chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	47319528	47319529	T	C	12	GENIC	heterozygous	53181713
8	47319725	47319726	C	T	10	GENIC	homozygous	53109389
8	47319891	47319892	C	T	13	GENIC	heterozygous	53181714
8	47319923	47319924	T	C	11	GENIC	heterozygous	53181715
8	47319931	47319932	T	C	10	GENIC	homozygous	53109390
8	47320614	47320615	G	A	15	GENIC	heterozygous	53181716
8	47320760	47320761	G	T	10	GENIC	heterozygous	53181717
8	47321519	47321526	GTGATAG	-------	21	GENIC	heterozygous	53181718
8	47322274	47322275	C	T	14	GENIC	heterozygous	53181722
8	47323092	47323093	T	C	11	GENIC	heterozygous	53181723
8	47323572	47323573	G	A	9	GENIC	heterozygous	53181724
8	47323584	47323585	C	T	12	GENIC	heterozygous	53181725
8	47324461	47324462	C	T	16	GENIC	heterozygous	53181726
8	47326295	47326296	C	T	11	GENIC	heterozygous	53181727
8	47326975	47326976	A	G	16	GENIC	heterozygous	53181728
8	47328395	47328396	A	G	17	GENIC	heterozygous	53181729
8	47329489	47329490	T	C	17	GENIC	heterozygous	53181731
8	47329935	47329936	G	A	19	GENIC	heterozygous	53181732
8	47330150	47330151	T	A	15	GENIC	heterozygous	53181733
8	47330294	47330295	A	G	11	GENIC	heterozygous	53181734