chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	34289588	34289589	A	G	22	GENIC	homozygous	109688959
2	34290977	34290978	T	C	35	GENIC	homozygous	109688961
2	34291897	34291898	G	T	30	GENIC	homozygous	109688963
2	34292766	34292767	C	T	35	GENIC	homozygous	109688965
2	34294419	34294420	A	G	2	GENIC	homozygous	109688967
2	34294773	34294774	C	A	17	GENIC	homozygous	109688969
2	34296901	34296902	G	A	17	GENIC	homozygous	109688971
2	34297319	34297320	G	A	33	GENIC	homozygous	109688973
2	34299239	34299240	C	T	24	GENIC	homozygous	109688975
2	34300619	34300620	G	T	27	GENIC	homozygous	109688979
2	34300766	34300767	T	C	21	GENIC	homozygous	109688981
2	34300940	34300941	A	G	32	GENIC	homozygous	109688983
2	34303953	34303954	C	T	30	GENIC	homozygous	109688985
2	34304163	34304164	C	T	34	GENIC	homozygous	109688987
2	34305043	34305044	T	A	27	GENIC	homozygous	109688989
2	34311966	34311967	A	T	25	GENIC	homozygous	109688991
2	34312402	34312403	T	A	18	GENIC	homozygous	109688993
2	34312922	34312923	T	C	11	GENIC	homozygous	109688995