chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	1725197	1725198	A	G	29	GENIC	heterozygous	119899446
X	1727406	1727407	A	G	26	GENIC	homozygous	108216148
X	1728343	1728344	A	G	23	GENIC	homozygous	119899447
X	1728355	1728356	C	G	24	GENIC	homozygous	119899448
X	1728390	1728391	A	G	22	GENIC	homozygous	119899449
X	1733840	1733841	A	T	31	GENIC	homozygous	108216152
X	1735102	1735103	T	C	33	GENIC	homozygous	108216154
X	1735375	1735376	A	G	23	GENIC	homozygous	108216157
X	1735609	1735610	A	G	14	GENIC	homozygous	108216159
X	1735692	1735693	G	A	15	GENIC	possibly homozygous	119899450
X	1736053	1736054	T	C	27	GENIC	homozygous	108216162
X	1736611	1736612	G	A	26	GENIC	homozygous	108216164
X	1739750	1739751	C	G	13	GENIC	homozygous	108216166
X	1741872	1741873	T	C	21	GENIC	homozygous	108216168
X	1743672	1743673	C	T	26	GENIC	homozygous	108216170