chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109972573	109972574	A	AGTGTGTGT	12	GENIC	homozygous	51600694
10	109972879	109972880	A	T	10	GENIC	homozygous	52331891
10	109973184	109973185	A	G	14	GENIC	homozygous	51600697
10	109973262	109973263	T	A	12	GENIC	homozygous	51600698
10	109973347	109973348	T	C	15	GENIC	homozygous	51600699
10	109973540	109973541	G	A	15	GENIC	homozygous	51600700
10	109974875	109974880	GTGTG	-----	21	GENIC	homozygous	51600701
10	109976247	109976248	G	C	13	GENIC	homozygous	51600705
10	109976639	109976640	T	C	20	GENIC	homozygous	51600710
10	109976655	109976656	C	T	20	GENIC	homozygous	51600711
10	109976941	109976942	G	A	19	GENIC	homozygous	51600712
10	109977040	109977044	CACA	----	14	GENIC	homozygous	51600713
10	109977462	109977463	G	A	30	GENIC	homozygous	51600715
10	109977776	109977777	C	T	20	GENIC	homozygous	51600716
10	109979045	109979046	A	G	12	GENIC	homozygous	51600719
10	109979053	109979054	G	GAACCC	14	GENIC	homozygous	51600720
10	109979055	109979056	T	C	14	GENIC	homozygous	52331893
10	109972864	109972865	G	GTTT	6	GENIC	heterozygous	52734752
10	109973421	109973422	C	T	14	GENIC	homozygous	51958322
10	109976379	109976391	TTTGTTTGTTTG	------------	9	GENIC	homozygous	51958325
10	109976678	109976679	C	T	13	GENIC	homozygous	51958328
10	109977023	109977024	C	A	20	GENIC	homozygous	51958331
10	109977804	109977805	G	A	18	GENIC	homozygous	51958334