chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115101969	115101971	AC	--	17	GENIC	homozygous	45312253
X	115113147	115113148	C	CT	9	GENIC	heterozygous	45198577
X	115113632	115113633	G	GT	8	GENIC	heterozygous	45198580
X	115113632	115113633	G	GTTTTTTTTTTTTT	8	GENIC	heterozygous	45521663
X	115122855	115122861	CACCAG	------	16	GENIC	homozygous	45198601
X	115125974	115125975	C	CTCTT	12	GENIC	possibly homozygous	45797604
X	115126885	115126886	C	CA	9	GENIC	heterozygous	45521669
X	115131886	115131887	A	-	11	INTERGENIC	heterozygous	45481513
X	115137092	115137093	G	-	8	INTERGENIC	heterozygous	45198644
X	115152129	115152130	A	AGTGT	8	GENIC	possibly homozygous	45312257
X	115155809	115155810	C	CT	5	GENIC	heterozygous	45521704
X	115156678	115156680	AC	--	18	GENIC	heterozygous	45521708
X	115160931	115160932	G	A	22	GENIC	heterozygous	45198719
X	115160969	115160970	G	-	22	GENIC	heterozygous	45198720
X	115163578	115163579	C	CA	4	INTERGENIC	heterozygous	45521710
X	115167695	115167699	TTTC	----	10	INTERGENIC	homozygous	45312260
X	115172819	115172820	A	C	9	INTERGENIC	heterozygous	45521725
X	115173894	115173895	T	-	3	INTERGENIC	heterozygous	45521727