chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50526172	50526173	C	CAT	19	GENIC	homozygous	52625945
8	50526178	50526179	T	C	19	GENIC	homozygous	52625947
8	50526553	50526554	T	TTG	21	GENIC	homozygous	52625949
8	50526658	50526659	T	TTGTGTG	2	GENIC	homozygous	53386002