chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40511610	40511611	C	T	26	GENIC	possibly homozygous	115383859
12	40514333	40514334	G	A	31	GENIC	homozygous	115477547
12	40517729	40517730	C	A	28	GENIC	homozygous	115477549
12	40517857	40517858	C	T	38	GENIC	homozygous	115477551
12	40518867	40518868	A	C	39	GENIC	homozygous	115328338
12	40519012	40519013	G	C	59	GENIC	homozygous	115477553
12	40521719	40521720	G	A	40	GENIC	homozygous	115441575
12	40524384	40524385	C	T	62	GENIC	homozygous	115441578
12	40527210	40527211	G	A	44	GENIC	homozygous	115477555
12	40527560	40527561	T	G	39	GENIC	homozygous	115328346
12	40518114	40518115	T	C	4	GENIC	homozygous	115543980
12	40525669	40525670	C	T	33	GENIC	homozygous	115543982
12	40525307	40525308	G	A	14	GENIC	homozygous	115622507