chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109972221	109972222	T	A	46	GENIC	homozygous	52272688
10	109972573	109972574	A	AGTGTGTGT	13	GENIC	homozygous	51600694
10	109973089	109973090	G	A	35	GENIC	possibly homozygous	52272690
10	109973184	109973185	A	G	59	GENIC	homozygous	51600697
10	109973262	109973263	T	A	47	GENIC	homozygous	51600698
10	109973347	109973348	T	C	54	GENIC	homozygous	51600699
10	109973540	109973541	G	A	59	GENIC	homozygous	51600700
10	109974600	109974601	G	A	36	GENIC	homozygous	52272692
10	109974875	109974880	GTGTG	-----	51	GENIC	homozygous	51600701
10	109975533	109975545	AGAGAAAGAGAG	------------	19	GENIC	possibly homozygous	51600703
10	109976247	109976248	G	C	30	GENIC	homozygous	51600705
10	109976380	109976387	TTGTTTG	-------	25	GENIC	heterozygous	51600708
10	109976383	109976391	TTTGTTTG	--------	12	GENIC	homozygous	51600709
10	109976655	109976656	C	T	48	GENIC	homozygous	51600711
10	109976774	109976775	A	G	41	GENIC	homozygous	52272694
10	109976941	109976942	G	A	45	GENIC	homozygous	51600712
10	109977064	109977065	C	T	41	GENIC	heterozygous	51600714
10	109977462	109977463	G	A	57	GENIC	homozygous	51600715
10	109977776	109977777	C	T	58	GENIC	homozygous	51600716
10	109979045	109979046	A	G	23	GENIC	possibly homozygous	51600719
10	109979053	109979054	G	GAACCC	17	GENIC	homozygous	51600720
10	109972864	109972865	G	GTT	12	GENIC	homozygous	52085308