chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	67403915	67403916	G	A	6	GENIC	homozygous	45256452
X	67403919	67403920	A	T	5	GENIC	homozygous	45256453
X	67404069	67404070	T	-	2	GENIC	homozygous	45256454
X	67404090	67404091	G	T	5	GENIC	homozygous	45305303
X	67404094	67404095	T	C	6	GENIC	homozygous	45305304
X	67404107	67404108	T	C	7	GENIC	homozygous	45256455
X	67404110	67404111	A	T	7	GENIC	homozygous	45256456
X	67404114	67404115	C	A	7	GENIC	homozygous	45256457
X	67404119	67404120	T	A	9	GENIC	homozygous	45256458
X	67404126	67404127	C	T	8	GENIC	homozygous	45256459
X	67404135	67404136	G	T	12	GENIC	homozygous	45256460
X	67404141	67404142	C	T	14	GENIC	homozygous	45256461
X	67404148	67404149	C	A	13	GENIC	homozygous	45256462
X	67404158	67404159	G	T	15	GENIC	homozygous	45145530
X	67404173	67404174	T	C	19	GENIC	homozygous	45145531
X	67404193	67404194	T	A	30	GENIC	homozygous	45145532
X	67404194	67404195	T	C	31	GENIC	homozygous	45145533
X	67422676	67422677	T	C	47	GENIC	homozygous	45256466
X	67422693	67422694	C	CA	55	GENIC	homozygous	45145535
X	67422804	67422805	C	G	50	GENIC	homozygous	45145536