chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25733929	25733930	A	T	13	GENIC	homozygous	50142671
12	25734265	25734266	C	CT	18	GENIC	heterozygous	50484314
12	25734282	25734283	A	G	15	GENIC	heterozygous	50142679
12	25734359	25734360	T	C	19	GENIC	homozygous	50296986
12	25734452	25734453	T	C	22	GENIC	homozygous	50142685
12	25734684	25734685	C	T	28	GENIC	homozygous	50142687
12	25734927	25734928	T	C	27	GENIC	homozygous	50142689
12	25735320	25735321	C	CA	5	GENIC	heterozygous	50539030
12	25736087	25736088	C	-	15	GENIC	homozygous	50142695
12	25736102	25736103	C	CG	16	GENIC	homozygous	50404322
12	25736917	25736918	A	G	24	GENIC	possibly homozygous	50142701
12	25736922	25736923	A	-	15	GENIC	possibly homozygous	50297000
12	25737166	25737169	GAA	---	19	GENIC	homozygous	50142703
12	25737620	25737621	T	TC	1	GENIC	homozygous	50142707
12	25737623	25737624	C	T	1	GENIC	homozygous	50614555
12	25737638	25737639	T	TTC	1	GENIC	homozygous	50142709
12	25738522	25738523	C	T	18	GENIC	homozygous	50484322
12	25739149	25739150	A	C	21	GENIC	homozygous	50484324
12	25739189	25739190	C	T	25	GENIC	homozygous	50297004
12	25739320	25739321	C	CAAAAAA	8	GENIC	homozygous	50142721
12	25740323	25740324	T	C	13	GENIC	homozygous	50142731
12	25740334	25740335	T	C	14	GENIC	homozygous	50142733
12	25740570	25740571	G	C	18	GENIC	homozygous	50297006