chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	11140465	11140466	T	G	14	GENIC	homozygous	108225743
X	11140538	11140539	C	G	22	GENIC	homozygous	108225745
X	11141277	11141278	G	T	8	GENIC	homozygous	108225747
X	11141280	11141281	G	T	8	GENIC	homozygous	108225749
X	11141440	11141441	T	C	14	GENIC	homozygous	108225751
X	11142137	11142138	T	C	9	GENIC	homozygous	108225753
X	11144419	11144420	G	A	17	GENIC	homozygous	108225757
X	11144728	11144729	C	A	22	GENIC	homozygous	108225759
X	11144773	11144774	T	C	16	GENIC	homozygous	108225762
X	11144850	11144851	C	G	17	GENIC	homozygous	108225764
X	11145063	11145064	G	A	11	GENIC	homozygous	108225766
X	11145141	11145142	G	A	5	GENIC	homozygous	108225768
X	11145350	11145351	C	T	11	GENIC	homozygous	108225770
X	11146025	11146026	C	A	9	GENIC	homozygous	108225774
X	11146842	11146843	G	A	12	GENIC	homozygous	108225776
X	11147502	11147503	C	T	10	GENIC	homozygous	108225778
X	11147695	11147696	C	A	6	GENIC	homozygous	108225780
X	11147831	11147832	C	G	14	GENIC	homozygous	108225782
X	11148492	11148493	C	A	14	GENIC	homozygous	108225784
X	11149684	11149685	C	T	10	GENIC	homozygous	108225786
X	11150337	11150338	A	C	10	GENIC	homozygous	108225788
X	11162186	11162187	T	C	9	GENIC	homozygous	108225790
X	11163546	11163547	A	T	7	GENIC	homozygous	108225792
X	11163695	11163696	G	C	12	GENIC	homozygous	108225794
X	11164009	11164010	T	C	15	GENIC	homozygous	108225796