chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	79660955	79660956	G	T	54	GENIC	homozygous	117928472
8	79665320	79665321	T	C	16	GENIC	homozygous	116844679
8	79665364	79665365	G	A	13	GENIC	homozygous	117047517
8	79665474	79665475	C	T	44	GENIC	homozygous	117928473
8	79665703	79665703		G	20	GENIC	possibly homozygous	132123038
8	79666869	79666870	C	G	65	GENIC	homozygous	117928474
8	79667024	79667025	C	T	53	GENIC	homozygous	126693205
8	79669232	79669233	T	C	50	GENIC	homozygous	116844681
8	79670174	79670175	T	C	56	GENIC	homozygous	116844683
8	79670545	79670546	T	C	57	GENIC	homozygous	116844685
8	79671820	79671821	A	C	55	GENIC	homozygous	116844686
8	79673316	79673317	G	A	42	GENIC	homozygous	117047519
8	79673387	79673388	C	A	49	GENIC	homozygous	117047520
8	79676328	79676329	C	T	54	GENIC	homozygous	117047522
8	79678354	79678355	A	G	49	GENIC	homozygous	116844690
8	79678625	79678626	A	C	62	GENIC	homozygous	116844691
8	79687212	79687213	G		31	GENIC	heterozygous	132123039
8	79687247	79687248	T	C	28	GENIC	heterozygous	126693207
8	79687379	79687380	G	C	40	GENIC	homozygous	132129282
8	79666300	79666300		AA	55	GENIC	homozygous	131050496
8	79681390	79681394	TACC		39	GENIC	homozygous	131050497
8	79681700	79681700		TGT	44	GENIC	homozygous	131050498
8	79672206	79672206		G	49	GENIC	homozygous	128605450
8	79687192	79687193	T	G	31	GENIC	heterozygous	132129277
8	79687213	79687214	G	A	32	GENIC	heterozygous	132129278
8	79687226	79687227	G	A	29	GENIC	heterozygous	132129279
8	79687375	79687376	G	C	39	GENIC	homozygous	132129280
8	79687377	79687378	G	C	39	GENIC	homozygous	132129281
8	79687381	79687382	G	C	41	GENIC	homozygous	132129283
8	79687383	79687384	G	C	39	GENIC	heterozygous	132129284
8	79690642	79690643	T	A	53	GENIC	homozygous	116844703
8	79691555	79691556	G	A	46	GENIC	homozygous	117047528
8	79691675	79691676	T	A	47	GENIC	homozygous	116844704