chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	46341222	46341223	C	CTG	37	INTERGENIC	homozygous	50218452
12	46374101	46374102	A	G	21	GENIC	homozygous	50218456
12	46376157	46376158	A	AG	28	GENIC	homozygous	50218457
12	46379985	46379987	TG	--	11	GENIC	heterozygous	50655340
12	46385776	46385777	C	CT	12	GENIC	homozygous	50218463
12	46394414	46394415	C	CA	8	GENIC	heterozygous	50615825
12	46396280	46396284	ACAC	----	8	GENIC	heterozygous	50615826
12	46417466	46417467	A	ATAT	6	GENIC	heterozygous	50655343
12	46428281	46428282	G	GAT	15	GENIC	homozygous	50218482
12	46428286	46428287	A	AG	17	GENIC	homozygous	50218485
12	46434092	46434093	C	-	19	GENIC	heterozygous	50387290
12	46446051	46446052	T	C	25	GENIC	homozygous	50611853
12	46446081	46446082	C	CCACCATCATCACCACCATCATCACCACCATCATCATCACCATCACCACCATCATCATCACCATCATCATCACCGTCACTGTCACCATCATCACCACCATCATCACCATCATCATCACCATCACCACCATCATCAT	6	GENIC	homozygous	50615829
12	46463401	46463405	TCTC	----	3	GENIC	heterozygous	50615831
12	46473010	46473012	TC	--	20	GENIC	homozygous	50218499
12	46473972	46473973	G	-	10	GENIC	heterozygous	50592811
12	46483281	46483282	A	AGT	31	GENIC	homozygous	50218502
12	46483311	46483312	C	-	28	GENIC	homozygous	50218504
12	46485108	46485109	C	T	25	GENIC	homozygous	50218506
12	46485134	46485135	C	G	19	GENIC	homozygous	50218507
12	46485237	46485240	GTG	---	34	GENIC	homozygous	50218509