chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4579874	4579875	A	G	18	GENIC	homozygous	109074755
20	4581986	4581987	G	A	32	GENIC	homozygous	109074761
20	4582119	4582120	C	T	24	GENIC	homozygous	109074763
20	4582624	4582625	C	T	19	GENIC	homozygous	109233527
20	4582721	4582722	T	A	23	GENIC	homozygous	109074765
20	4582830	4582831	G	A	32	GENIC	homozygous	109074767
20	4582956	4582957	G	T	32	GENIC	homozygous	109074769
20	4582995	4582996	G	A	26	GENIC	possibly homozygous	109074771
20	4583257	4583258	C	T	24	GENIC	homozygous	109074773
20	4583468	4583469	C	A	33	GENIC	homozygous	109074775
20	4583562	4583563	G	T	22	GENIC	possibly homozygous	109074777
20	4586338	4586339	G	A	28	GENIC	homozygous	109074781
20	4586724	4586725	A	G	24	GENIC	homozygous	109074789
20	4586822	4586823	G	A	21	GENIC	homozygous	109296144
20	4587736	4587737	T	G	26	GENIC	homozygous	109296148
20	4588080	4588081	G	A	22	GENIC	homozygous	109329588
20	4588106	4588107	G	A	24	GENIC	homozygous	109329590
20	4589025	4589026	G	A	25	GENIC	homozygous	109074793
20	4589422	4589423	T	C	13	GENIC	possibly homozygous	109074797
20	4591221	4591222	C	T	20	GENIC	homozygous	109329592
20	4591761	4591762	G	A	32	GENIC	homozygous	109329594