chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124917277	124917278	G	T	24	GENIC	homozygous	45216454
X	124919782	124919783	C	CTT	4	GENIC	heterozygous	45440602
X	124921854	124921855	T	TGTGTGA	10	GENIC	possibly homozygous	45482420
X	124922291	124922292	A	-	27	GENIC	homozygous	45216456
X	124922491	124922492	A	AATAC	17	GENIC	homozygous	45482422
X	124924939	124924942	TTT	---	16	GENIC	homozygous	45525449
X	124925592	124925593	C	CTTAAATA	21	GENIC	homozygous	45216458
X	124926212	124926213	A	T	23	GENIC	homozygous	45216459
X	124926321	124926322	C	G	24	GENIC	homozygous	45216460
X	124928275	124928276	C	T	22	GENIC	homozygous	45216461
X	124928503	124928504	G	GTGTA	19	GENIC	possibly homozygous	45216462
X	124928807	124928808	T	C	26	GENIC	homozygous	45216463
X	124929265	124929266	G	GA	11	GENIC	homozygous	45216464
X	124931109	124931110	A	G	25	GENIC	homozygous	45216465
X	124931553	124931554	G	A	22	GENIC	homozygous	45216466
X	124931970	124931971	C	T	29	GENIC	homozygous	45216467
X	124934546	124934547	A	-	11	GENIC	homozygous	45216468
X	124938495	124938500	AAAAC	-----	21	GENIC	homozygous	45216470
X	124940941	124940942	A	-	29	GENIC	homozygous	45216471
X	124941196	124941197	C	CGT	26	GENIC	homozygous	45216472
X	124941268	124941269	C	T	26	GENIC	homozygous	45216473
X	124942883	124942884	A	C	17	GENIC	homozygous	45216474
X	124946353	124946354	C	CT	14	GENIC	homozygous	45216475
X	124946907	124946908	C	CA	10	GENIC	homozygous	45216476
X	124946985	124946986	C	T	22	GENIC	homozygous	45216477
X	124948825	124948826	G	GAGAGGA	19	GENIC	homozygous	45216478
X	124950135	124950136	C	CA	26	GENIC	homozygous	45216479
X	124950649	124950661	TCTGTCTGTCTC	------------	6	GENIC	homozygous	45525451
X	124950665	124950675	TGTGTGTGTG	----------	4	GENIC	heterozygous	45216480
X	124951981	124951982	G	A	23	GENIC	homozygous	45216481
X	124952335	124952336	G	GTGTCCTCTTGAC	40	GENIC	homozygous	45216482