chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	135664103	135664104	G	T	18	GENIC	homozygous	118845740
5	135664105	135664106	G	T	19	GENIC	homozygous	118858469
5	135664210	135664211	C	A	23	GENIC	heterozygous	119213628
5	135664804	135664805	C	T	25	GENIC	homozygous	114442540
5	135665105	135665106	G	T	12	GENIC	possibly homozygous	114442542
5	135666369	135666370	C	T	22	GENIC	homozygous	114442544
5	135668452	135668453	T	C	19	GENIC	homozygous	114442546
5	135669118	135669119	T	C	29	GENIC	homozygous	114144692
5	135669568	135669569	A	G	19	GENIC	homozygous	114018310
5	135669593	135669594	G	A	22	GENIC	homozygous	114144693
5	135669628	135669629	T	C	29	GENIC	homozygous	114144694
5	135669823	135669824	T	C	20	GENIC	homozygous	114144695
5	135669857	135669858	A	C	29	GENIC	homozygous	114144696
5	135672173	135672174	T	C	21	GENIC	homozygous	114144699
5	135673053	135673054	G	A	20	GENIC	homozygous	114144702
5	135673187	135673188	A	G	17	GENIC	homozygous	114144703
5	135673910	135673911	A	G	19	GENIC	homozygous	114144704
5	135673963	135673964	C	T	16	GENIC	homozygous	114442548
5	135674186	135674187	G	A	14	GENIC	homozygous	114442550
5	135674254	135674255	A	G	17	GENIC	homozygous	114144705
5	135674298	135674299	C	T	17	GENIC	homozygous	114144706
5	135674436	135674437	T	C	29	GENIC	homozygous	114144707
5	135674786	135674787	T	C	15	GENIC	homozygous	114144708
5	135674974	135674975	T	C	11	GENIC	homozygous	114144709
5	135675084	135675085	C	T	14	GENIC	homozygous	114144710