chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115104789	115104790	C	T	6	GENIC	heterozygous	45726868
X	115107617	115107618	T	A	8	GENIC	heterozygous	45198561
X	115107850	115107851	G	A	18	GENIC	heterozygous	45726870
X	115115630	115115631	A	G	103	GENIC	heterozygous	45726889
X	115116084	115116085	C	A	247	GENIC	heterozygous	46000362
X	115116104	115116105	A	T	243	GENIC	heterozygous	46000363
X	115116134	115116135	T	C	201	GENIC	heterozygous	46000364
X	115118823	115118824	T	-	39	GENIC	heterozygous	45198592
X	115121883	115121884	A	T	112	GENIC	heterozygous	45265051
X	115121903	115121904	T	C	106	GENIC	heterozygous	45265052
X	115121970	115121971	G	-	71	GENIC	heterozygous	46000365
X	115143800	115143801	T	TTTC	59	INTERGENIC	heterozygous	45920575
X	115143801	115143802	A	G	60	INTERGENIC	heterozygous	45920576
X	115144386	115144387	G	C	233	GENIC	heterozygous	45198669
X	115144388	115144389	A	G	236	GENIC	heterozygous	45198670
X	115144939	115144940	G	T	33	GENIC	heterozygous	45265054
X	115145689	115145690	A	G	37	GENIC	heterozygous	46000582
X	115146738	115146739	C	T	16	GENIC	heterozygous	46000366
X	115147468	115147469	C	T	23	GENIC	heterozygous	46000367
X	115149120	115149121	A	C	9	GENIC	heterozygous	45198675
X	115149177	115149178	T	G	12	GENIC	heterozygous	45198676
X	115149178	115149179	C	G	12	GENIC	heterozygous	45198677
X	115154870	115154871	A	G	166	GENIC	heterozygous	45949517