chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	41676594	41676595	G	T	23	GENIC	homozygous	109889717
19	41679526	41679527	T	C	69	GENIC	heterozygous	109976997
19	41679572	41679573	C	A	77	GENIC	heterozygous	109976999
19	41679653	41679654	C	T	66	GENIC	heterozygous	109977003
19	41679719	41679720	C	T	54	GENIC	heterozygous	109977005
19	41679765	41679766	G	A	56	GENIC	heterozygous	109977009
19	41679888	41679889	C	A	38	GENIC	heterozygous	109977011
19	41680036	41680039	TAT		37	GENIC	homozygous	129609390
19	41679389	41679390	C	T	56	GENIC	heterozygous	109702383
19	41679957	41679963	TGGGGG		12	GENIC	heterozygous	129609388
19	41680034	41680034		G	32	GENIC	homozygous	129609389
19	41680054	41680054		G	47	GENIC	homozygous	129609391
19	41680058	41680059	A		46	GENIC	homozygous	129609392
19	41680092	41680092		CTTGCCA	45	GENIC	homozygous	129609393
19	41680096	41680096		TGGG	45	GENIC	homozygous	129609394
19	41680122	41680122		T	46	GENIC	homozygous	129609395
19	41680143	41680144	C		39	GENIC	homozygous	129609396
19	41680163	41680163		C	46	GENIC	homozygous	129609397
19	41680088	41680089	G	A	45	GENIC	homozygous	109782225
19	41680089	41680090	G	A	45	GENIC	homozygous	109817114