chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	135006860	135006861	C	G	4	GENIC	homozygous	120013112
X	135010004	135010005	C	T	18	GENIC	homozygous	108583559
X	135010654	135010655	A	C	21	GENIC	homozygous	108509489
X	135012103	135012104	T	C	16	GENIC	homozygous	108509491
X	135016733	135016734	T	C	21	GENIC	homozygous	108509495
X	135016822	135016823	C	T	11	GENIC	homozygous	108583563
X	135017317	135017318	G	A	18	GENIC	homozygous	108583565
X	135022587	135022588	T	C	19	GENIC	homozygous	108583569
X	135023304	135023305	T	G	24	GENIC	homozygous	108583571
X	135025100	135025101	A	G	13	GENIC	homozygous	108583573
X	135025422	135025423	C	T	9	GENIC	homozygous	108583575
X	135030594	135030595	G	A	5	GENIC	homozygous	108583577
X	135011648	135011649	T	A	6	GENIC	homozygous	108818840
X	135016786	135016787	C	G	8	GENIC	heterozygous	125170776
X	135031463	135031464	T	C	8	GENIC	homozygous	108509503
X	135031466	135031467	G	A	9	GENIC	homozygous	108509505
X	135031566	135031567	G	C	6	GENIC	homozygous	108583579
X	135032346	135032347	T	C	9	GENIC	homozygous	108583581
X	135032502	135032503	A	C	13	GENIC	homozygous	108583583
X	135032779	135032780	A	T	21	GENIC	homozygous	108509513
X	135032951	135032952	T	A	18	GENIC	homozygous	108509515
X	135033806	135033807	C	T	12	GENIC	homozygous	108583585
X	135035289	135035290	A	G	15	GENIC	homozygous	108509517
X	135036004	135036005	A	T	15	GENIC	homozygous	108509519
X	135036831	135036832	A	G	7	GENIC	homozygous	125170777
X	135037614	135037615	C	A	14	GENIC	homozygous	108583587
X	135037871	135037872	G	T	28	GENIC	homozygous	108583589
X	135038088	135038089	A	G	15	GENIC	homozygous	108583591