chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130007320	130007321	T	G	26	GENIC	homozygous	54110045
7	130007450	130007451	G	A	28	GENIC	homozygous	54110046
7	130008122	130008123	C	A	26	GENIC	homozygous	54110047
7	130008199	130008200	C	T	36	GENIC	homozygous	54110048
7	130008272	130008273	C	T	29	GENIC	homozygous	54110049
7	130008467	130008468	A	C	27	GENIC	possibly homozygous	54110050
7	130008963	130008964	C	T	15	GENIC	homozygous	54110051
7	130009502	130009503	T	G	24	GENIC	homozygous	54110052
7	130009564	130009565	T	C	28	GENIC	homozygous	54110053
7	130009628	130009629	T	A	37	GENIC	homozygous	54110054
7	130009970	130009971	G	GCCCCCC	5	GENIC	homozygous	55010290
7	130010067	130010068	G	A	29	GENIC	homozygous	54110058
7	130010091	130010092	C	T	31	GENIC	homozygous	54110059
7	130010247	130010248	C	T	19	GENIC	homozygous	54110060
7	130010305	130010306	C	A	19	GENIC	homozygous	54110061
7	130010709	130010710	G	A	41	GENIC	homozygous	54110062
7	130010727	130010728	T	C	39	GENIC	homozygous	54110063
7	130011098	130011099	C	T	30	GENIC	homozygous	54110064
7	130011398	130011399	C	T	20	GENIC	homozygous	54110065
7	130011637	130011638	C	T	9	GENIC	homozygous	54110066
7	130011760	130011761	C	T	17	GENIC	homozygous	54110067