chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	23916775	23916775		T	49	GENIC	homozygous	140383123
19	23917415	23917415		C	38	GENIC	homozygous	140383124
19	23917424	23917424		G	36	GENIC	homozygous	140383125
19	23917732	23917732		C	48	GENIC	homozygous	140383126
19	23918231	23918231		C	53	GENIC	homozygous	140383127
19	23918299	23918300	G		45	GENIC	homozygous	140383128
19	23918372	23918372		C	42	GENIC	homozygous	140383129
19	23918380	23918380		C	45	GENIC	homozygous	140383130
19	23918508	23918508		C	37	GENIC	homozygous	140383131
19	23918582	23918582		C	31	GENIC	homozygous	140383132
19	23918620	23918621	C		30	GENIC	homozygous	140383133
19	23918755	23918756	C		30	GENIC	homozygous	140383134
19	23918772	23918773	T		32	GENIC	homozygous	140383135
19	23918853	23918854	C	T	25	GENIC	homozygous	145072442
19	23918861	23918862	G	A	22	GENIC	homozygous	145072443
19	23918932	23918933	G		22	GENIC	homozygous	140383136
19	23919073	23919074	C		37	GENIC	homozygous	140383137
19	23919090	23919092	TG		38	GENIC	homozygous	140383138