chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	50112631	50112632	C	-	12	GENIC	homozygous	46153383
19	50112642	50112643	T	C	9	GENIC	possibly homozygous	46408165
19	50112644	50112645	C	A	9	GENIC	possibly homozygous	46408167
19	50112647	50112648	C	A	8	GENIC	possibly homozygous	46153384
19	50113789	50113790	T	-	14	GENIC	heterozygous	46153389
19	50120411	50120412	G	GGT	4	GENIC	homozygous	46408171