chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	22223448	22223450	TC		18	GENIC	homozygous	129727058
X	22227394	22227394		A	28	GENIC	homozygous	129727061
X	22227427	22227428	T		26	GENIC	homozygous	129727062
X	22227449	22227450	C		28	GENIC	homozygous	129727063
X	22227457	22227458	C		28	GENIC	homozygous	129727064
X	22227466	22227467	G		29	GENIC	homozygous	129727065
X	22227471	22227472	C		29	GENIC	homozygous	129727066
X	22227478	22227478		A	30	GENIC	homozygous	129727067
X	22227533	22227534	T		26	GENIC	homozygous	129727068
X	22227538	22227539	G		26	GENIC	homozygous	129727069
X	22227543	22227544	C		26	GENIC	homozygous	129727070
X	22227547	22227547		A	27	GENIC	homozygous	129727071
X	22252491	22252491		G	21	GENIC	homozygous	129727074
X	22252615	22252616	T		21	GENIC	homozygous	129727075
X	22252670	22252671	C		17	GENIC	homozygous	129727076
X	22252734	22252735	T		2	GENIC	homozygous	129727077
X	22252740	22252740		A	2	GENIC	homozygous	129727078
X	22257363	22257364	T	C	23	GENIC	homozygous	120024288
X	22271757	22271757		CTTT	21	GENIC	homozygous	133793155
X	22280839	22280839		AA	26	GENIC	homozygous	129727089