chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	225521652	225521653	C	T	27	GENIC	homozygous	61102160
1	225521658	225521660	CA	--	24	GENIC	homozygous	61102161
1	225521659	225521661	AT	--	24	GENIC	homozygous	61102162
1	225521689	225521693	GTGC	----	20	GENIC	heterozygous	61102163
1	225521693	225521699	GTGTGT	------	12	GENIC	heterozygous	61102164
1	225521736	225521737	C	CAA	18	GENIC	possibly homozygous	61102165
1	225521736	225521737	C	CA	18	GENIC	heterozygous	61102166
1	225521818	225521819	A	-	37	GENIC	homozygous	61102167
1	225521952	225521953	C	T	43	GENIC	homozygous	61102168
1	225522107	225522108	C	CT	18	GENIC	possibly homozygous	61102169
1	225522446	225522447	G	A	49	GENIC	homozygous	61102170
1	225522545	225522548	TGG	---	31	GENIC	homozygous	61102171
1	225522654	225522655	G	-	36	GENIC	homozygous	61102172
1	225522827	225522828	C	CATAT	42	GENIC	homozygous	61102173
1	225523336	225523337	C	T	64	GENIC	homozygous	61102174
1	225523711	225523712	C	T	53	GENIC	homozygous	61102175
1	225523968	225523969	T	A	40	GENIC	homozygous	61102176
1	225524273	225524274	T	G	49	GENIC	homozygous	61102177
1	225524917	225524918	T	C	47	GENIC	homozygous	61102178
1	225525442	225525443	A	G	56	GENIC	homozygous	61102179