chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	71340070	71340125	CTCTCCTCTCCTCTCCTTTCCTCTCCTCTCCTCTCCTCTCCTCTCCTCTCCTCTC	-------------------------------------------------------	7	GENIC	heterozygous	45588195
X	71356307	71356308	C	CTCTT	7	GENIC	homozygous	45588197
X	71361083	71361087	GTGT	----	10	GENIC	heterozygous	45511838
X	71361085	71361087	GT	--	10	GENIC	heterozygous	45569728
X	71369035	71369037	AC	--	12	GENIC	heterozygous	45511840
X	71372026	71372027	A	G	28	GENIC	homozygous	45260118
X	71372027	71372028	G	T	28	GENIC	homozygous	45478617
X	71372039	71372040	A	-	25	GENIC	homozygous	45146764
X	71372044	71372045	A	AG	25	GENIC	homozygous	45146765
X	71372771	71372772	T	C	24	GENIC	homozygous	45146766
X	71377390	71377392	AC	--	5	GENIC	heterozygous	45588199
X	71381701	71381703	GT	--	9	GENIC	homozygous	45511842
X	71396407	71396409	CA	--	8	GENIC	heterozygous	45511844
X	71397065	71397066	A	AG	31	GENIC	homozygous	45146773
X	71401900	71401901	G	T	26	GENIC	homozygous	45146774
X	71418177	71418207	TGGAAGCAACCCCCAGTGTTGCTGATTATG	------------------------------	8	GENIC	homozygous	45511848
X	71424548	71424555	GTTGATG	-------	14	GENIC	heterozygous	45588201
X	71424591	71424600	ATGAAGCCT	---------	11	GENIC	heterozygous	45146777
X	71429432	71429433	A	ATG	9	GENIC	heterozygous	45260191
X	71429432	71429433	A	ATGTGTGTGTGTGTGTGTGTG	9	GENIC	heterozygous	45588203