chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	121216039	121216040	T	C	75	GENIC	homozygous	116225113
7	121216540	121216541	T		53	GENIC	homozygous	131433743
7	121216978	121216979	G	A	50	GENIC	homozygous	118418033
7	121217552	121217553	A	G	51	GENIC	homozygous	118418034
7	121218065	121218066	A	G	62	GENIC	homozygous	118418035
7	121219627	121219628	T	G	54	GENIC	homozygous	116225115
7	121220402	121220404	AG		43	GENIC	homozygous	131433744
7	121221512	121221513	A	G	56	GENIC	possibly homozygous	116225116
7	121221952	121221953	A	G	55	GENIC	homozygous	116225117
7	121224631	121224632	G	A	42	GENIC	homozygous	118321938
7	121227221	121227222	A	G	43	GENIC	homozygous	115858114
7	121218535	121218536	A	G	45	GENIC	homozygous	115858106
7	121223317	121223318	C	T	46	GENIC	homozygous	115858110
7	121226093	121226094	A	G	48	GENIC	homozygous	115858112
7	121221329	121221329		AC	52	GENIC	homozygous	128512707
7	121227630	121227631	A	C	27	GENIC	homozygous	115858116
7	121228566	121228566		ACAGAC	46	GENIC	homozygous	128512708
7	121228748	121228752	GCCT		55	GENIC	homozygous	131433745
7	121229029	121229030	A	T	45	GENIC	homozygous	115858124
7	121229898	121229898		C	36	GENIC	homozygous	131433746
7	121231601	121231602	A	G	48	GENIC	homozygous	115858130