chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	41676594	41676595	G	T	21	GENIC	possibly homozygous	109889717
19	41680054	41680054		G	34	GENIC	homozygous	129609391
19	41680034	41680034		G	31	GENIC	homozygous	129609389
19	41680036	41680039	TAT		31	GENIC	homozygous	129609390
19	41680058	41680059	A		34	GENIC	homozygous	129609392
19	41680092	41680092		CTTGCCA	37	GENIC	homozygous	129609393
19	41680096	41680096		TGGG	39	GENIC	homozygous	129609394
19	41680122	41680122		T	42	GENIC	homozygous	129609395
19	41680143	41680144	C		46	GENIC	homozygous	129609396
19	41680163	41680163		C	48	GENIC	homozygous	129609397
19	41680088	41680089	G	A	34	GENIC	homozygous	109782225
19	41680089	41680090	G	A	34	GENIC	homozygous	109817114