chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	140876237	140876238	G	A	3	GENIC	homozygous	108455983
X	140876558	140876559	A	G	3	GENIC	homozygous	108347404
X	140876903	140876904	T	C	9	GENIC	homozygous	108455985
X	140877384	140877385	C	G	4	GENIC	homozygous	108347406
X	140878408	140878409	A	G	9	GENIC	homozygous	108347408
X	140878413	140878414	C	G	8	GENIC	homozygous	108347410
X	140881236	140881237	C	T	6	GENIC	homozygous	108347412
X	140883256	140883257	A		13	GENIC	possibly homozygous	131971016
X	140884219	140884220	G	A	9	GENIC	homozygous	108347414
X	140883107	140883108	A		8	GENIC	homozygous	129796528
X	140884598	140884599	T		9	GENIC	homozygous	129796529
X	140885858	140885859	G	A	17	GENIC	homozygous	108553359
X	140886025	140886026	G	T	9	GENIC	homozygous	108347420
X	140886446	140886447	T	C	5	GENIC	homozygous	108347424
X	140886772	140886773	A	G	5	GENIC	homozygous	108347426
X	140886836	140886839	TTC		7	GENIC	homozygous	129796531
X	140887772	140887773	C	G	5	GENIC	homozygous	108347428
X	140887956	140887957	C	T	6	GENIC	homozygous	108347430