chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40511610	40511611	C	T	60	GENIC	homozygous	115383859
12	40513202	40513203	G	A	59	GENIC	homozygous	115383861
12	40514602	40514603	A	T	60	GENIC	homozygous	115383863
12	40516663	40516664	A	G	45	GENIC	homozygous	115328334
12	40512478	40512482	TTTA		47	GENIC	homozygous	128989610
12	40516113	40516113		CACG	62	GENIC	homozygous	128989611
12	40518867	40518868	A	C	52	GENIC	homozygous	115328338
12	40519011	40519012	C	G	58	GENIC	homozygous	115383867
12	40520522	40520522		CAGGTCT	56	GENIC	homozygous	128989614
12	40520601	40520602	G	A	59	GENIC	homozygous	115383869
12	40524228	40524228		CAGCAGGGGTGGATCCGATGCCAGCCTGTGTCTTTCTCACACATAAGC	11	GENIC	homozygous	128989615
12	40524856	40524860	TGAA		44	GENIC	homozygous	128989616
12	40524911	40524912	C	T	50	GENIC	homozygous	115328342
12	40526616	40526617	A	G	60	GENIC	homozygous	115328344
12	40527560	40527561	T	G	70	GENIC	homozygous	115328346
12	40519314	40519315	G		59	GENIC	homozygous	133765604
12	40524710	40524711	T	C	15	GENIC	homozygous	118270553