chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	27017139	27017140	T	A	9	GENIC	homozygous	108245760
X	27017510	27017511	C	T	25	GENIC	homozygous	108245762
X	27018863	27018864	C	T	15	GENIC	homozygous	120066354
X	27020827	27020828	T	C	17	GENIC	homozygous	120066355
X	27021190	27021191	G	C	6	GENIC	homozygous	108682663
X	27021204	27021205	T	A	8	GENIC	homozygous	108682664
X	27021206	27021207	A	T	8	GENIC	homozygous	108682665
X	27021208	27021209	A	T	9	GENIC	homozygous	108682666
X	27021290	27021291	G	C	21	GENIC	homozygous	108245766
X	27022589	27022590	A	G	15	GENIC	homozygous	108245770
X	27023250	27023251	C	T	39	GENIC	homozygous	108376287
X	27021626	27021627	A	G	16	GENIC	homozygous	108376279
X	27022922	27022923	G	A	21	GENIC	homozygous	108376281
X	27022927	27022928	G	A	22	GENIC	homozygous	108376283
X	27023016	27023017	G	T	24	GENIC	homozygous	108376285
X	27021686	27021687	T	C	15	GENIC	homozygous	108440853
X	27021692	27021693	C	A	16	GENIC	possibly homozygous	108440855
X	27023385	27023386	C	T	30	GENIC	homozygous	108245772
X	27023740	27023741	G	A	25	GENIC	homozygous	108245774
X	27024368	27024369	A	G	17	GENIC	homozygous	108245776
X	27025504	27025505	T	A	25	GENIC	homozygous	108376289
X	27025505	27025506	C	A	24	GENIC	homozygous	108376291
X	27025684	27025685	A	C	33	GENIC	homozygous	108245780
X	27026196	27026197	C	T	19	GENIC	homozygous	108245782
X	27026729	27026730	A	G	24	GENIC	homozygous	108245784
X	27029159	27029160	G	C	26	GENIC	homozygous	108245786
X	27031720	27031721	T	G	13	GENIC	homozygous	108766445