chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	107587188	107587189	A	G	58	GENIC	homozygous	116073734
7	107589389	107589390	G	A	43	GENIC	homozygous	116073736
7	107589794	107589795	C	T	40	GENIC	homozygous	116073738
7	107590151	107590152	T	G	47	GENIC	homozygous	118332046
7	107590152	107590153	G	T	47	GENIC	homozygous	118332048
7	107590154	107590155	C	A	49	GENIC	homozygous	118332050
7	107590155	107590156	C	G	49	GENIC	homozygous	116392954
7	107593587	107593588	G	A	54	GENIC	homozygous	116073740
7	107593814	107593815	T	C	55	GENIC	homozygous	115807770
7	107595323	107595324	T	C	39	GENIC	homozygous	115807772
7	107597099	107597100	G	A	50	GENIC	homozygous	116073742
7	107599156	107599157	G	A	43	GENIC	homozygous	116073746
7	107602599	107602600	A	G	42	GENIC	homozygous	116073748
7	107602721	107602722	A	G	52	GENIC	homozygous	115807780
7	107603946	107603947	C	T	63	GENIC	possibly homozygous	115807782
7	107593261	107593265	TTCA		51	GENIC	homozygous	131023360
7	107590953	107590954	T		54	GENIC	possibly homozygous	132656962
7	107600467	107600467		TTC	51	GENIC	homozygous	132656963