chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	107306459	107306461	TA	--	25	GENIC	homozygous	45328359
X	107306500	107306501	A	T	48	GENIC	homozygous	45328360
X	107307317	107307318	C	T	48	GENIC	homozygous	45328361
X	107307419	107307420	T	A	43	GENIC	homozygous	45328362
X	107308477	107308478	A	G	58	GENIC	possibly homozygous	45328363
X	107308554	107308555	T	G	68	GENIC	possibly homozygous	45328364
X	107308568	107308569	T	TA	52	GENIC	homozygous	45328365
X	107309201	107309202	C	A	42	GENIC	homozygous	45328366
X	107309593	107309594	T	TC	56	GENIC	homozygous	45192660
X	107309598	107309599	T	C	60	GENIC	possibly homozygous	45192661
X	107309727	107309728	C	CA	25	GENIC	homozygous	45192662
X	107309983	107309984	A	G	57	GENIC	possibly homozygous	45328367
X	107311859	107311860	C	T	61	GENIC	homozygous	45328368
X	107312819	107312820	C	T	46	GENIC	homozygous	45328369
X	107317511	107317512	A	T	19	GENIC	possibly homozygous	45328378
X	107313101	107313102	A	G	48	GENIC	homozygous	45328370
X	107315351	107315352	C	A	29	GENIC	homozygous	45328371
X	107315387	107315388	T	TC	30	GENIC	homozygous	45328372
X	107316951	107316952	C	T	47	GENIC	homozygous	45328373
X	107317051	107317052	T	C	42	GENIC	possibly homozygous	45328374
X	107317101	107317102	A	T	42	GENIC	homozygous	45328375
X	107317392	107317396	TGTT	----	34	GENIC	homozygous	45328376
X	107317451	107317452	T	C	23	GENIC	possibly homozygous	45328377
X	107317401	107317402	G	A	37	GENIC	heterozygous	45356171
X	107318079	107318080	G	C	55	GENIC	homozygous	45328379
X	107318222	107318223	C	T	45	GENIC	homozygous	45328380
X	107318376	107318377	T	-	55	GENIC	homozygous	45328381
X	107319504	107319505	A	G	27	GENIC	homozygous	45328382
X	107323219	107323220	A	C	57	GENIC	homozygous	45328383