chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	70010066	70010067	A	G	37	GENIC	homozygous	47177361
17	70010198	70010199	G	A	50	GENIC	homozygous	47177362
17	70010449	70010450	C	A	39	GENIC	homozygous	47177363
17	70010468	70010469	A	G	32	GENIC	homozygous	47177364
17	70010492	70010493	C	T	30	GENIC	homozygous	47177365
17	70010522	70010526	AATT	----	20	GENIC	homozygous	47177366
17	70010688	70010689	T	C	23	GENIC	homozygous	47177367
17	70010744	70010745	C	T	28	GENIC	homozygous	47177368
17	70010759	70010760	T	G	33	GENIC	homozygous	47177369
17	70010916	70010917	A	G	31	GENIC	homozygous	47177370
17	70011208	70011209	A	G	44	GENIC	homozygous	47177371
17	70011319	70011320	T	G	40	GENIC	possibly homozygous	47177372
17	70011402	70011403	A	C	40	GENIC	homozygous	47177373
17	70011478	70011479	G	A	48	GENIC	homozygous	47177374
17	70011490	70011491	G	A	50	GENIC	homozygous	47177375
17	70011682	70011684	AC	--	35	GENIC	homozygous	47177376
17	70011754	70011755	C	CTCTCTCTT	7	GENIC	homozygous	47177377
17	70011774	70011775	A	G	31	GENIC	possibly homozygous	47177378
17	70012200	70012201	G	T	59	GENIC	homozygous	47177379
17	70012376	70012377	C	A	49	GENIC	possibly homozygous	47177380
17	70012672	70012673	A	C	60	GENIC	homozygous	47177381
17	70012731	70012732	G	A	64	GENIC	homozygous	47177382
17	70012902	70012903	G	T	35	GENIC	homozygous	47177383
17	70012991	70012992	A	-	22	GENIC	homozygous	47177384
17	70013403	70013404	A	C	49	GENIC	homozygous	47177385
17	70013405	70013406	G	GT	54	GENIC	homozygous	47177386