chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	22005200	22005201	G	C	23	GENIC	homozygous	140622550
X	22005274	22005275	T	C	25	GENIC	homozygous	140622551
X	22012195	22012196	T	C	21	GENIC	homozygous	140622552
X	22012948	22012949	T	G	26	GENIC	homozygous	140622553
X	22013068	22013069	A		19	GENIC	homozygous	140578813
X	22015229	22015230	C	T	29	GENIC	homozygous	140622554
X	22015544	22015545	G	A	19	GENIC	homozygous	140622555
X	22016116	22016116		T	14	GENIC	homozygous	140578814
X	22017476	22017477	A	G	25	GENIC	homozygous	140622556
X	22018268	22018269	T	C	22	GENIC	homozygous	140622557
X	22018802	22018803	T		11	GENIC	homozygous	140578815
X	22019183	22019184	A		25	GENIC	possibly homozygous	140578816
X	22022567	22022568	A	C	24	GENIC	homozygous	140622558
X	22022935	22022935		A	21	GENIC	possibly homozygous	140578817
X	22023394	22023395	A	G	17	GENIC	homozygous	140622559
X	22024154	22024155	T	A	15	GENIC	homozygous	140622560
X	22024906	22024907	C	A	20	GENIC	homozygous	140622561
X	22025744	22025750	TCCCTC		21	GENIC	homozygous	140578818
X	22025756	22025780	TCCTTCTCCCTCTCCCTCTCCCTC		22	GENIC	homozygous	140578819
X	22026015	22026016	G	A	18	GENIC	homozygous	140622562
X	22026097	22026098	A	G	21	GENIC	homozygous	140622563
X	22026716	22026717	G	A	12	GENIC	homozygous	140622564