chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	71673650	71673651	C	CTT	5	GENIC	heterozygous	46629085
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	71689632	71689633	T	-	5	GENIC	heterozygous	46510911
18	71695535	71695536	T	-	15	GENIC	heterozygous	46668004
18	71695632	71695634	TG	--	4	GENIC	heterozygous	46510928
18	71698600	71698601	G	T	15	GENIC	possibly homozygous	46629088
18	71701085	71701087	GT	--	17	GENIC	heterozygous	46822000
18	71722278	71722279	G	A	27	GENIC	homozygous	46822003
18	71722279	71722280	C	CTCTT	27	GENIC	homozygous	46822004
18	71722281	71722282	T	TA	26	GENIC	homozygous	46822005
18	71722282	71722283	G	GTTATT	27	GENIC	homozygous	46822006
18	71722286	71722287	A	ATGGT	26	GENIC	homozygous	46822007
18	71722287	71722288	C	CTTGAGAGTGAGTAGCATATAAAGTTGT	26	GENIC	homozygous	46822008
18	71724759	71724760	A	-	10	GENIC	heterozygous	46822012
18	71726632	71726633	C	CT	11	GENIC	heterozygous	46510998
18	71726633	71726634	T	-	11	GENIC	heterozygous	46510999
18	71733692	71733694	AA	--	7	GENIC	heterozygous	46880421
18	71733693	71733694	A	-	7	GENIC	heterozygous	46830236