chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	106727066	106727067	A	G	13	GENIC	homozygous	45327733
X	106727161	106727162	T	TA	11	GENIC	homozygous	45191189
X	106727552	106727553	A	-	19	GENIC	homozygous	45327734
X	106727670	106727671	G	A	12	GENIC	homozygous	45327735
X	106728886	106728887	T	C	13	GENIC	possibly homozygous	45327736
X	106730253	106730254	G	A	13	GENIC	homozygous	45327737
X	106730289	106730290	C	T	11	GENIC	homozygous	45327738
X	106730450	106730451	C	CAA	9	GENIC	homozygous	45327739
X	106730517	106730518	C	T	14	GENIC	homozygous	45887664
X	106731315	106731316	T	-	6	GENIC	homozygous	45327740
X	106732344	106732345	T	C	14	GENIC	homozygous	45327741
X	106732537	106732538	C	G	9	GENIC	homozygous	45327742
X	106732654	106732655	T	-	9	GENIC	homozygous	45327743
X	106733024	106733025	C	G	10	GENIC	homozygous	45327744
X	106733038	106733039	T	C	10	GENIC	homozygous	45327745
X	106733727	106733728	T	C	10	GENIC	homozygous	45327746
X	106734124	106734125	T	C	13	GENIC	homozygous	45327747
X	106735554	106735558	CACA	----	6	GENIC	homozygous	45770414
X	106735831	106735832	A	G	13	GENIC	homozygous	45887665
X	106735921	106735922	A	AAAC	11	GENIC	homozygous	45327749
X	106736389	106736390	C	CA	9	GENIC	homozygous	45327750
X	106736422	106736423	C	CA	13	GENIC	homozygous	45191190
X	106736483	106736484	A	G	7	GENIC	homozygous	45887666
X	106736816	106736919	AAAATTCCCTGGGATTATGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCTCAAGGCCCTGGGTTCGGTCCCCAGCTCCCCAAAAAAAAA	-------------------------------------------------------------------------------------------------------	6	GENIC	homozygous	45669296
X	106737442	106737444	AA	--	4	GENIC	homozygous	45669297
X	106737529	106737530	A	AT	11	GENIC	homozygous	45327752
X	106738990	106738991	A	-	7	GENIC	homozygous	45327753
X	106739264	106739265	C	T	11	GENIC	homozygous	45327754
X	106739473	106739474	G	C	9	GENIC	homozygous	45327755
X	106736065	106736080	TTGTTGTTGTTGTTG	---------------	5	GENIC	homozygous	45614406