chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	78862027	78862028	G	C	52	GENIC	homozygous	117575812
9	78863346	78863347	A	G	52	GENIC	homozygous	117575816
9	78863517	78863518	T	C	48	GENIC	homozygous	117575818
9	78863664	78863664		T	40	GENIC	possibly homozygous	133210497
9	78864688	78864689	G	C	55	GENIC	homozygous	117575820
9	78866242	78866242		A	52	GENIC	homozygous	128726712
9	78869366	78869367	A	G	37	GENIC	homozygous	117575832
9	78869456	78869457	T		34	GENIC	homozygous	133210498
9	78871694	78871695	T	A	35	GENIC	homozygous	117575838
9	78875570	78875571	T	C	38	GENIC	homozygous	117575852
9	78875761	78875762	C	T	45	GENIC	homozygous	117594026
9	78868288	78868289	C		44	GENIC	homozygous	130773421
9	78869833	78869834	A	T	46	GENIC	homozygous	117847477
9	78875427	78875428	C	T	55	GENIC	possibly homozygous	117847478
9	78875744	78875745	T	A	45	GENIC	homozygous	117594020
9	78875754	78875755	G	C	47	GENIC	homozygous	117594022
9	78875759	78875760	G	A	46	GENIC	homozygous	117594024
9	78875766	78875767	C	A	48	GENIC	homozygous	117594028
9	78875891	78875892	C	A	45	GENIC	homozygous	117847479
9	78876183	78876184	G	A	18	GENIC	homozygous	132688115