chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	72192047	72192048	C	T	64	GENIC	heterozygous	46000227
X	72192050	72192051	C	T	63	GENIC	heterozygous	46000228
X	72192184	72192185	T	A	43	GENIC	heterozygous	45939956
X	72192185	72192186	C	A	43	GENIC	heterozygous	46000229
X	72192190	72192196	CTAGGG	------	43	GENIC	heterozygous	46000540
X	72192201	72192202	G	C	45	GENIC	heterozygous	45939958
X	72192208	72192213	GGCAC	-----	47	GENIC	heterozygous	46000541
X	72192223	72192224	G	A	50	GENIC	heterozygous	46000230
X	72192227	72192228	G	T	50	GENIC	heterozygous	46012670
X	72192239	72192240	C	CA	41	GENIC	heterozygous	46014332
X	72192244	72192245	C	CAA	41	GENIC	heterozygous	46000542
X	72192260	72192261	G	T	44	GENIC	heterozygous	46000543
X	72192280	72192281	C	T	43	GENIC	heterozygous	46012672
X	72192683	72192684	G	T	20	GENIC	heterozygous	45146964
X	72192684	72192685	C	T	20	GENIC	heterozygous	45146965
X	72192801	72192802	C	T	46	GENIC	heterozygous	45146970
X	72192823	72192824	A	G	38	GENIC	heterozygous	45146971
X	72192827	72192828	A	T	38	GENIC	heterozygous	45146972
X	72192844	72192845	C	T	30	GENIC	heterozygous	46012515