chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	105680783	105680784	A	T	6	GENIC	homozygous	117617153
9	105680788	105680789	T	G	6	GENIC	homozygous	117617155
9	105680918	105680919	C	G	15	GENIC	homozygous	117617157
9	105681005	105681006	C	T	4	GENIC	homozygous	117617159
9	105681095	105681096	A	G	9	GENIC	homozygous	117617161
9	105681195	105681196	C	A	9	GENIC	homozygous	117617163
9	105681317	105681318	T	A	7	GENIC	homozygous	117617165
9	105681357	105681358	A	G	8	GENIC	homozygous	117617167
9	105681454	105681455	T	C	11	GENIC	homozygous	117617169
9	105681589	105681590	A	C	13	GENIC	homozygous	117617171
9	105681805	105681806	A	G	13	GENIC	homozygous	117617173
9	105681950	105681951	C	T	14	GENIC	homozygous	117617175
9	105682136	105682137	C	G	16	GENIC	homozygous	117617177
9	105682269	105682270	A	G	10	GENIC	homozygous	117617179
9	105682498	105682499	T	C	12	GENIC	homozygous	117617183
9	105682550	105682551	C	T	13	GENIC	homozygous	117632332
9	105682659	105682660	C	T	4	GENIC	homozygous	117617185
9	105682692	105682693	A	G	7	GENIC	homozygous	117617187
9	105683031	105683032	C	T	7	GENIC	homozygous	117617189
9	105683035	105683036	A	G	7	GENIC	homozygous	117617191
9	105683131	105683132	T	C	7	GENIC	homozygous	117617193
9	105683203	105683204	C	G	9	GENIC	homozygous	117617195
9	105683284	105683285	T	C	10	GENIC	homozygous	117617197
9	105683328	105683329	G	C	11	GENIC	homozygous	117617199
9	105683342	105683343	C	T	10	GENIC	homozygous	117632334
9	105683729	105683730	C	T	9	GENIC	homozygous	117617203
9	105684305	105684306	A	G	15	GENIC	homozygous	117735013
9	105685101	105685102	T	C	10	GENIC	homozygous	117617211
9	105689895	105689896	A	G	7	GENIC	homozygous	117617231
9	105690173	105690174	A	G	7	GENIC	homozygous	117735015
9	105691287	105691288	T	C	11	GENIC	homozygous	117617239