chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5056908	5056909	G	A	17	GENIC	homozygous	109076241
20	5056922	5056923	C	T	16	GENIC	homozygous	109076243
20	5056951	5056952	A	G	17	GENIC	homozygous	109076245
20	5056957	5056958	C	T	17	GENIC	homozygous	109076247
20	5057311	5057312	C	T	24	GENIC	homozygous	109233770
20	5057339	5057340	G	A	28	GENIC	homozygous	109076249
20	5057419	5057420	T	C	29	GENIC	homozygous	109076251
20	5057603	5057604	T	G	19	GENIC	homozygous	109076253
20	5057833	5057834	G	A	25	GENIC	homozygous	109233771
20	5058174	5058175	G	A	20	GENIC	possibly homozygous	109233772
20	5058251	5058252	C	G	29	GENIC	homozygous	109076258
20	5058626	5058627	G	A	32	GENIC	homozygous	109233773
20	5058688	5058689	C	T	27	GENIC	homozygous	109233774
20	5058917	5058918	G	C	15	GENIC	homozygous	109076260
20	5059479	5059480	A	G	32	GENIC	homozygous	109076262
20	5059592	5059593	A	G	24	GENIC	homozygous	109233775
20	5059619	5059620	G	A	25	GENIC	homozygous	109076264
20	5059696	5059697	T	C	26	GENIC	homozygous	109076266
20	5060363	5060364	C	T	24	GENIC	homozygous	109233776