chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	123713979	123713980	G	T	12	GENIC	homozygous	125117028
X	123714355	123714356	G	A	8	GENIC	homozygous	125117029
X	123714647	123714648	G	A	10	GENIC	homozygous	125117030
X	123715707	123715708	A	T	5	GENIC	homozygous	125117031
X	123716414	123716415	G	C	6	GENIC	homozygous	125117032
X	123717720	123717721	G	T	14	GENIC	homozygous	125117033
X	123720424	123720425	T	G	14	GENIC	homozygous	125117034
X	123721424	123721425	G	A	13	GENIC	homozygous	125117035
X	123725671	123725672	C	T	17	GENIC	homozygous	125117036
X	123719987	123719988	C	T	5	GENIC	homozygous	125136026
X	123728245	123728246	A	C	4	GENIC	homozygous	125117037