chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	159705062	159705063	G	C	39	GENIC	homozygous	108355462
X	159705254	159705255	G	A	34	GENIC	homozygous	108355464
X	159705374	159705375	C	T	29	GENIC	homozygous	108355466
X	159707465	159707466	A	G	40	GENIC	homozygous	108355468
X	159708024	159708025	A	G	35	GENIC	homozygous	108355470
X	159709077	159709078	G	A	27	GENIC	homozygous	108355472
X	159710314	159710315	G	A	30	GENIC	homozygous	108355474
X	159711476	159711477	G	A	27	GENIC	homozygous	108355476
X	159712372	159712373	T	C	22	GENIC	homozygous	108355478
X	159712457	159712458	A	G	23	GENIC	homozygous	108355480