chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	114958860	114958861	C	CCGTA	5	GENIC	heterozygous	45198192
X	114958991	114958993	AC	--	12	GENIC	homozygous	45198193
X	114959301	114959302	A	G	12	GENIC	homozygous	45198194
X	114960289	114960290	A	-	2	GENIC	homozygous	45198195
X	114960745	114960746	A	G	6	GENIC	homozygous	45198196
X	114961156	114961157	A	G	10	GENIC	homozygous	45198197
X	114961174	114961175	C	T	12	GENIC	homozygous	45198198
X	114961905	114961906	T	TA	1	GENIC	homozygous	45198201
X	114961914	114961915	A	AT	1	GENIC	homozygous	45198202
X	114965341	114965342	C	T	4	GENIC	homozygous	45198208
X	114966744	114966745	G	A	15	GENIC	possibly homozygous	45198209
X	114967693	114967694	A	G	10	GENIC	homozygous	45198211
X	114967725	114967726	A	C	13	GENIC	homozygous	45198212
X	114967813	114967814	T	A	5	GENIC	homozygous	45198213
X	114968161	114968179	CCTGTGCTGTCTCTCCAG	------------------	6	GENIC	homozygous	45198215
X	114968264	114968265	C	T	20	GENIC	homozygous	45198216
X	114968289	114968290	G	A	22	GENIC	homozygous	45198217
X	114968603	114968604	G	C	2	GENIC	homozygous	45198218
X	114968998	114968999	T	C	9	GENIC	homozygous	45198219
X	114969012	114969013	G	A	13	GENIC	homozygous	45198220
X	114969266	114969268	TT	--	1	GENIC	homozygous	45198221
X	114969552	114969553	G	-	3	GENIC	homozygous	45198222
X	114970246	114970247	T	C	26	GENIC	possibly homozygous	45198223
X	114970619	114970620	A	G	14	GENIC	homozygous	45198226
X	114972560	114972561	C	T	21	GENIC	possibly homozygous	45198233
X	114973041	114973042	G	C	7	GENIC	heterozygous	45198234
X	114973560	114973561	T	C	5	GENIC	heterozygous	45198235
X	114975474	114975475	C	T	4	GENIC	homozygous	45198237
X	114975667	114975668	G	T	9	GENIC	homozygous	45198238
X	114975704	114975705	C	T	12	GENIC	possibly homozygous	45198239
X	114975947	114975951	GGTG	----	7	GENIC	heterozygous	45198240