chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	75774474	75774476	CT	--	7	GENIC	heterozygous	45512944
X	75797794	75797796	AC	--	5	GENIC	heterozygous	45151440
X	75816654	75816655	G	-	5	GENIC	homozygous	45151444
X	75829071	75829072	A	-	7	GENIC	homozygous	45151446
X	75829087	75829088	A	-	5	GENIC	homozygous	45151447
X	75829102	75829103	G	-	5	GENIC	homozygous	45151448
X	75829119	75829120	G	T	7	GENIC	homozygous	45151449
X	75829127	75829128	T	-	9	GENIC	homozygous	45151450
X	75829138	75829139	A	C	9	GENIC	homozygous	45151451
X	75829153	75829154	C	T	8	GENIC	homozygous	45151452
X	75829160	75829161	C	-	9	GENIC	homozygous	45151453
X	75829165	75829166	G	C	9	GENIC	homozygous	45151454
X	75829168	75829169	A	C	9	GENIC	homozygous	45151455
X	75829170	75829171	A	AC	9	GENIC	homozygous	45151456
X	75829173	75829174	C	T	10	GENIC	homozygous	45260834
X	75829176	75829177	A	C	9	GENIC	homozygous	45151457
X	75829181	75829182	A	-	8	GENIC	homozygous	45151458
X	75829185	75829186	A	T	9	GENIC	homozygous	45151459
X	75829188	75829189	G	C	11	GENIC	homozygous	45151460