chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	42096376	42096377	C	T	34	GENIC	homozygous	109703121
19	42096735	42096736	G	A	38	GENIC	homozygous	109817593
19	42097001	42097001		A	64	GENIC	homozygous	132235469
19	42097057	42097058	A	T	63	GENIC	homozygous	109817595
19	42097068	42097069	G	A	56	GENIC	homozygous	109817597
19	42097112	42097113	T	A	55	GENIC	homozygous	109817599
19	42097359	42097360	G	A	53	GENIC	homozygous	109817601
19	42097604	42097605	G	A	63	GENIC	homozygous	109817603
19	42097632	42097633	A	T	62	GENIC	homozygous	109817605
19	42097677	42097678	G	A	52	GENIC	homozygous	109817607
19	42098220	42098221	C	T	61	GENIC	homozygous	109817609
19	42099384	42099385	A	G	42	GENIC	homozygous	109817611
19	42099670	42099671	T	C	48	GENIC	homozygous	109817613
19	42100591	42100592	G	A	50	GENIC	homozygous	109817615
19	42097685	42097691	CAGAGG		59	GENIC	homozygous	129609579
19	42098676	42098677	G	A	46	GENIC	homozygous	132239465