chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26322686	26322687	A	T	49	GENIC	homozygous	50147542
12	26323334	26323335	T	-	28	GENIC	homozygous	50298885
12	26323401	26323402	G	T	27	GENIC	possibly homozygous	50298887
12	26323407	26323408	G	T	24	GENIC	possibly homozygous	50298889
12	26323970	26323971	T	C	43	GENIC	homozygous	50147550
12	26325403	26325404	C	G	73	GENIC	homozygous	50147554
12	26325626	26325631	TTTTT	-----	16	GENIC	heterozygous	50147556
12	26326225	26326226	T	C	57	GENIC	homozygous	50147558
12	26326415	26326416	A	G	59	GENIC	possibly homozygous	50147560
12	26326905	26326906	A	C	71	GENIC	homozygous	50147562
12	26327304	26327306	GG	--	60	GENIC	homozygous	50298891
12	26328596	26328597	G	T	49	GENIC	possibly homozygous	50147564
12	26329440	26329441	T	C	49	GENIC	homozygous	50147566
12	26329634	26329635	A	AT	49	GENIC	homozygous	50298893
12	26329856	26329857	G	A	51	GENIC	possibly homozygous	50298895
12	26332375	26332376	G	A	47	GENIC	homozygous	50298897
12	26332744	26332745	C	T	58	GENIC	homozygous	50298899
12	26333315	26333316	G	A	41	GENIC	homozygous	50298901
12	26333453	26333454	G	A	61	GENIC	possibly homozygous	50147572
12	26334167	26334168	T	C	58	GENIC	homozygous	50147576
12	26334750	26334757	GACCTGT	-------	31	GENIC	homozygous	50298903
12	26334825	26334826	C	A	53	GENIC	possibly homozygous	50147578
12	26336017	26336018	T	TACAC	39	GENIC	homozygous	50147580