chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	140179068	140179069	T	C	49	GENIC	homozygous	69178650
7	140179069	140179070	T	C	49	GENIC	homozygous	69178651
7	140179682	140179683	A	G	46	GENIC	homozygous	69178652
7	140179761	140179762	G	T	32	GENIC	possibly homozygous	69178653
7	140179766	140179767	C	T	32	GENIC	possibly homozygous	69178654
7	140179792	140179793	C	T	28	GENIC	possibly homozygous	69178655
7	140179812	140179813	G	T	21	GENIC	possibly homozygous	69178656
7	140179818	140179819	T	A	20	GENIC	possibly homozygous	69178657
7	140179824	140179825	C	A	25	GENIC	heterozygous	69178658
7	140179837	140179838	T	C	22	GENIC	homozygous	69178659
7	140179838	140179839	G	A	22	GENIC	homozygous	69178660
7	140180453	140180454	T	C	90	GENIC	heterozygous	69178661
7	140180511	140180512	G	A	86	GENIC	heterozygous	69178662
7	140180523	140180524	C	T	80	GENIC	heterozygous	69178663
7	140180537	140180538	C	T	88	GENIC	heterozygous	69178664
7	140180568	140180569	C	T	76	GENIC	heterozygous	69178665
7	140180679	140180680	T	C	56	GENIC	heterozygous	69178666
7	140181496	140181497	T	C	36	GENIC	homozygous	69178667
7	140182372	140182373	G	T	43	GENIC	homozygous	69178668