chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	6557017	6557018	T	A	35	GENIC	homozygous	108219743
X	6558301	6558302	C	G	28	GENIC	homozygous	108219745
X	6559089	6559090	G	A	31	GENIC	homozygous	108219747
X	6562629	6562630	A	T	24	GENIC	homozygous	108219749
X	6566431	6566432	T	C	26	GENIC	homozygous	108219751
X	6570967	6570967		C	21	GENIC	homozygous	129717662
X	6562539	6562539		A	24	GENIC	homozygous	129717661
X	6571215	6571216	A	G	31	GENIC	homozygous	108219753
X	6573162	6573162		T	14	GENIC	possibly homozygous	129717663
X	6573165	6573165		T	13	GENIC	possibly homozygous	129717664
X	6573658	6573658		T	2	GENIC	homozygous	129717665
X	6577193	6577194	A	T	30	GENIC	homozygous	108219755
X	6577570	6577571	A	T	32	GENIC	homozygous	108219757
X	6578442	6578443	A	T	27	GENIC	homozygous	108219759
X	6579342	6579347	GTATG		23	GENIC	possibly homozygous	129717666
X	6573052	6573053	A	G	10	GENIC	homozygous	119983717
X	6583184	6583185	G		10	GENIC	homozygous	129717667
X	6583186	6583189	TAG		10	GENIC	homozygous	129717668
X	6585493	6585494	A		12	GENIC	homozygous	129717669
X	6585621	6585622	T	C	26	GENIC	homozygous	119901820
X	6589306	6589307	G	A	23	GENIC	homozygous	108219761
X	6589455	6589456	T		27	GENIC	homozygous	129717670
X	6596237	6596237		G	9	GENIC	heterozygous	129717671
X	6598539	6598540	C	T	32	GENIC	homozygous	108219763
X	6602277	6602278	G	T	27	GENIC	homozygous	108219765
X	6602283	6602284	G	T	28	GENIC	homozygous	108219767
X	6602287	6602288	T		28	GENIC	homozygous	129717673
X	6607251	6607252	C		28	GENIC	homozygous	129717674
X	6612098	6612098		T	27	GENIC	heterozygous	129717675
X	6615262	6615263	T		25	GENIC	homozygous	129717676