chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	108301687	108301688	T	C	65	GENIC	homozygous	138177686
7	108302002	108302003	C	T	54	GENIC	homozygous	138177687
7	108302141	108302142	G	A	65	GENIC	possibly homozygous	138177688
7	108303510	108303511	A	G	58	GENIC	possibly homozygous	138177689
7	108304764	108304765	G	A	45	GENIC	homozygous	138177690
7	108305330	108305331	C	T	45	GENIC	homozygous	138177691
7	108305407	108305408	A	G	47	GENIC	homozygous	138177692
7	108305558	108305559	G	A	55	GENIC	homozygous	138177693
7	108305755	108305756	T	C	56	GENIC	homozygous	138177694
7	108308454	108308455	A	T	55	GENIC	homozygous	138177695
7	108312850	108312851	C	G	59	GENIC	homozygous	138177699
7	108309283	108309283		T	31	GENIC	possibly homozygous	137973304
7	108311534	108311535	G		54	GENIC	homozygous	137973305
7	108312844	108312844		CCTTGGGTAGGAGCAGCA	54	GENIC	homozygous	137973306
7	108308469	108308470	T	A	53	GENIC	homozygous	138177696
7	108311927	108311928	G	C	66	GENIC	homozygous	138177697
7	108312093	108312094	A	G	54	GENIC	homozygous	138177698
7	108313484	108313485	G	A	69	GENIC	homozygous	138177700
7	108313546	108313547	A	T	57	GENIC	homozygous	138177701
7	108316041	108316042	C	T	71	GENIC	homozygous	138177702
7	108317309	108317309		G	43	GENIC	homozygous	137973307
7	108317738	108317739	C	A	55	GENIC	homozygous	138177703
7	108317862	108317863	T	C	64	GENIC	homozygous	138177704
7	108317974	108317975	C	T	75	GENIC	homozygous	138177705
7	108318304	108318305	T	G	64	GENIC	homozygous	138177706
7	108319088	108319089	G	A	65	GENIC	homozygous	138177707
7	108319239	108319240	G	A	70	GENIC	homozygous	138177708