chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	80461041	80461042	G	A	56	GENIC	homozygous	114690444
13	80461470	80461472	AA		66	GENIC	homozygous	131504773
13	80462079	80462080	C	G	48	GENIC	homozygous	114566815
13	80465263	80465264	C	T	53	GENIC	homozygous	114566816
13	80465744	80465745	T	C	67	GENIC	homozygous	114405658
13	80465991	80465992	G	A	58	GENIC	homozygous	114566817
13	80466750	80466751	A	G	47	GENIC	homozygous	114405662
13	80469274	80469274		T	50	GENIC	homozygous	131504774
13	80469636	80469637	T	C	50	GENIC	homozygous	114405668
13	80469639	80469640	C	T	49	GENIC	homozygous	114405670
13	80470027	80470027		T	63	GENIC	homozygous	129078119
13	80470175	80470176	C	T	62	GENIC	homozygous	114405674
13	80470455	80470456	C	T	46	GENIC	homozygous	114566818
13	80471417	80471418	T	C	46	GENIC	homozygous	114405676
13	80472888	80472889	C	T	54	GENIC	homozygous	114405677
13	80474139	80474139		TG	42	GENIC	homozygous	129078121
13	80474363	80474364	G	C	45	GENIC	homozygous	114405679
13	80474649	80474649		A	25	GENIC	homozygous	131504775
13	80474688	80474689	C	T	41	GENIC	homozygous	114405681
13	80474865	80474865		A	66	GENIC	homozygous	129078122
13	80478355	80478356	T	C	59	GENIC	homozygous	114566819
13	80479341	80479341		T	46	GENIC	possibly homozygous	131504776