chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	61680609	61680610	C	T	51	GENIC	heterozygous	117358697
9	61680719	61680719		TGGTATA	26	GENIC	heterozygous	128717798
9	61680978	61680979	T	C	43	GENIC	heterozygous	123186964
9	61680998	61680999	A	C	43	GENIC	heterozygous	117543049
9	61681007	61681008	C	T	43	GENIC	heterozygous	117875728
9	61681009	61681010	T	C	43	GENIC	heterozygous	123186965
9	61681084	61681085	G	A	32	GENIC	heterozygous	120278184
9	61681119	61681120	G	A	27	GENIC	heterozygous	133565660
9	61681247	61681247		A	27	GENIC	homozygous	128717799
9	61681450	61681451	T	C	38	GENIC	homozygous	117358698
9	61681820	61681822	GC		29	GENIC	possibly homozygous	128717800
9	61681893	61681894	C	T	22	GENIC	homozygous	117570289
9	61681949	61681950	G	A	23	GENIC	homozygous	117570291
9	61682251	61682252	T	G	19	GENIC	homozygous	117570293
9	61683065	61683066	A	G	30	GENIC	homozygous	117570295
9	61683128	61683129	T	G	29	GENIC	homozygous	117358703
9	61683541	61683542	T	C	28	GENIC	homozygous	117570297
9	61683702	61683703	G	A	24	GENIC	homozygous	117570299
9	61683825	61683826	C	T	33	GENIC	homozygous	117570301
9	61685656	61685656		TGAGACCCTGTCTCAAAAACATGACTACACAA	21	GENIC	homozygous	128717801
9	61687541	61687542	C	T	33	GENIC	homozygous	117570303
9	61687637	61687638	A	G	33	GENIC	homozygous	117570305