chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	81767766	81767767	G	C	9	GENIC	homozygous	116529681
8	81768081	81768082	T	G	21	GENIC	homozygous	116529683
8	81768309	81768310	C	T	12	GENIC	homozygous	116529685
8	81769048	81769049	T	C	12	GENIC	homozygous	117928648
8	81769536	81769537	A	G	31	GENIC	homozygous	116529687
8	81771843	81771844	T	C	19	GENIC	homozygous	116529689
8	81771854	81771855	C	T	19	GENIC	homozygous	116529691
8	81773635	81773636	A	G	27	GENIC	homozygous	116529693
8	81773822	81773823	A	G	21	GENIC	homozygous	116529695
8	81778870	81778871	A	G	21	GENIC	homozygous	117928649
8	81780226	81780227	T	C	26	GENIC	homozygous	117928650
8	81783372	81783373	T	C	8	GENIC	homozygous	117928651
8	81783430	81783431	C	A	11	GENIC	homozygous	117113508
8	81784880	81784881	C	A	29	GENIC	homozygous	116529709
8	81785238	81785239	A	G	19	GENIC	homozygous	117928652
8	81788323	81788324	A	G	39	GENIC	homozygous	117928653
8	81789385	81789386	T	C	36	GENIC	homozygous	116529713
8	81789552	81789553	G	A	35	GENIC	homozygous	117928654
8	81790322	81790323	G	A	16	GENIC	homozygous	117928655
8	81790658	81790659	A	G	23	GENIC	homozygous	116529715
8	81792159	81792160	C	A	4	GENIC	homozygous	117928656
8	81792160	81792161	A	C	4	GENIC	homozygous	117928657
8	81794999	81795000	C	T	30	GENIC	homozygous	117928658