chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	69012988	69012989	T	A	48	GENIC	homozygous	71537746
4	69013196	69013197	C	T	33	GENIC	homozygous	70798263
4	69013256	69013257	C	G	29	GENIC	homozygous	71537748
4	69013415	69013416	C	A	40	GENIC	homozygous	71537750
4	69013416	69013417	C	T	40	GENIC	homozygous	71537752
4	69013521	69013522	A	G	53	GENIC	possibly homozygous	71537754
4	69013628	69013629	A	G	44	GENIC	homozygous	71537755
4	69013750	69013751	C	T	54	GENIC	homozygous	71537757
4	69013990	69013991	C	A	48	GENIC	homozygous	71537759
4	69014053	69014054	G	C	35	GENIC	homozygous	71537761
4	69014089	69014090	A	C	37	GENIC	homozygous	71537763
4	69014213	69014214	C	G	29	GENIC	homozygous	71537765
4	69014477	69014478	C	A	77	GENIC	homozygous	71537767
4	69014508	69014509	G	A	82	GENIC	homozygous	70798266
4	69014589	69014590	A	G	70	GENIC	heterozygous	71537769
4	69014882	69014883	C	T	27	GENIC	homozygous	71537771
4	69015004	69015005	A	G	41	GENIC	homozygous	71537773
4	69015041	69015042	A	G	48	GENIC	homozygous	71537775
4	69015144	69015145	G	A	67	GENIC	homozygous	71537777
4	69015229	69015230	G	A	50	GENIC	heterozygous	71537779