chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	1619232	1619232		A	8	GENIC	homozygous	140574091
X	1621411	1621412	C	T	8	GENIC	homozygous	140602322
X	1621490	1621491	T	C	9	GENIC	homozygous	140602323
X	1621553	1621554	T	C	7	GENIC	heterozygous	403473563
X	1621549	1621550	T		7	GENIC	homozygous	403473560
X	1621549	1621550	T	C	7	GENIC	heterozygous	403473561
X	1621553	1621554	T		7	GENIC	homozygous	403473562
X	1621581	1621582	T		7	GENIC	homozygous	403473564
X	1621581	1621582	T	C	7	GENIC	heterozygous	403473565
X	1621601	1621602	T		7	GENIC	homozygous	403473566
X	1621601	1621602	T	C	7	GENIC	heterozygous	403473567
X	1624310	1624311	C	G	4	GENIC	homozygous	140602324
X	1626156	1626157	G	A	6	GENIC	homozygous	140602325
X	1627022	1627023	G	C	3	GENIC	homozygous	140602326
X	1633574	1633575	A	G	6	GENIC	homozygous	140602330
X	1634289	1634290	G	A	7	GENIC	homozygous	140602331
X	1634384	1634385	T	G	5	GENIC	homozygous	140602332
X	1625678	1625678		T	8	GENIC	homozygous	140574093