chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50039964	50039965	G	A	24	GENIC	possibly homozygous	50236010
12	50040008	50040009	C	T	20	GENIC	possibly homozygous	50236012
12	50040397	50040398	A	G	21	GENIC	homozygous	50236014
12	50041955	50041956	C	T	49	GENIC	homozygous	50236016
12	50042556	50042557	T	C	71	GENIC	homozygous	50236018
12	50043246	50043247	C	CTGTG	20	GENIC	homozygous	50236020
12	50043249	50043250	C	CCAGGATGCCCAA	15	GENIC	homozygous	50236022
12	50043669	50043670	C	T	60	GENIC	possibly homozygous	50236024
12	50043880	50043881	C	CGA	16	GENIC	possibly homozygous	50236026
12	50043890	50043892	AC	--	18	GENIC	possibly homozygous	50236028
12	50043895	50043896	C	G	31	GENIC	possibly homozygous	50236030
12	50043899	50043900	C	G	31	GENIC	heterozygous	50236032
12	50043903	50043904	C	G	30	GENIC	heterozygous	50236034
12	50043904	50043912	AGACAGAT	--------	18	GENIC	homozygous	50236036