chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	117688687	117688688	A	G	53	GENIC	homozygous	115847943
7	117689117	117689118	G	T	20	GENIC	homozygous	118258926
7	117689911	117689912	C	A	64	GENIC	homozygous	115847949
7	117690326	117690327	C	A	55	GENIC	homozygous	115847951
7	117690388	117690389	T	C	59	GENIC	homozygous	115847953
7	117691535	117691536	C	A	53	GENIC	homozygous	115847955
7	117691541	117691542	C	T	54	GENIC	homozygous	115847957
7	117692538	117692539	G	T	58	GENIC	homozygous	115847959
7	117692677	117692678	C	T	55	GENIC	homozygous	115847961
7	117693000	117693001	T	C	62	GENIC	homozygous	115847965
7	117693023	117693024	T	G	74	GENIC	homozygous	115847967
7	117693844	117693845	G	T	38	GENIC	homozygous	115847969
7	117694013	117694014	T	G	70	GENIC	homozygous	115847971
7	117694816	117694817	T	C	66	GENIC	homozygous	115847973
7	117696183	117696184	A	G	63	GENIC	homozygous	115847975
7	117697243	117697244	A	G	48	GENIC	homozygous	115847977
7	117697852	117697853	G	C	46	GENIC	homozygous	115847979
7	117698209	117698210	C	T	55	GENIC	homozygous	115847981
7	117698224	117698225	G	A	49	GENIC	homozygous	115847983
7	117698395	117698396	C	T	68	GENIC	homozygous	115847985
7	117698957	117698958	A	G	30	GENIC	homozygous	115847987
7	117698989	117698989		C	34	GENIC	homozygous	128510679
7	117689122	117689123	T		20	GENIC	homozygous	128510676
7	117690354	117690361	AATAAAT		49	GENIC	homozygous	128510677
7	117694044	117694048	GCTG		69	GENIC	homozygous	128510678
7	117689135	117689136	T	C	16	GENIC	homozygous	116080610
7	117701313	117701314	C	T	46	GENIC	homozygous	115847991
7	117703041	117703044	CCG		42	GENIC	homozygous	128510685
7	117698994	117698994		G	31	GENIC	homozygous	128510680
7	117699037	117699037		T	29	GENIC	homozygous	128510681
7	117699065	117699065		C	26	GENIC	homozygous	128510682
7	117699311	117699311		G	7	GENIC	homozygous	128510684