chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	115103202	115103203	T	TGAAGCTCCTA	13	GENIC	heterozygous	45198546
X	115118714	115118715	G	A	44	GENIC	heterozygous	45198591
X	115118823	115118824	T	-	37	GENIC	heterozygous	45198592
X	115121851	115121852	G	A	82	GENIC	heterozygous	45198599
X	115122527	115122528	G	T	75	GENIC	heterozygous	45198600
X	115122663	115122664	A	G	105	GENIC	heterozygous	46000581
X	115144316	115144317	G	T	250	GENIC	heterozygous	45198668
X	115144386	115144387	G	C	217	GENIC	heterozygous	45198669
X	115144388	115144389	A	G	219	GENIC	heterozygous	45198670
X	115144939	115144940	G	T	39	GENIC	heterozygous	45265054
X	115145015	115145016	C	G	85	GENIC	heterozygous	45265055
X	115149120	115149121	A	C	17	GENIC	heterozygous	45198675
X	115149177	115149178	T	G	22	GENIC	heterozygous	45198676
X	115149178	115149179	C	G	22	GENIC	heterozygous	45198677
X	115159739	115159740	G	GC	25	GENIC	heterozygous	45198713
X	115161791	115161792	A	G	6	INTERGENIC	heterozygous	45198734