chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	61082329	61082330	A	G	9	GENIC	homozygous	112355776
16	61083241	61083242	G	A	15	GENIC	homozygous	112005882
16	61083675	61083676	T	C	21	GENIC	homozygous	112005884
16	61084065	61084066	A	G	9	GENIC	homozygous	112355778
16	61084164	61084165	A	G	11	GENIC	homozygous	112005886
16	61084311	61084312	A	G	16	GENIC	homozygous	112005888
16	61085482	61085483	C	A	8	GENIC	homozygous	112005892
16	61085947	61085948	T	G	9	GENIC	homozygous	112005894
16	61086031	61086032	C	T	10	GENIC	homozygous	112005896
16	61086151	61086152	G	A	12	GENIC	homozygous	112005900
16	61086279	61086280	T	G	18	GENIC	homozygous	112005902
16	61086393	61086394	G	A	19	GENIC	homozygous	112005904
16	61086676	61086677	C	T	12	GENIC	homozygous	112005906
16	61086751	61086752	T	C	26	GENIC	homozygous	112005908
16	61086834	61086835	C	T	11	GENIC	homozygous	112005910
16	61087062	61087063	G	A	13	GENIC	homozygous	112005912
16	61087105	61087106	A	G	11	GENIC	homozygous	112005914
16	61087260	61087261	T	C	21	GENIC	homozygous	112005916
16	61088084	61088085	G	A	7	GENIC	homozygous	112355780
16	61088687	61088688	T	C	7	GENIC	homozygous	112005924