chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15360101	15360102	G	T	9	INTERGENIC	homozygous	62914165
X	15360367	15360368	A	C	16	INTERGENIC	homozygous	62914166
X	15360438	15360439	A	C	18	INTERGENIC	homozygous	62914167
X	15362092	15362093	C	T	8	INTERGENIC	heterozygous	62914169
X	15365945	15365946	A	G	6	INTERGENIC	homozygous	62914170
X	15368764	15368765	A	C	16	INTERGENIC	homozygous	62914171
X	15374318	15374319	A	G	9	INTERGENIC	homozygous	62914172
X	15377439	15377440	A	C	7	INTERGENIC	homozygous	62914173
X	15377973	15377974	C	G	5	INTERGENIC	homozygous	62914174
X	15381451	15381452	G	C	2	INTERGENIC	homozygous	62914177
X	15381534	15381535	C	T	11	INTERGENIC	homozygous	62914178
X	15382500	15382501	G	C	2	INTERGENIC	heterozygous	62914179
X	15382501	15382502	G	A	2	INTERGENIC	heterozygous	62914180
X	15382519	15382520	C	T	1	INTERGENIC	homozygous	62914182
X	15385718	15385719	C	G	11	INTERGENIC	homozygous	62914192
X	15387004	15387005	A	C	2	INTERGENIC	homozygous	62914193
X	15387443	15387444	A	T	9	INTERGENIC	homozygous	62914194
X	15387909	15387910	A	G	8	INTERGENIC	possibly homozygous	62914195
X	15389125	15389126	C	T	13	INTERGENIC	homozygous	62914196
X	15391023	15391024	C	T	8	INTERGENIC	homozygous	62914197