chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	123633922	123633923	T	TG	2	GENIC	homozygous	45598802
X	123634096	123634097	C	CT	8	GENIC	possibly homozygous	45362260
X	123634514	123634515	G	GATAT	17	GENIC	homozygous	45267626
X	123634639	123634640	T	-	3	GENIC	heterozygous	45524987
X	123635820	123635821	C	CT	2	GENIC	heterozygous	45214577
X	123636485	123636487	TT	--	4	GENIC	homozygous	45214578
X	123638142	123638143	C	CGT	2	GENIC	homozygous	45524989
X	123638970	123638971	C	T	18	GENIC	possibly homozygous	45362261
X	123639476	123639516	AATGATTGTACTGGTGTTTTAGTGAAGTACTTTGTGAGTC	----------------------------------------	1	GENIC	homozygous	45482319
X	123639567	123639568	G	GTT	2	GENIC	homozygous	45362262
X	123640639	123640640	T	C	12	GENIC	homozygous	45214581