chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	157100649	157100650	G	A	22	GENIC	homozygous	108354164
X	157110384	157110385	G	T	29	GENIC	heterozygous	133046286
X	157110369	157110370	C	T	32	GENIC	heterozygous	133046285
X	157109857	157109858	A	G	39	GENIC	heterozygous	129832317
X	157109878	157109879	A	C	41	GENIC	heterozygous	130204069
X	157109895	157109896	A	G	43	GENIC	heterozygous	130204070
X	157109919	157109920	G	A	43	GENIC	heterozygous	130516041
X	157110406	157110407	T	G	32	GENIC	heterozygous	120038258
X	157110436	157110437	G	A	33	GENIC	heterozygous	133697497
X	157110666	157110667	C	A	38	GENIC	heterozygous	133657182
X	157110697	157110698	C	A	33	GENIC	heterozygous	133657183