chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59771158	59771159	A	C	41	GENIC	heterozygous	134015665
8	59771164	59771165	A	C	41	GENIC	heterozygous	133964840
8	59771171	59771172	T	A	40	GENIC	heterozygous	133964841
8	59777571	59777572	T	C	53	GENIC	homozygous	116513164
8	59779155	59779156	T	C	61	GENIC	homozygous	116513166
8	59779942	59779943	G	T	73	GENIC	possibly homozygous	116513168
8	59781665	59781666	C	T	46	GENIC	homozygous	116513174
8	59782444	59782445	G	T	66	GENIC	homozygous	116513176
8	59782884	59782885	C	T	74	GENIC	homozygous	116513178
8	59783210	59783211	C	G	52	GENIC	homozygous	116513180
8	59783221	59783222	A	G	58	GENIC	homozygous	116513182
8	59783401	59783402	A	G	58	GENIC	homozygous	116513184
8	59783498	59783500	TC		44	GENIC	heterozygous	134061244
8	59783918	59783919	T	A	75	GENIC	homozygous	116513186
8	59784254	59784255	T	C	67	GENIC	homozygous	116513192
8	59784854	59784855	T	C	42	GENIC	possibly homozygous	134139051
8	59784922	59784923	C	A	60	GENIC	homozygous	116513194
8	59785172	59785173	T	C	55	GENIC	homozygous	116513198
8	59785184	59785185	T	C	58	GENIC	homozygous	116513200
8	59785508	59785509	C	T	49	GENIC	homozygous	116513202
8	59774845	59774846	C	T	49	GENIC	homozygous	118146249
8	59780189	59780190	C	T	62	GENIC	possibly homozygous	118146251
8	59778380	59778380		T	63	GENIC	homozygous	128595777
8	59778381	59778381		T	63	GENIC	homozygous	128595778