chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53572503	53572504	G	A	16	GENIC	possibly homozygous	52057756
10	53574075	53574076	C	CT	1	GENIC	homozygous	51455635
10	53574895	53574896	C	A	15	GENIC	homozygous	52057758
10	53575623	53575624	T	TA	6	GENIC	heterozygous	52057760
10	53575794	53575795	C	A	13	GENIC	possibly homozygous	52057762
10	53576440	53576441	C	G	21	GENIC	possibly homozygous	52057764
10	53580671	53580672	C	T	16	GENIC	possibly homozygous	51648519
10	53580727	53580728	A	C	23	GENIC	homozygous	51648520
10	53583921	53583922	T	G	9	GENIC	homozygous	51648528
10	53583926	53583927	A	G	9	GENIC	homozygous	51648529
10	53584505	53584506	A	C	24	GENIC	homozygous	52057766
10	53585640	53585641	G	A	21	GENIC	possibly homozygous	52057768
10	53585667	53585681	ACCCCACACCTTGT	--------------	6	GENIC	heterozygous	52057770
10	53586028	53586029	A	G	19	GENIC	homozygous	51648534
10	53586217	53586218	G	T	10	GENIC	possibly homozygous	52057772
10	53586518	53586519	G	A	24	GENIC	possibly homozygous	52057774
10	53586651	53586652	C	T	26	GENIC	possibly homozygous	51648536
10	53586739	53586740	G	A	27	GENIC	homozygous	52057776
10	53588786	53588787	C	G	20	GENIC	homozygous	51648542
10	53588886	53588887	C	T	8	GENIC	possibly homozygous	51648544
10	53589090	53589091	G	T	1	GENIC	homozygous	52057778
10	53597425	53597426	A	AC	5	GENIC	heterozygous	51648552
10	53598306	53598307	G	GT	6	GENIC	heterozygous	51648554