chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	16959067	16959068	T	G	15	INTERGENIC	homozygous	62915312
X	16959479	16959480	C	T	15	INTERGENIC	heterozygous	62915313
X	16965057	16965058	T	A	12	INTERGENIC	possibly homozygous	62915315
X	16965484	16965485	A	C	47	INTERGENIC	heterozygous	62915316
X	16966569	16966570	T	C	50	INTERGENIC	homozygous	62915317
X	16967732	16967733	A	G	23	INTERGENIC	possibly homozygous	86090289
X	16968876	16968877	A	T	16	INTERGENIC	heterozygous	62915318
X	16970717	16970718	A	C	15	INTERGENIC	possibly homozygous	63030971
X	16972806	16972807	A	T	8	INTERGENIC	possibly homozygous	62915321
X	16974704	16974705	A	T	8	INTERGENIC	homozygous	62915322
X	16974927	16974928	T	C	12	INTERGENIC	homozygous	62915323
X	16975118	16975119	C	G	8	INTERGENIC	heterozygous	86090293
X	16975120	16975121	C	G	8	INTERGENIC	heterozygous	63303257
X	16975122	16975123	C	G	8	INTERGENIC	heterozygous	63303258
X	16975124	16975125	C	G	8	INTERGENIC	heterozygous	63303259
X	16975126	16975127	C	G	8	INTERGENIC	heterozygous	86090295
X	16977054	16977055	T	C	5	INTERGENIC	homozygous	62915324