chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	123516888	123516889	A	G	31	GENIC	homozygous	54090238
7	123516890	123516891	A	AG	30	GENIC	homozygous	54090239
7	123517385	123517386	C	CAAA	13	GENIC	homozygous	54090241
7	123517388	123517389	C	CAACA	18	GENIC	homozygous	54090244
7	123518177	123518178	A	-	19	GENIC	heterozygous	54921460
7	123518850	123518851	T	A	15	GENIC	homozygous	54090245
7	123520676	123520677	A	T	12	GENIC	homozygous	54090247
7	123520731	123520732	T	A	15	GENIC	homozygous	54090248
7	123521354	123521355	C	T	23	GENIC	homozygous	54090250
7	123521573	123521574	G	C	15	GENIC	homozygous	54090251
7	123521875	123521876	C	CA	2	GENIC	homozygous	54090252
7	123522131	123522132	A	G	20	GENIC	homozygous	54090253
7	123522192	123522193	G	-	15	GENIC	homozygous	54090255
7	123522481	123522482	C	T	23	GENIC	homozygous	54090256
7	123522732	123522733	C	CA	15	GENIC	possibly homozygous	54090257
7	123523040	123523041	A	G	18	GENIC	homozygous	54090259
7	123523513	123523514	T	G	19	GENIC	homozygous	54090260
7	123524801	123524802	C	T	34	GENIC	homozygous	54090263
7	123526743	123526744	A	ATGGTGG	10	GENIC	possibly homozygous	55144977
7	123526767	123526768	A	G	10	GENIC	homozygous	54090267
7	123528914	123528915	G	GC	4	GENIC	homozygous	54236497
7	123529168	123529170	GT	--	20	GENIC	heterozygous	55059741
7	123529269	123529271	TG	--	13	GENIC	homozygous	54090268