chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	41315973	41315974	A	-	28	GENIC	heterozygous	52370735
10	41315978	41315979	T	-	27	GENIC	heterozygous	52316689
10	41316432	41316433	G	A	8	GENIC	homozygous	51427448
10	41316443	41316444	A	C	7	GENIC	homozygous	51427449
10	41316451	41316452	T	C	5	GENIC	heterozygous	51427450
10	41316482	41316483	T	A	9	GENIC	possibly homozygous	51427452
10	41316497	41316498	G	C	10	GENIC	homozygous	51427453
10	41316624	41316625	C	CAG	7	GENIC	homozygous	51427454
10	41316652	41316653	A	G	10	GENIC	homozygous	51427455
10	41316709	41316710	A	-	1	GENIC	homozygous	51427456
10	41316781	41316782	T	G	3	GENIC	homozygous	52370739
10	41316933	41316934	C	G	12	GENIC	heterozygous	51427470
10	41317021	41317022	G	T	12	GENIC	possibly homozygous	51427472
10	41317094	41317095	C	T	6	GENIC	heterozygous	51427474
10	41317214	41317215	C	T	7	GENIC	heterozygous	51427487
10	41317215	41317216	C	G	8	GENIC	heterozygous	51427488
10	41317282	41317283	A	T	32	GENIC	heterozygous	51427490