chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	81935918	81935919	C	T	12	GENIC	possibly homozygous	52680746
8	81936123	81936124	G	T	12	GENIC	homozygous	52680748
8	81936381	81936382	G	A	4	GENIC	heterozygous	52680753
8	81936548	81936549	T	C	16	GENIC	possibly homozygous	52680756
8	81937378	81937379	A	G	25	GENIC	homozygous	52680758
8	81937611	81937612	C	T	18	GENIC	homozygous	52680759
8	81938346	81938347	G	T	22	GENIC	possibly homozygous	52680762
8	81939715	81939716	C	A	17	GENIC	homozygous	52680767
8	81939967	81939968	G	GAAAA	2	GENIC	heterozygous	52680769
8	81940016	81940017	C	G	8	GENIC	homozygous	53401130
8	81941015	81941016	C	T	29	GENIC	homozygous	53401131
8	81944402	81944403	A	G	13	GENIC	homozygous	52680772
8	81944573	81944574	A	-	8	GENIC	homozygous	52680773
8	81945982	81945983	T	C	26	GENIC	possibly homozygous	52680776
8	81946053	81946054	G	A	32	GENIC	possibly homozygous	52680778
8	81946624	81946625	A	G	23	GENIC	possibly homozygous	52680779
8	81947653	81947654	C	A	10	GENIC	possibly homozygous	52680781
8	81948475	81948476	T	-	12	GENIC	homozygous	52680782
8	81948672	81948673	A	G	31	GENIC	homozygous	52680784
8	81949897	81949905	AAAGAAAG	--------	1	GENIC	homozygous	53401134
8	81951323	81951324	C	T	7	GENIC	possibly homozygous	52680794
8	81951451	81951452	T	TG	7	GENIC	heterozygous	52680796
8	81952860	81952861	G	T	33	GENIC	homozygous	52680797