chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	23149358	23149359	G	A	10	GENIC	homozygous	108239664
X	23149769	23149770	G	A	5	GENIC	homozygous	108239666
X	23150421	23150422	G	C	12	GENIC	homozygous	108239669
X	23151503	23151504	G	A	8	GENIC	homozygous	108239671
X	23151677	23151678	A	G	14	GENIC	homozygous	108239673
X	23151801	23151802	A	T	13	GENIC	homozygous	108239675
X	23152929	23152930	T	C	10	GENIC	homozygous	108373204
X	23153018	23153019	T	C	8	GENIC	homozygous	108373206
X	23153154	23153155	C	T	9	GENIC	homozygous	108239677
X	23153613	23153614	G	A	6	GENIC	homozygous	108239679
X	23153853	23153854	A	C	6	GENIC	homozygous	108239681
X	23154356	23154357	C	T	12	GENIC	homozygous	108239683
X	23155407	23155408	A	T	5	GENIC	homozygous	108373210
X	23162755	23162756	G	A	8	GENIC	homozygous	108239685
X	23162804	23162805	T	C	7	GENIC	homozygous	108239687
X	23163318	23163319	C	A	23	GENIC	homozygous	108239689
X	23163617	23163618	C	T	17	GENIC	homozygous	108239691
X	23163745	23163746	G	A	15	GENIC	homozygous	108239693
X	23163758	23163759	A	G	17	GENIC	homozygous	108239695
X	23164037	23164038	A	G	16	GENIC	homozygous	108239697
X	23164288	23164289	T	C	11	GENIC	homozygous	108239699
X	23165316	23165317	T	C	6	GENIC	homozygous	108239701
X	23165633	23165634	G	T	12	GENIC	homozygous	108239703