chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	14579138	14579139	T	C	7	GENIC	homozygous	125100681
X	14579359	14579360	C	T	7	GENIC	homozygous	125100682
X	14580079	14580080	G	A	7	GENIC	homozygous	125100683
X	14582999	14583000	T	C	17	GENIC	homozygous	125100684
X	14586171	14586172	C	T	15	GENIC	homozygous	125100685
X	14586330	14586331	T	C	12	GENIC	homozygous	125100686
X	14586398	14586399	T	C	9	GENIC	homozygous	125100687
X	14587747	14587748	A	G	10	GENIC	homozygous	125100688
X	14589409	14589410	G	A	9	GENIC	homozygous	125100689
X	14590445	14590446	A	G	11	GENIC	homozygous	125100690
X	14591304	14591305	A	G	6	GENIC	homozygous	125100691
X	14591578	14591579	G	A	12	GENIC	homozygous	125100692
X	14592182	14592183	G	A	11	GENIC	homozygous	125100693
X	14594954	14594955	A	G	15	GENIC	homozygous	125100694
X	14599072	14599073	T	C	12	GENIC	heterozygous	125100698
X	14596985	14596986	T	C	4	GENIC	homozygous	125100695
X	14599043	14599044	G	T	5	GENIC	homozygous	125100696
X	14599071	14599072	C	T	12	GENIC	heterozygous	125100697
X	14600551	14600552	T	C	10	GENIC	homozygous	125100699
X	14602816	14602817	C	A	4	GENIC	heterozygous	125100700
X	14608294	14608295	T	G	7	GENIC	homozygous	125100701
X	14608464	14608465	C	T	6	GENIC	homozygous	125100702
X	14609447	14609448	T	A	4	GENIC	homozygous	125100703
X	14609831	14609832	A	C	8	GENIC	homozygous	125100704