chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109528931	109528932	A	G	42	GENIC	homozygous	116718537
10	109530659	109530660	G	C	26	GENIC	homozygous	116718543
10	109530904	109530905	G	A	28	GENIC	homozygous	116909571
10	109531729	109531730	T	C	17	GENIC	homozygous	116909572
10	109531858	109531859	A	C	32	GENIC	homozygous	116718545
10	109532324	109532325	A	G	29	GENIC	homozygous	116718547
10	109532860	109532861	G	A	32	GENIC	homozygous	116718549
10	109533199	109533200	T	C	25	GENIC	homozygous	116718551
10	109534380	109534381	A	C	33	GENIC	homozygous	116909573
10	109534587	109534588	G	A	41	GENIC	homozygous	116718553
10	109534704	109534705	T	C	33	GENIC	homozygous	116718555
10	109535271	109535272	G	A	41	GENIC	homozygous	116909574
10	109535688	109535689	A	G	26	GENIC	homozygous	116718559
10	109535798	109535799	G	A	27	GENIC	possibly homozygous	116909575
10	109535847	109535848	C	G	34	GENIC	homozygous	116718561
10	109535940	109535941	T	G	24	GENIC	homozygous	116718563
10	109539700	109539701	G	A	17	GENIC	homozygous	116909576
10	109539942	109539943	G	A	25	GENIC	homozygous	116909577