chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15576427	15576428	C	T	14	GENIC	homozygous	108233510
X	15579360	15579361	A	G	15	GENIC	homozygous	108233514
X	15581144	15581145	C	T	9	GENIC	homozygous	108472250
X	15579984	15579985	G	A	13	GENIC	homozygous	108472242
X	15580065	15580066	C	T	11	GENIC	homozygous	108472244
X	15580080	15580081	C	T	13	GENIC	homozygous	108472246
X	15580703	15580704	C	A	10	GENIC	homozygous	108472248
X	15581272	15581273	C	T	10	GENIC	homozygous	108472252
X	15581301	15581302	T	C	5	GENIC	homozygous	108472254
X	15582161	15582162	G	A	11	GENIC	homozygous	108472256
X	15582281	15582282	A	G	9	GENIC	homozygous	108472258
X	15582352	15582353	A	C	9	GENIC	homozygous	108472260
X	15585039	15585040	G	A	8	GENIC	homozygous	108472263
X	15585404	15585405	T	G	8	GENIC	homozygous	108472265
X	15585550	15585551	G	T	22	GENIC	homozygous	108472267
X	15585605	15585606	C	T	17	GENIC	homozygous	108472269
X	15586433	15586434	C	T	11	GENIC	homozygous	108472271