chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	72131312	72131313	T	TC	38	GENIC	homozygous	45146932
X	72131358	72131359	G	-	28	GENIC	homozygous	45146933
X	72131374	72131375	G	-	27	GENIC	homozygous	45146934
X	72131376	72131377	G	-	27	GENIC	homozygous	45146935
X	72131383	72131384	G	-	23	GENIC	homozygous	45146936
X	72131386	72131387	G	-	21	GENIC	homozygous	45146937
X	72131398	72131399	G	-	22	GENIC	homozygous	45146938
X	72131403	72131404	A	-	22	GENIC	homozygous	45146939