chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	33139333	33139333		CAAGA	47	GENIC	homozygous	140387006
19	33139341	33139341		CTCTCCATAACAGG	44	GENIC	homozygous	140387007
19	33139642	33139643	A	G	34	GENIC	homozygous	140446777
19	33139753	33139754	G	A	34	GENIC	homozygous	140446778
19	33139847	33139847		TTGG	10	GENIC	homozygous	140387008
19	33140042	33140043	G	T	47	GENIC	homozygous	140446779
19	33140268	33140269	A	G	53	GENIC	homozygous	140446780
19	33140680	33140681	G	C	41	GENIC	homozygous	140446781
19	33141141	33141142	G		8	GENIC	homozygous	140387009
19	33141141	33141142	G	A	8	GENIC	heterozygous	404101097
19	33141144	33141145	G		8	GENIC	homozygous	140387010
19	33141144	33141145	G	A	8	GENIC	heterozygous	404101098
19	33141147	33141148	G	A	7	GENIC	homozygous	404571960
19	33141994	33141995	A	C	39	GENIC	possibly homozygous	140446782
19	33141995	33141996	A	T	39	GENIC	possibly homozygous	140446783
19	33142326	33142327	G	C	58	GENIC	homozygous	140446784