chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	13527032	13527032		AGGCGAA	18	GENIC	homozygous	129721498
X	13527352	13527353	C	A	7	GENIC	possibly homozygous	119903651
X	13527384	13527385	C		7	GENIC	homozygous	129721499
X	13527390	13527390		A	7	GENIC	homozygous	129721500
X	13527695	13527696	C	A	20	GENIC	possibly homozygous	108229260
X	13553316	13553317	G	A	16	GENIC	homozygous	108369399
X	13557818	13557819	C	A	21	GENIC	homozygous	108369401
X	13561084	13561085	G	A	15	GENIC	homozygous	108470684
X	13546696	13546697	A	G	23	GENIC	homozygous	108561926
X	13563522	13563523	C	T	27	GENIC	homozygous	108561930
X	13555086	13555086		G	7	GENIC	homozygous	130718803
X	13562788	13562789	A	T	5	GENIC	heterozygous	132253934
X	13578532	13578533	G	A	18	GENIC	homozygous	108561933
X	13583440	13583441	G	A	21	GENIC	homozygous	108561935
X	13594335	13594336	C	T	5	GENIC	homozygous	120785881
X	13594413	13594414	T	C	9	GENIC	homozygous	129808182
X	13594417	13594418	T	C	9	GENIC	homozygous	129808183
X	13594614	13594614		TCTGTATTTGCTGTATTCTGGCTGTGTCTCTCAGGAGAGATCTACATCCGGTTCCTG	2	GENIC	homozygous	129721529
X	13596538	13596538		A	17	GENIC	homozygous	133860793
X	13594325	13594326	C	T	6	GENIC	homozygous	120046621
X	13594320	13594321	C	A	6	GENIC	homozygous	120046620