chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40511610	40511611	C	T	60	GENIC	homozygous	115383859
12	40511960	40511961	A	G	33	GENIC	homozygous	115328328
12	40512478	40512482	TTTA		53	GENIC	homozygous	128989610
12	40516113	40516113		CACG	48	GENIC	homozygous	128989611
12	40516305	40516306	G	A	48	GENIC	homozygous	115328332
12	40516547	40516547		TTG	25	GENIC	heterozygous	128989612
12	40516548	40516548		TG	25	GENIC	heterozygous	128989613
12	40516663	40516664	A	G	52	GENIC	homozygous	115328334
12	40518792	40518793	C	T	51	GENIC	homozygous	115328336
12	40518867	40518868	A	C	41	GENIC	homozygous	115328338
12	40519011	40519012	C	G	57	GENIC	homozygous	115383867
12	40520522	40520522		CAGGTCT	34	GENIC	homozygous	128989614
12	40520601	40520602	G	A	40	GENIC	homozygous	115383869
12	40521940	40521941	G	C	46	GENIC	homozygous	115328340
12	40524710	40524711	T	C	18	GENIC	homozygous	118270553
12	40524856	40524860	TGAA		44	GENIC	homozygous	128989616
12	40524911	40524912	C	T	49	GENIC	homozygous	115328342
12	40526616	40526617	A	G	58	GENIC	homozygous	115328344
12	40527560	40527561	T	G	48	GENIC	homozygous	115328346