chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94486866	94486867	G	C	25	GENIC	homozygous	52053563
9	94486898	94486899	G	C	26	GENIC	heterozygous	52053567
9	94486902	94486903	G	C	28	GENIC	heterozygous	52280660
9	94487063	94487064	C	T	31	GENIC	homozygous	52280661
9	94487322	94487323	C	T	26	GENIC	homozygous	52280662
9	94487529	94487530	C	T	52	GENIC	homozygous	52280663
9	94488368	94488369	G	T	41	GENIC	homozygous	52280664
9	94489668	94489669	C	T	46	GENIC	homozygous	52280665
9	94490270	94490271	A	AG	35	GENIC	homozygous	52280666
9	94490375	94490376	T	C	39	GENIC	possibly homozygous	52280667
9	94490669	94490670	C	A	56	GENIC	possibly homozygous	52053575
9	94490672	94490674	AA	--	20	GENIC	heterozygous	52280668
9	94490673	94490674	A	-	20	GENIC	possibly homozygous	52053577
9	94491050	94491051	A	G	31	GENIC	homozygous	52053579
9	94491093	94491099	ACACAC	------	13	GENIC	heterozygous	52280669
9	94491382	94491383	T	C	45	GENIC	homozygous	52053583
9	94491966	94491967	A	G	45	GENIC	heterozygous	52280670
9	94491969	94491970	A	G	45	GENIC	possibly homozygous	52280671
9	94491972	94491973	A	G	45	GENIC	possibly homozygous	52280672
9	94492018	94492019	T	A	46	GENIC	homozygous	52280673
9	94492047	94492048	G	A	42	GENIC	homozygous	52280674
9	94492281	94492282	C	A	55	GENIC	possibly homozygous	52053589
9	94492466	94492467	C	T	59	GENIC	homozygous	52280675
9	94492497	94492498	G	GCA	54	GENIC	homozygous	52053593
9	94492893	94492894	G	-	28	GENIC	homozygous	52280676
9	94492908	94492923	TTTTTTTTTGGGGTT	---------------	20	GENIC	homozygous	52280677
9	94492921	94492923	TT	--	11	GENIC	heterozygous	52053594
9	94492922	94492923	T	-	11	GENIC	heterozygous	52053596
9	94493500	94493506	ACACAC	------	12	GENIC	homozygous	52280678
9	94493516	94493517	A	G	38	GENIC	heterozygous	52280679
9	94493522	94493523	A	G	34	GENIC	heterozygous	52280680
9	94494024	94494025	G	C	23	GENIC	possibly homozygous	52280681
9	94494050	94494051	C	G	18	GENIC	homozygous	52280682
9	94494774	94494775	C	G	51	GENIC	homozygous	52280683
9	94494796	94494797	A	G	49	GENIC	possibly homozygous	52053600
9	94494956	94494957	C	CTG	4	GENIC	heterozygous	52053602