chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	118728126	118728127	G	T	13	GENIC	homozygous	108316647
X	118734195	118734196	C	T	5	GENIC	homozygous	108316651
X	118736194	118736195	A	G	10	GENIC	homozygous	108316653
X	118736708	118736709	T	A	8	GENIC	homozygous	108316655
X	118743458	118743459	C	T	9	GENIC	homozygous	108316658
X	118743803	118743804	T	G	8	GENIC	homozygous	108419888
X	118743807	118743808	A	T	8	GENIC	homozygous	108419890
X	118743814	118743815	G	C	8	GENIC	homozygous	108419892
X	118744367	118744368	T	C	5	GENIC	homozygous	108316660
X	118745427	118745428	C	A	11	GENIC	homozygous	108316662
X	118747434	118747435	C	T	26	GENIC	homozygous	108316664
X	118750741	118750742	C	A	9	GENIC	homozygous	108419910
X	118755357	118755358	T	A	12	GENIC	homozygous	108316666
X	118757164	118757165	G	T	9	GENIC	homozygous	108316672
X	118763192	118763193	A	T	9	GENIC	homozygous	108316674
X	118766238	118766239	T	C	6	GENIC	homozygous	108316676