chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95286762	95286763	T	C	23	GENIC	homozygous	117606909
9	95287623	95287624	A	G	15	GENIC	homozygous	117392238
9	95291196	95291197	T	C	14	GENIC	homozygous	117606911
9	95291607	95291608	T	C	19	GENIC	homozygous	117606913
9	95291766	95291767	A	G	21	GENIC	homozygous	117606915
9	95293121	95293122	C	T	24	GENIC	homozygous	117606917
9	95293235	95293236	A	G	23	GENIC	homozygous	117606919
9	95295006	95295007	G	T	17	GENIC	homozygous	117606921
9	95295532	95295533	G	A	21	GENIC	homozygous	117606923
9	95297143	95297144	A	G	18	GENIC	homozygous	117606929
9	95296496	95296497	C	T	26	GENIC	homozygous	117606927
9	95297313	95297314	C	T	19	GENIC	homozygous	117602913
9	95297677	95297678	T	A	24	GENIC	homozygous	117606931
9	95297885	95297886	A	G	19	GENIC	heterozygous	117606933
9	95298065	95298066	G	T	15	GENIC	homozygous	117606935
9	95298086	95298087	A	G	16	GENIC	homozygous	117606937
9	95298115	95298116	G	A	26	GENIC	homozygous	117606939
9	95298157	95298158	G	C	25	GENIC	homozygous	117606941
9	95298171	95298172	C	T	18	GENIC	homozygous	117606943
9	95298823	95298824	T	C	15	GENIC	homozygous	117606945
9	95299438	95299439	T	A	7	GENIC	homozygous	117829024
9	95299726	95299727	C	A	22	GENIC	homozygous	117602915
9	95300735	95300736	A	T	20	GENIC	heterozygous	117602917
9	95302314	95302315	A	T	7	GENIC	homozygous	117606953