chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	123599390	123599391	C	T	54	GENIC	homozygous	116082471
7	123599399	123599400	T	C	50	GENIC	homozygous	116082472
7	123599415	123599416	C	T	39	GENIC	homozygous	116082473
7	123599420	123599421	C	T	42	GENIC	homozygous	116082474
7	123599707	123599708	A	G	55	GENIC	heterozygous	115863714
7	123599738	123599739	A	G	52	GENIC	possibly homozygous	115863718
7	123599749	123599750	C	T	54	GENIC	possibly homozygous	115863720
7	123599765	123599766	G	A	49	GENIC	homozygous	116082475
7	123600051	123600052	C	T	62	GENIC	heterozygous	115863724
7	123600485	123600486	C	G	56	GENIC	homozygous	116082476
7	123600610	123600611	C	T	49	GENIC	homozygous	115863728
7	123601433	123601434	T	C	60	GENIC	homozygous	115863730
7	123601878	123601879	G	T	47	GENIC	homozygous	116082477
7	123602044	123602045	A	G	55	GENIC	homozygous	115863736
7	123602354	123602355	C	A	52	GENIC	homozygous	115863738
7	123604361	123604362	A	G	48	GENIC	homozygous	115863742
7	123604744	123604745	C	T	45	GENIC	homozygous	116082478
7	123605417	123605418	C	T	25	GENIC	heterozygous	116082479
7	123607488	123607489	T	C	14	GENIC	heterozygous	116082480
7	123607492	123607493	T	C	15	GENIC	heterozygous	116082481