chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26322005	26322006	C	T	15	GENIC	homozygous	50147535
12	26322628	26322630	TT	--	38	GENIC	heterozygous	50147539
12	26322629	26322630	T	-	38	GENIC	heterozygous	50147540
12	26322686	26322687	A	T	35	GENIC	homozygous	50147542
12	26323097	26323098	A	C	39	GENIC	homozygous	50147544
12	26323265	26323266	G	-	46	GENIC	homozygous	50147548
12	26323970	26323971	T	C	34	GENIC	homozygous	50147550
12	26324285	26324286	C	T	35	GENIC	homozygous	50147552
12	26325403	26325404	C	G	40	GENIC	possibly homozygous	50147554
12	26325626	26325631	TTTTT	-----	6	GENIC	heterozygous	50147556
12	26326225	26326226	T	C	29	GENIC	homozygous	50147558
12	26326415	26326416	A	G	44	GENIC	homozygous	50147560
12	26326905	26326906	A	C	33	GENIC	homozygous	50147562
12	26328596	26328597	G	T	48	GENIC	possibly homozygous	50147564
12	26329440	26329441	T	C	38	GENIC	homozygous	50147566
12	26329635	26329636	T	-	33	GENIC	homozygous	50147568
12	26333171	26333172	C	T	36	GENIC	homozygous	50147570
12	26333453	26333454	G	A	37	GENIC	homozygous	50147572
12	26333483	26333484	C	T	43	GENIC	homozygous	50147574
12	26334167	26334168	T	C	34	GENIC	homozygous	50147576
12	26334825	26334826	C	A	52	GENIC	homozygous	50147578
12	26331353	26331354	C	T	38	GENIC	homozygous	50419556
12	26336017	26336018	T	TACAC	39	GENIC	homozygous	50147580