chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	14996485	14996486	T	C	7	GENIC	homozygous	108232976
X	14996548	14996549	A	T	10	GENIC	homozygous	108232978
X	14996559	14996560	A	G	10	GENIC	homozygous	108232980
X	14997397	14997398	G	A	9	GENIC	homozygous	108595021
X	14997561	14997562	A	G	10	GENIC	homozygous	108232984
X	14997783	14997784	A		14	GENIC	homozygous	133793067
X	14998198	14998200	TT		8	GENIC	homozygous	133793068
X	14998684	14998685	C	T	12	GENIC	homozygous	108595023
X	14999039	14999040	A	C	16	GENIC	homozygous	108232986
X	14999245	14999246	A	G	10	GENIC	homozygous	108232988
X	15001151	15001151		GGA	4	GENIC	homozygous	133793069
X	15004224	15004225	A	G	10	GENIC	homozygous	108232994
X	15004256	15004257	T	C	10	GENIC	homozygous	108232996
X	14997860	14997861	G		13	GENIC	homozygous	129722312
X	14997879	14997879		TAACAGATCC	12	GENIC	homozygous	129722313
X	15003728	15003729	A		9	GENIC	homozygous	129722315
X	15004281	15004282	G		9	GENIC	homozygous	129722316
X	15004365	15004366	T	C	12	GENIC	homozygous	108369806
X	15005203	15005204	C	A	12	GENIC	homozygous	108595025
X	15005331	15005333	AT		10	GENIC	homozygous	133793070
X	15005466	15005467	A	G	22	GENIC	homozygous	108595027