chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	80461222	80461223	C	T	4	GENIC	homozygous	114776387
13	80462378	80462379	T	G	6	GENIC	homozygous	114776389
13	80462712	80462713	G	A	8	GENIC	homozygous	114405654
13	80465744	80465745	T	C	3	GENIC	homozygous	114405658
13	80465843	80465844	C	T	7	GENIC	homozygous	114900978
13	80466132	80466133	C	G	6	GENIC	homozygous	114900980
13	80466750	80466751	A	G	4	GENIC	homozygous	114405662
13	80467088	80467089	G	A	3	GENIC	homozygous	114900992
13	80468415	80468416	T	C	4	GENIC	homozygous	114901002
13	80469513	80469514	G	A	3	GENIC	homozygous	114901010
13	80469639	80469640	C	T	4	GENIC	homozygous	114405670
13	80470034	80470035	T	C	8	GENIC	homozygous	115119872
13	80470048	80470049	G	A	10	GENIC	homozygous	114405672
13	80470175	80470176	C	T	7	GENIC	homozygous	114405674
13	80470585	80470586	G	A	8	GENIC	homozygous	114901014
13	80471099	80471100	A	G	7	GENIC	homozygous	114901016
13	80471417	80471418	T	C	7	GENIC	homozygous	114405676
13	80472888	80472889	C	T	4	GENIC	homozygous	114405677
13	80474363	80474364	G	C	3	GENIC	homozygous	114405679
13	80478355	80478356	T	C	8	GENIC	homozygous	114566819
13	80468093	80468094	C	T	3	GENIC	homozygous	115184286
13	80468883	80468884	G	T	2	GENIC	homozygous	115184288
13	80475107	80475108	T	G	10	GENIC	homozygous	115184290
13	80476657	80476658	G	A	7	GENIC	homozygous	115184292
13	80483182	80483183	C	T	5	GENIC	homozygous	115184294
13	80469100	80469101	A	G	2	GENIC	homozygous	115221639