chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	153561408	153561409	A	T	6	GENIC	homozygous	125124346
X	153561689	153561690	G	T	6	GENIC	homozygous	125124347
X	153563062	153563063	G	C	10	GENIC	heterozygous	125124348
X	153568757	153568758	G	T	3	GENIC	heterozygous	125171934
X	153719364	153719365	A	T	12	GENIC	homozygous	125124353
X	153719374	153719375	A	T	11	GENIC	homozygous	125124354
X	153719399	153719400	T	A	4	GENIC	homozygous	125168307
X	153719436	153719437	C	T	12	GENIC	homozygous	125124355
X	153719491	153719492	T	C	8	GENIC	homozygous	125124356
X	153719493	153719494	C	T	7	GENIC	homozygous	125124357
X	153723221	153723222	T	C	11	GENIC	homozygous	125127370
X	153719484	153719485	A	G	7	GENIC	homozygous	125127368
X	153719485	153719486	G	A	7	GENIC	homozygous	125127369
X	153719311	153719312	G	A	6	GENIC	homozygous	125147324
X	153730957	153730958	C	G	9	GENIC	heterozygous	125154007
X	153730959	153730960	T	C	9	GENIC	heterozygous	125154008
X	153731005	153731006	A	T	14	GENIC	heterozygous	125124358
X	153755316	153755317	G	C	12	GENIC	homozygous	125127372
X	153802093	153802094	G	T	10	GENIC	heterozygous	125124360
X	153817525	153817526	G	A	11	GENIC	homozygous	125124362
X	153913999	153914000	A	G	13	GENIC	heterozygous	125124364
X	153914008	153914009	A	T	17	GENIC	heterozygous	125124365
X	153914489	153914490	A	G	14	GENIC	homozygous	125124366