chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	153994032	153994033	T	G	16	GENIC	heterozygous	45990861
X	153994060	153994061	A	T	13	GENIC	heterozygous	45990863
X	153994186	153994187	A	T	9	GENIC	heterozygous	45971111
X	153994199	153994200	G	A	9	GENIC	heterozygous	45971112
X	153994356	153994357	G	-	28	GENIC	heterozygous	45990865
X	153994373	153994374	G	A	26	GENIC	heterozygous	45990867
X	153994386	153994387	A	C	23	GENIC	heterozygous	45990869
X	153994387	153994388	C	A	23	GENIC	heterozygous	45990871
X	153994393	153994394	G	T	21	GENIC	heterozygous	45990873
X	153994407	153994408	T	A	18	GENIC	heterozygous	45990875
X	154009945	154009946	C	A	15	GENIC	heterozygous	45955018
X	154009959	154009960	A	G	15	GENIC	heterozygous	45955019
X	154009960	154009961	C	T	15	GENIC	heterozygous	45955020
X	154052692	154052693	C	G	12	GENIC	heterozygous	45249310
X	154052700	154052701	A	G	14	GENIC	heterozygous	45249311
X	154052708	154052709	G	A	13	GENIC	heterozygous	45249312
X	154052746	154052747	C	G	12	GENIC	heterozygous	45955022