chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109528931	109528932	A	G	20	GENIC	homozygous	116718537
10	109529995	109529996	C	A	7	GENIC	homozygous	116718539
10	109530529	109530530	G	A	19	GENIC	homozygous	116718541
10	109530659	109530660	G	C	10	GENIC	homozygous	116718543
10	109531858	109531859	A	C	20	GENIC	homozygous	116718545
10	109532324	109532325	A	G	11	GENIC	homozygous	116718547
10	109532860	109532861	G	A	10	GENIC	homozygous	116718549
10	109533199	109533200	T	C	5	GENIC	homozygous	116718551
10	109534587	109534588	G	A	16	GENIC	homozygous	116718553
10	109534704	109534705	T	C	10	GENIC	homozygous	116718555
10	109535201	109535202	C	T	9	GENIC	homozygous	116718557
10	109535688	109535689	A	G	22	GENIC	homozygous	116718559
10	109535769	109535770	A	G	5	GENIC	homozygous	126391751
10	109535798	109535799	G	A	26	GENIC	homozygous	116909575
10	109535847	109535848	C	G	17	GENIC	homozygous	116718561
10	109535940	109535941	T	G	21	GENIC	homozygous	116718563
10	109539468	109539469	G	C	17	GENIC	homozygous	116718565