chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	171013233	171013234	C	A	49	GENIC	homozygous	112205368
3	171014426	171014427	G	T	36	GENIC	homozygous	112205370
3	171014979	171014980	G	A	40	GENIC	homozygous	112205372
3	171014988	171014989	G	A	42	GENIC	homozygous	112205374
3	171015072	171015073	T	A	45	GENIC	homozygous	112205376
3	171017029	171017030	T	G	36	GENIC	heterozygous	112433098
3	171017607	171017608	A	T	56	GENIC	possibly homozygous	112205378
3	171017664	171017665	G	A	51	GENIC	homozygous	112205380
3	171017778	171017779	A	G	44	GENIC	possibly homozygous	112205382
3	171021220	171021221	A	G	49	GENIC	homozygous	112205384
3	171022119	171022120	G	A	71	GENIC	homozygous	112205386
3	171022152	171022153	T	G	52	GENIC	possibly homozygous	112205388
3	171022817	171022818	G	A	43	GENIC	homozygous	112205390
3	171023037	171023038	A	G	46	GENIC	homozygous	112205392
3	171025463	171025464	G	A	36	GENIC	homozygous	112205394
3	171026720	171026721	G	T	46	GENIC	homozygous	112205396
3	171027491	171027492	G	A	52	GENIC	homozygous	112205398
3	171027675	171027676	A	G	27	GENIC	possibly homozygous	112258371