chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17211816	17211817	C	A	23	GENIC	homozygous	116500493
10	17213383	17213384	T	C	19	GENIC	homozygous	116500495
10	17214355	17214356	G	A	25	GENIC	possibly homozygous	116500496
10	17215772	17215773	G	A	29	GENIC	homozygous	116500500
10	17216526	17216527	T	C	26	GENIC	homozygous	116500502
10	17216896	17216897	T	G	37	GENIC	homozygous	116500504
10	17216963	17216964	G	T	24	GENIC	homozygous	116500506
10	17217967	17217968	A	C	33	GENIC	homozygous	116500510
10	17217980	17217981	A	G	38	GENIC	homozygous	116500512
10	17218025	17218026	T	C	41	GENIC	homozygous	116500514
10	17218221	17218222	C	T	27	GENIC	homozygous	116500516
10	17218239	17218240	C	T	25	GENIC	homozygous	116500518
10	17218682	17218683	T	C	28	GENIC	homozygous	116500520
10	17219509	17219510	C	T	45	GENIC	homozygous	116500522
10	17220528	17220529	G	A	27	GENIC	homozygous	116500526
10	17220905	17220906	C	G	11	GENIC	homozygous	116500528
10	17221379	17221380	C	T	42	GENIC	homozygous	116500530
10	17234071	17234072	C	G	31	GENIC	homozygous	116500532
10	17265994	17265995	T	G	24	GENIC	homozygous	116500534