chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15041831	15041832	C	T	12	GENIC	homozygous	108233018
X	15042314	15042315	A	G	4	GENIC	homozygous	108233020
X	15042671	15042672	A	G	14	GENIC	homozygous	108233022
X	15044809	15044810	A	G	18	GENIC	homozygous	108369814
X	15045449	15045450	A	T	1	GENIC	homozygous	108766286
X	15045729	15045730	G	T	10	GENIC	homozygous	108471978
X	15045759	15045760	G	A	12	GENIC	homozygous	108233024
X	15045760	15045761	A	G	12	GENIC	homozygous	108233026
X	15045784	15045785	G	C	14	GENIC	homozygous	108233028
X	15045786	15045787	T	G	15	GENIC	homozygous	108233030
X	15045787	15045788	G	C	16	GENIC	homozygous	108233032
X	15047190	15047191	T	G	10	GENIC	homozygous	108233034
X	15047282	15047283	C	G	6	GENIC	homozygous	108233036
X	15047290	15047291	C	A	6	GENIC	homozygous	108233038
X	15047316	15047317	A	G	5	GENIC	homozygous	108233040
X	15047374	15047375	G	A	5	GENIC	homozygous	108233042
X	15047384	15047385	C	A	5	GENIC	homozygous	108233044
X	15047385	15047386	G	A	5	GENIC	homozygous	108233046
X	15047392	15047393	C	A	4	GENIC	homozygous	108233048