chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	98446162	98446163	C	T	28	GENIC	homozygous	117613256
9	98446163	98446164	A	G	29	GENIC	homozygous	117613258
9	98447120	98447121	A	G	17	GENIC	homozygous	117761059
9	98448236	98448237	T	C	29	GENIC	homozygous	117761061
9	98448617	98448618	G	A	34	GENIC	homozygous	117613262
9	98448709	98448710	T	G	25	GENIC	homozygous	117761063
9	98448761	98448762	A	G	31	GENIC	homozygous	117761064
9	98449201	98449202	C	T	29	GENIC	homozygous	117761067
9	98449379	98449380	T	C	39	GENIC	homozygous	117761069
9	98450439	98450440	A	C	30	GENIC	homozygous	117613268
9	98451673	98451674	T	A	15	GENIC	homozygous	117761072
9	98453018	98453019	G	A	31	GENIC	homozygous	117613274
9	98453497	98453498	T	C	31	GENIC	possibly homozygous	117613276
9	98453622	98453623	G	A	28	GENIC	homozygous	117761074
9	98454044	98454045	A	G	19	GENIC	homozygous	117613278
9	98454509	98454510	C	T	27	GENIC	homozygous	117761075
9	98454571	98454572	T	C	26	GENIC	homozygous	117761077
9	98455013	98455014	G	A	32	GENIC	homozygous	117761079
9	98455035	98455036	T	C	29	GENIC	possibly homozygous	117761080
9	98455670	98455671	G	A	27	GENIC	homozygous	117761082
9	98455900	98455901	C	T	13	GENIC	homozygous	117761084
9	98455987	98455988	T	C	14	GENIC	homozygous	117613280
9	98457198	98457199	A	G	31	GENIC	homozygous	117613282
9	98458063	98458064	C	T	23	GENIC	homozygous	117896206
9	98458179	98458180	T	C	31	GENIC	homozygous	117613288