chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	27421821	27421822	T	A	13	GENIC	heterozygous	45113693
X	27422192	27422193	C	T	22	GENIC	possibly homozygous	45113694
X	27423382	27423383	G	GCTAGGTGATTTTCATCAGTCTAGGTATAACTCCGTCATAAGTGAAGGAGCAT	2	GENIC	heterozygous	45504437
X	27423387	27423388	G	GTAATATGCACTGTTTGT	2	GENIC	heterozygous	45475550
X	27423398	27423399	G	GA	3	GENIC	homozygous	45113697
X	27425972	27425973	G	C	7	GENIC	homozygous	45113708
X	27426308	27426309	A	G	7	GENIC	homozygous	45378052
X	27426368	27426369	T	C	5	GENIC	homozygous	45378054
X	27426374	27426375	C	A	6	GENIC	homozygous	45378056
X	27426600	27426604	GTGG	----	6	GENIC	heterozygous	45113709
X	27427271	27427272	A	G	19	GENIC	possibly homozygous	45113711
X	27427604	27427605	G	A	9	GENIC	homozygous	45378058
X	27427609	27427610	G	A	10	GENIC	homozygous	45378060
X	27427698	27427699	G	T	22	GENIC	homozygous	45378062
X	27427932	27427933	C	T	26	GENIC	homozygous	45378064
X	27428067	27428068	C	T	25	GENIC	possibly homozygous	45113712
X	27428422	27428423	G	A	20	GENIC	possibly homozygous	45113713
X	27429050	27429051	A	G	32	GENIC	heterozygous	45113714
X	27430186	27430187	T	A	2	GENIC	homozygous	45378066
X	27430187	27430188	C	A	2	GENIC	homozygous	45378068
X	27430366	27430367	A	C	19	GENIC	possibly homozygous	45113716
X	27430878	27430879	C	T	19	GENIC	possibly homozygous	45113717
X	27431411	27431412	A	G	26	GENIC	possibly homozygous	45113718
X	27432879	27432880	A	-	4	GENIC	heterozygous	45378070
X	27433841	27433842	G	C	18	GENIC	heterozygous	45113720
X	27434070	27434071	A	AT	3	GENIC	heterozygous	45113721
X	27434070	27434071	A	ATT	3	GENIC	heterozygous	45324160