chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	34896381	34896382	G	A	28	GENIC	homozygous	148992834
X	35012994	35012995	T		8	GENIC	heterozygous	142743799
X	35048229	35048230	G	A	5	GENIC	homozygous	145102473
X	35048233	35048234	G	A	5	GENIC	homozygous	148992835
X	35118346	35118347	C	A	19	GENIC	homozygous	403479242
X	35048242	35048243	A		5	GENIC	heterozygous	403479221
X	35048242	35048243	A	G	5	GENIC	homozygous	403479222
X	35048246	35048247	A		5	GENIC	heterozygous	403479223
X	35048246	35048247	A	G	5	GENIC	homozygous	403479224
X	35118346	35118347	C		19	GENIC	heterozygous	403479243
X	35138779	35138780	A	T	17	GENIC	heterozygous	155173756
X	35138779	35138780	A		17	GENIC	heterozygous	403479244
X	35192641	35192642	C		6	GENIC	heterozygous	403479258
X	35161954	35161955	A	C	6	GENIC	homozygous	140635131
X	35196565	35196566	T	G	20	GENIC	homozygous	140635132
X	35161954	35161955	A		6	GENIC	heterozygous	403870031
X	35192641	35192642	C	T	6	GENIC	homozygous	141124665
X	35192642	35192643	T	C	5	GENIC	homozygous	141124666