chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15939137	15939138	T	C	24	GENIC	possibly homozygous	45097831
X	15940285	15940287	AC	--	6	GENIC	heterozygous	45097833
X	15942121	15942122	G	A	5	GENIC	heterozygous	45097836
X	15942703	15942704	C	-	5	GENIC	homozygous	45097837
X	15942713	15942714	G	-	7	GENIC	homozygous	45097838
X	15942725	15942726	C	G	9	GENIC	homozygous	45252136
X	15942764	15942765	G	T	4	GENIC	heterozygous	45097839
X	15942850	15942851	T	C	5	GENIC	heterozygous	45097842
X	15944801	15944802	G	A	1	GENIC	homozygous	45097845
X	15944950	15944951	C	T	19	GENIC	possibly homozygous	45097847
X	15945752	15945753	C	T	19	GENIC	homozygous	45473937
X	15943415	15943421	ACTGTG	------	6	GENIC	homozygous	45473927
X	15944771	15944772	C	T	16	GENIC	possibly homozygous	45473929
X	15944917	15944918	C	CT	6	GENIC	homozygous	45473931
X	15945038	15945039	A	C	21	GENIC	possibly homozygous	45473933
X	15945281	15945282	G	A	20	GENIC	homozygous	45473935