chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	104572200	104572201	C	CT	7	GENIC	heterozygous	45614016
X	104584747	104584751	ATAT	----	7	GENIC	heterozygous	45724698
X	104584967	104584968	T	TGTATGTGGTGGTTACTGTCCAAGTA	18	GENIC	homozygous	45480785
X	104585193	104585194	G	T	14	GENIC	homozygous	45480787
X	104585197	104585198	C	CA	13	GENIC	homozygous	45189968
X	104585198	104585199	C	T	13	GENIC	homozygous	45480789
X	104585203	104585204	C	T	13	GENIC	homozygous	45189970
X	104585211	104585212	G	GT	12	GENIC	homozygous	45189971
X	104585213	104585214	G	GA	12	GENIC	homozygous	45189972
X	104585221	104585222	T	TC	11	GENIC	homozygous	45189973
X	104585242	104585243	A	T	9	GENIC	homozygous	45519563
X	104585243	104585244	A	ACC	9	GENIC	homozygous	45189974
X	104585246	104585247	G	T	10	GENIC	homozygous	45189975
X	104585248	104585249	G	T	10	GENIC	homozygous	45189976
X	104585239	104585240	C	G	9	GENIC	homozygous	45264085
X	104585192	104585193	A	G	18	GENIC	homozygous	45264083
X	104585237	104585238	T	G	8	GENIC	homozygous	45264084