chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	64891560	64891561	C	G	14	GENIC	homozygous	108271424
X	64895132	64895133	G	T	25	GENIC	homozygous	108383821
X	64895565	64895566	G	A	16	GENIC	homozygous	108383823
X	64896970	64896971	G	A	20	GENIC	homozygous	108383825
X	64897008	64897009	C	A	19	GENIC	homozygous	108665795
X	64897030	64897031	A	G	19	GENIC	possibly homozygous	108665798
X	64897272	64897273	C	T	34	GENIC	possibly homozygous	108383827
X	64898349	64898350	T	A	12	GENIC	homozygous	108383829
X	64898819	64898820	C	T	26	GENIC	homozygous	108383830
X	64899272	64899273	C	T	27	GENIC	homozygous	108383832
X	64899479	64899480	T	A	20	GENIC	homozygous	108665800
X	64899637	64899638	A	G	22	GENIC	homozygous	108271428
X	64899639	64899640	A	G	21	GENIC	homozygous	108383834
X	64900289	64900290	A	G	20	GENIC	homozygous	108383838
X	64901853	64901854	A	C	29	GENIC	homozygous	108271430
X	64902046	64902047	G	C	18	GENIC	homozygous	108383840
X	64902280	64902281	A	C	22	GENIC	homozygous	108383842
X	64902931	64902932	G	A	13	GENIC	homozygous	108665802
X	64905490	64905491	C	T	12	GENIC	homozygous	108665804
X	64905515	64905516	A	G	12	GENIC	homozygous	108665806
X	64907392	64907393	A	C	18	GENIC	homozygous	108383844