chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46314908	46314909	T	C	11	GENIC	homozygous	116772488
10	46315925	46315926	G	A	19	GENIC	homozygous	116772490
10	46315930	46315931	T	G	21	GENIC	homozygous	116772492
10	46316163	46316164	G	T	29	GENIC	homozygous	116877695
10	46317257	46317258	T	C	17	GENIC	homozygous	116772494
10	46317610	46317611	A	G	41	GENIC	homozygous	116877697
10	46317840	46317841	G	A	40	GENIC	homozygous	116772496
10	46318819	46318820	C	A	35	GENIC	homozygous	116772498
10	46319250	46319251	A	G	15	GENIC	homozygous	116772500
10	46319716	46319717	A	G	32	GENIC	homozygous	116772502
10	46319738	46319739	A	C	19	GENIC	homozygous	116772504
10	46319886	46319887	G	A	38	GENIC	homozygous	116772508
10	46320125	46320126	G	A	29	GENIC	homozygous	116772510
10	46320760	46320761	A	G	26	GENIC	homozygous	116772512
10	46321844	46321845	C	T	30	GENIC	homozygous	116772514
10	46323312	46323313	T	C	32	GENIC	homozygous	116772516
10	46323452	46323453	T	C	42	GENIC	homozygous	116772518
10	46324115	46324116	C	T	29	GENIC	possibly homozygous	116877699
10	46324321	46324322	T	G	27	GENIC	homozygous	116772522
10	46324323	46324324	G	T	27	GENIC	homozygous	116772524
10	46324332	46324333	C	T	27	GENIC	homozygous	116772526
10	46324455	46324456	A	G	29	GENIC	homozygous	116772528
10	46324684	46324685	C	G	35	GENIC	homozygous	116772530
10	46325626	46325627	C	T	24	GENIC	homozygous	116877701
10	46326813	46326814	G	C	37	GENIC	possibly homozygous	116772532
10	46327139	46327140	G	A	29	GENIC	possibly homozygous	116772534
10	46327182	46327183	A	G	22	GENIC	homozygous	116772536
10	46327242	46327243	G	A	39	GENIC	possibly homozygous	116772538
10	46328517	46328518	C	T	28	GENIC	homozygous	116772542
10	46329155	46329156	G	T	41	GENIC	homozygous	116877703
10	46329282	46329283	C	T	52	GENIC	possibly homozygous	116772544
10	46327616	46327617	T	G	28	GENIC	homozygous	116585675
10	46324176	46324177	T	C	19	GENIC	homozygous	116585671