chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	113001632	113001634	TT	--	6	GENIC	homozygous	45197069
X	113001638	113001639	T	TGC	6	GENIC	homozygous	45197070
X	113001648	113001649	A	C	8	GENIC	homozygous	45197071
X	113001653	113001654	G	T	9	GENIC	homozygous	45197072
X	113001676	113001677	A	AGAG	11	GENIC	homozygous	45197073
X	113001678	113001679	A	AGAAGT	11	GENIC	homozygous	45521073
X	113001680	113001687	CACCCCC	-------	11	GENIC	homozygous	45521075
X	113001688	113001689	C	T	10	GENIC	homozygous	45521077
X	113006153	113006154	C	T	9	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	3	GENIC	heterozygous	45595068
X	113020742	113020743	C	CATGT	7	GENIC	homozygous	45197077
X	113022240	113022241	G	GT	10	GENIC	possibly homozygous	45197078
X	113025705	113025707	AC	--	1	GENIC	homozygous	45550712
X	113029087	113029089	AC	--	1	GENIC	homozygous	45573193
X	113032671	113032672	T	TTTGCCCGGAAACCGGGAAAGGGAATAACACTCGAAATGTATACAAGAAATACTCAAGTTAATAAAAAAAA	3	GENIC	homozygous	45481356
X	113038797	113038799	CT	--	3	GENIC	heterozygous	45550714
X	113039630	113039631	C	CT	13	GENIC	homozygous	45197079
X	113042986	113042987	T	TC	8	GENIC	homozygous	45197080
X	113050929	113050930	T	C	8	GENIC	heterozygous	45889076
X	113053253	113053255	TG	--	7	GENIC	heterozygous	45311835
X	113060883	113060884	C	-	6	GENIC	homozygous	45481358
X	113065201	113065203	AC	--	2	GENIC	homozygous	45595084
X	113082299	113082300	C	CGGTTAGGGGGATTTTGGTCTGGAAACAGGGAAG	1	GENIC	homozygous	45521088
X	113100084	113100086	AA	--	5	GENIC	heterozygous	45573195
X	113100085	113100086	A	-	5	GENIC	heterozygous	45550716