chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	33108099	33108100	T	C	46	GENIC	homozygous	112671662
15	33108452	33108453	G	A	39	GENIC	homozygous	112671664
15	33108614	33108615	C	T	38	GENIC	homozygous	112671666
15	33109092	33109095	CTC		40	GENIC	homozygous	131159116
15	33109571	33109573	CC		44	GENIC	homozygous	131159117
15	33109718	33109719	A	G	42	GENIC	homozygous	112671668
15	33110852	33110853	T	C	27	GENIC	homozygous	112671670
15	33111166	33111170	TCTT		30	GENIC	homozygous	131159118
15	33113360	33113361	C	T	54	GENIC	homozygous	112671672
15	33113444	33113445	G	A	56	GENIC	homozygous	112671674
15	33114678	33114679	T	A	40	GENIC	homozygous	112671676
15	33114088	33114089	C	T	59	GENIC	homozygous	112806787
15	33111269	33111270	T	C	41	GENIC	homozygous	112806785