chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	138231172	138231173	T	G	16	GENIC	homozygous	108344494
X	138231184	138231185	C	A	18	GENIC	homozygous	108344496
X	138231199	138231200	A	T	17	GENIC	homozygous	108344498
X	138231223	138231224	G	T	23	GENIC	homozygous	108344500
X	138231234	138231235	A	G	23	GENIC	homozygous	108344502
X	138231237	138231238	T	C	23	GENIC	homozygous	108344504
X	138231279	138231280	T	G	25	GENIC	homozygous	108344506
X	138231294	138231295	T	A	21	GENIC	homozygous	108428323
X	138231295	138231296	G	A	21	GENIC	homozygous	108428325
X	138231320	138231321	T	A	20	GENIC	homozygous	108428327
X	138231321	138231322	G	A	20	GENIC	homozygous	108428329
X	138231330	138231331	A	G	22	GENIC	homozygous	108428331
X	138231342	138231343	G	A	22	GENIC	homozygous	108428333
X	138231347	138231348	C	T	21	GENIC	homozygous	108428335
X	138231371	138231372	C	G	30	GENIC	homozygous	108344508
X	138231377	138231378	T	A	24	GENIC	homozygous	108428337
X	138231378	138231379	T	G	23	GENIC	homozygous	108428339
X	138231385	138231386	T	A	23	GENIC	homozygous	108428341
X	138231387	138231388	T	A	23	GENIC	homozygous	108583846
X	138231388	138231389	G	A	23	GENIC	homozygous	108428343
X	138231467	138231468	T	G	28	GENIC	homozygous	108344510
X	138231472	138231473	G	T	27	GENIC	homozygous	108344512
X	138231479	138231480	C	G	24	GENIC	homozygous	108344514
X	138231481	138231482	C	A	25	GENIC	homozygous	108344516
X	138231486	138231487	G	C	26	GENIC	homozygous	108344518