chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	153632002	153632003	G	-	2	GENIC	homozygous	45248875
X	153633802	153633803	T	-	3	GENIC	homozygous	45322105
X	153634613	153634614	C	CTGAAGCTGTGGGGTAAGGGTGGACAAAGTTTTGCTGGACACAGTGGCTTATGCCTGTAATTCTAGCATTT	1	GENIC	homozygous	45486709
X	153642544	153642545	A	-	2	GENIC	heterozygous	45248886
X	153647900	153647901	C	CA	3	GENIC	homozygous	45248889
X	153647907	153647908	C	CA	3	GENIC	homozygous	45248890
X	153655014	153655015	C	A	3	GENIC	homozygous	45248894
X	153655051	153655052	G	-	2	GENIC	homozygous	45248895
X	153655058	153655059	C	-	2	GENIC	homozygous	45248896
X	153655068	153655069	C	-	2	GENIC	homozygous	45248897
X	153655098	153655099	C	-	1	GENIC	homozygous	45248898
X	153655120	153655121	T	-	2	GENIC	homozygous	45248899
X	153655125	153655126	G	A	2	GENIC	homozygous	45248900
X	153665824	153665825	A	AGTGT	2	GENIC	heterozygous	45248914
X	153667839	153667840	A	-	2	GENIC	homozygous	45322133