chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	51156712	51156713	T	C	6	GENIC	homozygous	108259338
X	51174651	51174652	T	A	7	GENIC	homozygous	108259375
X	51176231	51176232	A	G	7	GENIC	homozygous	108381633
X	51176242	51176243	C	G	8	GENIC	homozygous	108381635
X	51180599	51180600	T	G	5	GENIC	homozygous	108381637
X	51181761	51181762	T	G	15	GENIC	possibly homozygous	108381639
X	51209458	51209459	A	T	13	GENIC	heterozygous	108259485
X	51209256	51209257	C	T	21	GENIC	heterozygous	108595954
X	51209459	51209460	T	A	13	GENIC	heterozygous	108259487
X	51228974	51228975	A	T	8	GENIC	homozygous	108381641
X	51236822	51236823	A	T	10	GENIC	homozygous	108381643
X	51240740	51240741	G	A	14	GENIC	homozygous	108259598
X	51240747	51240748	C	T	15	GENIC	homozygous	108259600
X	51650863	51650864	A	C	15	GENIC	heterozygous	108446814
X	52159935	52159936	C	A	9	GENIC	heterozygous	108446824
X	52169313	52169314	T	C	7	GENIC	homozygous	108595956
X	52395079	52395080	G	T	5	GENIC	homozygous	108262080
X	52655800	52655801	A	C	9	GENIC	heterozygous	108446826
X	52979010	52979011	T	A	20	GENIC	homozygous	108595958
X	53335871	53335872	T	A	10	GENIC	homozygous	108595960