chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	84000517	84000518	A	T	14	GENIC	possibly homozygous	46543838
18	84000598	84000599	T	C	10	GENIC	homozygous	46543839
18	84000694	84000695	T	C	7	GENIC	homozygous	46543840
18	84000727	84000729	TT	--	4	GENIC	homozygous	46543841
18	84000750	84000752	TT	--	2	GENIC	homozygous	46543842
18	84000948	84000949	C	A	1	GENIC	homozygous	46543843
18	84001185	84001186	G	C	11	GENIC	homozygous	46543844
18	84001395	84001396	A	T	10	GENIC	heterozygous	46543845
18	84001396	84001397	A	T	11	GENIC	heterozygous	46543846
18	84001474	84001475	G	C	8	GENIC	homozygous	46543847
18	84001589	84001590	A	AAT	7	GENIC	homozygous	46543848
18	84001895	84001896	A	AT	16	GENIC	possibly homozygous	46543849
18	84002039	84002040	A	-	7	GENIC	homozygous	46543850
18	84002085	84002086	C	T	7	GENIC	homozygous	46543851
18	84002821	84002822	A	G	12	GENIC	heterozygous	46543852
18	84002913	84002914	A	G	8	GENIC	homozygous	46543853
18	84003067	84003068	G	A	16	GENIC	possibly homozygous	46543854
18	84003303	84003304	T	G	1	GENIC	homozygous	46543855
18	84003305	84003306	C	-	1	GENIC	homozygous	46543856