chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	37475482	37475483	G	T	79	GENIC	homozygous	108256567
X	37475515	37475516	A	T	91	GENIC	homozygous	108256569
X	37475681	37475682	G	A	83	GENIC	homozygous	108256571
X	37475907	37475908	C	A	89	GENIC	homozygous	108380360
X	37476036	37476037	C	A	54	GENIC	homozygous	108256573
X	37489689	37489690	T	C	73	GENIC	homozygous	108256575
X	37495239	37495240	G	T	71	GENIC	possibly homozygous	108256577
X	37507402	37507403	C	T	80	GENIC	homozygous	108256579
X	37507484	37507485	G	T	98	GENIC	homozygous	108256581
X	37507572	37507573	A	G	63	GENIC	possibly homozygous	108256583
X	37507706	37507707	C	T	68	GENIC	homozygous	108256585
X	37508786	37508787	A	T	59	GENIC	possibly homozygous	108702602
X	37542979	37542980	G	A	68	GENIC	heterozygous	119916600
X	37500344	37500345	C	G	21	GENIC	homozygous	119995052
X	37507779	37507780	G	A	42	GENIC	homozygous	119916596
X	37508820	37508821	A	T	50	GENIC	homozygous	119916597
X	37542972	37542973	A	T	68	GENIC	heterozygous	119916599
X	37558353	37558354	C	G	131	GENIC	heterozygous	119995053
X	37558416	37558417	G	A	103	GENIC	heterozygous	119916604
X	37558421	37558422	T	C	99	GENIC	heterozygous	119916605
X	37560645	37560646	G	A	134	GENIC	heterozygous	119995054
X	37560649	37560650	T	G	131	GENIC	heterozygous	119995055
X	37560719	37560720	T	C	198	GENIC	heterozygous	119995056
X	37560751	37560752	A	T	183	GENIC	heterozygous	119995057
X	37560783	37560784	G	T	144	GENIC	heterozygous	119916607
X	37560800	37560801	G	C	111	GENIC	heterozygous	119995058
X	37564526	37564527	G	C	122	GENIC	heterozygous	119995059