chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	64235265	64235266	C	CATG	15	GENIC	homozygous	45141655
X	64237819	64237820	A	-	12	GENIC	homozygous	45141660
X	64239412	64239413	T	TG	15	GENIC	homozygous	45141662
X	64239978	64239979	C	A	5	GENIC	homozygous	45141663
X	64247201	64247202	G	GT	17	GENIC	homozygous	45141675
X	64247207	64247208	G	GT	17	GENIC	homozygous	45141676
X	64259218	64259219	T	A	18	GENIC	homozygous	45141678
X	64261242	64261243	G	GA	3	GENIC	heterozygous	45141682
X	64261889	64261894	AAGTA	-----	13	GENIC	heterozygous	45478312
X	64266648	64266649	T	TTGCTGTTTTGGTTTTTGTTCCAAATTAGCTGCCTTTGTTTTCCCCAATTAAGTAAGTTGCCTGCAGGCAGGGCCCACAAGATCTACTTTTCTACTTAATGCAACCTAGTCCAGTGCCA	23	GENIC	homozygous	45478314
X	64266826	64266827	C	T	15	GENIC	homozygous	45141688
X	64266835	64266836	C	-	15	GENIC	homozygous	45478316
X	64266836	64266837	C	G	15	GENIC	homozygous	45510264
X	64266838	64266839	C	CA	16	GENIC	homozygous	45478318
X	64266844	64266845	C	A	15	GENIC	homozygous	45141691
X	64266859	64266860	C	T	14	GENIC	homozygous	45141692
X	64266860	64266861	C	A	14	GENIC	homozygous	45141693
X	64266863	64266864	C	A	12	GENIC	homozygous	45141694
X	64271651	64271652	C	CTTTT	4	GENIC	heterozygous	45510266