chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	116059955	116059956	C	CA	8	GENIC	possibly homozygous	45727517
X	116059955	116059956	C	CAA	8	GENIC	heterozygous	45727518
X	116059975	116059976	C	A	11	GENIC	homozygous	45200601
X	116060012	116060014	TT	--	3	GENIC	heterozygous	45200602
X	116060013	116060014	T	-	3	GENIC	heterozygous	45598161
X	116060596	116060597	A	AGTGTGTGTGTGTGTGT	8	GENIC	heterozygous	45788916
X	116060603	116060605	GT	--	8	GENIC	heterozygous	45817832
X	116062520	116062521	A	ATG	16	GENIC	homozygous	45817833
X	116062673	116062674	T	TGTGCTTGTGTGTGTGTGTGTGTGTGTGTGTTCATATGAGTAC	5	GENIC	heterozygous	45889534
X	116064252	116064253	T	C	18	GENIC	homozygous	45200612
X	116064948	116064949	C	CGTGTGT	2	GENIC	homozygous	45797666
X	116060601	116060605	GTGT	----	8	GENIC	heterozygous	45522227
X	116065411	116065412	A	-	9	GENIC	homozygous	45727522
X	116066902	116066903	G	GAC	7	GENIC	heterozygous	45634437
X	116066904	116066905	G	GAC	9	GENIC	possibly homozygous	45817834
X	116065151	116065152	A	ATG	5	GENIC	homozygous	45481652