chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	61694794	61694795	C	T	39	GENIC	possibly homozygous	117358709
9	61697178	61697179	T	G	30	GENIC	homozygous	117358710
9	61702380	61702381	C	T	38	GENIC	homozygous	117358711
9	61702524	61702525	T	C	31	GENIC	homozygous	117358712
9	61703519	61703520	C	T	36	GENIC	possibly homozygous	117358713
9	61706833	61706834	G	A	48	GENIC	homozygous	117358714
9	61707311	61707312	T	G	39	GENIC	heterozygous	117358715
9	61708519	61708520	C	T	36	GENIC	homozygous	117358716
9	61712172	61712173	C	T	55	GENIC	homozygous	117358717
9	61715402	61715403	A	G	37	GENIC	heterozygous	117358718
9	61715503	61715504	C	T	25	GENIC	heterozygous	117358719
9	61715667	61715668	A	G	30	GENIC	heterozygous	117358720
9	61719399	61719400	A	G	51	GENIC	heterozygous	117358725
9	61723758	61723759	A	G	44	GENIC	homozygous	117358726