chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	82654974	82654975	T	G	93	GENIC	possibly homozygous	108280370
X	82660489	82660490	A	T	63	GENIC	homozygous	108280372
X	82667015	82667016	G	A	62	GENIC	homozygous	108280374
X	82671335	82671336	G	A	72	GENIC	homozygous	108280376
X	82673089	82673090	A	G	92	GENIC	possibly homozygous	108280378
X	82674414	82674415	C	G	6	GENIC	heterozygous	120004432
X	82678960	82678961	C	T	78	GENIC	possibly homozygous	108280380
X	82701022	82701023	T	C	92	GENIC	possibly homozygous	108280382
X	82694310	82694311	G	A	26	GENIC	heterozygous	119930774
X	82702387	82702388	C	T	191	GENIC	heterozygous	119930776
X	82700676	82700677	T	C	66	GENIC	possibly homozygous	108396573
X	82703094	82703095	G	A	98	GENIC	heterozygous	119930779
X	82703138	82703139	A	G	111	GENIC	heterozygous	119930780
X	82703796	82703797	T	C	58	GENIC	heterozygous	120004433
X	82703838	82703839	A	T	47	GENIC	heterozygous	119930781
X	82703843	82703844	T	A	49	GENIC	heterozygous	119930782
X	82707697	82707698	C	T	82	GENIC	homozygous	108280384
X	82710357	82710358	C	T	111	GENIC	heterozygous	119930785
X	82710360	82710361	A	T	112	GENIC	heterozygous	119930786
X	82710387	82710388	T	A	102	GENIC	heterozygous	119930787
X	82713139	82713140	T	C	103	GENIC	heterozygous	119930788
X	82714836	82714837	A	G	53	GENIC	homozygous	108396575
X	82716304	82716305	G	C	51	GENIC	homozygous	108280386
X	82723954	82723955	T	G	34	GENIC	possibly homozygous	108280388
X	82729273	82729274	C	A	88	GENIC	homozygous	108280392
X	82738510	82738511	T	A	71	GENIC	homozygous	108280396
X	82743653	82743654	T	C	51	GENIC	homozygous	108280398