chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124722798	124722799	T	A	7	GENIC	homozygous	108811688
X	124725082	124725083	A	G	7	GENIC	homozygous	108326273
X	124726205	124726206	G	A	9	GENIC	homozygous	108326275
X	124729053	124729054	A	G	9	GENIC	homozygous	131249534
X	124731446	124731447	T	C	8	GENIC	homozygous	108811694
X	124731973	124731974	A	C	12	GENIC	homozygous	108326277
X	124732732	124732733	C	T	8	GENIC	homozygous	108811696
X	124733723	124733724	A	T	10	GENIC	homozygous	131249535
X	124733992	124733993	T	C	7	GENIC	homozygous	108811698
X	124741491	124741492	T	C	5	GENIC	homozygous	108326281
X	124743397	124743398	C	T	9	GENIC	homozygous	131249536
X	124743427	124743428	A	C	8	GENIC	homozygous	108326283
X	124743935	124743936	A	G	3	GENIC	homozygous	108326285
X	124744963	124744964	C	G	6	GENIC	homozygous	108811714
X	124747331	124747332	G	A	17	GENIC	homozygous	108326293
X	124748552	124748553	T	A	10	GENIC	homozygous	108326295
X	124725318	124725320	AC		8	GENIC	homozygous	131243821
X	124725325	124725340	GGTTTCAATGCCACA		8	GENIC	homozygous	131243822
X	124728513	124728513		AAAAAAAC	3	GENIC	homozygous	131243823
X	124725898	124725899	C	G	4	GENIC	homozygous	108424725
X	124742681	124742682	A	G	6	GENIC	homozygous	108424727
X	124750926	124750926		A	6	GENIC	homozygous	129787178
X	124750979	124750979		T	7	GENIC	homozygous	129787179
X	124751603	124751604	G	A	10	GENIC	homozygous	108811718
X	124754472	124754473	A		7	GENIC	homozygous	129787182
X	124755361	124755362	A	G	5	GENIC	homozygous	108811720
X	124755922	124755923	C	T	4	GENIC	homozygous	131249537
X	124757067	124757067		TTT	4	GENIC	homozygous	131243824
X	124757735	124757736	A	G	3	GENIC	homozygous	108326311
X	124760191	124760198	AACAGCG		7	GENIC	homozygous	131243825
X	124762063	124762064	G	A	5	GENIC	homozygous	131249538
X	124762180	124762181	T	C	6	GENIC	homozygous	131249539
X	124756799	124756800	A	G	1	GENIC	homozygous	108635320