chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95286762	95286763	T	C	63	GENIC	homozygous	117606909
9	95287623	95287624	A	G	49	GENIC	homozygous	117392238
9	95287713	95287714	C		43	GENIC	possibly homozygous	128733787
9	95291196	95291197	T	C	44	GENIC	homozygous	117606911
9	95291607	95291608	T	C	52	GENIC	homozygous	117606913
9	95291766	95291767	A	G	58	GENIC	homozygous	117606915
9	95293121	95293122	C	T	53	GENIC	homozygous	117606917
9	95293235	95293236	A	G	47	GENIC	homozygous	117606919
9	95294721	95294722	T		45	GENIC	homozygous	128733788
9	95295006	95295007	G	T	38	GENIC	homozygous	117606921
9	95295031	95295032	A		31	GENIC	homozygous	129960041
9	95295035	95295036	A		30	GENIC	homozygous	129960042
9	95295037	95295038	A	T	29	GENIC	homozygous	123216269
9	95295040	95295041	C	T	27	GENIC	homozygous	123216270
9	95295043	95295044	A		25	GENIC	homozygous	129960043
9	95295532	95295533	G	A	39	GENIC	homozygous	117606923
9	95295613	95295614	C	G	38	GENIC	homozygous	117606925
9	95296496	95296497	C	T	51	GENIC	homozygous	117606927
9	95297143	95297144	A	G	41	GENIC	homozygous	117606929
9	95297677	95297678	T	A	42	GENIC	homozygous	117606931
9	95297885	95297886	A	G	55	GENIC	homozygous	117606933
9	95298065	95298066	G	T	51	GENIC	homozygous	117606935
9	95298086	95298087	A	G	49	GENIC	homozygous	117606937
9	95298115	95298116	G	A	42	GENIC	homozygous	117606939
9	95298157	95298158	G	C	46	GENIC	homozygous	117606941
9	95298171	95298172	C	T	44	GENIC	homozygous	117606943
9	95298823	95298824	T	C	72	GENIC	homozygous	117606945
9	95299218	95299222	ACTT		39	GENIC	homozygous	128733789
9	95299494	95299495	T	C	49	GENIC	possibly homozygous	117606947
9	95299505	95299506	G	C	51	GENIC	possibly homozygous	117606949
9	95300043	95300044	C	T	45	GENIC	homozygous	117606951
9	95300120	95300122	AG		28	GENIC	homozygous	128733790
9	95302314	95302315	A	T	58	GENIC	homozygous	117606953
9	95302741	95302742	A	G	56	GENIC	homozygous	117606955