chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	70324818	70324819	G	A	14	GENIC	homozygous	108390028
X	70326806	70326807	G	A	13	GENIC	homozygous	108449443
X	70333328	70333329	G	T	10	GENIC	homozygous	108449445
X	70336318	70336319	G	A	18	GENIC	homozygous	108449447
X	70336331	70336332	G	A	19	GENIC	homozygous	108390030
X	70337294	70337295	A	G	22	GENIC	homozygous	108390034
X	70340171	70340172	T	C	21	GENIC	homozygous	108449449
X	70340577	70340578	A	T	22	GENIC	homozygous	108449451
X	70341315	70341316	G	A	15	GENIC	homozygous	108449453
X	70342027	70342028	T	C	17	GENIC	homozygous	108390036
X	70342465	70342466	G	T	9	GENIC	homozygous	108449455
X	70342709	70342710	G	A	10	GENIC	homozygous	108449457