chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	80461041	80461042	G	A	56	GENIC	homozygous	114690444
13	80465744	80465745	T	C	56	GENIC	homozygous	114405658
13	80461470	80461472	AA		46	GENIC	homozygous	131504773
13	80462079	80462080	C	G	41	GENIC	homozygous	114566815
13	80465263	80465264	C	T	54	GENIC	homozygous	114566816
13	80465991	80465992	G	A	58	GENIC	homozygous	114566817
13	80463372	80463373	T	G	27	GENIC	heterozygous	133433044
13	80466750	80466751	A	G	64	GENIC	homozygous	114405662
13	80469274	80469274		T	43	GENIC	homozygous	131504774
13	80469636	80469637	T	C	60	GENIC	homozygous	114405668
13	80469639	80469640	C	T	59	GENIC	homozygous	114405670
13	80470027	80470027		T	43	GENIC	homozygous	129078119
13	80470175	80470176	C	T	53	GENIC	homozygous	114405674
13	80470455	80470456	C	T	43	GENIC	homozygous	114566818
13	80471417	80471418	T	C	56	GENIC	homozygous	114405676
13	80472888	80472889	C	T	68	GENIC	homozygous	114405677
13	80474139	80474139		TG	29	GENIC	homozygous	129078121
13	80474363	80474364	G	C	50	GENIC	homozygous	114405679
13	80474649	80474649		A	30	GENIC	possibly homozygous	131504775
13	80474688	80474689	C	T	44	GENIC	homozygous	114405681
13	80474865	80474865		A	43	GENIC	possibly homozygous	129078122
13	80478355	80478356	T	C	55	GENIC	homozygous	114566819
13	80479341	80479341		T	26	GENIC	homozygous	131504776
13	80474591	80474597	TTTTTG		16	GENIC	heterozygous	133430777