chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	1619232	1619232		A	14	GENIC	homozygous	140574091
X	1621411	1621412	C	T	15	GENIC	homozygous	140602322
X	1621490	1621491	T	C	18	GENIC	homozygous	140602323
X	1622360	1622361	A		16	GENIC	homozygous	140574092
X	1624310	1624311	C	G	13	GENIC	homozygous	140602324
X	1625678	1625678		T	36	GENIC	possibly homozygous	140574093
X	1626156	1626157	G	A	32	GENIC	homozygous	140602325
X	1627022	1627023	G	C	23	GENIC	homozygous	140602326
X	1631446	1631447	G	C	10	GENIC	homozygous	140602327
X	1631448	1631449	G	C	10	GENIC	homozygous	140602328
X	1631450	1631451	G	C	10	GENIC	homozygous	140602329
X	1633574	1633575	A	G	28	GENIC	homozygous	140602330
X	1634289	1634290	G	A	24	GENIC	homozygous	140602331
X	1634384	1634385	T	G	23	GENIC	possibly homozygous	140602332