chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	151609986	151609988	AG		21	GENIC	heterozygous	140600385
X	151612611	151612612	C	T	16	GENIC	homozygous	140712198
X	151613790	151613790		C	12	GENIC	homozygous	140600386
X	151617501	151617502	C	G	17	GENIC	homozygous	140712199
X	151617503	151617505	CC		17	GENIC	homozygous	140600387
X	151617504	151617505	C	T	17	GENIC	heterozygous	403490226
X	151613799	151613800	A		16	GENIC	heterozygous	148137593
X	151613799	151613800	A	C	16	GENIC	homozygous	155209997
X	151617504	151617505	C		17	GENIC	homozygous	403490225
X	151617511	151617512	C	G	18	GENIC	homozygous	140712200
X	151617528	151617530	TG		10	GENIC	heterozygous	140600388
X	151617529	151617530	G		10	GENIC	heterozygous	403490227
X	151617529	151617530	G	C	10	GENIC	heterozygous	403490228
X	151617540	151617541	C	T	12	GENIC	homozygous	140712201
X	151617540	151617541	C		12	GENIC	heterozygous	403490229