chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	121351511	121351512	A	C	5	GENIC	homozygous	115858512
7	121351659	121351660	A	G	13	GENIC	homozygous	115858514
7	121351666	121351667	G	A	17	GENIC	homozygous	115858516
7	121352112	121352113	A	G	18	GENIC	homozygous	115858518
7	121352821	121352822	A	G	6	GENIC	homozygous	115858520
7	121354407	121354408	A	G	10	GENIC	homozygous	115858522
7	121354414	121354415	C	T	9	GENIC	homozygous	115858524
7	121354892	121354893	A	C	15	GENIC	homozygous	115858526
7	121355445	121355446	T	A	6	GENIC	homozygous	115858528
7	121357005	121357006	T	G	18	GENIC	homozygous	115858530
7	121364820	121364821	C	T	14	GENIC	homozygous	115858536
7	121365669	121365670	T	C	17	GENIC	homozygous	115858540
7	121367352	121367353	T	C	20	GENIC	homozygous	115858542
7	121367375	121367376	G	A	22	GENIC	homozygous	115858544
7	121369373	121369374	A	G	17	GENIC	homozygous	115858546
7	121370431	121370432	T	C	20	GENIC	homozygous	115858548
7	121370678	121370679	C	T	26	GENIC	homozygous	115858550
7	121371103	121371104	G	A	12	GENIC	homozygous	115858552
7	121372869	121372870	T	C	19	GENIC	homozygous	115858554
7	121373043	121373044	T	C	26	GENIC	possibly homozygous	115858556
7	121374131	121374132	A	G	22	GENIC	homozygous	115858558
7	121374767	121374768	C	T	6	GENIC	homozygous	115858560
7	121376233	121376234	T	C	21	GENIC	homozygous	115858562
7	121377740	121377741	C	T	22	GENIC	homozygous	115858564
7	121378332	121378333	T	C	33	GENIC	possibly homozygous	115858566
7	121379448	121379449	G	A	17	GENIC	homozygous	115858568
7	121380634	121380635	T	C	18	GENIC	homozygous	115858570
7	121382028	121382029	G	A	18	GENIC	homozygous	115858574