chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	116768971	116768972	G		39	GENIC	homozygous	129782357
X	116768984	116768985	T		36	GENIC	homozygous	129782358
X	116768990	116768991	T		36	GENIC	homozygous	129782359
X	116768994	116768995	A	C	39	GENIC	homozygous	108313442
X	116768998	116768999	C	G	38	GENIC	homozygous	108313444
X	116769021	116769022	T		31	GENIC	homozygous	129782360
X	116769027	116769028	C	A	31	GENIC	homozygous	108313446
X	116769031	116769032	C	A	31	GENIC	homozygous	108313448
X	116769033	116769034	G	A	31	GENIC	homozygous	108313450
X	116769034	116769035	A	G	31	GENIC	homozygous	108313452
X	116778169	116778170	G		41	GENIC	homozygous	129782362
X	116778180	116778180		A	38	GENIC	homozygous	129782363
X	116808178	116808178		A	31	GENIC	homozygous	129782364