chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	111100718	111100719	G	A	14	GENIC	homozygous	108506964
X	111101862	111101863	T	C	10	GENIC	homozygous	108506966
X	111102445	111102446	G	A	8	GENIC	homozygous	108506968
X	111104332	111104333	A	T	17	GENIC	homozygous	108506970
X	111105238	111105239	T	C	12	GENIC	homozygous	108506972
X	111105603	111105604	A	G	16	GENIC	homozygous	108506974
X	111106606	111106607	A	G	12	GENIC	homozygous	108416650
X	111108354	111108355	G	A	22	GENIC	homozygous	108506976
X	111109509	111109510	T	C	16	GENIC	homozygous	108506978
X	111109817	111109818	C	A	10	GENIC	homozygous	108452441
X	111113222	111113223	T	C	11	GENIC	homozygous	108506980
X	111113230	111113231	A	G	11	GENIC	homozygous	108506982
X	111113947	111113948	A	G	49	GENIC	heterozygous	120033228
X	111109021	111109022	A	G	10	GENIC	heterozygous	120033225
X	111109233	111109234	G	A	10	GENIC	homozygous	120033226
X	111113916	111113917	G	A	8	GENIC	homozygous	120033227
X	111113953	111113954	A	G	56	GENIC	heterozygous	120033229
X	111114009	111114010	G	T	60	GENIC	heterozygous	120033230
X	111114019	111114020	G	A	67	GENIC	heterozygous	120033231
X	111114024	111114025	G	T	64	GENIC	heterozygous	120033232
X	111114204	111114205	T	C	10	GENIC	homozygous	108506984
X	111114643	111114644	A	G	15	GENIC	homozygous	108416652