chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	46339678	46339681	TGA	---	8	INTERGENIC	heterozygous	50218451
12	46341222	46341223	C	CTG	28	INTERGENIC	homozygous	50218452
12	46363044	46363045	C	CCTAT	22	GENIC	possibly homozygous	50886449
12	46374101	46374102	A	G	20	GENIC	homozygous	50218456
12	46376157	46376158	A	AG	34	GENIC	homozygous	50218457
12	46385776	46385777	C	CT	21	GENIC	homozygous	50218463
12	46405733	46405734	C	-	24	GENIC	heterozygous	50575089
12	46428029	46428033	AGAT	----	15	GENIC	heterozygous	50899847
12	46428281	46428282	G	GAT	28	GENIC	homozygous	50218482
12	46428286	46428287	A	AG	25	GENIC	homozygous	50218485
12	46446051	46446052	T	C	32	GENIC	homozygous	50611853
12	46446081	46446082	C	CCACCATCATCACCACCATCATCACCACCATCATCATCACCATCACCACCATCATCATCACCATCATCATCACCGTCACTGTCACCATCATCACCACCATCATCACCATCATCATCACCATCACCACCATCATCAT	7	GENIC	possibly homozygous	50615829
12	46463401	46463405	TCTC	----	5	GENIC	heterozygous	50615831
12	46470350	46470352	GT	--	2	GENIC	heterozygous	50218495
12	46473010	46473012	TC	--	24	GENIC	homozygous	50218499
12	46473972	46473973	G	-	9	GENIC	heterozygous	50592811
12	46482038	46482040	GT	--	10	GENIC	heterozygous	50218501
12	46483281	46483282	A	AGT	28	GENIC	homozygous	50218502
12	46483311	46483312	C	-	39	GENIC	homozygous	50218504
12	46485108	46485109	C	T	30	GENIC	homozygous	50218506
12	46485134	46485135	C	G	38	GENIC	homozygous	50218507
12	46485237	46485240	GTG	---	35	GENIC	homozygous	50218509
12	46488640	46488642	GT	--	19	GENIC	heterozygous	50949628