chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39952419	39952420	G	C	57	GENIC	homozygous	50202251
12	39952655	39952656	T	A	81	GENIC	possibly homozygous	50202253
12	39953219	39953220	C	T	23	GENIC	heterozygous	50202255
12	39953221	39953222	G	A	23	GENIC	heterozygous	50202257
12	39953270	39953271	C	T	42	GENIC	homozygous	50202259
12	39953357	39953358	T	C	45	GENIC	possibly homozygous	50202261
12	39953364	39953365	A	T	46	GENIC	heterozygous	50202263
12	39954012	39954013	A	-	50	GENIC	homozygous	50202265
12	39954275	39954276	A	G	75	GENIC	homozygous	50202267
12	39954283	39954284	G	A	72	GENIC	homozygous	50202269
12	39954588	39954591	TTC	---	27	GENIC	homozygous	50202271
12	39954650	39954651	T	C	29	GENIC	possibly homozygous	50202273
12	39954840	39954841	C	G	52	GENIC	homozygous	50202275
12	39954970	39954971	C	A	59	GENIC	homozygous	50202277
12	39955001	39955002	G	A	67	GENIC	homozygous	50202279
12	39955889	39955890	A	G	52	GENIC	homozygous	50202281
12	39956087	39956088	C	G	34	GENIC	heterozygous	50323177
12	39956202	39956206	GAAG	----	20	GENIC	heterozygous	50202285
12	39956210	39956211	G	GC	26	GENIC	heterozygous	50202287
12	39956211	39956212	A	C	30	GENIC	heterozygous	50202289
12	39956211	39956212	A	AGGC	28	GENIC	heterozygous	50202291
12	39956789	39956790	G	A	55	GENIC	homozygous	50202293
12	39958244	39958245	C	T	53	GENIC	possibly homozygous	50202299