chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115415440	115415441	A	G	34	GENIC	homozygous	45199596
X	115415853	115415854	A	G	37	GENIC	homozygous	45199597
X	115416058	115416059	C	T	44	GENIC	homozygous	45199598
X	115416159	115416160	T	C	41	GENIC	homozygous	45199599
X	115418477	115418480	TGC	---	19	GENIC	homozygous	45199600
X	115419256	115419257	G	A	28	GENIC	homozygous	45199601
X	115419611	115419612	C	T	34	GENIC	possibly homozygous	45199602
X	115419627	115419628	C	G	28	GENIC	homozygous	45199603
X	115419834	115419835	T	C	44	GENIC	possibly homozygous	45199604
X	115419894	115419895	A	G	40	GENIC	homozygous	45199605
X	115421241	115421242	C	T	34	GENIC	homozygous	45199606
X	115421396	115421397	T	C	27	GENIC	homozygous	45199607
X	115422482	115422483	G	A	26	GENIC	possibly homozygous	45199609
X	115422839	115422840	C	CAAAAAAAA	2	GENIC	homozygous	45199610
X	115422896	115422899	CTT	---	15	GENIC	homozygous	45199611
X	115423317	115423318	A	C	44	GENIC	homozygous	45199612