chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	45605563	45605564	T	C	38	GENIC	homozygous	117865987
9	45606606	45606607	A	G	24	GENIC	possibly homozygous	117507782
9	45607900	45607901	T	C	34	GENIC	homozygous	117507784
9	45608064	45608065	G	A	12	GENIC	homozygous	117865988
9	45608150	45608151	T	C	4	GENIC	homozygous	120425630
9	45612680	45612681	A	G	18	GENIC	homozygous	117507792
9	45612805	45612806	G	A	30	GENIC	homozygous	117865989
9	45613598	45613599	G	A	23	GENIC	homozygous	117865990
9	45612607	45612608	A	T	33	GENIC	homozygous	117539245
9	45612602	45612603	A	T	35	GENIC	homozygous	117333823
9	45612604	45612605	A	C	34	GENIC	homozygous	117333824
9	45614863	45614864	G	A	34	GENIC	homozygous	117539253
9	45616550	45616551	C	A	45	GENIC	homozygous	117507794