chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	111887887	111887888	A	T	2	GENIC	homozygous	45550635
X	111887891	111887892	T	TGGTAGAGCG	3	GENIC	homozygous	45550637
X	111887893	111887894	T	TTG	3	GENIC	homozygous	45573151
X	111887897	111887898	A	AGCAAG	3	GENIC	homozygous	45573153
X	111887900	111887901	G	-	3	GENIC	homozygous	45573155
X	111891965	111891966	C	CA	10	GENIC	heterozygous	45195286
X	111893839	111893840	G	-	4	GENIC	homozygous	45195291
X	111895577	111895578	T	TA	14	GENIC	heterozygous	45195296
X	111899846	111899847	T	-	19	GENIC	homozygous	45195304
X	111899925	111899927	CA	--	10	GENIC	heterozygous	45520860
X	111901060	111901061	T	G	5	GENIC	homozygous	45195309
X	111901908	111901909	G	T	17	GENIC	homozygous	45195311
X	111902561	111902565	CACA	----	3	GENIC	heterozygous	45520862
X	111902563	111902565	CA	--	3	GENIC	heterozygous	45520864
X	111904539	111904541	AC	--	20	GENIC	heterozygous	45520866
X	111910906	111910907	T	TAA	3	GENIC	heterozygous	45195322
X	111918855	111918856	A	-	16	GENIC	heterozygous	45520868
X	111944105	111944106	T	-	10	INTERGENIC	heterozygous	45550639
X	111899923	111899927	CACA	----	10	GENIC	heterozygous	45594972