chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	31817781	31817782	C	T	7	INTERGENIC	homozygous	45118379
X	31825667	31825668	C	G	12	INTERGENIC	homozygous	45505438
X	31825668	31825669	C	T	12	INTERGENIC	homozygous	45505440
X	31825672	31825675	AAT	---	12	INTERGENIC	homozygous	45118408
X	31825710	31825711	C	A	15	INTERGENIC	homozygous	45475815
X	31825711	31825712	A	C	15	INTERGENIC	homozygous	45475817
X	31825720	31825721	A	-	14	INTERGENIC	homozygous	45118409
X	31825748	31825749	T	-	13	INTERGENIC	homozygous	45118410
X	31825758	31825759	G	-	13	INTERGENIC	homozygous	45118411
X	31825760	31825761	T	TAA	11	INTERGENIC	homozygous	45118412
X	31825777	31825778	C	CCA	10	INTERGENIC	homozygous	45253818
X	31825779	31825780	T	TTTAC	11	INTERGENIC	homozygous	45253819
X	31825787	31825788	A	AG	12	INTERGENIC	homozygous	45253820
X	31825789	31825790	A	ATAGC	12	INTERGENIC	homozygous	45253821
X	31825821	31825822	T	TGG	12	INTERGENIC	homozygous	45118413
X	31825823	31825824	T	TAA	13	INTERGENIC	homozygous	45118414
X	31825826	31825827	T	TGC	13	INTERGENIC	homozygous	45118415
X	31825832	31825833	A	AAGG	13	INTERGENIC	homozygous	45118416
X	31825844	31825845	C	CT	15	INTERGENIC	homozygous	45118417
X	31825845	31825846	A	ATC	16	INTERGENIC	homozygous	45118418
X	31825849	31825850	G	GGT	16	INTERGENIC	homozygous	45118419
X	31825854	31825855	G	GT	17	INTERGENIC	homozygous	45118420