chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	61680609	61680610	C	T	87	GENIC	heterozygous	117358697
9	61680938	61680939	C	T	91	GENIC	heterozygous	123186962
9	61681247	61681247		A	62	GENIC	homozygous	128717799
9	61681450	61681451	T	C	70	GENIC	homozygous	117358698
9	61681820	61681822	GC		45	GENIC	homozygous	128717800
9	61680927	61680928	T	G	89	GENIC	heterozygous	130387438
9	61680955	61680956	G		85	GENIC	heterozygous	130379108
9	61681893	61681894	C	T	36	GENIC	homozygous	117570289
9	61681949	61681950	G	A	53	GENIC	homozygous	117570291
9	61682251	61682252	T	G	61	GENIC	homozygous	117570293
9	61683065	61683066	A	G	64	GENIC	homozygous	117570295
9	61683128	61683129	T	G	61	GENIC	possibly homozygous	117358703
9	61683541	61683542	T	C	51	GENIC	homozygous	117570297
9	61683702	61683703	G	A	53	GENIC	homozygous	117570299
9	61683825	61683826	C	T	42	GENIC	homozygous	117570301
9	61685656	61685656		TGAGACCCTGTCTCAAAAACATGACTACACAA	46	GENIC	homozygous	128717801
9	61687541	61687542	C	T	58	GENIC	homozygous	117570303
9	61687637	61687638	A	G	42	GENIC	homozygous	117570305