chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109972573	109972574	A	AGTGTGTGTGTGTGT	8	GENIC	heterozygous	52410206
10	109972573	109972574	A	AGTGTGTGTGTGTGTGT	8	GENIC	heterozygous	52410208
10	109972864	109972865	G	GTT	10	GENIC	heterozygous	52085308
10	109972879	109972880	A	T	21	GENIC	homozygous	52331891
10	109972904	109972905	A	G	16	GENIC	homozygous	51600696
10	109973184	109973185	A	G	38	GENIC	homozygous	51600697
10	109973262	109973263	T	A	36	GENIC	homozygous	51600698
10	109973347	109973348	T	C	34	GENIC	homozygous	51600699
10	109973540	109973541	G	A	48	GENIC	homozygous	51600700
10	109974875	109974880	GTGTG	-----	53	GENIC	homozygous	51600701
10	109976102	109976103	G	A	23	GENIC	homozygous	51600704
10	109976247	109976248	G	C	24	GENIC	homozygous	51600705
10	109976371	109976372	G	-	26	GENIC	homozygous	51600706
10	109976380	109976387	TTGTTTG	-------	27	GENIC	homozygous	51600708
10	109976639	109976640	T	C	27	GENIC	homozygous	51600710
10	109976655	109976656	C	T	28	GENIC	homozygous	51600711
10	109976941	109976942	G	A	51	GENIC	homozygous	51600712
10	109977040	109977044	CACA	----	32	GENIC	homozygous	51600713
10	109977462	109977463	G	A	27	GENIC	homozygous	51600715
10	109977776	109977777	C	T	50	GENIC	homozygous	51600716
10	109972864	109972865	G	GTTT	10	GENIC	heterozygous	52734752
10	109978463	109978464	G	A	41	GENIC	homozygous	51600717
10	109978962	109978963	C	CA	30	GENIC	possibly homozygous	51600718
10	109979045	109979046	A	G	38	GENIC	homozygous	51600719
10	109979053	109979054	G	GAACCC	37	GENIC	homozygous	51600720
10	109979055	109979056	T	C	41	GENIC	homozygous	52331893