chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10172683	10172684	G	A	9	GENIC	homozygous	120293568
9	10175917	10175918	A	G	13	GENIC	homozygous	117244155
9	10176926	10176927	T	C	5	GENIC	homozygous	117244156
9	10181131	10181132	G	A	19	GENIC	homozygous	117244157
9	10181781	10181782	T	C	23	GENIC	homozygous	117244158
9	10184126	10184127	T	C	17	GENIC	homozygous	117244160
9	10186860	10186861	A	G	10	GENIC	possibly homozygous	120352092
9	10186861	10186862	T	C	10	GENIC	possibly homozygous	120352093
9	10188117	10188118	A	T	20	GENIC	homozygous	117244163
9	10189350	10189351	A	G	16	GENIC	homozygous	117244164
9	10193680	10193681	C	A	29	GENIC	homozygous	117244168
9	10195092	10195093	G	T	18	GENIC	homozygous	117244169
9	10195346	10195347	A	G	11	GENIC	homozygous	117244171
9	10195968	10195969	A	T	13	GENIC	homozygous	117244172
9	10196035	10196036	C	T	20	GENIC	homozygous	117244173
9	10198777	10198778	A	T	14	GENIC	homozygous	117244177
9	10200834	10200835	A	G	7	GENIC	homozygous	117244178
9	10202151	10202152	T	A	17	GENIC	homozygous	117244179
9	10203028	10203029	T	C	13	GENIC	homozygous	117244180