chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	170992597	170992598	A	T	36	GENIC	homozygous	112205319
3	170993406	170993406		TTT	38	GENIC	homozygous	130915302
3	170993939	170993940	T	C	31	GENIC	homozygous	121921478
3	170993941	170993942	T	C	31	GENIC	homozygous	119888936
3	170993944	170993945	C		29	GENIC	homozygous	127961061
3	170993888	170993890	CT		36	GENIC	homozygous	127961057
3	170993892	170993892		T	37	GENIC	homozygous	127961058
3	170993919	170993921	GC		34	GENIC	homozygous	127961059
3	170993937	170993938	T		31	GENIC	homozygous	127961060
3	170993925	170993926	T	G	34	GENIC	homozygous	112047073
3	170993947	170993947		G	29	GENIC	homozygous	127961062
3	170994927	170994928	C	T	49	GENIC	homozygous	112205323
3	170997182	170997183	C	T	46	GENIC	homozygous	112371397
3	170997802	170997803	G	A	53	GENIC	homozygous	112205325
3	170999831	170999831		CAGGGACCTTAT	51	GENIC	homozygous	130915305
3	171002325	171002326	C	A	65	GENIC	homozygous	112205331
3	171008059	171008060	A	G	71	GENIC	homozygous	112205336
3	171008073	171008074	T	A	69	GENIC	homozygous	112205338
3	171008117	171008118	A	C	66	GENIC	homozygous	112205340
3	171008197	171008317	CACAGACCCAGTACACACAGACCCAGTACACACAGAGATAGTATACTTAGACCCAGTACACACAGACCCAGTACACACAGACCCAGTACACACAGAGATAGTATACTTAGACCCAGTACA		39	GENIC	homozygous	130915306
3	170994617	170994618	T	A	25	GENIC	possibly homozygous	119705742