chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41831451	41831452	C	T	20	GENIC	homozygous	50207932
12	41831662	41831664	AC	--	2	GENIC	homozygous	50207933
12	41831740	41831741	A	G	20	GENIC	homozygous	50207934
12	41832877	41832878	C	T	35	GENIC	homozygous	50207935
12	41833183	41833184	T	-	1	GENIC	homozygous	50207936
12	41833199	41833200	C	-	11	GENIC	heterozygous	50207937
12	41833540	41833541	C	-	3	GENIC	homozygous	50325878
12	41833664	41833665	C	G	13	GENIC	homozygous	50207938
12	41833673	41833674	T	A	14	GENIC	possibly homozygous	50207939
12	41833680	41833681	T	TAA	15	GENIC	heterozygous	50207940
12	41833680	41833681	T	TAAA	15	GENIC	possibly homozygous	50207941
12	41834185	41834186	C	A	34	GENIC	homozygous	50207942
12	41835416	41835422	AAAAAA	------	1	GENIC	homozygous	50207943
12	41835701	41835702	T	TG	21	GENIC	homozygous	50207944