chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	99411725	99411726	T	G	31	GENIC	homozygous	54491181
7	99411833	99411834	T	-	39	GENIC	homozygous	54491183
7	99412196	99412197	T	C	39	GENIC	homozygous	54491185
7	99412954	99412955	T	C	41	GENIC	homozygous	54491187
7	99413118	99413119	A	G	48	GENIC	homozygous	54491189
7	99413184	99413185	A	G	57	GENIC	homozygous	54491191
7	99413317	99413318	T	C	62	GENIC	homozygous	54491193
7	99413364	99413368	CAAA	----	42	GENIC	homozygous	54491195
7	99413878	99413879	T	C	46	GENIC	homozygous	54491197
7	99414680	99414681	G	T	61	GENIC	homozygous	54491199
7	99414997	99414998	T	C	46	GENIC	homozygous	54491201
7	99415013	99415014	T	C	46	GENIC	homozygous	54491203
7	99415933	99415934	T	C	35	GENIC	homozygous	54491205
7	99416088	99416089	A	-	1	GENIC	homozygous	54491207
7	99416632	99416633	A	G	43	GENIC	homozygous	54491209
7	99417133	99417134	C	A	51	GENIC	homozygous	54491211
7	99417191	99417192	C	T	51	GENIC	homozygous	54491213
7	99417425	99417426	C	A	49	GENIC	possibly homozygous	54491215
7	99417577	99417578	A	G	69	GENIC	homozygous	54491217
7	99414226	99414227	C	G	34	GENIC	heterozygous	54830724