chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	104735515	104735516	C	T	24	GENIC	homozygous	108779356
X	104736709	104736710	A	G	18	GENIC	homozygous	108666971
X	104738424	104738425	C	T	19	GENIC	homozygous	108666975
X	104739898	104739899	G	A	16	GENIC	homozygous	108779358
X	104740267	104740268	C	G	27	GENIC	homozygous	108666977
X	104740713	104740714	T	G	21	GENIC	homozygous	108666979
X	104741041	104741042	G	T	30	GENIC	homozygous	108666981
X	104741731	104741732	G	C	30	GENIC	homozygous	108779360
X	104742318	104742319	C	T	19	GENIC	homozygous	108779362
X	104742526	104742527	A	G	15	GENIC	homozygous	108779364
X	104744190	104744191	A	T	29	GENIC	homozygous	108779366
X	104745297	104745298	G	A	27	GENIC	homozygous	108779368
X	104745805	104745806	G	A	24	GENIC	homozygous	108779370
X	104746321	104746322	A	T	13	GENIC	homozygous	108666987
X	104747794	104747795	A	G	22	GENIC	homozygous	108666991
X	104752030	104752031	A	G	18	GENIC	homozygous	108666995
X	104758087	104758088	C	T	23	GENIC	homozygous	108779372
X	104759307	104759308	C	T	22	GENIC	homozygous	108779374