chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5459584	5459585	A	C	39	GENIC	homozygous	109078066
20	5460329	5460330	G	A	35	GENIC	homozygous	109390300
20	5461035	5461036	C	G	34	GENIC	possibly homozygous	109234069
20	5461226	5461227	T	C	28	GENIC	homozygous	109078074
20	5461370	5461371	T	G	32	GENIC	homozygous	109078076
20	5461632	5461633	C	T	24	GENIC	possibly homozygous	109390301
20	5461772	5461773	T	A	36	GENIC	possibly homozygous	109420464
20	5461924	5461925	T	C	41	GENIC	homozygous	109078078
20	5464254	5464255	T	A	21	GENIC	homozygous	109078080
20	5464507	5464508	T	C	29	GENIC	homozygous	109078084
20	5465595	5465596	G	A	44	GENIC	homozygous	109390306
20	5465949	5465950	A	T	38	GENIC	homozygous	109463151
20	5466167	5466168	C	T	23	GENIC	homozygous	109463152
20	5466597	5466598	G	A	41	GENIC	homozygous	109420466