chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	32648851	32648852	T	C	10	GENIC	homozygous	50175787
12	32649167	32649168	A	G	8	GENIC	homozygous	50175789
12	32652761	32652762	C	T	15	GENIC	homozygous	50444967
12	32652996	32652997	T	-	8	GENIC	homozygous	50444969
12	32653360	32653361	G	A	10	GENIC	homozygous	50444971
12	32654142	32654143	T	C	17	GENIC	homozygous	50444973
12	32655303	32655304	G	C	7	GENIC	homozygous	50444977
12	32657087	32657088	G	GC	9	GENIC	homozygous	50175795
12	32657096	32657098	GA	--	9	GENIC	homozygous	50175796
12	32658485	32658486	T	C	13	GENIC	homozygous	50444987
12	32658733	32658734	G	A	8	GENIC	homozygous	50444989
12	32659670	32659671	C	A	17	GENIC	homozygous	50444991
12	32659672	32659673	C	T	17	GENIC	homozygous	50444993
12	32659916	32659917	C	A	15	GENIC	homozygous	50444995
12	32661110	32661111	T	C	13	GENIC	homozygous	50444997
12	32661156	32661157	C	CAG	10	GENIC	homozygous	50444999
12	32662720	32662721	A	G	7	GENIC	homozygous	50445004