chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	55306937	55306938	G	A	37	GENIC	homozygous	49760774
13	55307628	55307629	C	T	23	GENIC	homozygous	49760781
13	55307885	55307886	C	CTTT	9	GENIC	heterozygous	49760783
13	55308525	55308526	A	-	20	GENIC	homozygous	50044979
13	55307585	55307586	G	A	20	GENIC	homozygous	50044973
13	55307885	55307886	C	CTTTTT	9	GENIC	possibly homozygous	50044975
13	55308096	55308097	G	A	32	GENIC	homozygous	50044977
13	55308537	55308538	T	C	23	GENIC	possibly homozygous	49760787
13	55308830	55308834	TTTT	----	3	GENIC	homozygous	50044981
13	55309291	55309292	T	C	25	GENIC	homozygous	49760788
13	55309406	55309407	A	G	20	GENIC	homozygous	50044983
13	55309510	55309511	A	G	25	GENIC	homozygous	49760789
13	55310195	55310198	TTT	---	20	GENIC	homozygous	49953127
13	55310568	55310569	T	C	9	GENIC	homozygous	50044985
13	55310690	55310691	C	T	13	GENIC	homozygous	49760792
13	55311280	55311281	A	G	21	GENIC	homozygous	50044987
13	55311285	55311286	A	C	22	GENIC	homozygous	50044990
13	55311341	55311342	T	TAATA	15	GENIC	homozygous	50044992
13	55312196	55312197	A	G	19	GENIC	homozygous	49760794