chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	82654974	82654975	T	G	9	GENIC	homozygous	108280370
X	82660489	82660490	A	T	11	GENIC	homozygous	108280372
X	82667015	82667016	G	A	27	GENIC	homozygous	108280374
X	82671335	82671336	G	A	18	GENIC	homozygous	108280376
X	82673089	82673090	A	G	14	GENIC	homozygous	108280378
X	82678960	82678961	C	T	9	GENIC	homozygous	108280380
X	82694310	82694311	G	A	20	GENIC	possibly homozygous	119930774
X	82700676	82700677	T	C	17	GENIC	homozygous	108396573
X	82701022	82701023	T	C	12	GENIC	homozygous	108280382
X	82702299	82702300	T	A	58	GENIC	heterozygous	119930775
X	82702387	82702388	C	T	157	GENIC	heterozygous	119930776
X	82703067	82703068	T	C	49	GENIC	heterozygous	119930777
X	82703086	82703087	A	C	67	GENIC	heterozygous	119930778
X	82703094	82703095	G	A	77	GENIC	heterozygous	119930779
X	82703138	82703139	A	G	77	GENIC	heterozygous	119930780
X	82703838	82703839	A	T	26	GENIC	heterozygous	119930781
X	82703843	82703844	T	A	23	GENIC	heterozygous	119930782
X	82707697	82707698	C	T	15	GENIC	homozygous	108280384
X	82710217	82710218	C	A	16	GENIC	heterozygous	119930783
X	82710264	82710265	T	G	41	GENIC	heterozygous	119930784
X	82710357	82710358	C	T	101	GENIC	heterozygous	119930785
X	82710360	82710361	A	T	95	GENIC	heterozygous	119930786
X	82710387	82710388	T	A	103	GENIC	heterozygous	119930787
X	82713139	82713140	T	C	25	GENIC	heterozygous	119930788
X	82713170	82713171	A	T	34	GENIC	heterozygous	119930789
X	82713255	82713256	T	C	10	GENIC	heterozygous	119930790
X	82714836	82714837	A	G	8	GENIC	homozygous	108396575
X	82716304	82716305	G	C	8	GENIC	homozygous	108280386
X	82729273	82729274	C	A	4	GENIC	homozygous	108280392
X	82732699	82732700	C	G	9	GENIC	homozygous	108280394
X	82738510	82738511	T	A	6	GENIC	homozygous	108280396
X	82743653	82743654	T	C	23	GENIC	homozygous	108280398