chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	123776640	123776641	C	T	15	GENIC	heterozygous	120011450
X	123776651	123776652	C	T	19	GENIC	heterozygous	120043824
X	123776925	123776926	T	A	38	GENIC	heterozygous	120043829
X	123782742	123782743	G	A	23	GENIC	homozygous	108325312
X	123786577	123786578	A	G	13	GENIC	homozygous	108325314
X	123786685	123786686	G	T	14	GENIC	homozygous	120073004
X	123786689	123786690	G	T	13	GENIC	homozygous	120073005
X	123786722	123786723	C	T	12	GENIC	homozygous	120073006
X	123786734	123786735	T	C	10	GENIC	heterozygous	119951333
X	123786738	123786739	T	C	10	GENIC	heterozygous	119951334
X	123786761	123786762	T	C	10	GENIC	homozygous	120073007
X	123788000	123788001	T	C	11	GENIC	homozygous	108678311
X	123785692	123785693	A	G	7	GENIC	possibly homozygous	108688545
X	123785721	123785722	C	T	4	GENIC	homozygous	108688547
X	123786180	123786181	G	A	11	GENIC	homozygous	108678307
X	123786836	123786837	C	G	14	GENIC	homozygous	108678308
X	123787238	123787239	G	A	13	GENIC	homozygous	108678309
X	123787472	123787473	G	T	10	GENIC	homozygous	108678310
X	123788057	123788058	C	T	15	GENIC	homozygous	108678312
X	123788456	123788457	G	A	20	GENIC	heterozygous	120073008
X	123788457	123788458	G	A	19	GENIC	heterozygous	120073009
X	123788505	123788506	A	G	27	GENIC	heterozygous	120073010
X	123788844	123788845	T	C	19	GENIC	homozygous	108325318