chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	86677848	86677849	G	GC	1	GENIC	homozygous	51528467
10	86678140	86678141	G	C	26	GENIC	homozygous	51528468
10	86678183	86678184	G	A	27	GENIC	homozygous	51528469
10	86678202	86678206	TGTG	----	18	GENIC	possibly homozygous	52444612
10	86679336	86679337	G	A	33	GENIC	homozygous	51528471
10	86679579	86679580	C	G	28	GENIC	homozygous	51528472
10	86680965	86680966	T	A	30	GENIC	homozygous	51528473
10	86681050	86681051	T	C	37	GENIC	homozygous	51528474
10	86681810	86681811	T	-	21	GENIC	homozygous	51528475
10	86684783	86684784	G	A	33	GENIC	possibly homozygous	51528476
10	86685277	86685278	G	A	36	GENIC	homozygous	51528477
10	86685335	86685336	C	T	27	GENIC	homozygous	51528478
10	86685428	86685429	G	T	31	GENIC	homozygous	51528479
10	86685567	86685568	C	A	37	GENIC	homozygous	51528480
10	86685583	86685586	TTA	---	28	GENIC	homozygous	52808355
10	86685599	86685600	T	G	29	GENIC	possibly homozygous	52808358
10	86685604	86685605	T	G	28	GENIC	possibly homozygous	52808361
10	86685609	86685611	TG	--	27	GENIC	possibly homozygous	52808363
10	86685616	86685617	T	G	21	GENIC	possibly homozygous	51528484
10	86685622	86685623	C	-	19	GENIC	possibly homozygous	51528485
10	86685964	86685965	G	A	29	GENIC	homozygous	51528486
10	86688553	86688554	T	G	19	GENIC	homozygous	51528487
10	86689161	86689162	G	C	29	GENIC	homozygous	51528488
10	86689169	86689170	A	C	29	GENIC	homozygous	51528489
10	86689733	86689734	G	-	5	GENIC	homozygous	51528490