chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	159015719	159015720	G	A	6	GENIC	homozygous	108646006
X	159015724	159015725	A	T	6	GENIC	homozygous	119965744
X	159015745	159015746	G	T	4	GENIC	homozygous	108429487
X	159023836	159023837	C	A	13	GENIC	homozygous	108354707
X	159023947	159023948	G	A	12	GENIC	homozygous	108354709
X	159032627	159032628	G	C	28	GENIC	possibly homozygous	108681841
X	159033153	159033154	C	A	7	GENIC	homozygous	119965754
X	159033803	159033804	A	T	19	GENIC	homozygous	119965756
X	159033806	159033807	C	A	20	GENIC	possibly homozygous	119965758
X	159033989	159033990	T	C	12	GENIC	homozygous	119965760
X	159034168	159034169	G	A	8	GENIC	homozygous	108681843
X	159034442	159034443	G	T	10	GENIC	homozygous	108354742
X	159034245	159034246	G	A	11	GENIC	homozygous	108692646
X	159034160	159034161	T	A	11	GENIC	homozygous	108609936