	GENIC	homozygous	112218588
3	176111006	176111007	C	A	68	GENIC	homozygous	119747763
3	176112128	176112129	C	T	68	GENIC	homozygous	133126219
3	176112755	176112756	C	T	59	GENIC	homozygous	119747765
3	176115486	176115487	G	A	59	GENIC	homozygous	112373516
3	176116451	176116452	G	C	38	GENIC	homozygous	112373517
3	176116477	176116478	A	G	39	GENIC	homozygous	119747767
3	176116525	176116526	C	A	38	GENIC	homozygous	112373518
3	176117903	176117904	C	T	37	GENIC	homozygous	119747769
3	176118191	176118192	T	G	55	GENIC	homozygous	112373519
3	176119260	176119261	T	A	54	GENIC	possibly homozygous	112218594
3	176119355	176119356	G	A	68	GENIC	homozygous	112373521
3	176119658	176119659	A	G	48	GENIC	homozygous	112218596
3	176120426	176120427	C	T	61	GENIC	homozygous	119747771
3	176120800	176120801	T	C	54	GENIC	homozygous	112373522
3	176121894	176121895	G	A	73	GENIC	homozygous	112373524
3	176122367	176122368	A	C	42	GENIC	possibly homozygous	112218598
3	176115141	176115142	T		77	GENIC	homozygous	133117591
3	176122920	176122920		G	48	GENIC	homozygous	127965215
3	176122923	176122924	A		51	GENIC	homozygous	127965216
3	176123114	176123114		ATGTACACGTACCACAGAACTAACGTAGGGATTAGAGGGCAACTTTGTGGAGTCAGTTCTCTTCTAATTTTACGTGGGTCCTGGACATTAAATTCGAGTTACCAGACTGGAGCAA	45	GENIC	possibly homozygous	127965217
3	176124808	176124809	A	C	59	GENIC	homozygous	112218600