chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	87663280	87663281	A	C	7	GENIC	homozygous	110950786
2	87663303	87663304	T	C	7	GENIC	homozygous	109896187
2	87663399	87663400	A	G	10	GENIC	homozygous	109896188
2	87663400	87663401	T	C	11	GENIC	homozygous	109896189
2	87663716	87663717	G	A	9	GENIC	homozygous	110950788
2	87663821	87663822	T	C	11	GENIC	homozygous	109896190
2	87663913	87663914	G	A	13	GENIC	homozygous	109896191
2	87663918	87663919	C	G	13	GENIC	homozygous	109896192
2	87664028	87664029	A	G	13	GENIC	homozygous	109896193
2	87664030	87664031	A	G	13	GENIC	homozygous	109896194
2	87664055	87664056	G	A	10	GENIC	homozygous	109896195
2	87664472	87664473	G	A	13	GENIC	homozygous	109896200
2	87664936	87664937	G	A	22	GENIC	homozygous	109896220
2	87664988	87664989	G	A	18	GENIC	homozygous	109896221
2	87665309	87665310	G	A	17	GENIC	homozygous	109896224
2	87665436	87665437	A	C	17	GENIC	homozygous	109896225
2	87665790	87665791	A	T	19	GENIC	homozygous	109896227
2	87665806	87665807	A	G	17	GENIC	homozygous	109896228
2	87666184	87666185	A	T	18	GENIC	homozygous	109896233
2	87666546	87666547	A	C	40	GENIC	homozygous	109896235
2	87666603	87666604	G	T	31	GENIC	homozygous	109896236
2	87666627	87666628	T	C	26	GENIC	homozygous	110950794
2	87666747	87666748	A	C	20	GENIC	homozygous	109896237
2	87666754	87666755	G	A	20	GENIC	homozygous	109896238
2	87666941	87666942	C	A	19	GENIC	homozygous	109896239
2	87667116	87667117	G	A	19	GENIC	homozygous	109896240
2	87667422	87667423	G	C	17	GENIC	homozygous	109896243