chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	30685819	30685820	A	G	18	GENIC	heterozygous	108249801
X	30685860	30685861	C	T	15	GENIC	heterozygous	108249803
X	30689480	30689481	A	C	7	GENIC	homozygous	108249837
X	30724347	30724348	A	G	5	GENIC	heterozygous	120081688
X	30729067	30729068	A	T	10	GENIC	homozygous	108249933
X	30757002	30757003	G	A	2	GENIC	homozygous	108249937
X	30770692	30770693	T	A	7	GENIC	homozygous	108478550
X	30790720	30790721	C	G	10	GENIC	homozygous	108249939
X	30791605	30791606	G	C	24	GENIC	heterozygous	120081690
X	30803807	30803808	T	C	9	GENIC	homozygous	108249945
X	30803884	30803885	T	C	14	GENIC	homozygous	108249948
X	30804113	30804114	G	A	14	GENIC	homozygous	108249950
X	30804144	30804145	A	G	12	GENIC	homozygous	108249952
X	30804181	30804182	C	A	12	GENIC	homozygous	108249954
X	30807508	30807509	A	C	4	GENIC	heterozygous	119913152
X	30807523	30807524	G	A	4	GENIC	homozygous	119913154
X	30807532	30807533	A	C	4	GENIC	homozygous	119913156
X	30807542	30807543	A	G	4	GENIC	homozygous	108249956
X	30807543	30807544	T	G	4	GENIC	homozygous	108249959
X	30807594	30807595	T	C	6	GENIC	homozygous	108249961
X	30819022	30819023	T	C	7	GENIC	homozygous	108478552
X	30827825	30827826	C	G	10	GENIC	homozygous	108478554
X	30804246	30804247	T	G	5	GENIC	homozygous	108595718