chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124723280	124723281	T	C	49	GENIC	homozygous	108326267
X	124725082	124725083	A	G	40	GENIC	homozygous	108326273
X	124725898	124725899	C	G	29	GENIC	homozygous	108424725
X	124726205	124726206	G	A	54	GENIC	homozygous	108326275
X	124731973	124731974	A	C	60	GENIC	homozygous	108326277
X	124734856	124734857	C	T	46	GENIC	homozygous	108326279
X	124741491	124741492	T	C	47	GENIC	possibly homozygous	108326281
X	124742681	124742682	A	G	43	GENIC	homozygous	108424727
X	124743427	124743428	A	C	49	GENIC	homozygous	108326283
X	124743935	124743936	A	G	50	GENIC	homozygous	108326285
X	124744332	124744333	A	C	15	GENIC	homozygous	108326287
X	124744963	124744964	C	G	42	GENIC	possibly homozygous	108811714
X	124745634	124745635	T	C	55	GENIC	homozygous	108326289
X	124746866	124746867	C	T	56	GENIC	homozygous	108326291
X	124747331	124747332	G	A	46	GENIC	homozygous	108326293
X	124748552	124748553	T	A	38	GENIC	homozygous	108326295
X	124749078	124749079	G	A	59	GENIC	homozygous	108326297
X	124753199	124753200	G	A	40	GENIC	homozygous	108326305
X	124753405	124753406	C	T	51	GENIC	homozygous	108326307
X	124756799	124756800	A	G	24	GENIC	heterozygous	108635320
X	124757222	124757223	T	G	44	GENIC	homozygous	108326309
X	124757735	124757736	A	G	58	GENIC	possibly homozygous	108326311
X	124759581	124759582	C	T	45	GENIC	possibly homozygous	108326313
X	124759853	124759854	C	T	54	GENIC	homozygous	108326315
X	124760647	124760648	T	A	50	GENIC	homozygous	108326317
X	124761379	124761380	G	A	42	GENIC	homozygous	108326319