chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	108301687	108301688	T	C	53	GENIC	homozygous	138177686
7	108302002	108302003	C	T	48	GENIC	homozygous	138177687
7	108302141	108302142	G	A	52	GENIC	homozygous	138177688
7	108303510	108303511	A	G	58	GENIC	homozygous	138177689
7	108304764	108304765	G	A	73	GENIC	homozygous	138177690
7	108305330	108305331	C	T	61	GENIC	homozygous	138177691
7	108305407	108305408	A	G	49	GENIC	homozygous	138177692
7	108305558	108305559	G	A	57	GENIC	possibly homozygous	138177693
7	108305755	108305756	T	C	43	GENIC	homozygous	138177694
7	108308454	108308455	A	T	47	GENIC	homozygous	138177695
7	108308469	108308470	T	A	48	GENIC	homozygous	138177696
7	108311927	108311928	G	C	46	GENIC	homozygous	138177697
7	108312093	108312094	A	G	63	GENIC	homozygous	138177698
7	108312850	108312851	C	G	65	GENIC	homozygous	138177699
7	108313484	108313485	G	A	60	GENIC	homozygous	138177700
7	108313546	108313547	A	T	50	GENIC	homozygous	138177701
7	108316041	108316042	C	T	58	GENIC	homozygous	138177702
7	108317738	108317739	C	A	58	GENIC	homozygous	138177703
7	108317862	108317863	T	C	60	GENIC	homozygous	138177704
7	108317974	108317975	C	T	42	GENIC	homozygous	138177705
7	108318304	108318305	T	G	57	GENIC	homozygous	138177706
7	108319088	108319089	G	A	68	GENIC	homozygous	138177707
7	108319239	108319240	G	A	57	GENIC	homozygous	138177708
7	108317309	108317309		G	43	GENIC	homozygous	137973307
7	108309283	108309283		T	38	GENIC	possibly homozygous	137973304
7	108311534	108311535	G		56	GENIC	homozygous	137973305
7	108312844	108312844		CCTTGGGTAGGAGCAGCA	64	GENIC	homozygous	137973306