chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5469183	5469184	C	T	23	GENIC	homozygous	109234075
20	5469453	5469454	C	T	12	GENIC	homozygous	109234077
20	5469497	5469498	A	G	11	GENIC	homozygous	109078098
20	5469538	5469539	A	C	5	GENIC	homozygous	109371238
20	5469832	5469833	C	A	34	GENIC	homozygous	109234078
20	5469863	5469864	G	A	34	GENIC	homozygous	109234079
20	5471183	5471184	C	T	38	GENIC	homozygous	109371240
20	5472093	5472094	G	A	34	GENIC	homozygous	109078106
20	5472841	5472842	A	G	25	GENIC	possibly homozygous	109234080
20	5472857	5472858	G	C	23	GENIC	homozygous	109234081
20	5472889	5472890	C	T	25	GENIC	homozygous	109078108
20	5473246	5473247	T	C	28	GENIC	homozygous	109234082
20	5473992	5473993	T	C	34	GENIC	homozygous	109078112
20	5474155	5474156	G	A	28	GENIC	homozygous	109234083
20	5474167	5474168	G	T	28	GENIC	homozygous	109078114
20	5474203	5474204	G	A	28	GENIC	homozygous	109078116
20	5475701	5475702	C	A	21	GENIC	homozygous	109371242
20	5475846	5475847	A	G	21	GENIC	homozygous	109078118