chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5063161	5063162	T	C	29	GENIC	homozygous	125176881
20	5063372	5063373	T	C	13	GENIC	homozygous	125176882
20	5063387	5063388	C	T	13	GENIC	homozygous	125200169
20	5063510	5063511	A	G	5	GENIC	homozygous	125200170
20	5063796	5063797	C	T	7	GENIC	heterozygous	125176884
20	5063893	5063894	A	G	21	GENIC	homozygous	125176885
20	5064074	5064075	G	C	5	GENIC	homozygous	125200171
20	5064078	5064079	C	T	4	GENIC	homozygous	125200172
20	5064083	5064084	C	A	4	GENIC	homozygous	125200173
20	5064498	5064499	C	G	6	GENIC	homozygous	125176887
20	5066280	5066281	C	G	7	GENIC	homozygous	125176897
20	5066921	5066922	T	G	10	GENIC	homozygous	125176899
20	5067129	5067130	C	T	15	GENIC	homozygous	125200174
20	5067365	5067366	A	G	11	GENIC	homozygous	125200175
20	5068268	5068269	A	G	6	GENIC	homozygous	125215791
20	5068274	5068275	C	G	8	GENIC	homozygous	125200176
20	5068853	5068854	T	G	22	GENIC	homozygous	125176922