chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95286762	95286763	T	C	36	GENIC	homozygous	117606909
9	95287623	95287624	A	G	27	GENIC	homozygous	117392238
9	95287652	95287653	C	T	27	GENIC	homozygous	117602909
9	95290983	95290984	G	A	31	GENIC	homozygous	117602911
9	95291196	95291197	T	C	36	GENIC	homozygous	117606911
9	95291607	95291608	T	C	29	GENIC	homozygous	117606913
9	95291766	95291767	A	G	22	GENIC	homozygous	117606915
9	95293121	95293122	C	T	24	GENIC	homozygous	117606917
9	95293235	95293236	A	G	27	GENIC	homozygous	117606919
9	95295006	95295007	G	T	23	GENIC	homozygous	117606921
9	95295037	95295038	A	T	18	GENIC	possibly homozygous	123216269
9	95295040	95295041	C	T	18	GENIC	possibly homozygous	123216270
9	95295532	95295533	G	A	28	GENIC	homozygous	117606923
9	95296496	95296497	C	T	29	GENIC	homozygous	117606927
9	95297143	95297144	A	G	28	GENIC	homozygous	117606929
9	95297313	95297314	C	T	33	GENIC	homozygous	117602913
9	95297677	95297678	T	A	23	GENIC	homozygous	117606931
9	95297885	95297886	A	G	27	GENIC	homozygous	117606933
9	95298065	95298066	G	T	25	GENIC	homozygous	117606935
9	95298086	95298087	A	G	30	GENIC	homozygous	117606937
9	95298115	95298116	G	A	31	GENIC	homozygous	117606939
9	95298157	95298158	G	C	31	GENIC	homozygous	117606941
9	95298171	95298172	C	T	31	GENIC	homozygous	117606943
9	95298823	95298824	T	C	27	GENIC	homozygous	117606945
9	95287713	95287714	C		31	GENIC	homozygous	128733787
9	95294721	95294722	T		19	GENIC	homozygous	128733788
9	95295031	95295032	A		17	GENIC	homozygous	129960041
9	95295035	95295036	A		18	GENIC	possibly homozygous	129960042
9	95295042	95295042		C	18	GENIC	possibly homozygous	131454231
9	95299726	95299727	C	A	21	GENIC	possibly homozygous	117602915
9	95300735	95300736	A	T	33	GENIC	homozygous	117602917
9	95302314	95302315	A	T	21	GENIC	homozygous	117606953