chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	72357111	72357112	C	T	12	GENIC	homozygous	142759131
X	72360694	72360695	T	G	6	GENIC	homozygous	142759132
X	72361039	72361039		A	5	GENIC	homozygous	142744935
X	72362919	72362920	G	C	10	GENIC	homozygous	140646181
X	72364917	72364918	A		7	GENIC	homozygous	141147790
X	72365816	72365817	G	A	8	GENIC	homozygous	142759133
X	72368030	72368031	A	G	5	GENIC	homozygous	142759134
X	72369183	72369184	G	A	3	GENIC	homozygous	142759135
X	72369862	72369863	A		12	GENIC	homozygous	142744936
X	72373426	72373427	A	T	11	GENIC	homozygous	142759136
X	72373978	72373979	G	T	3	GENIC	homozygous	140646182
X	72379050	72379051	G	A	9	GENIC	homozygous	140646183
X	72381262	72381263	T	C	8	GENIC	homozygous	140646184
X	72382683	72382684	A	G	11	GENIC	homozygous	142759137
X	72383117	72383118	A	G	4	GENIC	homozygous	142759138
X	72385086	72385087	T	C	12	GENIC	homozygous	142759139
X	72385431	72385432	C	T	3	GENIC	homozygous	142759140
X	72387656	72387657	G	A	8	GENIC	possibly homozygous	142759141
X	72389370	72389371	T	A	4	GENIC	homozygous	142759142
X	72390787	72390788	T		10	GENIC	homozygous	403481651
X	72390785	72390786	T		10	GENIC	homozygous	403481649
X	72390785	72390786	T	C	10	GENIC	heterozygous	403481650
X	72390787	72390788	T	C	10	GENIC	heterozygous	155185770
X	72390789	72390790	T	C	10	GENIC	heterozygous	155185771
X	72390789	72390790	T		10	GENIC	homozygous	403481652
X	72393168	72393169	A	G	6	GENIC	homozygous	142759143
X	72394854	72394855	C	A	13	GENIC	homozygous	142759144
X	72391555	72391556	A		5	GENIC	homozygous	140584364