chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	26738390	26738391	T	G	21	GENIC	homozygous	47355898
16	26738946	26738947	T	C	51	GENIC	homozygous	47355899
16	26740682	26740683	G	A	45	GENIC	homozygous	47355900
16	26741832	26741833	C	T	27	GENIC	homozygous	47355901
16	26741946	26741947	T	-	19	GENIC	heterozygous	47355902
16	26741947	26741949	AA	--	10	GENIC	heterozygous	47355903
16	26741948	26741949	A	-	10	GENIC	heterozygous	47355904
16	26742812	26742813	A	C	50	GENIC	homozygous	47355905
16	26745512	26745513	G	A	30	GENIC	homozygous	47355906
16	26745646	26745647	C	CT	16	GENIC	possibly homozygous	47355907
16	26745753	26745754	A	-	1	GENIC	homozygous	47633565
16	26745902	26745903	G	C	10	GENIC	heterozygous	47355909
16	26747682	26747683	T	C	26	GENIC	homozygous	47355910
16	26748822	26748823	C	T	40	GENIC	possibly homozygous	47355911
16	26748874	26748875	C	G	42	GENIC	homozygous	47355912
16	26748909	26748910	C	A	49	GENIC	possibly homozygous	47355913
16	26748970	26748971	G	A	47	GENIC	homozygous	47355914
16	26749300	26749301	C	T	47	GENIC	possibly homozygous	47355915
16	26750006	26750007	C	T	39	GENIC	possibly homozygous	47355916
16	26750744	26750745	C	A	28	GENIC	homozygous	47355918
16	26751452	26751454	CA	--	45	GENIC	homozygous	47355919
16	26751516	26751517	T	G	48	GENIC	homozygous	47355920
16	26751853	26751854	T	TAC	18	GENIC	possibly homozygous	47355921
16	26751866	26751867	T	A	34	GENIC	heterozygous	47355922
16	26751866	26751867	T	TCACA	10	GENIC	heterozygous	47355923
16	26752095	26752096	T	C	51	GENIC	homozygous	47355924
16	26753162	26753163	A	G	49	GENIC	homozygous	47355925
16	26753187	26753188	T	C	52	GENIC	homozygous	47355926
16	26753281	26753282	T	C	61	GENIC	homozygous	47355927
16	26753587	26753588	T	C	51	GENIC	homozygous	47355928
16	26753596	26753597	C	-	51	GENIC	homozygous	47355929
16	26754728	26754729	G	A	51	GENIC	homozygous	47355930