chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	151612611	151612612	C	T	16	GENIC	possibly homozygous	140712198
X	151613799	151613800	A		11	GENIC	heterozygous	148137593
X	151613799	151613800	A	C	11	GENIC	homozygous	155209997
X	151617501	151617502	C	G	20	GENIC	homozygous	140712199
X	151617509	151617510	C	G	12	GENIC	heterozygous	141102293
X	151617511	151617512	C	G	12	GENIC	heterozygous	140712200
X	151617540	151617541	C	T	21	GENIC	homozygous	140712201
X	151617540	151617541	C		21	GENIC	heterozygous	403490229
X	151617503	151617505	CC		12	GENIC	heterozygous	140600387
X	151617504	151617505	C		12	GENIC	heterozygous	403490225
X	151617504	151617505	C	T	12	GENIC	heterozygous	403490226
X	151617529	151617530	G		18	GENIC	heterozygous	403490227
X	151617529	151617530	G	C	18	GENIC	homozygous	403490228