chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10009859	10009860	C	T	36	GENIC	homozygous	117243938
9	10009862	10009863	C	T	37	GENIC	homozygous	117243939
9	10009865	10009866	C	T	37	GENIC	homozygous	117243940
9	10010052	10010053	C	A	40	GENIC	possibly homozygous	117243942
9	10010121	10010122	C	G	16	GENIC	homozygous	117243943
9	10010123	10010124	C	T	17	GENIC	homozygous	117243944
9	10010129	10010130	C	G	16	GENIC	homozygous	117243945
9	10010131	10010132	C	G	16	GENIC	homozygous	117243946
9	10010134	10010135	C	A	18	GENIC	possibly homozygous	117243947
9	10010141	10010142	C	A	44	GENIC	homozygous	117243948
9	10010162	10010163	C	G	47	GENIC	homozygous	117243949
9	10010178	10010179	C	G	36	GENIC	homozygous	117243950
9	10010193	10010194	C	G	44	GENIC	homozygous	117243951