chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10009859	10009860	C	T	16	GENIC	homozygous	117243938
9	10009862	10009863	C	T	17	GENIC	homozygous	117243939
9	10009865	10009866	C	T	15	GENIC	homozygous	117243940
9	10010052	10010053	C	A	19	GENIC	homozygous	117243942
9	10010055	10010055		C	19	GENIC	homozygous	128678564
9	10010077	10010077		T	19	GENIC	homozygous	128678565
9	10010097	10010097		T	20	GENIC	homozygous	128678566
9	10010105	10010105		T	21	GENIC	homozygous	128678567
9	10010111	10010112	G	T	21	GENIC	homozygous	123119234
9	10010112	10010113	T	G	21	GENIC	homozygous	120405983
9	10010121	10010122	C	G	21	GENIC	homozygous	117243943
9	10010123	10010124	C	T	21	GENIC	homozygous	117243944
9	10010129	10010130	C	G	21	GENIC	homozygous	117243945
9	10010131	10010132	C	G	22	GENIC	homozygous	117243946
9	10010134	10010135	C	A	22	GENIC	homozygous	117243947
9	10010141	10010142	C	A	22	GENIC	homozygous	117243948
9	10010162	10010163	C	G	21	GENIC	homozygous	117243949
9	10010171	10010172	A	T	21	GENIC	homozygous	120405984
9	10010172	10010173	C	A	21	GENIC	homozygous	120424219
9	10010173	10010174	C	T	21	GENIC	homozygous	120424220
9	10010178	10010179	C	G	19	GENIC	homozygous	117243950
9	10010193	10010194	C	G	20	GENIC	homozygous	117243951