chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	176102336	176102337	T	G	23	GENIC	homozygous	111841336
3	176102701	176102702	C	T	32	GENIC	homozygous	112218573
3	176102816	176102817	G	A	28	GENIC	homozygous	112218574
3	176103374	176103375	A	G	30	GENIC	homozygous	112218575
3	176103386	176103387	G	A	36	GENIC	homozygous	112218576
3	176103575	176103576	T	C	30	GENIC	homozygous	112218577
3	176104030	176104031	T	C	43	GENIC	homozygous	112218578
3	176104070	176104071	A	G	41	GENIC	homozygous	112218579
3	176104830	176104831	A	G	43	GENIC	homozygous	112218580
3	176105076	176105077	T	A	38	GENIC	homozygous	112218581
3	176105119	176105120	G	A	31	GENIC	homozygous	112218582
3	176105681	176105682	A	G	40	GENIC	homozygous	112218583
3	176106121	176106122	G	A	36	GENIC	homozygous	112218584
3	176107498	176107499	T	C	29	GENIC	homozygous	112218585
3	176107507	176107508	C	A	26	GENIC	homozygous	112218586
3	176108587	176108588	T	G	23	GENIC	possibly homozygous	112218587
3	176108922	176108923	A	T	31	GENIC	homozygous	112218588
3	176111220	176111221	T	C	34	GENIC	homozygous	112218589
3	176111558	176111559	G	A	37	GENIC	homozygous	112218590
3	176112118	176112119	C	T	38	GENIC	homozygous	112218591
3	176115936	176115937	C	T	34	GENIC	possibly homozygous	112218592
3	176116130	176116131	T	C	27	GENIC	heterozygous	112218593
3	176119260	176119261	T	A	29	GENIC	homozygous	112218594
3	176119574	176119575	G	A	31	GENIC	homozygous	112218595
3	176119658	176119659	A	G	28	GENIC	homozygous	112218596
3	176120899	176120900	C	T	33	GENIC	possibly homozygous	112218597
3	176122367	176122368	A	C	34	GENIC	possibly homozygous	112218598
3	176123555	176123556	T	C	41	GENIC	possibly homozygous	112218599
3	176124808	176124809	A	C	38	GENIC	homozygous	112218600