chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5120505	5120506	A	G	25	GENIC	homozygous	109077024
20	5120516	5120517	C	T	23	GENIC	homozygous	109077028
20	5120550	5120551	C	T	14	GENIC	homozygous	109296835
20	5120569	5120570	A	G	17	GENIC	homozygous	109077029
20	5120645	5120646	A	G	14	GENIC	homozygous	109077031
20	5120791	5120792	G	A	26	GENIC	homozygous	109077033
20	5120891	5120892	C	G	26	GENIC	homozygous	109077037
20	5121310	5121311	C	T	19	GENIC	possibly homozygous	109296837
20	5121476	5121477	C	T	23	GENIC	homozygous	109077039
20	5122012	5122013	A	G	16	GENIC	homozygous	109077041
20	5122179	5122180	G	A	25	GENIC	homozygous	109077043
20	5122283	5122284	C	T	18	GENIC	homozygous	109077045
20	5122291	5122292	C	T	20	GENIC	homozygous	109296839
20	5122376	5122377	A	T	12	GENIC	homozygous	109077047
20	5122397	5122398	C	T	12	GENIC	homozygous	109077049
20	5122532	5122533	C	T	16	GENIC	homozygous	109077051
20	5122618	5122619	G	A	20	GENIC	homozygous	109077053
20	5122907	5122908	A	G	15	GENIC	homozygous	109077059
20	5123062	5123063	T	C	18	GENIC	homozygous	109077061