chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	75434745	75434746	G	C	10	GENIC	homozygous	108392208
X	75434747	75434748	T	A	9	GENIC	homozygous	108392210
X	75435273	75435274	A	C	11	GENIC	homozygous	108392212
X	75436298	75436299	C	T	10	GENIC	homozygous	108392214
X	75436796	75436797	C	T	7	GENIC	homozygous	108392216
X	75437619	75437620	A	G	9	GENIC	homozygous	108392218
X	75438312	75438313	G	A	13	GENIC	homozygous	108392220
X	75441489	75441490	A	C	9	GENIC	homozygous	108392222
X	75441921	75441922	T	C	6	GENIC	homozygous	108392224
X	75442859	75442860	A	G	5	GENIC	homozygous	108392226
X	75449460	75449461	T	A	6	GENIC	homozygous	108392228
X	75452969	75452970	C	T	13	GENIC	homozygous	108392230
X	75453015	75453016	C	G	13	GENIC	homozygous	108392232
X	75453724	75453725	A	C	7	GENIC	homozygous	108392234
X	75493556	75493557	C	T	9	GENIC	homozygous	108274881
X	75512124	75512125	G	T	12	GENIC	homozygous	108392236