chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39952419	39952420	G	C	25	GENIC	homozygous	50202251
12	39952655	39952656	T	A	38	GENIC	homozygous	50202253
12	39953219	39953223	CAGC	----	2	GENIC	homozygous	50571498
12	39953224	39953271	GCTGCACTTACACTGCTGTTGGTCATTACACAGCATGCCTCGGCAAC	-----------------------------------------------	33	GENIC	possibly homozygous	50512178
12	39953357	39953358	T	C	14	GENIC	homozygous	50202261
12	39954012	39954013	A	-	26	GENIC	homozygous	50202265
12	39954275	39954276	A	G	30	GENIC	homozygous	50202267
12	39954283	39954284	G	A	33	GENIC	homozygous	50202269
12	39954586	39954587	C	-	16	GENIC	heterozygous	50599277
12	39954588	39954591	TTC	---	5	GENIC	heterozygous	50202271
12	39954650	39954651	T	C	4	GENIC	homozygous	50202273
12	39954840	39954841	C	G	27	GENIC	homozygous	50202275
12	39954970	39954971	C	A	26	GENIC	possibly homozygous	50202277
12	39955001	39955002	G	A	14	GENIC	homozygous	50202279
12	39955889	39955890	A	G	34	GENIC	homozygous	50202281
12	39956087	39956088	C	CAGGG	3	GENIC	homozygous	50512180
12	39956210	39956211	G	GC	1	GENIC	homozygous	50202287
12	39956789	39956790	G	A	31	GENIC	homozygous	50202293
12	39957320	39957321	T	TACACACACACACAC	3	GENIC	heterozygous	50543428
12	39957323	39957325	AC	--	3	GENIC	heterozygous	50571500
12	39958244	39958245	C	T	23	GENIC	homozygous	50202299