chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	86136200	86136201	T	C	61	GENIC	homozygous	112946395
15	86136850	86136851	T	C	47	GENIC	possibly homozygous	112570541
15	86136974	86136975	T	C	66	GENIC	homozygous	112570543
15	86137377	86137378	A	T	60	GENIC	possibly homozygous	112570545
15	86138168	86138169	T	C	46	GENIC	homozygous	112570547
15	86138405	86138406	G	A	53	GENIC	homozygous	112570549
15	86138832	86138833	T	C	44	GENIC	homozygous	112570551
15	86138923	86138924	A	C	57	GENIC	homozygous	112570552
15	86139051	86139052	A	G	53	GENIC	homozygous	112570554
15	86139098	86139099	A	T	53	GENIC	homozygous	112570556
15	86139755	86139756	G	A	58	GENIC	homozygous	112570558
15	86139779	86139780	A	G	60	GENIC	homozygous	112570561
15	86139964	86139965	G	T	48	GENIC	homozygous	112570563
15	86140034	86140035	C	T	43	GENIC	homozygous	112570565
15	86140339	86140340	C	T	56	GENIC	homozygous	112570567
15	86140453	86140454	G	C	43	GENIC	homozygous	112570569
15	86141546	86141547	G	C	55	GENIC	homozygous	112570571
15	86141724	86141725	G	A	46	GENIC	homozygous	112570573
15	86138099	86138099		G	50	GENIC	homozygous	129278622
15	86138379	86138380	A		56	GENIC	homozygous	129278623
15	86140613	86140614	A		46	GENIC	homozygous	129278624