chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	258966873	258966874	T	C	37	GENIC	heterozygous	110417336
2	258969902	258969903	C	G	33	GENIC	homozygous	110417338
2	258969903	258969904	T	A	34	GENIC	homozygous	110417340
2	258969920	258969921	G	A	33	GENIC	homozygous	110417342
2	258974132	258974133	C	T	47	GENIC	homozygous	110417344
2	258976678	258976679	A	C	44	GENIC	homozygous	110417346
2	258976713	258976714	A	G	43	GENIC	possibly homozygous	110417348
2	258977137	258977138	G	A	44	GENIC	homozygous	110417350
2	258977265	258977266	T	C	61	GENIC	homozygous	110417352
2	258977293	258977294	A	G	50	GENIC	possibly homozygous	110417354
2	258978187	258978188	T	C	56	GENIC	homozygous	110417356
2	258979107	258979108	A	G	81	GENIC	heterozygous	110417360
2	258979115	258979116	G	A	75	GENIC	heterozygous	110417362
2	258979118	258979119	T	C	70	GENIC	heterozygous	110417364
2	258979660	258979661	A	G	56	GENIC	homozygous	110417366
2	258980432	258980433	A	G	66	GENIC	possibly homozygous	110417368
2	258981036	258981037	A	G	45	GENIC	homozygous	110417370
2	258981521	258981522	A	G	39	GENIC	heterozygous	110417372
2	258983570	258983571	A	C	50	GENIC	homozygous	110417376
2	258983915	258983916	C	T	44	GENIC	homozygous	110417378
2	258984343	258984344	T	C	44	GENIC	possibly homozygous	110417380