chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124723280	124723281	T	C	8	GENIC	homozygous	108326267
X	124725082	124725083	A	G	8	GENIC	homozygous	108326273
X	124725898	124725899	C	G	11	GENIC	homozygous	108424725
X	124726205	124726206	G	A	21	GENIC	homozygous	108326275
X	124731973	124731974	A	C	10	GENIC	homozygous	108326277
X	124734856	124734857	C	T	14	GENIC	homozygous	108326279
X	124741491	124741492	T	C	11	GENIC	homozygous	108326281
X	124742681	124742682	A	G	12	GENIC	homozygous	108424727
X	124743427	124743428	A	C	16	GENIC	homozygous	108326283
X	124743935	124743936	A	G	9	GENIC	homozygous	108326285
X	124745634	124745635	T	C	14	GENIC	homozygous	108326289
X	124746866	124746867	C	T	16	GENIC	homozygous	108326291
X	124748552	124748553	T	A	14	GENIC	homozygous	108326295
X	124749078	124749079	G	A	16	GENIC	homozygous	108326297
X	124753199	124753200	G	A	9	GENIC	homozygous	108326305
X	124753405	124753406	C	T	15	GENIC	homozygous	108326307
X	124757222	124757223	T	G	16	GENIC	homozygous	108326309
X	124757735	124757736	A	G	7	GENIC	homozygous	108326311
X	124759581	124759582	C	T	13	GENIC	homozygous	108326313
X	124759853	124759854	C	T	20	GENIC	homozygous	108326315
X	124760647	124760648	T	A	11	GENIC	homozygous	108326317
X	124761379	124761380	G	A	14	GENIC	homozygous	108326319