chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	46341222	46341223	C	CTG	28	INTERGENIC	homozygous	50218452
12	46349215	46349217	CA	--	9	INTERGENIC	heterozygous	50615823
12	46374101	46374102	A	G	21	GENIC	homozygous	50218456
12	46376157	46376158	A	AG	22	GENIC	homozygous	50218457
12	46385776	46385777	C	CT	21	GENIC	homozygous	50218463
12	46394414	46394415	C	CA	8	GENIC	heterozygous	50615825
12	46396280	46396284	ACAC	----	7	GENIC	heterozygous	50615826
12	46428281	46428282	G	GAT	18	GENIC	homozygous	50218482
12	46428286	46428287	A	AG	16	GENIC	homozygous	50218485
12	46441733	46441734	G	T	2	GENIC	homozygous	50387293
12	46441741	46441742	G	T	8	GENIC	homozygous	50218488
12	46446051	46446052	T	C	27	GENIC	homozygous	50611853
12	46446081	46446082	C	CCACCATCATCACCACCATCATCACCACCATCATCATCACCATCACCACCATCATCATCACCATCATCATCACCGTCACTGTCACCATCATCACCACCATCATCACCATCATCATCACCATCACCACCATCATCAT	4	GENIC	homozygous	50615829
12	46463401	46463405	TCTC	----	1	GENIC	homozygous	50615831
12	46473010	46473012	TC	--	22	GENIC	homozygous	50218499
12	46482038	46482040	GT	--	4	GENIC	heterozygous	50218501
12	46483281	46483282	A	AGT	42	GENIC	homozygous	50218502
12	46483311	46483312	C	-	44	GENIC	homozygous	50218504
12	46485108	46485109	C	T	25	GENIC	homozygous	50218506
12	46485134	46485135	C	G	27	GENIC	homozygous	50218507
12	46485237	46485240	GTG	---	21	GENIC	homozygous	50218509
12	46488638	46488642	GTGT	----	22	GENIC	heterozygous	50341258
12	46488640	46488642	GT	--	22	GENIC	heterozygous	50949628