chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	51882760	51882761	T	A	19	GENIC	heterozygous	116490684
8	51885476	51885477	T	G	41	GENIC	homozygous	116490686
8	51901841	51901842	A	C	44	GENIC	homozygous	116490688
8	51901853	51901854	A	G	42	GENIC	homozygous	116490690
8	51901860	51901861	A	G	40	GENIC	homozygous	116490692
8	51901873	51901874	C	T	30	GENIC	homozygous	116490694
8	51901877	51901878	A	T	29	GENIC	homozygous	116490696
8	51902548	51902549	C	A	40	GENIC	homozygous	116490698
8	51902551	51902552	G	T	40	GENIC	possibly homozygous	116490700
8	51902559	51902560	G	T	33	GENIC	homozygous	116490702
8	51902675	51902676	G	T	4	GENIC	homozygous	116490704
8	51924482	51924483	T	C	46	GENIC	homozygous	116490706
8	51948605	51948606	T	C	49	GENIC	homozygous	116490708
8	51950779	51950780	G	A	22	GENIC	heterozygous	116490710
8	52003117	52003118	T	A	23	GENIC	homozygous	116490712
8	52003247	52003248	C	T	61	GENIC	homozygous	116490714
8	52007845	52007846	C	G	30	GENIC	homozygous	116490716
8	52007890	52007891	C	A	16	GENIC	homozygous	116490718
8	52007906	52007907	G	A	12	GENIC	homozygous	116490720
8	52007907	52007908	G	A	12	GENIC	homozygous	116490722
8	52068121	52068122	C	T	29	GENIC	homozygous	116490724
8	52072885	52072886	T	A	124	GENIC	heterozygous	116490726
8	52073156	52073157	A	G	3	GENIC	homozygous	116490727
8	52073167	52073168	C	T	3	GENIC	homozygous	116490729
8	52073168	52073169	A	G	3	GENIC	homozygous	116490731
8	52073200	52073201	A	T	6	GENIC	homozygous	116490733
8	52089954	52089955	C	T	41	GENIC	homozygous	116490735
8	52096225	52096226	T	A	34	GENIC	heterozygous	116490737