chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	70010066	70010067	A	G	23	GENIC	homozygous	47177361
17	70010198	70010199	G	A	14	GENIC	homozygous	47177362
17	70010449	70010450	C	A	21	GENIC	homozygous	47177363
17	70010468	70010469	A	G	22	GENIC	homozygous	47177364
17	70010492	70010493	C	T	20	GENIC	homozygous	47177365
17	70010522	70010526	AATT	----	19	GENIC	homozygous	47177366
17	70010688	70010689	T	C	21	GENIC	homozygous	47177367
17	70010744	70010745	C	T	19	GENIC	homozygous	47177368
17	70010759	70010760	T	G	16	GENIC	homozygous	47177369
17	70010916	70010917	A	G	18	GENIC	homozygous	47177370
17	70011208	70011209	A	G	14	GENIC	homozygous	47177371
17	70011319	70011320	T	G	16	GENIC	homozygous	47177372
17	70011402	70011403	A	C	20	GENIC	homozygous	47177373
17	70011478	70011479	G	A	17	GENIC	homozygous	47177374
17	70011490	70011491	G	A	15	GENIC	homozygous	47177375
17	70011754	70011755	C	CTCTCTCTCTT	14	GENIC	homozygous	48160318
17	70011758	70011759	G	C	14	GENIC	homozygous	47338313
17	70011774	70011775	A	G	17	GENIC	homozygous	47177378
17	70012200	70012201	G	T	10	GENIC	homozygous	47177379
17	70012376	70012377	C	A	11	GENIC	homozygous	47177380
17	70012672	70012673	A	C	15	GENIC	homozygous	47177381
17	70012731	70012732	G	A	20	GENIC	homozygous	47177382
17	70012902	70012903	G	T	26	GENIC	homozygous	47177383
17	70012991	70012992	A	-	23	GENIC	homozygous	47177384
17	70013403	70013404	A	C	26	GENIC	homozygous	47177385
17	70013405	70013406	G	GT	26	GENIC	homozygous	47177386