chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120393432	120393433	G	A	47	GENIC	homozygous	115856040
7	120394124	120394125	T	C	26	GENIC	homozygous	115856042
7	120394877	120394878	A	G	47	GENIC	homozygous	115856044
7	120395692	120395693	C	T	29	GENIC	homozygous	115856046
7	120395790	120395791	A	G	23	GENIC	homozygous	115856048
7	120395896	120395897	A	G	17	GENIC	homozygous	115856050
7	120396479	120396480	A	G	24	GENIC	homozygous	115856052
7	120396571	120396572	G	C	28	GENIC	homozygous	115856056
7	120397035	120397036	C	T	49	GENIC	homozygous	115856058
7	120397110	120397111	T	C	41	GENIC	homozygous	115856060
7	120397353	120397354	A	G	29	GENIC	homozygous	115856062
7	120397963	120397964	A	G	20	GENIC	homozygous	115856064
7	120398405	120398406	G	A	31	GENIC	homozygous	115856066
7	120398897	120398898	C	T	38	GENIC	homozygous	115856068
7	120399459	120399460	G	A	31	GENIC	homozygous	116409449
7	120399932	120399933	T	C	35	GENIC	homozygous	115856070
7	120400980	120400981	T	C	26	GENIC	homozygous	115856072
7	120401106	120401107	T	C	17	GENIC	homozygous	115856074
7	120401127	120401128	T	G	15	GENIC	homozygous	115856076
7	120401624	120401625	T	C	35	GENIC	homozygous	115856078