chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	47375537	47375538	G	A	26	GENIC	homozygous	53181759
8	47377245	47377246	G	C	46	GENIC	homozygous	53181760
8	47377885	47377886	A	G	28	GENIC	homozygous	53181761
8	47378306	47378307	A	-	20	GENIC	possibly homozygous	53109412
8	47378307	47378308	T	TG	20	GENIC	possibly homozygous	53109413
8	47378313	47378314	T	A	28	GENIC	possibly homozygous	53109414
8	47378444	47378445	T	TG	26	GENIC	homozygous	53181762
8	47378519	47378520	G	GT	16	GENIC	heterozygous	52620250
8	47379845	47379853	TCTCTCTC	--------	5	GENIC	homozygous	53109415
8	47379850	47379851	C	G	9	GENIC	possibly homozygous	53109416
8	47379856	47379857	C	G	10	GENIC	heterozygous	53181763
8	47379874	47379892	CTCACACACACACACACA	------------------	10	GENIC	heterozygous	53109417
8	47381859	47381860	A	-	6	GENIC	homozygous	52620252
8	47382124	47382125	T	-	19	GENIC	heterozygous	53109418
8	47382892	47382893	A	G	52	GENIC	homozygous	53109419
8	47384288	47384289	T	G	34	GENIC	homozygous	53109420