chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	129708044	129708045	A	AT	15	GENIC	homozygous	57670662
3	129708285	129708286	A	AG	18	GENIC	homozygous	57670664
3	129708608	129708609	G	T	30	GENIC	homozygous	57670666
3	129708637	129708638	A	G	30	GENIC	homozygous	57670668
3	129708791	129708792	A	T	25	GENIC	homozygous	57670670
3	129708793	129708794	A	AGCTGTC	25	GENIC	homozygous	57670672
3	129708795	129708796	G	C	25	GENIC	homozygous	57670674
3	129709753	129709754	C	CGTGTGTGTGT	6	GENIC	heterozygous	57670676
3	129709753	129709754	C	CGTGTGTGT	6	GENIC	heterozygous	58695712
3	129709807	129709808	T	C	16	GENIC	homozygous	57670678
3	129710892	129710893	C	T	22	GENIC	homozygous	57670682
3	129711221	129711222	G	A	20	GENIC	homozygous	57670684
3	129711437	129711438	C	T	23	GENIC	homozygous	57670686
3	129711716	129711717	T	A	13	GENIC	homozygous	57670688
3	129712146	129712147	T	G	26	GENIC	homozygous	57670692
3	129712681	129712682	C	CATGCCT	28	GENIC	homozygous	57670694
3	129712774	129712775	C	T	25	GENIC	homozygous	57670696
3	129713653	129713654	A	T	13	GENIC	homozygous	57670699
3	129714047	129714048	A	G	20	GENIC	homozygous	57670701
3	129714069	129714072	CTT	---	22	GENIC	homozygous	57670703
3	129714073	129714076	TAT	---	23	GENIC	homozygous	57670705
3	129714078	129714079	A	-	20	GENIC	homozygous	57670707
3	129714079	129714080	T	G	20	GENIC	homozygous	58695714
3	129715054	129715055	G	A	19	GENIC	homozygous	57670709
3	129715229	129715230	C	CA	10	GENIC	heterozygous	57670711
3	129715270	129715271	A	G	20	GENIC	homozygous	57670713
3	129715333	129715334	T	TAG	22	GENIC	homozygous	57670715
3	129715518	129715519	C	T	25	GENIC	homozygous	57670717
3	129715599	129715600	G	A	24	GENIC	homozygous	57670719
3	129716465	129716466	C	CCTGCCT	19	GENIC	homozygous	57670721
3	129716495	129716497	TT	--	21	GENIC	possibly homozygous	58695715
3	129717971	129717985	TCAAACATGGTGTG	--------------	9	GENIC	homozygous	57670723
3	129717987	129717994	GGGGCCC	-------	8	GENIC	homozygous	57670725