chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	46346747	46346748	T	C	13	GENIC	homozygous	51935677
9	46363331	46363332	G	T	52	GENIC	heterozygous	51935680
9	46375793	46375794	C	CGTGT	28	GENIC	homozygous	51935684
9	46385707	46385708	G	GTATA	5	GENIC	heterozygous	51935687
9	46395772	46395773	A	C	28	GENIC	homozygous	51935690
9	46396959	46396967	GTGTGTGT	--------	2	GENIC	heterozygous	51935693
9	46396965	46396967	GT	--	2	GENIC	heterozygous	51935697
9	46414121	46414122	G	T	46	GENIC	homozygous	51935698
9	46414140	46414141	A	T	42	GENIC	homozygous	51935701
9	46414143	46414144	G	GT	38	GENIC	homozygous	51935704
9	46414147	46414148	A	G	44	GENIC	possibly homozygous	51935707
9	46414148	46414149	G	C	44	GENIC	possibly homozygous	51935711
9	46417426	46417428	CA	--	11	GENIC	heterozygous	51935714
9	46428824	46428825	G	-	2	GENIC	homozygous	51935717
9	46429097	46429098	A	G	68	GENIC	heterozygous	51935720
9	46429341	46429342	A	T	113	GENIC	heterozygous	51935723
9	46429879	46429880	G	C	135	GENIC	heterozygous	51935726
9	46429967	46429968	C	T	118	GENIC	heterozygous	51935729
9	46429979	46429980	G	C	104	GENIC	heterozygous	51935732
9	46429985	46429986	T	G	102	GENIC	heterozygous	51935735
9	46429992	46429993	G	C	92	GENIC	heterozygous	51935738
9	46434466	46434467	G	GATCT	14	GENIC	heterozygous	51935741