chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	116842507	116842508	C	T	35	GENIC	homozygous	54076698
7	116842792	116842793	A	T	20	GENIC	homozygous	54920732
7	116843165	116843166	G	T	36	GENIC	homozygous	54076699
7	116843590	116843591	C	T	39	GENIC	homozygous	54076700
7	116844718	116844719	C	T	50	GENIC	homozygous	54076701
7	116844795	116844796	T	C	44	GENIC	homozygous	54076702
7	116845276	116845277	C	T	32	GENIC	homozygous	54076703
7	116846268	116846269	G	GA	20	GENIC	homozygous	54076704
7	116846285	116846286	A	-	27	GENIC	possibly homozygous	54076706
7	116846286	116846287	A	C	29	GENIC	possibly homozygous	54920734
7	116847057	116847058	A	-	35	GENIC	homozygous	54076707
7	116847164	116847165	C	CT	27	GENIC	homozygous	54076708
7	116847340	116847341	G	GT	21	GENIC	possibly homozygous	54076709