chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	151612611	151612612	C	T	14	GENIC	homozygous	140712198
X	151613790	151613790		C	7	GENIC	heterozygous	140600386
X	151613799	151613800	A		8	GENIC	heterozygous	148137593
X	151613799	151613800	A	C	8	GENIC	homozygous	155209997
X	151617501	151617502	C	G	21	GENIC	homozygous	140712199
X	151617503	151617505	CC		21	GENIC	homozygous	140600387
X	151617511	151617512	C	G	19	GENIC	homozygous	140712200
X	151617540	151617541	C	T	18	GENIC	homozygous	140712201
X	151617504	151617505	C		21	GENIC	homozygous	403490225
X	151617504	151617505	C	T	21	GENIC	heterozygous	403490226
X	151617529	151617530	G		16	GENIC	heterozygous	403490227
X	151617529	151617530	G	C	16	GENIC	homozygous	403490228
X	151617540	151617541	C		18	GENIC	heterozygous	403490229