chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	118733741	118733742	T	C	17	GENIC	homozygous	108718039
X	118736194	118736195	A	G	17	GENIC	homozygous	108316653
X	118743344	118743345	T	C	11	GENIC	homozygous	108718041
X	118743458	118743459	C	T	10	GENIC	homozygous	108316658
X	118743803	118743804	T	G	5	GENIC	homozygous	108419888
X	118743807	118743808	A	T	7	GENIC	homozygous	108419890
X	118743814	118743815	G	C	7	GENIC	homozygous	108419892
X	118747434	118747435	C	T	21	GENIC	homozygous	108316664
X	118748649	118748650	G	A	12	GENIC	homozygous	108718043
X	118750435	118750436	A	G	16	GENIC	homozygous	108419908
X	118755163	118755164	G	A	10	GENIC	homozygous	108718045
X	118755807	118755808	G	C	7	GENIC	homozygous	108718047
X	118763192	118763193	A	T	15	GENIC	homozygous	108316674
X	118765683	118765684	A	G	13	GENIC	homozygous	108718049
X	118766024	118766025	T	G	14	GENIC	homozygous	108508128