chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	146532084	146532085	T	C	31	GENIC	heterozygous	120063067
X	146532139	146532140	T	C	34	GENIC	heterozygous	120063068
X	146532178	146532179	T	C	36	GENIC	heterozygous	120063069
X	146532230	146532231	G	A	23	GENIC	heterozygous	120063070
X	146532250	146532251	T	C	21	GENIC	heterozygous	120063071
X	146532260	146532261	T	C	21	GENIC	heterozygous	120063072
X	146532293	146532294	A	G	20	GENIC	heterozygous	120063073
X	146532316	146532318	AT		19	GENIC	heterozygous	133357271
X	146532319	146532332	CATGGATGCACCA		21	GENIC	heterozygous	133357272
X	146532340	146532341	T	C	19	GENIC	heterozygous	133365993
X	146532544	146532545	C	G	22	GENIC	heterozygous	133365995
X	146533028	146533029	G	C	24	GENIC	heterozygous	133365996
X	146533043	146533044	C	G	27	GENIC	heterozygous	120063074
X	146533058	146533059	G	A	24	GENIC	heterozygous	120063075
X	146533122	146533123	A	T	18	GENIC	heterozygous	120063076
X	146533144	146533145	C	G	25	GENIC	heterozygous	120063077
X	146532398	146532399	G	A	15	GENIC	homozygous	134771574