chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	64315672	64315673	C	T	25	GENIC	homozygous	110594928
18	64316431	64316432	A	G	28	GENIC	homozygous	110594930
18	64317232	64317233	C	T	22	GENIC	homozygous	110594932
18	64319666	64319667	C	T	32	GENIC	homozygous	110594934
18	64324771	64324772	T	A	22	GENIC	homozygous	110594936
18	64325042	64325043	T	C	23	GENIC	homozygous	110594938
18	64325924	64325925	A	T	23	GENIC	homozygous	110594940
18	64326395	64326396	A	G	21	GENIC	homozygous	110594942
18	64329816	64329817	T	G	14	GENIC	homozygous	110383267
18	64330424	64330425	C	T	18	GENIC	homozygous	110594944
18	64332357	64332358	C	A	18	GENIC	homozygous	110594946
18	64332435	64332436	T	A	21	GENIC	homozygous	110594948
18	64332527	64332528	C	T	33	GENIC	homozygous	110594950
18	64332569	64332570	T	C	31	GENIC	homozygous	110594952
18	64332599	64332600	A	C	27	GENIC	homozygous	110594954
18	64332668	64332669	C	T	40	GENIC	homozygous	110594956
18	64332985	64332986	C	T	31	GENIC	homozygous	110594958
18	64333003	64333004	A	C	32	GENIC	homozygous	110594960
18	64333277	64333278	T	C	23	GENIC	homozygous	110594962
18	64333594	64333595	C	T	16	GENIC	homozygous	110594964