chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	58754028	58754029	T	C	40	GENIC	homozygous	51464511
10	58759542	58759543	C	CGT	34	GENIC	homozygous	51464513
10	58760250	58760251	T	C	45	GENIC	homozygous	51662101
10	58761362	58761363	A	G	29	GENIC	homozygous	51464518
10	58761531	58761532	C	T	42	GENIC	homozygous	51662103
10	58766149	58766150	C	CAA	117	GENIC	possibly homozygous	51464520
10	58766240	58766242	AC	--	81	GENIC	homozygous	51464521
10	58766648	58766649	A	G	37	GENIC	homozygous	51662111
10	58767110	58767112	AA	--	8	GENIC	homozygous	51464523
10	58769701	58769702	A	AT	10	GENIC	homozygous	51662115
10	58774126	58774127	C	T	28	GENIC	possibly homozygous	51662117
10	58776213	58776219	CACACA	------	5	GENIC	heterozygous	52503326
10	58777682	58777683	C	T	21	GENIC	homozygous	51662121
10	58783639	58783640	T	TCAGAGTGGCAGCCATGGAGTCAC	42	GENIC	homozygous	51464530
10	58787431	58787435	CACA	----	11	GENIC	heterozygous	53103357
10	58787433	58787435	CA	--	11	GENIC	heterozygous	52378774
10	58788429	58788430	G	-	20	GENIC	homozygous	51464534
10	58787430	58787431	T	TCA	11	GENIC	heterozygous	52801424
10	58770833	58770834	C	T	53	GENIC	homozygous	52061808
10	58782761	58782762	G	A	30	GENIC	homozygous	52061812