chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	51428940	51428941	G		6	GENIC	heterozygous	403871098
X	51428940	51428941	G	C	6	GENIC	heterozygous	403871099
X	51886987	51886988	T		8	GENIC	homozygous	140582661
X	51545537	51545538	A		12	GENIC	heterozygous	141101114
X	51946097	51946098	C		5	GENIC	homozygous	140582664
X	52083281	52083282	C	A	10	GENIC	heterozygous	144216314
X	52002078	52002079	A	C	3	GENIC	homozygous	140640381
X	52037741	52037742	A	G	11	GENIC	heterozygous	144216310
X	52037743	52037744	A	T	11	GENIC	heterozygous	144216311
X	52083249	52083250	C	T	9	GENIC	heterozygous	144216312
X	52083252	52083253	G	A	9	GENIC	heterozygous	144216313
X	52083286	52083287	A	C	10	GENIC	heterozygous	144216315
X	52404084	52404084		A	4	GENIC	homozygous	140582670
X	52421814	52421815	A		8	GENIC	homozygous	140582671
X	52553456	52553457	T	G	4	GENIC	homozygous	140640386
X	52553458	52553459	C	T	4	GENIC	homozygous	140640387
X	52553461	52553461		GCTTCTCAGGA	4	GENIC	homozygous	140582674
X	52083292	52083293	G		10	GENIC	heterozygous	144211958
X	52803705	52803706	G		6	GENIC	heterozygous	141147726
X	52803705	52803706	G	T	6	GENIC	heterozygous	403685225
X	52852833	52852834	T		8	GENIC	homozygous	140582678
X	52859703	52859704	C		15	GENIC	heterozygous	404758809
X	52859703	52859704	C	G	15	GENIC	heterozygous	404758810