chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	23670649	23670650	G	C	20	GENIC	possibly homozygous	108373364
X	23670723	23670724	T	C	23	GENIC	possibly homozygous	108373366
X	23672065	23672066	G	A	24	GENIC	homozygous	108373368
X	23677644	23677645	T	C	22	GENIC	homozygous	108240494
X	23678397	23678398	T	G	10	GENIC	homozygous	108240496
X	23679488	23679489	G	A	18	GENIC	homozygous	108373370
X	23680678	23680679	C	T	9	GENIC	homozygous	108240498
X	23680993	23680994	G	A	15	GENIC	homozygous	108240500
X	23682925	23682926	A	G	18	GENIC	homozygous	108240502
X	23683717	23683718	T	C	14	GENIC	homozygous	108240504
X	23688014	23688015	A	C	14	GENIC	homozygous	108240507
X	23690353	23690354	C	A	20	GENIC	homozygous	108240513
X	23691203	23691227	TCCTTCTCCCTCTCCCTCTCCCTC		14	GENIC	homozygous	129728248
X	23678517	23678518	A		16	GENIC	homozygous	129728242
X	23681565	23681565		T	14	GENIC	homozygous	129728243
X	23684251	23684252	T		15	GENIC	homozygous	129728244
X	23684632	23684633	A		14	GENIC	homozygous	129728245
X	23691191	23691197	TCCCTC		13	GENIC	homozygous	129728247
X	23679308	23679309	C	T	23	GENIC	homozygous	108563523
X	23681944	23681945	C	T	16	GENIC	homozygous	108631123
X	23691462	23691463	G	A	15	GENIC	homozygous	108240515
X	23691544	23691545	A	G	21	GENIC	homozygous	108240517
X	23692163	23692164	G	A	18	GENIC	homozygous	108240519