chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	138035388	138035389	C	G	3	GENIC	homozygous	108816572
X	138038853	138038854	G	A	3	GENIC	homozygous	108691373
X	138039553	138039554	T	C	4	GENIC	homozygous	108816576
X	138040548	138040549	C	T	2	GENIC	homozygous	108816578
X	138042213	138042214	G	C	4	GENIC	homozygous	108816580
X	138050005	138050006	A	G	5	GENIC	homozygous	108691378
X	138051093	138051094	T	C	7	GENIC	homozygous	108816582
X	138052689	138052690	C	A	6	GENIC	homozygous	108816584
X	138052942	138052943	C	T	2	GENIC	homozygous	108816586
X	138056179	138056180	C	T	2	GENIC	homozygous	108816590
X	138056916	138056917	C	A	3	GENIC	homozygous	108691385
X	138056945	138056946	A	C	3	GENIC	homozygous	108816594
X	138057722	138057723	A	G	2	GENIC	homozygous	108816596
X	138060704	138060705	G	A	3	GENIC	homozygous	108818903
X	138063256	138063257	G	T	6	GENIC	homozygous	108344450
X	138063299	138063300	T	A	2	GENIC	homozygous	108344452
X	138063302	138063303	C	T	2	GENIC	homozygous	108344454
X	138063734	138063735	A	G	2	GENIC	homozygous	108691387
X	138068741	138068742	C	G	2	GENIC	homozygous	108816600
X	138073651	138073652	T	C	3	GENIC	homozygous	108691420
X	138074288	138074289	C	T	4	GENIC	homozygous	108816603
X	138075571	138075572	T	C	2	GENIC	homozygous	108691432
X	138079366	138079367	G	T	4	GENIC	homozygous	108816611
X	138079637	138079638	T	C	2	GENIC	homozygous	108816613
X	138083445	138083446	G	T	2	GENIC	homozygous	108816615
X	138093350	138093351	A	G	2	GENIC	homozygous	108691463
X	138093806	138093807	A	C	2	GENIC	homozygous	108691465
X	138094653	138094654	A	G	2	GENIC	homozygous	108816626
X	138095661	138095662	T	C	2	GENIC	homozygous	108816630
X	138095743	138095744	C	A	5	GENIC	homozygous	108816632
X	138095950	138095951	G	A	2	GENIC	homozygous	108816633
X	138069124	138069125	C	G	3	GENIC	homozygous	108455695