chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40511610	40511611	C	T	32	GENIC	homozygous	115383859
12	40511960	40511961	A	G	36	GENIC	possibly homozygous	115328328
12	40511961	40511962	T	G	42	GENIC	possibly homozygous	115328330
12	40516305	40516306	G	A	44	GENIC	homozygous	115328332
12	40516663	40516664	A	G	47	GENIC	homozygous	115328334
12	40518792	40518793	C	T	62	GENIC	homozygous	115328336
12	40518867	40518868	A	C	46	GENIC	homozygous	115328338
12	40519011	40519012	C	G	59	GENIC	homozygous	115383867
12	40520601	40520602	G	A	61	GENIC	homozygous	115383869
12	40521940	40521941	G	C	37	GENIC	homozygous	115328340
12	40524911	40524912	C	T	58	GENIC	homozygous	115328342
12	40526616	40526617	A	G	59	GENIC	homozygous	115328344
12	40527560	40527561	T	G	41	GENIC	homozygous	115328346
12	40524710	40524711	T	C	24	GENIC	homozygous	118270553