chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39952289	39952290	C	T	16	GENIC	homozygous	50422071
12	39952444	39952445	T	C	19	GENIC	homozygous	50422072
12	39952655	39952656	T	A	25	GENIC	homozygous	50202253
12	39953171	39953222	CTGCTGCACTTACACTGCTGTTGGTCATTACACAGCATGCCTCGGCAACAG	---------------------------------------------------	7	GENIC	homozygous	50543424
12	39953357	39953358	T	C	21	GENIC	homozygous	50202261
12	39953362	39953363	A	AAT	15	GENIC	heterozygous	50543425
12	39953548	39953549	G	GGA	12	GENIC	homozygous	50422073
12	39953549	39953550	C	G	12	GENIC	homozygous	50543426
12	39953835	39953836	G	A	13	GENIC	homozygous	50422074
12	39954012	39954013	A	-	13	GENIC	possibly homozygous	50202265
12	39954275	39954276	A	G	18	GENIC	homozygous	50202267
12	39954283	39954284	G	A	18	GENIC	homozygous	50202269
12	39954590	39954591	C	-	7	GENIC	heterozygous	50543427
12	39954650	39954651	T	C	6	GENIC	homozygous	50202273
12	39955001	39955002	G	A	21	GENIC	homozygous	50202279
12	39955889	39955890	A	G	8	GENIC	homozygous	50202281
12	39956067	39956068	T	TA	10	GENIC	homozygous	50422075
12	39956087	39956088	C	CAGGG	10	GENIC	homozygous	50512180
12	39956167	39956168	G	A	10	GENIC	homozygous	50422076
12	39956202	39956206	GAAG	----	5	GENIC	homozygous	50202285
12	39957320	39957321	T	TACACACACACACAC	2	GENIC	homozygous	50543428
12	39957377	39957378	G	GT	12	GENIC	heterozygous	50202295
12	39957377	39957378	G	GTT	12	GENIC	heterozygous	50563453
12	39958244	39958245	C	T	22	GENIC	homozygous	50202299
12	39958725	39958726	A	G	22	GENIC	homozygous	50422077
12	39958936	39958937	C	A	20	GENIC	homozygous	50422078
12	39957365	39957366	G	GT	9	GENIC	heterozygous	50381035