chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	41315973	41315974	A	-	13	GENIC	homozygous	52370735
10	41315975	41315976	C	-	13	GENIC	homozygous	52370737
10	41315978	41315979	T	-	14	GENIC	homozygous	52316689
10	41316237	41316238	A	C	42	GENIC	homozygous	52188014
10	41316395	41316396	G	T	36	GENIC	heterozygous	52145828
10	41316387	41316388	A	-	35	GENIC	heterozygous	52145826
10	41316432	41316433	G	A	30	GENIC	homozygous	51427448
10	41316443	41316444	A	C	27	GENIC	homozygous	51427449
10	41316451	41316452	T	C	27	GENIC	homozygous	51427450
10	41316482	41316483	T	A	19	GENIC	homozygous	51427452
10	41316497	41316498	G	C	20	GENIC	homozygous	51427453
10	41316624	41316625	C	CAG	16	GENIC	homozygous	51427454
10	41316652	41316653	A	G	19	GENIC	homozygous	51427455
10	41316709	41316710	A	-	13	GENIC	homozygous	51427456
10	41316713	41316716	GGG	---	16	GENIC	heterozygous	51427457
10	41316781	41316782	T	G	27	GENIC	possibly homozygous	52370739
10	41316787	41316789	TC	--	30	GENIC	heterozygous	51865270
10	41316831	41316834	GGT	---	71	GENIC	heterozygous	52370741
10	41316834	41316835	G	GCA	68	GENIC	heterozygous	52370743
10	41316933	41316934	C	G	69	GENIC	heterozygous	51427470
10	41317021	41317022	G	T	47	GENIC	heterozygous	51427472
10	41317094	41317095	C	T	18	GENIC	homozygous	51427474
10	41317098	41317099	T	-	18	GENIC	heterozygous	51427475
10	41317103	41317104	A	AC	18	GENIC	heterozygous	51427476
10	41317157	41317158	A	-	20	GENIC	heterozygous	51427481
10	41317173	41317174	T	TG	29	GENIC	heterozygous	52370745
10	41317214	41317215	C	T	52	GENIC	heterozygous	51427487
10	41317215	41317216	C	G	53	GENIC	heterozygous	51427488
10	41317282	41317283	A	T	57	GENIC	heterozygous	51427490