chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	171013233	171013234	C	A	28	GENIC	homozygous	112205368
3	171014426	171014427	G	T	23	GENIC	homozygous	112205370
3	171014816	171014817	T	A	27	GENIC	homozygous	119653089
3	171014979	171014980	G	A	28	GENIC	homozygous	112205372
3	171014988	171014989	G	A	30	GENIC	homozygous	112205374
3	171015072	171015073	T	A	38	GENIC	homozygous	112205376
3	171017607	171017608	A	T	33	GENIC	homozygous	112205378
3	171017664	171017665	G	A	26	GENIC	homozygous	112205380
3	171017778	171017779	A	G	35	GENIC	homozygous	112205382
3	171021220	171021221	A	G	38	GENIC	homozygous	112205384
3	171022119	171022120	G	A	30	GENIC	homozygous	112205386
3	171022152	171022153	T	G	23	GENIC	homozygous	112205388
3	171022817	171022818	G	A	37	GENIC	homozygous	112205390
3	171023037	171023038	A	G	39	GENIC	homozygous	112205392
3	171025463	171025464	G	A	54	GENIC	homozygous	112205394
3	171026720	171026721	G	T	27	GENIC	homozygous	112205396
3	171027491	171027492	G	A	38	GENIC	homozygous	112205398
3	171030259	171030260	G	A	38	GENIC	homozygous	119686538