chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	80267737	80267738	A	G	13	GENIC	homozygous	109874239
2	80267957	80267958	G	A	18	GENIC	homozygous	109874241
2	80268193	80268194	A	G	20	GENIC	homozygous	109874243
2	80268661	80268662	C	T	17	GENIC	homozygous	109874245
2	80269122	80269123	G	T	22	GENIC	homozygous	109874246
2	80269571	80269572	A	G	22	GENIC	homozygous	109874248
2	80270443	80270444	G	A	15	GENIC	homozygous	109874250
2	80271138	80271139	T	C	19	GENIC	homozygous	109874252
2	80271306	80271307	A	G	26	GENIC	homozygous	109874254
2	80271797	80271798	A	G	22	GENIC	homozygous	109874256
2	80271977	80271978	T	C	30	GENIC	possibly homozygous	109874258
2	80272372	80272373	G	A	23	GENIC	homozygous	109874260
2	80272692	80272693	A	G	15	GENIC	homozygous	109874262
2	80273349	80273350	C	A	16	GENIC	homozygous	109874264
2	80273405	80273406	C	A	22	GENIC	homozygous	109874266
2	80273471	80273472	T	G	30	GENIC	possibly homozygous	109874268
2	80273627	80273628	A	G	14	GENIC	homozygous	109874269
2	80273880	80273881	T	C	24	GENIC	homozygous	109874271
2	80274232	80274233	C	T	19	GENIC	homozygous	109874273
2	80275203	80275204	C	T	20	GENIC	homozygous	109874275
2	80275686	80275687	T	C	23	GENIC	homozygous	109874277
2	80275787	80275788	T	C	31	GENIC	possibly homozygous	109874279
2	80276238	80276239	T	C	30	GENIC	homozygous	109874281
2	80281095	80281096	T	C	27	GENIC	homozygous	109874284
2	80281914	80281915	C	T	24	GENIC	homozygous	109874286
2	80284504	80284505	C	A	29	GENIC	homozygous	109874288
2	80287041	80287042	C	T	17	GENIC	homozygous	109874290
2	80287721	80287722	A	G	15	GENIC	homozygous	109874292
2	80290115	80290116	A	G	21	GENIC	homozygous	109874294
2	80290890	80290891	A	G	15	GENIC	homozygous	109874296
2	80291176	80291177	A	G	20	GENIC	homozygous	109874298
2	80291755	80291756	A	T	24	GENIC	homozygous	109874300
2	80293194	80293195	T	C	36	GENIC	homozygous	109874302