chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	37793662	37793663	T	G	14	GENIC	homozygous	108256603
X	37793695	37793696	T	G	12	GENIC	homozygous	108256605
X	37824978	37824979	T	G	3	GENIC	homozygous	108256615
X	37931796	37931797	G	T	5	GENIC	homozygous	108256617
X	37937467	37937468	C	T	12	GENIC	homozygous	108256619
X	37937725	37937726	C	T	5	GENIC	homozygous	108256621
X	37937726	37937727	T	C	5	GENIC	homozygous	108256623
X	37967463	37967464	T	G	10	GENIC	homozygous	108256625
X	37995918	37995919	G	T	15	GENIC	homozygous	108256629
X	37998333	37998334	G	A	9	GENIC	homozygous	108256631
X	37998337	37998338	G	A	10	GENIC	homozygous	108256633
X	37998339	37998340	G	A	10	GENIC	homozygous	108256635
X	37998344	37998345	G	A	10	GENIC	homozygous	108256637
X	38005081	38005082	G	T	6	GENIC	homozygous	108380368
X	38013955	38013956	A	T	4	GENIC	homozygous	108380370
X	38062539	38062540	A	T	8	GENIC	homozygous	108380372
X	38062630	38062631	A	T	4	GENIC	homozygous	108380374
X	38062658	38062659	C	A	2	GENIC	homozygous	108380376
X	38135890	38135891	A	C	6	GENIC	homozygous	108380378
X	38170422	38170423	T	G	13	GENIC	homozygous	108256639