chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	71020914	71020915	A	G	14	GENIC	homozygous	108501753
X	71020970	71020971	G	T	14	GENIC	homozygous	108391205
X	71021161	71021162	T	G	5	GENIC	homozygous	108273180
X	71021227	71021228	G	A	9	GENIC	homozygous	108273182
X	71044799	71044800	A	T	10	GENIC	homozygous	108391207
X	71044964	71044965	C	T	11	GENIC	homozygous	108273188
X	71044965	71044966	T	C	11	GENIC	homozygous	108273190
X	71045055	71045056	A	C	16	GENIC	homozygous	108273194
X	71045146	71045147	C	G	15	GENIC	homozygous	108273196
X	71045173	71045174	C	G	14	GENIC	homozygous	108273198
X	71045304	71045305	G	T	12	GENIC	homozygous	108273200
X	71045609	71045610	C	A	7	GENIC	homozygous	108391213
X	71051476	71051477	G	A	3	GENIC	homozygous	108391215
X	71051494	71051495	G	A	4	GENIC	homozygous	108391217
X	71051497	71051498	C	A	5	GENIC	homozygous	108391219
X	71051506	71051507	G	A	4	GENIC	homozygous	108391221
X	71051510	71051511	G	A	6	GENIC	homozygous	108391223
X	71051546	71051547	G	A	7	GENIC	homozygous	108449787
X	71051547	71051548	A	G	7	GENIC	homozygous	108391225
X	71051557	71051558	C	T	8	GENIC	homozygous	108273212
X	71079576	71079577	C	T	11	GENIC	homozygous	108501755
X	71079583	71079584	G	T	12	GENIC	homozygous	108501757