chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109904042	109904042		G	41	GENIC	homozygous	128860841
10	109904073	109904073		G	38	GENIC	homozygous	128860842
10	109904099	109904100	G		35	GENIC	homozygous	128860843
10	109904104	109904105	G	C	36	GENIC	homozygous	116843120
10	109904106	109904106		G	38	GENIC	homozygous	128860844
10	109904119	109904119		G	35	GENIC	homozygous	128860845
10	109904184	109904185	C		37	GENIC	homozygous	128860846
10	109904235	109904235		C	48	GENIC	homozygous	128860847
10	109904237	109904238	A		48	GENIC	homozygous	128860848
10	109904244	109904244		C	48	GENIC	homozygous	128860849
10	109904251	109904251		CC	52	GENIC	homozygous	128860850
10	109904290	109904291	A		49	GENIC	homozygous	128860851
10	109905640	109905641	A	G	39	GENIC	homozygous	116719306