chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	31816996	31816997	T	C	5	GENIC	homozygous	108251403
X	31819959	31819960	T	C	9	GENIC	homozygous	108791959
X	31821096	31821097	T	C	12	GENIC	homozygous	108251407
X	31822486	31822487	C	T	10	GENIC	homozygous	108791961
X	31826669	31826670	T	C	11	GENIC	homozygous	108251413
X	31827717	31827718	G	C	8	GENIC	homozygous	108791963
X	31828331	31828332	G	C	11	GENIC	homozygous	108791965
X	31828451	31828452	C	T	4	GENIC	heterozygous	108550357
X	31830198	31830199	T	G	7	GENIC	homozygous	108251417
X	31832656	31832657	T	C	7	GENIC	homozygous	108251425
X	31833120	31833121	G	A	7	GENIC	homozygous	108791969
X	31834719	31834720	C	T	10	GENIC	homozygous	108791971
X	31835241	31835242	T	C	11	GENIC	homozygous	108791973
X	31837394	31837395	C	T	4	GENIC	homozygous	108819577
X	31839715	31839716	G	T	7	GENIC	heterozygous	125103157
X	31839738	31839739	G	C	5	GENIC	heterozygous	125103158
X	31842923	31842924	A	C	12	GENIC	homozygous	108478725
X	31842998	31842999	C	T	13	GENIC	homozygous	108251429
X	31843139	31843140	T	C	8	GENIC	homozygous	108791979
X	31843262	31843263	G	A	7	GENIC	homozygous	108791981
X	31843544	31843545	C	G	8	GENIC	homozygous	108791983
X	31844234	31844235	T	G	8	GENIC	homozygous	108251431
X	31847200	31847201	G	T	7	GENIC	homozygous	108791989
X	31844291	31844292	A	C	11	GENIC	homozygous	108791985
X	31844416	31844417	G	A	10	GENIC	heterozygous	108251433
X	31845738	31845739	G	C	6	GENIC	homozygous	108251435
X	31846722	31846723	G	T	7	GENIC	homozygous	108791987
X	31841458	31841459	A	G	4	GENIC	heterozygous	125161001
X	31847811	31847812	A	C	9	GENIC	homozygous	125161002
X	31848693	31848694	T	C	4	GENIC	homozygous	108791991
X	31851190	31851191	G	T	13	GENIC	homozygous	108251445
X	31851345	31851346	G	C	8	GENIC	homozygous	108791993