chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37814071	37814072	A	G	17	GENIC	homozygous	51419651
10	37814102	37814103	A	T	23	GENIC	homozygous	51419655
10	37814193	37814194	A	T	21	GENIC	possibly homozygous	52140666
10	37814997	37814998	C	-	17	GENIC	possibly homozygous	52140668
10	37815114	37815115	C	T	8	GENIC	homozygous	52140669
10	37815166	37815167	T	C	19	GENIC	heterozygous	51419657
10	37815298	37815299	T	C	21	GENIC	possibly homozygous	51419659
10	37815390	37815391	G	A	24	GENIC	homozygous	51419661
10	37815437	37815438	T	C	23	GENIC	homozygous	51419663
10	37815509	37815515	ACACAC	------	3	GENIC	heterozygous	51419667
10	37815701	37815702	A	AC	1	GENIC	homozygous	51850904
10	37815813	37815814	G	A	17	GENIC	heterozygous	52140675
10	37816960	37816961	T	C	27	GENIC	homozygous	51419673
10	37817649	37817650	T	C	12	GENIC	possibly homozygous	51419677
10	37818049	37818050	A	T	8	GENIC	possibly homozygous	51419679
10	37818050	37818051	A	C	9	GENIC	possibly homozygous	51419681
10	37818652	37818653	A	T	23	GENIC	homozygous	51419685
10	37821086	37821087	T	C	20	GENIC	possibly homozygous	52140679
10	37821117	37821118	G	A	19	GENIC	homozygous	52140681
10	37821213	37821222	GGGTTTACG	---------	2	GENIC	homozygous	52140683
10	37819511	37819512	T	C	22	GENIC	possibly homozygous	51419687
10	37822088	37822089	A	G	22	GENIC	homozygous	51419695
10	37822613	37822614	T	C	20	GENIC	possibly homozygous	51419704
10	37823000	37823001	T	TG	9	GENIC	homozygous	51419708
10	37823367	37823368	T	C	17	GENIC	possibly homozygous	51419712
10	37824150	37824151	G	-	23	GENIC	homozygous	51419716
10	37824387	37824388	T	C	15	GENIC	possibly homozygous	51419718
10	37825824	37825825	T	G	7	GENIC	homozygous	51419728
10	37826428	37826429	T	C	26	GENIC	homozygous	51419730
10	37826998	37827000	CT	--	14	GENIC	homozygous	52140685
10	37822107	37822108	A	AACACACACACACACACACAC	2	GENIC	heterozygous	52316340