chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	129501912	129501913	G	A	14	GENIC	homozygous	54108861
7	129501942	129501943	A	G	16	GENIC	homozygous	54108862
7	129502762	129502763	A	G	19	GENIC	homozygous	54108864
7	129503510	129503511	G	T	15	GENIC	homozygous	54108865
7	129503570	129503571	G	A	19	GENIC	homozygous	54108866
7	129503775	129503776	C	T	11	GENIC	homozygous	54108867
7	129503952	129503953	C	T	14	GENIC	homozygous	54108868
7	129504033	129504034	T	C	12	GENIC	homozygous	54108869
7	129504153	129504154	A	-	11	GENIC	homozygous	54108870
7	129504193	129504194	T	-	14	GENIC	homozygous	54108871
7	129504226	129504227	G	T	16	GENIC	homozygous	54108872
7	129504250	129504251	C	A	21	GENIC	homozygous	54108873
7	129504265	129504266	T	TG	23	GENIC	homozygous	54108874
7	129504713	129504714	C	T	17	GENIC	homozygous	54108875
7	129505002	129505003	C	T	21	GENIC	homozygous	54108876
7	129505220	129505221	C	T	13	GENIC	homozygous	54108877
7	129505485	129505486	G	A	15	GENIC	homozygous	54108878
7	129505772	129505773	T	TC	14	GENIC	homozygous	54108879
7	129506029	129506030	G	A	12	GENIC	homozygous	54108880
7	129506082	129506083	A	G	11	GENIC	homozygous	54108881
7	129506448	129506449	G	A	13	GENIC	homozygous	54108882
7	129507673	129507674	T	C	18	GENIC	homozygous	54108883
7	129508151	129508153	AT	--	9	GENIC	homozygous	54108884