chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	91667950	91667951	A	G	60	GENIC	homozygous	117385753
9	91667962	91667963	A	G	55	GENIC	homozygous	117385754
9	91668559	91668560	T	C	32	GENIC	homozygous	117385755
9	91668758	91668759	G	A	32	GENIC	homozygous	117385756
9	91668930	91668931	G	T	25	GENIC	homozygous	117385757
9	91669320	91669321	T	C	32	GENIC	homozygous	117385758
9	91669751	91669752	G	A	35	GENIC	homozygous	117385759
9	91670355	91670356	A	T	27	GENIC	heterozygous	117385760
9	91670733	91670734	T	C	45	GENIC	homozygous	117385761
9	91671005	91671006	T	C	51	GENIC	homozygous	117385762
9	91671133	91671134	C	T	47	GENIC	homozygous	117385763
9	91671301	91671302	G	A	42	GENIC	homozygous	117385764
9	91672326	91672327	C	T	38	GENIC	homozygous	117385765
9	91672608	91672609	T	C	47	GENIC	homozygous	117385766
9	91673061	91673062	A	C	31	GENIC	homozygous	117385767
9	91673144	91673145	A	G	28	GENIC	homozygous	117385768
9	91673184	91673185	C	T	24	GENIC	homozygous	117385769
9	91673598	91673599	G	A	52	GENIC	homozygous	117385770
9	91673604	91673605	T	C	55	GENIC	possibly homozygous	117385771
9	91674712	91674713	A	G	31	GENIC	homozygous	117385772
9	91675541	91675542	A	C	37	GENIC	homozygous	117385773
9	91675647	91675648	C	T	26	GENIC	homozygous	117385774
9	91676234	91676235	C	T	10	GENIC	homozygous	117385775
9	91677786	91677787	T	G	30	GENIC	homozygous	117385776
9	91680722	91680723	G	A	54	GENIC	homozygous	117385777
9	91682179	91682180	C	T	27	GENIC	homozygous	117385778
9	91683123	91683124	G	A	27	GENIC	homozygous	117385779
9	91683221	91683222	C	T	29	GENIC	homozygous	117385780