chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	115761506	115761507	C	T	24	GENIC	homozygous	52826692
8	115762581	115762582	T	C	21	GENIC	possibly homozygous	52826694
8	115765168	115765169	T	-	1	GENIC	homozygous	53050710
8	115765572	115765573	G	A	22	GENIC	possibly homozygous	52826698
8	115766980	115766981	C	T	10	GENIC	possibly homozygous	52826701
8	115767195	115767196	A	T	8	GENIC	heterozygous	52826702
8	115767357	115767358	T	C	18	GENIC	possibly homozygous	52826703
8	115767612	115767613	T	C	24	GENIC	homozygous	52826704
8	115768827	115768830	TCT	---	14	GENIC	heterozygous	52826705
8	115769039	115769040	T	G	26	GENIC	homozygous	52826706
8	115769090	115769091	G	GCTGGAAGGTC	2	GENIC	homozygous	52826707
8	115769867	115769868	T	C	14	GENIC	homozygous	52826708
8	115771862	115771863	A	G	24	GENIC	homozygous	52826709
8	115772007	115772008	C	CA	3	GENIC	heterozygous	52826710
8	115772285	115772286	G	A	38	GENIC	possibly homozygous	52826711
8	115772876	115772877	T	C	13	GENIC	possibly homozygous	52826712
8	115775106	115775107	C	A	25	GENIC	possibly homozygous	52826714
8	115775284	115775285	C	T	20	GENIC	possibly homozygous	52826715
8	115775702	115775704	GT	--	1	GENIC	homozygous	52826716
8	115775872	115775873	G	A	21	GENIC	possibly homozygous	52826718
8	115775944	115775945	G	A	23	GENIC	possibly homozygous	52826719
8	115776245	115776246	C	T	28	GENIC	possibly homozygous	52826720
8	115776408	115776409	A	G	18	GENIC	heterozygous	52826721
8	115776409	115776410	T	C	17	GENIC	heterozygous	52826722
8	115776604	115776605	A	G	9	GENIC	homozygous	52826723
8	115777815	115777816	G	-	5	GENIC	homozygous	52826724
8	115778201	115778202	T	C	19	GENIC	homozygous	52826725
8	115778236	115778237	C	A	24	GENIC	homozygous	52826726
8	115778902	115778903	A	G	24	GENIC	homozygous	52826727