chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	47347534	47347535	A	G	12	GENIC	homozygous	46437760
18	47349596	47349597	T	C	16	GENIC	possibly homozygous	46437761
18	47349861	47349864	TTT	---	1	GENIC	homozygous	46437762
18	47350681	47350682	G	A	21	GENIC	possibly homozygous	46437765
18	47350749	47350750	G	A	15	GENIC	homozygous	46437766
18	47352637	47352638	A	G	19	GENIC	homozygous	46437768
18	47353659	47353660	G	A	14	GENIC	homozygous	46437770
18	47354647	47354648	G	A	18	GENIC	possibly homozygous	46437771
18	47355001	47355002	C	T	15	GENIC	homozygous	46437772
18	47356367	47356368	G	C	7	GENIC	homozygous	46437775
18	47356377	47356378	C	T	7	GENIC	homozygous	46437776
18	47356999	47357000	C	T	8	GENIC	homozygous	46437777
18	47357344	47357345	A	AG	8	GENIC	homozygous	46437778
18	47358621	47358622	G	T	21	GENIC	homozygous	46437779
18	47359065	47359066	A	T	1	GENIC	homozygous	46437780
18	47359357	47359358	A	G	7	GENIC	possibly homozygous	46437783
18	47359606	47359607	A	G	6	GENIC	homozygous	46437784
18	47361794	47361795	G	A	12	GENIC	heterozygous	46437788
18	47362309	47362311	CT	--	10	GENIC	homozygous	46437789
18	47364215	47364219	TTTG	----	2	GENIC	homozygous	46437792
18	47365252	47365253	G	A	7	GENIC	heterozygous	46437795
18	47367584	47367585	A	T	27	GENIC	homozygous	46437797
18	47368889	47368890	A	G	13	GENIC	possibly homozygous	46437799
18	47369419	47369420	C	CA	3	GENIC	homozygous	46437800
18	47371789	47371790	C	G	19	GENIC	possibly homozygous	46437808
18	47372228	47372229	C	T	21	GENIC	homozygous	46437809
18	47372320	47372321	A	G	16	GENIC	homozygous	46437810
18	47374121	47374122	C	G	12	GENIC	homozygous	46437811
18	47377277	47377278	T	-	17	GENIC	possibly homozygous	46437814
18	47383280	47383281	T	C	15	GENIC	homozygous	46437820
18	47384908	47384909	A	G	10	GENIC	possibly homozygous	46437821