chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	26808766	26808767	T	C	17	GENIC	homozygous	111011112
17	26813393	26813394	G	A	11	GENIC	homozygous	111011114
17	26816336	26816337	C	T	26	GENIC	homozygous	111011116
17	26817997	26817998	T	G	22	GENIC	homozygous	111011118
17	26818667	26818668	A	T	21	GENIC	homozygous	111011120
17	26824134	26824135	G	C	14	GENIC	homozygous	111011122
17	26824258	26824259	A	G	18	GENIC	homozygous	111011124
17	26825132	26825133	A	G	20	GENIC	homozygous	111011126
17	26825473	26825474	C	T	19	GENIC	homozygous	111011128
17	26825476	26825477	C	T	18	GENIC	homozygous	111011130
17	26825558	26825559	C	T	18	GENIC	homozygous	111011132
17	26824904	26824904		AC	17	GENIC	homozygous	129439376
17	26826697	26826697		TACCAACT	21	GENIC	homozygous	129439377
17	26826699	26826699		GCT	22	GENIC	homozygous	129439378
17	26827565	26827573	ATACATAC		3	GENIC	homozygous	129439379
17	26829848	26829980	GCTCCCACTGCCTGCTCACACCCAGTACACTGCGCTCCCGCTGCCTGCTCACACCCAGTACACTGTGCTCCCACTGCCTGCTCACACCCAGTACACTGTGCTCCCGCTGCCTGCTCACACCCAGTACACTGT		7	GENIC	homozygous	129439380
17	26830006	26830007	C	G	10	GENIC	homozygous	119271367
17	26830016	26830017	T	C	12	GENIC	heterozygous	119271368
17	26830188	26830188		T	19	GENIC	homozygous	129439381
17	26831822	26831823	A	G	31	GENIC	homozygous	111011134
17	26830095	26830096	G	T	29	GENIC	possibly homozygous	111445952