chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479572	42479573	T	C	2	GENIC	homozygous	50209155
12	42484707	42484708	C	T	16	GENIC	homozygous	50209161
12	42487665	42487666	A	C	17	GENIC	homozygous	50209167
12	42487706	42487707	C	T	12	GENIC	possibly homozygous	50209168
12	42487729	42487730	T	C	18	GENIC	homozygous	50209169
12	42488972	42488973	G	A	15	GENIC	homozygous	50209174
12	42490347	42490348	T	A	15	GENIC	homozygous	50209175
12	42490538	42490539	A	G	19	GENIC	homozygous	50209176
12	42490657	42490658	C	T	12	GENIC	possibly homozygous	50209180
12	42491236	42491237	A	-	8	GENIC	heterozygous	50327525
12	42494101	42494102	C	A	12	INTERGENIC	heterozygous	50209183
12	42494157	42494158	A	G	19	INTERGENIC	homozygous	50209184