chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	10250558	10250559	A	T	49	GENIC	homozygous	111722469
16	10250572	10250573	C	G	50	GENIC	homozygous	111722471
16	10250711	10250712	G	A	42	GENIC	homozygous	111722473
16	10250724	10250726	TA		39	GENIC	homozygous	129332666
16	10250727	10250727		CT	40	GENIC	homozygous	129332667
16	10251029	10251030	T	G	57	GENIC	homozygous	111722475
16	10251145	10251146	T	A	25	GENIC	homozygous	111933016
16	10251186	10251186		GG	22	GENIC	homozygous	129332668
16	10251276	10251277	A	G	42	GENIC	homozygous	111722477
16	10251756	10251757	G	A	54	GENIC	homozygous	111722479
16	10252343	10252344	T		48	GENIC	homozygous	129332669
16	10253019	10253020	T	C	55	GENIC	homozygous	111722481
16	10254630	10254631	C	T	45	GENIC	homozygous	111722483
16	10254745	10254746	C	A	60	GENIC	homozygous	111722485
16	10255171	10255172	C	T	61	GENIC	homozygous	111722487
16	10255989	10255990	G	T	63	GENIC	possibly homozygous	111722489
16	10256222	10256223	C	T	59	GENIC	homozygous	111722491
16	10256613	10256614	C	T	54	GENIC	homozygous	119094935
16	10256934	10256938	ATAA		54	GENIC	possibly homozygous	129332670
16	10256990	10256994	ATAA		55	GENIC	possibly homozygous	129332671
16	10257589	10257590	T	C	62	GENIC	homozygous	111722497
16	10256735	10256736	G	A	43	GENIC	possibly homozygous	111722493
16	10256768	10256769	G	A	47	GENIC	possibly homozygous	111722495
16	10256925	10256926	G	A	55	GENIC	homozygous	119094936
16	10257953	10257954	A	G	45	GENIC	homozygous	119094937
16	10257988	10258000	TAATAATAATAG		49	GENIC	homozygous	129332672
16	10258017	10258017		A	47	GENIC	homozygous	129332673
16	10258406	10258406		AGG	58	GENIC	homozygous	129332674
16	10258467	10258468	G	C	58	GENIC	homozygous	111722499
16	10258481	10258482	A	G	63	GENIC	homozygous	111722501
16	10258647	10258647		GAG	59	GENIC	homozygous	129332675
16	10259880	10259881	T		60	GENIC	possibly homozygous	129332676
16	10260820	10260820		C	49	GENIC	homozygous	129332677