chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62407983	62407984	C	T	52	GENIC	homozygous	116836505
8	62409362	62409363	C	A	43	GENIC	homozygous	116836507
8	62410739	62410740	C	G	56	GENIC	possibly homozygous	116836509
8	62411008	62411009	A	G	69	GENIC	homozygous	116836511
8	62411425	62411426	T	G	13	GENIC	heterozygous	116836513
8	62411429	62411430	T	G	10	GENIC	heterozygous	116836515
8	62411463	62411464	A	G	16	GENIC	heterozygous	116836517
8	62412604	62412605	C	T	38	GENIC	homozygous	116836519
8	62412971	62412972	T	A	42	GENIC	possibly homozygous	116836521
8	62412972	62412973	G	A	43	GENIC	homozygous	116836523
8	62415986	62415987	G	A	55	GENIC	possibly homozygous	116836525
8	62415989	62415990	T	C	55	GENIC	possibly homozygous	116836527
8	62416036	62416037	T	C	54	GENIC	homozygous	116836529
8	62416535	62416536	G	A	63	GENIC	homozygous	116836531
8	62417509	62417510	A	G	58	GENIC	homozygous	116836533
8	62417823	62417824	T	G	49	GENIC	possibly homozygous	116836535
8	62418793	62418794	A	G	61	GENIC	homozygous	116836537
8	62419689	62419690	G	A	59	GENIC	homozygous	116836539
8	62419706	62419707	T	C	53	GENIC	homozygous	116836541
8	62421110	62421111	A	T	42	GENIC	homozygous	116836543
8	62421662	62421663	G	A	53	GENIC	possibly homozygous	116836545
8	62421823	62421824	A	G	55	GENIC	homozygous	116836547