chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	25283589	25283590	T	C	37	GENIC	homozygous	136661418
3	25283917	25283918	A	C	31	GENIC	possibly homozygous	145403166
3	25283958	25283959	A	G	33	GENIC	homozygous	136661419
3	25284496	25284497	A	G	44	GENIC	homozygous	136661423
3	25284682	25284683	T		41	GENIC	possibly homozygous	140984845
3	25284755	25284756	C	T	56	GENIC	homozygous	145403167
3	25285133	25285134	G	A	59	GENIC	homozygous	145403168
3	25285762	25285763	C	T	51	GENIC	homozygous	145403169
3	25285790	25285791	A	C	42	GENIC	homozygous	145403170
3	25286102	25286103	G	C	56	GENIC	homozygous	136661430
3	25286343	25286344	C	G	42	GENIC	homozygous	136661436
3	25286528	25286529	T	G	30	GENIC	homozygous	136661438
3	25286998	25286999	G	A	48	GENIC	homozygous	145403171
3	25287000	25287001	C	T	48	GENIC	homozygous	145403172
3	25287263	25287264	G	A	48	GENIC	homozygous	145403173
3	25287371	25287372	A	T	46	GENIC	homozygous	145403174
3	25287545	25287546	C	T	31	GENIC	homozygous	145403175
3	25287653	25287654	A	T	30	GENIC	homozygous	136661442
3	25288733	25288734	C	T	51	GENIC	homozygous	145403176
3	25288774	25288775	T	A	41	GENIC	homozygous	136661445
3	25288809	25288811	AG		41	GENIC	homozygous	136553338
3	25288959	25288960	C	T	46	GENIC	homozygous	136661446
3	25288963	25288964	C	G	45	GENIC	homozygous	136661447
3	25289633	25289634	C	A	41	GENIC	possibly homozygous	145403177
3	25289694	25289695	A	T	45	GENIC	homozygous	136661449
3	25289819	25289820	G	A	39	GENIC	homozygous	145403178
3	25290016	25290017	G	A	39	GENIC	homozygous	136661451
3	25284957	25284959	GA		37	GENIC	homozygous	145390763
3	25286101	25286102	G		56	GENIC	heterozygous	136553335
3	25286101	25286102	G	T	56	GENIC	homozygous	154072712