chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	71673650	71673651	C	CTT	8	GENIC	heterozygous	46629085
18	71673651	71673652	T	-	8	GENIC	heterozygous	46629086
18	71674856	71674857	A	G	34	GENIC	homozygous	46510871
18	71680101	71680102	T	TTGTGTGTGTG	10	GENIC	homozygous	46833281
18	71681721	71681723	GA	--	1	GENIC	homozygous	46821994
18	71681724	71681725	G	GCTT	1	GENIC	homozygous	46821995
18	71681729	71681730	A	AGG	1	GENIC	homozygous	46510890
18	71681737	71681738	G	GCTCTACCAC	4	GENIC	homozygous	46821996
18	71689632	71689633	T	-	7	GENIC	heterozygous	46510911
18	71690452	71690453	A	AT	21	GENIC	possibly homozygous	46969127
18	71695631	71695632	C	CTGTGTGTGTG	10	GENIC	homozygous	46821999
18	71696951	71696952	A	G	23	GENIC	homozygous	46969128
18	71698600	71698601	G	T	11	GENIC	possibly homozygous	46629088
18	71699682	71699683	C	CGTGTGT	10	GENIC	homozygous	46888411
18	71701085	71701087	GT	--	7	GENIC	possibly homozygous	46822000
18	71722278	71722279	G	A	42	GENIC	homozygous	46822003
18	71722279	71722280	C	CTCTT	42	GENIC	homozygous	46822004
18	71722281	71722282	T	TA	43	GENIC	homozygous	46822005
18	71722282	71722283	G	GTTATT	43	GENIC	homozygous	46822006
18	71722286	71722287	A	ATGGT	43	GENIC	homozygous	46822007
18	71722287	71722288	C	CTTGAGAGTGAGTAGCATATAAAGTTGT	43	GENIC	homozygous	46822008
18	71723790	71723791	G	C	16	GENIC	homozygous	46510991
18	71723989	71723990	A	-	8	GENIC	homozygous	46822009
18	71723992	71723996	CATT	----	9	GENIC	homozygous	46822010
18	71723999	71724000	G	GTGGT	5	GENIC	homozygous	46822011
18	71724759	71724760	A	-	15	GENIC	heterozygous	46822012
18	71724745	71724746	A	G	17	GENIC	homozygous	46510995
18	71724758	71724760	AA	--	15	GENIC	heterozygous	46510996
18	71732292	71732293	C	CT	9	GENIC	heterozygous	46511003
18	71732293	71732294	T	-	9	GENIC	heterozygous	46830235
18	71732461	71732462	G	GTGTGTC	3	GENIC	heterozygous	46969129
18	71733692	71733694	AA	--	10	GENIC	heterozygous	46880421
18	71733693	71733694	A	-	10	GENIC	heterozygous	46830236