chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	118445539	118445540	T	C	8	GENIC	homozygous	108316156
X	118447932	118447933	C	T	7	GENIC	homozygous	108316158
X	118447933	118447934	T	G	7	GENIC	homozygous	108316160
X	118448630	118448631	G	A	8	GENIC	homozygous	108316162
X	118452010	118452011	G	A	11	GENIC	homozygous	108316164
X	118452626	118452627	G	A	9	GENIC	homozygous	108316166
X	118452880	118452881	G	C	8	GENIC	homozygous	108316168
X	118456045	118456046	C	T	8	GENIC	homozygous	108316170
X	118462153	118462154	T	A	6	GENIC	homozygous	108316172
X	118467279	118467280	A	G	7	GENIC	homozygous	108316174
X	118469922	118469923	G	A	14	GENIC	homozygous	108316176
X	118472970	118472971	G	A	7	GENIC	homozygous	108316178
X	118483734	118483735	T	G	5	GENIC	homozygous	108316180
X	118492842	118492843	A	G	9	GENIC	homozygous	108316182
X	118493383	118493384	G	C	8	GENIC	homozygous	108316184
X	118495775	118495776	C	T	10	GENIC	homozygous	108316186
X	118503022	118503023	C	T	12	GENIC	homozygous	108316188
X	118503074	118503075	C	T	16	GENIC	homozygous	108316190
X	118503647	118503648	G	A	9	GENIC	homozygous	108316192
X	118503671	118503672	T	C	5	GENIC	homozygous	108316194
X	118504183	118504184	G	C	8	GENIC	homozygous	108316196
X	118504333	118504334	C	T	6	GENIC	homozygous	108316198
X	118504354	118504355	C	A	6	GENIC	homozygous	108316200
X	118504356	118504357	G	A	5	GENIC	homozygous	108316202
X	118505392	118505393	G	A	4	GENIC	homozygous	108316204
X	118508081	118508082	C	G	11	GENIC	homozygous	108316206
X	118508088	118508089	T	A	12	GENIC	homozygous	108316208
X	118508401	118508402	G	A	7	GENIC	homozygous	108316210
X	118511529	118511530	A	G	9	GENIC	homozygous	108316212
X	118513958	118513959	T	C	6	GENIC	homozygous	108316214
X	118473328	118473329	A	G	7	GENIC	homozygous	108419830
X	118514352	118514353	A	G	7	GENIC	homozygous	108419834
X	118475134	118475135	T	A	10	GENIC	homozygous	108419832