chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	153628373	153628375	GT	--	23	GENIC	heterozygous	45532309
X	153632002	153632003	G	-	18	GENIC	homozygous	45248875
X	153632108	153632110	CA	--	2	GENIC	homozygous	45532311
X	153633802	153633803	T	-	14	GENIC	homozygous	45322105
X	153634613	153634614	C	CTGAAGCTGTGGGGTAAGGGTGGACAAAGTTTTGCTGGACACAGTGGCTTATGCCTGTAATTCTAGCATTT	20	GENIC	possibly homozygous	45486709
X	153647276	153647278	AC	--	3	GENIC	heterozygous	45270322
X	153647900	153647901	C	CA	27	GENIC	homozygous	45248889
X	153647907	153647908	C	CA	29	GENIC	homozygous	45248890
X	153655014	153655015	C	A	25	GENIC	homozygous	45248894
X	153655051	153655052	G	-	26	GENIC	homozygous	45248895
X	153655058	153655059	C	-	26	GENIC	homozygous	45248896
X	153655068	153655069	C	-	30	GENIC	homozygous	45248897
X	153655098	153655099	C	-	29	GENIC	homozygous	45248898
X	153655120	153655121	T	-	25	GENIC	homozygous	45248899
X	153655125	153655126	G	A	23	GENIC	homozygous	45248900
X	153665825	153665827	GT	--	5	GENIC	heterozygous	45532315
X	153667839	153667840	A	-	9	GENIC	heterozygous	45322133
X	153668312	153668314	TG	--	5	GENIC	heterozygous	45248916
X	153668711	153668713	GT	--	7	GENIC	heterozygous	45574559