chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	41315851	41315852	T	C	14	GENIC	heterozygous	51427431
10	41315874	41315875	A	T	18	GENIC	heterozygous	51427432
10	41315893	41315894	G	T	17	GENIC	heterozygous	52188008
10	41315924	41315925	G	T	16	GENIC	heterozygous	52188010
10	41315973	41315974	A	-	15	GENIC	heterozygous	52370735
10	41315976	41315978	CA	--	12	GENIC	heterozygous	53581919
10	41315978	41315979	T	A	12	GENIC	heterozygous	53581920
10	41316025	41316026	T	C	47	GENIC	heterozygous	51427434
10	41316825	41316826	C	G	45	GENIC	heterozygous	51427462
10	41316830	41316831	G	-	45	GENIC	heterozygous	51427463
10	41316831	41316832	G	C	45	GENIC	heterozygous	53568144
10	41316833	41316834	T	C	44	GENIC	heterozygous	51427464
10	41316834	41316835	G	A	45	GENIC	heterozygous	53568145
10	41316880	41316881	T	A	49	GENIC	heterozygous	51427465
10	41316883	41316884	G	A	48	GENIC	heterozygous	51427466
10	41316899	41316900	C	A	42	GENIC	heterozygous	51427467
10	41316912	41316913	A	G	41	GENIC	heterozygous	51427468
10	41316916	41316917	T	C	38	GENIC	heterozygous	51427469
10	41317185	41317186	A	G	57	GENIC	heterozygous	51427483
10	41317191	41317192	G	A	58	GENIC	heterozygous	51427484
10	41317201	41317202	T	G	53	GENIC	heterozygous	51427486
10	41317214	41317215	C	T	54	GENIC	heterozygous	51427487
10	41317215	41317216	C	G	54	GENIC	heterozygous	51427488