chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	86948911	86948912	T	C	20	GENIC	homozygous	108882976
1	86949424	86949425	C	T	17	GENIC	homozygous	120560196
1	86951763	86951764	T	C	25	GENIC	homozygous	108882981
1	86951985	86951986	C	T	17	GENIC	homozygous	120869394
1	86954218	86954219	G	A	24	GENIC	possibly homozygous	120560198
1	86954679	86954680	G	T	20	GENIC	homozygous	108882988
1	86955974	86955975	G	T	16	GENIC	possibly homozygous	120560200
1	86959347	86959348	G	A	8	GENIC	homozygous	120869395
1	86960803	86960804	G	A	23	GENIC	homozygous	120560202
1	86952596	86952596		T	14	GENIC	homozygous	131259587
1	86959942	86959950	CTGACTGA		21	GENIC	homozygous	131259588
1	86963237	86963238	A	G	19	GENIC	homozygous	108883006
1	86963497	86963498	A	C	19	GENIC	homozygous	108883007
1	86963503	86963504	T	C	19	GENIC	homozygous	108883008
1	86963527	86963527		G	15	GENIC	homozygous	131259589
1	86965707	86965708	T	G	15	GENIC	homozygous	120560204
1	86965793	86965794	C	T	15	GENIC	homozygous	120560206
1	86966390	86966391	G	A	25	GENIC	homozygous	120560208
1	86966523	86966524	A	G	24	GENIC	homozygous	108883009
1	86968484	86968485	G	C	26	GENIC	homozygous	108883010
1	86969333	86969334	T	C	15	GENIC	homozygous	108883011
1	86969828	86969828		TATG	13	GENIC	homozygous	131259590
1	86971587	86971588	C	A	22	GENIC	homozygous	108883012
1	86971760	86971761	T	C	15	GENIC	homozygous	108883013
1	86971793	86971794	T	C	16	GENIC	homozygous	108883014