chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25733929	25733930	A	T	35	GENIC	homozygous	50142671
12	25734096	25734097	C	T	34	GENIC	homozygous	50142673
12	25734262	25734263	G	GC	29	GENIC	heterozygous	50142677
12	25734282	25734283	A	G	36	GENIC	heterozygous	50142679
12	25734320	25734321	A	G	34	GENIC	heterozygous	50142683
12	25734452	25734453	T	C	40	GENIC	homozygous	50142685
12	25734684	25734685	C	T	46	GENIC	homozygous	50142687
12	25734927	25734928	T	C	36	GENIC	homozygous	50142689
12	25734928	25734929	G	A	36	GENIC	homozygous	50142691
12	25736087	25736088	C	-	16	GENIC	homozygous	50142695
12	25736132	25736133	G	GAAAA	16	GENIC	possibly homozygous	50142697
12	25736132	25736133	G	GAAA	16	GENIC	heterozygous	50142699
12	25736917	25736918	A	G	29	GENIC	heterozygous	50142701
12	25737166	25737169	GAA	---	29	GENIC	homozygous	50142703
12	25737618	25737620	TT	--	6	GENIC	homozygous	50142705
12	25737620	25737621	T	TC	8	GENIC	heterozygous	50142707
12	25737638	25737639	T	TTC	6	GENIC	homozygous	50142709
12	25737700	25737701	T	C	22	GENIC	homozygous	50142711
12	25737989	25737990	C	G	34	GENIC	homozygous	50142713
12	25738041	25738042	G	A	44	GENIC	homozygous	50142715
12	25738490	25738491	G	A	48	GENIC	homozygous	50142717
12	25738943	25738944	A	G	39	GENIC	homozygous	50142719
12	25739320	25739321	C	CAAAAAA	9	GENIC	homozygous	50142721
12	25739324	25739325	G	GA	12	GENIC	possibly homozygous	50142723
12	25739327	25739328	A	AAAG	15	GENIC	heterozygous	50142725
12	25739340	25739341	C	A	20	GENIC	homozygous	50142727
12	25740082	25740083	C	T	49	GENIC	homozygous	50142729
12	25740323	25740324	T	C	30	GENIC	homozygous	50142731
12	25740334	25740335	T	C	25	GENIC	homozygous	50142733