chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10173187	10173188	C	T	73	GENIC	homozygous	117244150
9	10174810	10174811	T	C	47	GENIC	homozygous	117244151
9	10174955	10174956	A	G	32	GENIC	possibly homozygous	117244153
9	10175405	10175406	G	A	51	GENIC	homozygous	117244154
9	10175917	10175918	A	G	70	GENIC	possibly homozygous	117244155
9	10176926	10176927	T	C	51	GENIC	homozygous	117244156
9	10181131	10181132	G	A	71	GENIC	possibly homozygous	117244157
9	10181781	10181782	T	C	71	GENIC	homozygous	117244158
9	10182185	10182186	A	G	39	GENIC	possibly homozygous	117244159
9	10184126	10184127	T	C	61	GENIC	homozygous	117244160
9	10185446	10185447	C	T	58	GENIC	homozygous	117244161
9	10186250	10186251	T	G	27	GENIC	heterozygous	117482604
9	10186277	10186278	G	A	32	GENIC	homozygous	117244162
9	10188117	10188118	A	T	67	GENIC	homozygous	117244163
9	10189350	10189351	A	G	48	GENIC	homozygous	117244164
9	10192672	10192673	G	T	31	GENIC	homozygous	117244165
9	10192787	10192788	G	A	60	GENIC	homozygous	117244166
9	10193580	10193581	G	A	50	GENIC	homozygous	117244167
9	10193680	10193681	C	A	66	GENIC	possibly homozygous	117244168
9	10195092	10195093	G	T	52	GENIC	possibly homozygous	117244169
9	10195194	10195195	T	C	45	GENIC	homozygous	117244170
9	10195346	10195347	A	G	44	GENIC	homozygous	117244171
9	10195968	10195969	A	T	69	GENIC	possibly homozygous	117244172
9	10196035	10196036	C	T	64	GENIC	possibly homozygous	117244173
9	10196269	10196270	T	G	2	GENIC	homozygous	117244174
9	10196310	10196311	T	C	46	GENIC	homozygous	117244175
9	10198444	10198445	C	T	35	GENIC	heterozygous	117244176
9	10198777	10198778	A	T	43	GENIC	homozygous	117244177
9	10200834	10200835	A	G	60	GENIC	homozygous	117244178
9	10202151	10202152	T	A	55	GENIC	homozygous	117244179
9	10203028	10203029	T	C	40	GENIC	possibly homozygous	117244180