chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	27421821	27421822	T	A	14	GENIC	homozygous	45113693
X	27422192	27422193	C	T	13	GENIC	homozygous	45113694
X	27423276	27423277	T	C	8	GENIC	homozygous	45113695
X	27423382	27423383	G	GCTAGGTGATTTTCATCAGTCTAGGTATAACTCCGTCATAAGTGAAGGAGCAT	7	GENIC	homozygous	45504437
X	27423387	27423388	G	GTAATATGCACTGTTTGT	8	GENIC	homozygous	45475550
X	27423398	27423399	G	GA	10	GENIC	homozygous	45113697
X	27425552	27425553	C	-	3	GENIC	heterozygous	45113698
X	27425821	27425822	C	CA	2	GENIC	homozygous	45113702
X	27425872	27425873	G	C	1	GENIC	homozygous	45113703
X	27425886	27425887	T	A	1	GENIC	homozygous	45113705
X	27425888	27425889	A	T	1	GENIC	homozygous	45113706
X	27425890	27425891	A	T	1	GENIC	homozygous	45113707
X	27425972	27425973	G	C	6	GENIC	homozygous	45113708
X	27426600	27426604	GTGG	----	6	GENIC	homozygous	45113709
X	27427094	27427095	A	G	4	GENIC	homozygous	45113710
X	27427271	27427272	A	G	7	GENIC	homozygous	45113711
X	27428067	27428068	C	T	16	GENIC	homozygous	45113712
X	27428422	27428423	G	A	15	GENIC	homozygous	45113713
X	27429050	27429051	A	G	5	GENIC	homozygous	45113714
X	27429362	27429363	C	G	16	GENIC	homozygous	45113715
X	27430366	27430367	A	C	7	GENIC	homozygous	45113716
X	27430878	27430879	C	T	7	GENIC	homozygous	45113717
X	27431411	27431412	A	G	7	GENIC	homozygous	45113718
X	27433492	27433493	C	T	3	GENIC	homozygous	45113719
X	27434070	27434071	A	ATT	9	GENIC	heterozygous	45324160
X	27436390	27436391	T	-	1	GENIC	homozygous	45279224
X	27433841	27433842	G	C	20	GENIC	homozygous	45113720
X	27434070	27434071	A	AT	9	GENIC	possibly homozygous	45113721
X	27434881	27434882	G	GTA	4	GENIC	heterozygous	45113722