chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40511610	40511611	C	T	45	GENIC	homozygous	115383859
12	40511960	40511961	A	G	64	GENIC	possibly homozygous	115328328
12	40516305	40516306	G	A	42	GENIC	homozygous	115328332
12	40516663	40516664	A	G	40	GENIC	homozygous	115328334
12	40512478	40512482	TTTA		52	GENIC	homozygous	128989610
12	40516113	40516113		CACG	39	GENIC	homozygous	128989611
12	40516547	40516547		TTG	21	GENIC	heterozygous	128989612
12	40516548	40516548		TG	21	GENIC	heterozygous	128989613
12	40518792	40518793	C	T	57	GENIC	homozygous	115328336
12	40518867	40518868	A	C	62	GENIC	homozygous	115328338
12	40519011	40519012	C	G	52	GENIC	homozygous	115383867
12	40520522	40520522		CAGGTCT	46	GENIC	homozygous	128989614
12	40520601	40520602	G	A	45	GENIC	homozygous	115383869
12	40521940	40521941	G	C	49	GENIC	homozygous	115328340
12	40524911	40524912	C	T	33	GENIC	homozygous	115328342
12	40526616	40526617	A	G	43	GENIC	possibly homozygous	115328344
12	40527560	40527561	T	G	42	GENIC	possibly homozygous	115328346
12	40524710	40524711	T	C	24	GENIC	homozygous	118270553
12	40524228	40524228		CAGCAGGGGTGGATCCGATGCCAGCCTGTGTCTTTCTCACACATAAGC	3	GENIC	homozygous	128989615
12	40524856	40524860	TGAA		39	GENIC	homozygous	128989616