chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	149261085	149261086	C	T	40	GENIC	homozygous	112880972
4	149261145	149261146	C	T	43	GENIC	homozygous	112880974
4	149261207	149261208	T	G	29	GENIC	homozygous	112880976
4	149261290	149261291	G	C	39	GENIC	possibly homozygous	112880978
4	149261302	149261303	G	C	43	GENIC	homozygous	112880980
4	149262475	149262476	G	T	35	GENIC	possibly homozygous	112880982
4	149262734	149262735	T	G	58	GENIC	possibly homozygous	112880983
4	149263191	149263192	A	G	49	GENIC	homozygous	112880985
4	149263832	149263833	C	G	32	GENIC	homozygous	112880986
4	149264140	149264141	T	C	60	GENIC	homozygous	112880988
4	149266190	149266191	C	G	30	GENIC	homozygous	112880990
4	149266735	149266736	A	T	24	GENIC	possibly homozygous	112880992
4	149267751	149267752	A	G	51	GENIC	homozygous	112880993
4	149268403	149268404	A	G	37	GENIC	possibly homozygous	112880995
4	149268735	149268736	G	A	58	GENIC	homozygous	112880997
4	149268750	149268751	G	C	56	GENIC	homozygous	112880999
4	149269079	149269080	G	C	36	GENIC	possibly homozygous	112881001
4	149269399	149269400	G	A	52	GENIC	homozygous	112881003
4	149269416	149269417	C	T	57	GENIC	homozygous	112881005
4	149269863	149269864	G	A	57	GENIC	homozygous	112881007
4	149270013	149270014	T	C	44	GENIC	homozygous	112881009
4	149270246	149270247	A	G	60	GENIC	possibly homozygous	112881011
4	149270298	149270299	T	G	57	GENIC	homozygous	112881013
4	149270389	149270390	C	T	47	GENIC	homozygous	112881015
4	149272089	149272090	A	G	58	GENIC	homozygous	112881017
4	149272209	149272210	A	G	58	GENIC	homozygous	112881019
4	149272287	149272288	C	T	45	GENIC	homozygous	112881020
4	149272346	149272347	C	G	38	GENIC	homozygous	112881022
4	149273082	149273083	G	T	47	GENIC	possibly homozygous	112881024
4	149273177	149273178	C	T	49	GENIC	homozygous	112881025
4	149273178	149273179	C	T	49	GENIC	homozygous	112881027
4	149273247	149273248	G	A	50	GENIC	possibly homozygous	112881028