chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50526172	50526173	C	CAT	37	GENIC	homozygous	52625945
8	50526178	50526179	T	C	37	GENIC	homozygous	52625947
8	50526553	50526554	T	TTG	29	GENIC	homozygous	52625949