chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	31788360	31788361	A	G	52	GENIC	homozygous	108251350
X	31789336	31789337	G	A	55	GENIC	homozygous	108251352
X	31789576	31789577	T	A	60	GENIC	homozygous	108251354
X	31791733	31791734	G	T	57	GENIC	homozygous	108251356
X	31792523	31792524	G	T	53	GENIC	possibly homozygous	108251358
X	31794250	31794251	G	A	89	GENIC	homozygous	108251360
X	31794330	31794331	T	C	75	GENIC	homozygous	108251362
X	31794992	31794993	A	G	63	GENIC	homozygous	108251364
X	31795908	31795909	A	T	83	GENIC	possibly homozygous	108251366
X	31798559	31798560	C	G	46	GENIC	homozygous	108251368