chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	58509952	58509953	C	A	52	GENIC	possibly homozygous	110534285
2	58510337	58510338	A	T	58	GENIC	possibly homozygous	109772505
2	58510357	58510358	T	C	67	GENIC	homozygous	109772507
2	58510921	58510922	C	G	59	GENIC	homozygous	109772509
2	58511819	58511820	A	C	63	GENIC	homozygous	109772511
2	58512633	58512634	G	A	77	GENIC	homozygous	109772513
2	58514798	58514799	G	A	51	GENIC	homozygous	109772515
2	58515682	58515683	C	T	44	GENIC	possibly homozygous	109772517
2	58518941	58518942	G	A	70	GENIC	homozygous	109772519
2	58519764	58519765	T	C	38	GENIC	possibly homozygous	109772521
2	58519848	58519849	T	A	48	GENIC	homozygous	109772523
2	58520051	58520052	C	T	59	GENIC	homozygous	109772525
2	58520718	58520719	C	T	42	GENIC	homozygous	109772529
2	58522782	58522783	G	A	69	GENIC	homozygous	109772531
2	58522934	58522935	C	T	51	GENIC	homozygous	109772533
2	58523051	58523052	T	C	63	GENIC	homozygous	109772535
2	58526540	58526541	C	T	57	GENIC	homozygous	109772537
2	58531840	58531841	T	C	72	GENIC	homozygous	109772539
2	58531883	58531884	T	C	57	GENIC	homozygous	109772541
2	58533267	58533268	G	A	51	GENIC	homozygous	109772542