chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	81427310	81427311	G	A	42	GENIC	possibly homozygous	117585125
9	81427345	81427346	A	T	39	GENIC	homozygous	117585127
9	81427665	81427666	T	G	42	GENIC	possibly homozygous	117585129
9	81428179	81428180	T	C	40	GENIC	heterozygous	117585131
9	81428181	81428182	T	C	38	GENIC	heterozygous	117585133
9	81428331	81428332	A	G	41	GENIC	homozygous	117585135
9	81428340	81428341	C	A	42	GENIC	homozygous	117585137
9	81428562	81428563	G	A	33	GENIC	homozygous	117585139
9	81429050	81429051	C	T	54	GENIC	possibly homozygous	117585141
9	81429305	81429306	G	T	52	GENIC	homozygous	117585143
9	81429342	81429343	T	C	63	GENIC	homozygous	117585145
9	81429772	81429773	T	C	51	GENIC	possibly homozygous	117585147
9	81430347	81430348	T	C	51	GENIC	homozygous	117585149
9	81430500	81430501	T	G	44	GENIC	possibly homozygous	117585151
9	81430624	81430625	A	C	49	GENIC	homozygous	117585153
9	81430639	81430640	A	C	49	GENIC	possibly homozygous	117585155
9	81430712	81430713	A	G	56	GENIC	homozygous	117585157
9	81430731	81430732	T	C	63	GENIC	homozygous	117585159
9	81430793	81430794	C	T	71	GENIC	homozygous	117585161
9	81430970	81430971	A	G	50	GENIC	homozygous	117585163
9	81431032	81431033	T	G	50	GENIC	homozygous	117585165
9	81432120	81432121	G	A	44	GENIC	homozygous	117585167
9	81432683	81432684	T	G	49	GENIC	possibly homozygous	117585169
9	81433424	81433425	C	T	47	GENIC	homozygous	117585171