chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	68892583	68892584	T	C	18	GENIC	homozygous	108388191
X	68892674	68892674		A	18	GENIC	homozygous	131242033
X	68892876	68892877	C	T	24	GENIC	homozygous	108388195
X	68893381	68893382	C	G	27	GENIC	homozygous	108388197
X	68893550	68893551	T	C	28	GENIC	homozygous	108388199
X	68893773	68893774	A	G	26	GENIC	homozygous	108388201
X	68894052	68894053	C		27	GENIC	homozygous	131242034
X	68894781	68894782	C	G	34	GENIC	homozygous	108388203
X	68897740	68897741	T		27	GENIC	homozygous	129752721
X	68898697	68898698	A	C	39	GENIC	homozygous	108448624
X	68893923	68893924	T	C	35	GENIC	homozygous	108448618
X	68896864	68896865	G	A	35	GENIC	homozygous	108448620
X	68897194	68897195	C	A	37	GENIC	homozygous	108448622
X	68903445	68903446	C	T	40	GENIC	homozygous	108501711
X	68899472	68899473	G	A	40	GENIC	homozygous	108448626
X	68902324	68902325	G	A	25	GENIC	homozygous	108448628