chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	87663280	87663281	A	C	13	GENIC	homozygous	110950786
2	87663303	87663304	T	C	17	GENIC	homozygous	109896187
2	87663716	87663717	G	A	18	GENIC	possibly homozygous	110950788
2	87663821	87663822	T	C	21	GENIC	homozygous	109896190
2	87663913	87663914	G	A	28	GENIC	homozygous	109896191
2	87663918	87663919	C	G	25	GENIC	homozygous	109896192
2	87664028	87664029	A	G	31	GENIC	homozygous	109896193
2	87664030	87664031	A	G	30	GENIC	homozygous	109896194
2	87664055	87664056	G	A	26	GENIC	homozygous	109896195
2	87664106	87664107	T	A	26	GENIC	homozygous	109896196
2	87664472	87664473	G	A	28	GENIC	homozygous	109896200
2	87664763	87664764	A	C	24	GENIC	homozygous	109896207
2	87664802	87664803	T	C	27	GENIC	homozygous	109896212
2	87664803	87664804	G	A	27	GENIC	homozygous	109896213
2	87664846	87664847	A	G	24	GENIC	homozygous	110950790
2	87664936	87664937	G	A	15	GENIC	homozygous	109896220
2	87665115	87665116	T	C	36	GENIC	homozygous	109896222
2	87665309	87665310	G	A	12	GENIC	homozygous	109896224
2	87665436	87665437	A	C	26	GENIC	homozygous	109896225
2	87665790	87665791	A	T	31	GENIC	homozygous	109896227
2	87665806	87665807	A	G	29	GENIC	homozygous	109896228
2	87666184	87666185	A	T	28	GENIC	homozygous	109896233
2	87666218	87666219	C	T	29	GENIC	possibly homozygous	110950792
2	87666426	87666427	A	T	23	GENIC	homozygous	109896234
2	87666546	87666547	A	C	21	GENIC	homozygous	109896235
2	87666603	87666604	G	T	28	GENIC	homozygous	109896236
2	87666627	87666628	T	C	19	GENIC	possibly homozygous	110950794
2	87666747	87666748	A	C	31	GENIC	homozygous	109896237
2	87666754	87666755	G	A	31	GENIC	homozygous	109896238
2	87666941	87666942	C	A	25	GENIC	homozygous	109896239
2	87667116	87667117	G	A	19	GENIC	homozygous	109896240
2	87667422	87667423	G	C	26	GENIC	homozygous	109896243