chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	117446969	117446970	T	C	30	GENIC	homozygous	115847199
7	117447155	117447156	T	C	27	GENIC	homozygous	115847201
7	117448631	117448632	C	T	21	GENIC	homozygous	118512036
7	117449020	117449021	T	C	40	GENIC	homozygous	115847205
7	117449425	117449426	A	T	37	GENIC	homozygous	115847207
7	117450576	117450577	G	T	26	GENIC	possibly homozygous	116302151
7	117451328	117451329	T	A	23	GENIC	homozygous	115847213
7	117452131	117452132	C	T	25	GENIC	homozygous	116302153
7	117452864	117452865	A	G	26	GENIC	possibly homozygous	116302155
7	117453020	117453021	C	T	35	GENIC	homozygous	116302156
7	117453265	117453266	C	T	29	GENIC	possibly homozygous	118512037
7	117454020	117454021	G	A	13	GENIC	homozygous	118512038
7	117455617	117455618	C	T	11	GENIC	homozygous	118512039
7	117455753	117455754	C	T	25	GENIC	homozygous	118512040
7	117455900	117455901	G	A	36	GENIC	possibly homozygous	118512041
7	117456219	117456220	G	A	27	GENIC	homozygous	115847219
7	117457226	117457227	C	T	48	GENIC	possibly homozygous	116302163
7	117457472	117457473	C	T	48	GENIC	possibly homozygous	118512042
7	117459228	117459229	C	T	30	GENIC	homozygous	116302165
7	117463871	117463872	A	G	31	GENIC	homozygous	118512043
7	117464541	117464542	A	G	21	GENIC	homozygous	115847241
7	117465018	117465019	A	G	23	GENIC	homozygous	115847243
7	117465714	117465715	T	C	43	GENIC	homozygous	115847245
7	117465978	117465979	C	T	30	GENIC	homozygous	116302170
7	117466098	117466099	A	G	36	GENIC	homozygous	115847247
7	117469166	117469167	T	C	26	GENIC	homozygous	115847253
7	117469554	117469555	G	A	28	GENIC	homozygous	116302172