chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	37793662	37793663	T	G	19	GENIC	homozygous	108256603
X	37793695	37793696	T	G	19	GENIC	homozygous	108256605
X	37931796	37931797	G	T	21	GENIC	homozygous	108256617
X	37937467	37937468	C	T	27	GENIC	homozygous	108256619
X	37937725	37937726	C	T	21	GENIC	homozygous	108256621
X	37937726	37937727	T	C	21	GENIC	homozygous	108256623
X	37967463	37967464	T	G	29	GENIC	homozygous	108256625
X	37995918	37995919	G	T	31	GENIC	homozygous	108256629
X	37998333	37998334	G	A	16	GENIC	homozygous	108256631
X	37998337	37998338	G	A	15	GENIC	homozygous	108256633
X	37998339	37998340	G	A	14	GENIC	homozygous	108256635
X	37998344	37998345	G	A	15	GENIC	homozygous	108256637
X	38005227	38005228	T	A	3	GENIC	homozygous	108443967
X	38005230	38005231	A	C	3	GENIC	homozygous	108443969
X	38170422	38170423	T	G	20	GENIC	homozygous	108256639