chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	127094670	127094671	G	A	9	GENIC	homozygous	140702742
X	127095791	127095792	T	C	11	GENIC	homozygous	140702743
X	127097654	127097655	T		14	GENIC	homozygous	140597182
X	127102371	127102372	T		9	GENIC	homozygous	140597183
X	127105770	127105770		TT	6	GENIC	homozygous	140597185
X	127105864	127105865	A	G	7	GENIC	homozygous	140702744
X	127110928	127110928		AGTC	8	GENIC	homozygous	140597186
X	127112978	127112979	A	G	8	GENIC	homozygous	140702745
X	127114132	127114133	A	T	9	GENIC	homozygous	140702746
X	127114338	127114339	C	T	8	GENIC	homozygous	140702747
X	127114447	127114448	A	T	6	GENIC	homozygous	140702748
X	127115029	127115030	C	G	8	GENIC	homozygous	140702749
X	127115143	127115144	T	C	13	GENIC	homozygous	140702750
X	127115696	127115697	A	T	6	GENIC	homozygous	140702751
X	127115749	127115750	G	A	7	GENIC	homozygous	140702752
X	127116439	127116440	A	C	8	GENIC	homozygous	140702753
X	127116887	127116888	T	G	9	GENIC	homozygous	140702754
X	127117147	127117148	C	T	8	GENIC	homozygous	140702755
X	127117604	127117605	C	T	7	GENIC	homozygous	140702756
X	127119989	127119990	C	T	8	GENIC	homozygous	140702757
X	127120669	127120670	A	C	8	GENIC	homozygous	140702758
X	127121056	127121057	T	A	12	GENIC	homozygous	140702759
X	127121643	127121644	T	G	14	GENIC	homozygous	140702760
X	127122368	127122369	C	T	12	GENIC	homozygous	140702761
X	127128479	127128480	G	A	10	GENIC	homozygous	140702762
X	127130399	127130400	A	G	10	GENIC	homozygous	140702763
X	127130455	127130456	A	T	12	GENIC	homozygous	140702764
X	127132623	127132623		T	9	GENIC	homozygous	140597187
X	127133993	127133994	G	T	8	GENIC	homozygous	140702765
X	127138814	127138815	A	G	11	GENIC	homozygous	140702766
X	127139427	127139428	G	A	9	GENIC	homozygous	140702767