chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	113000567	113000569	TG	--	1	GENIC	homozygous	45619290
X	113001632	113001634	TT	--	10	GENIC	homozygous	45197069
X	113001638	113001639	T	TGC	10	GENIC	homozygous	45197070
X	113001648	113001649	A	C	9	GENIC	homozygous	45197071
X	113001653	113001654	G	T	7	GENIC	homozygous	45197072
X	113001676	113001677	A	AGAG	10	GENIC	homozygous	45197073
X	113001678	113001679	A	AGAAGT	10	GENIC	homozygous	45521073
X	113001680	113001687	CACCCCC	-------	10	GENIC	homozygous	45521075
X	113001688	113001689	C	T	10	GENIC	homozygous	45521077
X	113006153	113006154	C	T	8	GENIC	homozygous	45521080
X	113006159	113006160	A	G	8	GENIC	homozygous	45197075
X	113006173	113006174	A	AC	6	GENIC	homozygous	45197076
X	113008983	113008984	G	GT	8	GENIC	heterozygous	45595068
X	113020742	113020743	C	CATGT	4	GENIC	homozygous	45197077
X	113022240	113022241	G	GT	10	GENIC	heterozygous	45197078
X	113039630	113039631	C	CT	11	GENIC	homozygous	45197079
X	113042986	113042987	T	TC	8	GENIC	homozygous	45197080
X	113022240	113022241	G	GTT	10	GENIC	heterozygous	45264863
X	113029087	113029089	AC	--	2	GENIC	heterozygous	45573193
X	113032671	113032672	T	TTTGCCCGGAAACCGGGAAAGGGAATAACACTCGAAATGTATACAAGAAATACTCAAGTTAATAAAAAAAA	6	GENIC	homozygous	45481356
X	113060883	113060884	C	-	8	GENIC	possibly homozygous	45481358
X	113079956	113079957	A	-	8	GENIC	heterozygous	45521086
X	113082299	113082300	C	CGGTTAGGGGGATTTTGGTCTGGAAACAGGGAAG	2	GENIC	homozygous	45521088
X	113097171	113097172	C	CA	7	GENIC	heterozygous	45264868