chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53572503	53572504	G	A	15	GENIC	homozygous	52057756
10	53574895	53574896	C	A	16	GENIC	homozygous	52057758
10	53575623	53575624	T	TA	19	GENIC	possibly homozygous	52057760
10	53575794	53575795	C	A	22	GENIC	homozygous	52057762
10	53576440	53576441	C	G	11	GENIC	homozygous	52057764
10	53580542	53580543	A	ATTGTTG	12	GENIC	homozygous	51648518
10	53580671	53580672	C	T	22	GENIC	homozygous	51648519
10	53580727	53580728	A	C	22	GENIC	homozygous	51648520
10	53583921	53583922	T	G	22	GENIC	homozygous	51648528
10	53583926	53583927	A	G	21	GENIC	homozygous	51648529
10	53584505	53584506	A	C	13	GENIC	homozygous	52057766
10	53585640	53585641	G	A	11	GENIC	homozygous	52057768
10	53585667	53585681	ACCCCACACCTTGT	--------------	10	GENIC	homozygous	52057770
10	53586028	53586029	A	G	13	GENIC	homozygous	51648534
10	53586217	53586218	G	T	16	GENIC	homozygous	52057772
10	53586518	53586519	G	A	18	GENIC	homozygous	52057774
10	53586651	53586652	C	T	16	GENIC	homozygous	51648536
10	53586739	53586740	G	A	19	GENIC	homozygous	52057776
10	53588786	53588787	C	G	22	GENIC	homozygous	51648542
10	53588886	53588887	C	T	18	GENIC	homozygous	51648544
10	53589090	53589091	G	T	26	GENIC	homozygous	52057778
10	53589111	53589112	T	C	24	GENIC	homozygous	52057780
10	53591711	53591712	G	-	13	GENIC	homozygous	51455640