chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15394525	15394526	G	A	16	GENIC	homozygous	117267718
9	15395292	15395293	A	G	31	GENIC	homozygous	117267719
9	15395608	15395609	C	T	22	GENIC	homozygous	117267720
9	15395855	15395856	C	T	28	GENIC	homozygous	117267721
9	15396053	15396054	C	T	45	GENIC	homozygous	117267722
9	15397929	15397930	T	G	32	GENIC	homozygous	117267723
9	15398229	15398230	T	C	27	GENIC	homozygous	117267724
9	15398347	15398348	G	T	32	GENIC	homozygous	117267725
9	15399001	15399002	C	T	25	GENIC	homozygous	117267726
9	15399028	15399029	A	C	30	GENIC	homozygous	117267727
9	15399845	15399846	C	T	28	GENIC	homozygous	117267728
9	15399850	15399851	A	G	29	GENIC	homozygous	117267729
9	15399987	15399988	G	T	21	GENIC	homozygous	117267730
9	15400015	15400016	C	G	28	GENIC	homozygous	117267731
9	15400393	15400394	A	G	23	GENIC	homozygous	117267732
9	15400519	15400520	G	A	23	GENIC	homozygous	117267733
9	15400625	15400626	C	T	31	GENIC	homozygous	117267734
9	15400769	15400770	A	G	40	GENIC	homozygous	117267735
9	15400862	15400863	G	A	27	GENIC	homozygous	117267736
9	15400958	15400959	A	G	22	GENIC	homozygous	117267737
9	15401020	15401021	C	T	17	GENIC	homozygous	117267738
9	15401315	15401316	C	T	29	GENIC	homozygous	117267739
9	15401422	15401423	T	C	32	GENIC	homozygous	117267740
9	15401493	15401494	T	A	30	GENIC	homozygous	117267741
9	15402352	15402353	C	T	35	GENIC	homozygous	117267742
9	15402464	15402465	A	G	28	GENIC	homozygous	117267743
9	15402531	15402532	T	C	36	GENIC	homozygous	117267744
9	15402713	15402714	G	A	36	GENIC	homozygous	117267745