chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	124635881	124635882	G	C	31	GENIC	homozygous	108326124
X	124636223	124636224	G	A	12	GENIC	homozygous	108326126
X	124637404	124637405	A	C	12	GENIC	heterozygous	119951603
X	124637429	124637430	G	A	9	GENIC	homozygous	119951604
X	124642068	124642069	A	G	44	GENIC	heterozygous	119951605
X	124642452	124642453	A	G	19	GENIC	homozygous	108326128
X	124643201	124643202	C	T	33	GENIC	homozygous	108326130
X	124644532	124644533	C	T	17	GENIC	homozygous	108326132
X	124644755	124644756	C	T	29	GENIC	homozygous	108326134
X	124648028	124648029	G	T	12	GENIC	homozygous	108326136
X	124648043	124648044	C	T	13	GENIC	homozygous	108326138
X	124648547	124648548	A	G	34	GENIC	homozygous	108326140
X	124648836	124648837	T	C	30	GENIC	homozygous	108326142
X	124651865	124651866	G	C	21	GENIC	homozygous	108326144
X	124651980	124651981	C	T	18	GENIC	homozygous	108326146
X	124642122	124642123	A	G	18	GENIC	heterozygous	108621613