chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5120505	5120506	A	G	32	GENIC	homozygous	109077024
20	5120516	5120517	C	T	38	GENIC	homozygous	109077028
20	5120520	5120521	C	T	36	GENIC	homozygous	109233849
20	5120569	5120570	A	G	36	GENIC	homozygous	109077029
20	5120645	5120646	A	G	43	GENIC	homozygous	109077031
20	5120791	5120792	G	A	55	GENIC	homozygous	109077033
20	5121476	5121477	C	T	36	GENIC	homozygous	109077039
20	5122012	5122013	A	G	41	GENIC	homozygous	109077041
20	5122062	5122063	A	G	49	GENIC	homozygous	109233850
20	5122179	5122180	G	A	49	GENIC	homozygous	109077043
20	5122376	5122377	A	T	39	GENIC	homozygous	109077047
20	5122397	5122398	C	T	32	GENIC	homozygous	109077049
20	5122532	5122533	C	T	24	GENIC	homozygous	109077051
20	5122618	5122619	G	A	30	GENIC	homozygous	109077053
20	5122643	5122644	G	A	28	GENIC	homozygous	109233851
20	5122730	5122731	G	A	23	GENIC	homozygous	109077055
20	5122907	5122908	A	G	50	GENIC	homozygous	109077059
20	5123062	5123063	T	C	35	GENIC	homozygous	109077061