chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	6034491	6034492	T	A	23	GENIC	homozygous	140605719
X	6035775	6035776	C	G	27	GENIC	homozygous	140605720
X	6036563	6036564	G	A	25	GENIC	homozygous	140605721
X	6040104	6040105	A	T	23	GENIC	homozygous	140605722
X	6043908	6043909	T	C	26	GENIC	homozygous	140605723
X	6048693	6048694	A	G	20	GENIC	homozygous	140605724
X	6050640	6050640		T	13	GENIC	homozygous	140574931
X	6050643	6050643		T	13	GENIC	heterozygous	140574932
X	6051136	6051136		T	12	GENIC	homozygous	140574933
X	6054668	6054669	A	T	18	GENIC	homozygous	140605725
X	6055045	6055046	A	T	19	GENIC	homozygous	140605726
X	6055917	6055918	A	T	14	GENIC	homozygous	140605727
X	6056817	6056822	GTATG		19	GENIC	homozygous	140574934
X	6060659	6060660	G		9	GENIC	homozygous	140574935
X	6060661	6060664	TAG		9	GENIC	homozygous	140574936
X	6062968	6062969	A		17	GENIC	homozygous	140574937
X	6063096	6063097	T	C	25	GENIC	homozygous	140605728
X	6066890	6066891	G	A	17	GENIC	homozygous	140605729
X	6067039	6067040	T		15	GENIC	homozygous	140574938
X	6076124	6076125	C	T	24	GENIC	homozygous	140605730
X	6077847	6077849	GC		18	GENIC	heterozygous	140574939
X	6084837	6084838	C		20	GENIC	homozygous	140574940
X	6092848	6092849	T		14	GENIC	homozygous	140574941
X	6060663	6060664	G		9	GENIC	homozygous	403474277
X	6077848	6077849	C	T	18	GENIC	heterozygous	155195719
X	6060663	6060664	G	C	9	GENIC	heterozygous	403474278
X	6077848	6077849	C		18	GENIC	heterozygous	403474279
X	6091301	6091302	C		12	GENIC	heterozygous	403474280
X	6091301	6091302	C	G	12	GENIC	heterozygous	403474281