chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	128897596	128897597	T	C	21	GENIC	homozygous	108332625
X	128898443	128898444	C	T	11	GENIC	homozygous	108332627
X	128898578	128898579	T	C	25	GENIC	homozygous	108332629
X	128901952	128901953	A	G	21	GENIC	homozygous	108332631
X	128907309	128907310	A	T	25	GENIC	homozygous	108332633
X	128898905	128898905		GATT	12	GENIC	homozygous	129789508
X	128901659	128901659		CTC	19	GENIC	homozygous	129789509
X	128901683	128901683		T	18	GENIC	homozygous	129789510
X	128907735	128907735		T	22	GENIC	homozygous	129789511
X	128909377	128909378	T	C	23	GENIC	homozygous	108332635
X	128909769	128909770	T		7	GENIC	homozygous	130195768
X	128910718	128910719	T	A	24	GENIC	homozygous	108332637
X	128911867	128911868	T	C	20	GENIC	homozygous	108332639
X	128912122	128912123	C		25	GENIC	homozygous	129789512
X	128913352	128913352		T	15	GENIC	homozygous	129789513
X	128914133	128914134	T	C	29	GENIC	homozygous	108332641
X	128916365	128916366	C	T	16	GENIC	homozygous	108332643
X	128916619	128916620	A	G	22	GENIC	homozygous	108332645
X	128921502	128921502		A	18	GENIC	homozygous	129789514
X	128924540	128924541	T		24	GENIC	possibly homozygous	129789515
X	128909772	128909773	T	C	7	GENIC	homozygous	108425753