chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	58749866	58749867	T	C	20	GENIC	homozygous	51896528
10	58750035	58750036	G	A	26	GENIC	heterozygous	51464508
10	58752745	58752746	C	T	26	GENIC	homozygous	51896531
10	58753670	58753671	A	C	28	GENIC	homozygous	51896534
10	58754028	58754029	T	C	36	GENIC	homozygous	51464511
10	58754395	58754396	C	T	32	GENIC	homozygous	51896537
10	58756209	58756210	T	C	20	GENIC	homozygous	51896540
10	58756699	58756700	C	T	22	GENIC	homozygous	51896543
10	58757382	58757383	T	C	30	GENIC	homozygous	51896546
10	58757737	58757738	G	A	40	GENIC	homozygous	51896549
10	58759542	58759543	C	CGT	33	GENIC	heterozygous	51464513
10	58759543	58759545	GT	--	33	GENIC	heterozygous	51464514
10	58759544	58759545	T	TGC	40	GENIC	homozygous	51464515
10	58759560	58759561	T	C	48	GENIC	possibly homozygous	51662099
10	58760250	58760251	T	C	33	GENIC	homozygous	51662101
10	58760281	58760282	G	A	32	GENIC	possibly homozygous	51896553
10	58761362	58761363	A	G	27	GENIC	homozygous	51464518
10	58762253	58762254	G	A	30	GENIC	homozygous	51896556
10	58766142	58766143	T	TCA	37	GENIC	homozygous	51464519
10	58766149	58766150	C	CAA	51	GENIC	homozygous	51464520
10	58766240	58766242	AC	--	56	GENIC	homozygous	51464521
10	58766648	58766649	A	G	22	GENIC	homozygous	51662111
10	58767108	58767112	AAAA	----	14	GENIC	homozygous	51896559
10	58767456	58767457	T	A	23	GENIC	possibly homozygous	51896562
10	58769701	58769702	A	AT	20	GENIC	homozygous	51662115
10	58770766	58770767	C	T	9	GENIC	homozygous	51896564
10	58777682	58777683	C	T	27	GENIC	homozygous	51662121
10	58780337	58780338	C	G	36	GENIC	homozygous	51896574
10	58780348	58780349	C	A	35	GENIC	homozygous	51896577
10	58783639	58783640	T	TCAGAGTGGCAGCCATGGAGTCAC	9	GENIC	homozygous	51464530
10	58785292	58785293	G	A	31	GENIC	homozygous	51896580
10	58788429	58788430	G	-	21	GENIC	homozygous	51464534
10	58788445	58788446	T	C	26	GENIC	homozygous	51464535
10	58788480	58788481	T	C	28	GENIC	homozygous	51464536