chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	114367214	114367215	G	T	12	GENIC	homozygous	108312332
X	114367418	114367419	A	C	21	GENIC	homozygous	108312334
X	114367612	114367613	G	T	22	GENIC	homozygous	108312336
X	114367696	114367697	A	T	28	GENIC	homozygous	108312338
X	114367697	114367698	A	C	28	GENIC	homozygous	108312340
X	114368334	114368335	G	A	40	GENIC	homozygous	108312342
X	114371893	114371894	G	A	22	GENIC	homozygous	108312346
X	114372312	114372313	C	T	12	GENIC	homozygous	108454005
X	114373248	114373249	G	A	11	GENIC	homozygous	108312348
X	114373322	114373323	C	T	10	GENIC	homozygous	108312350
X	114374627	114374628	G	A	37	GENIC	homozygous	108312352
X	114375835	114375836	A	G	34	GENIC	homozygous	108312354
X	114376129	114376130	T	G	26	GENIC	homozygous	108312356
X	114377249	114377250	G	A	20	GENIC	homozygous	108312358