chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97969033	97969034	G	A	43	GENIC	homozygous	116828051
10	97970360	97970361	C	T	41	GENIC	homozygous	116695462
10	97973978	97973979	C	T	19	GENIC	heterozygous	118010458
10	97973995	97973996	T	C	26	GENIC	heterozygous	117230389
10	97983055	97983056	T	C	55	GENIC	homozygous	116695534
10	98001792	98001793	G	C	58	GENIC	homozygous	116695660
10	98001813	98001814	A	G	60	GENIC	possibly homozygous	116828053
10	98002245	98002246	A	C	38	GENIC	homozygous	116828055
10	98002269	98002270	C	A	42	GENIC	homozygous	116828057
10	98002379	98002380	T	C	15	GENIC	possibly homozygous	118010482
10	98002939	98002940	T	A	6	GENIC	homozygous	118010483
10	98002962	98002963	T	G	13	GENIC	homozygous	118010484
10	98003004	98003005	C	A	18	GENIC	homozygous	118010485
10	98007297	98007298	C	T	39	GENIC	possibly homozygous	116828059
10	98010431	98010432	A	C	43	GENIC	homozygous	116695672
10	98013256	98013257	T	C	65	GENIC	homozygous	116695678
10	98013736	98013737	A	G	73	GENIC	homozygous	116695680
10	98013917	98013918	T	C	29	GENIC	homozygous	116828061
10	98014214	98014215	T	C	47	GENIC	possibly homozygous	116828063
10	98015247	98015248	G	A	49	GENIC	homozygous	116695682
10	98015261	98015262	C	T	49	GENIC	homozygous	116695684
10	98015433	98015434	A	G	57	GENIC	possibly homozygous	116695688
10	98015751	98015752	T	C	64	GENIC	homozygous	116828065
10	98016446	98016447	A	G	61	GENIC	homozygous	116828067
10	98016602	98016603	G	T	61	GENIC	homozygous	116695690
10	97973960	97973961	C	T	42	GENIC	heterozygous	118051826
10	97996317	97996318	A	G	11	GENIC	possibly homozygous	118051828
10	97997293	97997294	T	A	154	GENIC	heterozygous	118051829