chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	61673545	61673546	G	A	69	GENIC	homozygous	52988298
8	61673862	61673863	T	C	53	GENIC	homozygous	52988300
8	61674113	61674114	C	CTTTTT	37	GENIC	possibly homozygous	52988302
8	61674113	61674114	C	CTT	37	GENIC	heterozygous	52988304
8	61674300	61674301	A	AG	66	GENIC	homozygous	52988306
8	61674312	61674313	A	G	64	GENIC	homozygous	52988308
8	61674594	61674595	G	T	70	GENIC	homozygous	52988310
8	61675093	61675094	C	T	56	GENIC	homozygous	52988312
8	61675532	61675533	A	ACCTTC	37	GENIC	homozygous	52988314
8	61675749	61675750	A	AAC	47	GENIC	homozygous	52988316
8	61675891	61675892	A	C	61	GENIC	homozygous	52988318