chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	14996380	14996381	T	C	29	GENIC	homozygous	108232974
X	14996485	14996486	T	C	18	GENIC	homozygous	108232976
X	14996548	14996549	A	T	15	GENIC	homozygous	108232978
X	14996559	14996560	A	G	10	GENIC	homozygous	108232980
X	14996943	14996944	C	T	19	GENIC	homozygous	108232982
X	14997561	14997562	A	G	14	GENIC	possibly homozygous	108232984
X	14999039	14999040	A	C	21	GENIC	homozygous	108232986
X	14999245	14999246	A	G	21	GENIC	homozygous	108232988
X	15000269	15000270	C	T	30	GENIC	homozygous	108232990
X	15004068	15004069	G	A	23	GENIC	homozygous	108232992
X	15004224	15004225	A	G	18	GENIC	homozygous	108232994
X	15004256	15004257	T	C	19	GENIC	homozygous	108232996
X	15004667	15004668	C	T	18	GENIC	homozygous	108369808
X	15001381	15001382	A	T	6	GENIC	homozygous	119905693
X	15003272	15003273	T	C	22	GENIC	homozygous	108439104
X	15004365	15004366	T	C	13	GENIC	homozygous	108369806