chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	153632002	153632003	G	-	9	GENIC	homozygous	45248875
X	153633802	153633803	T	-	3	GENIC	homozygous	45322105
X	153647276	153647278	AC	--	6	GENIC	heterozygous	45270322
X	153647900	153647901	C	CA	9	GENIC	homozygous	45248889
X	153647907	153647908	C	CA	12	GENIC	homozygous	45248890
X	153655014	153655015	C	A	10	GENIC	homozygous	45248894
X	153655051	153655052	G	-	9	GENIC	homozygous	45248895
X	153655058	153655059	C	-	8	GENIC	homozygous	45248896
X	153655068	153655069	C	-	8	GENIC	homozygous	45248897
X	153655098	153655099	C	-	6	GENIC	homozygous	45248898
X	153655120	153655121	T	-	9	GENIC	homozygous	45248899
X	153655125	153655126	G	A	10	GENIC	homozygous	45248900
X	153655715	153655716	T	-	6	GENIC	heterozygous	45532313
X	153665825	153665827	GT	--	2	GENIC	heterozygous	45532315
X	153668312	153668314	TG	--	4	GENIC	heterozygous	45248916
X	153634613	153634614	C	CTGAAGCTGTGGGGTAAGGGTGGACAAAGTTTTGCTGGACACAGTGGCTTATGCCTGTAATTCTAGCATTT	5	GENIC	heterozygous	45486709
X	153668311	153668312	C	CTGTGTGTG	4	GENIC	heterozygous	45600965