chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	110793698	110793699	T	C	7	GENIC	homozygous	108416410
X	110794268	110794269	C	A	5	GENIC	homozygous	108416412
X	110794272	110794273	T	G	5	GENIC	homozygous	108416414
X	110796367	110796368	A	G	10	GENIC	homozygous	108416416
X	110798756	110798757	C	T	7	GENIC	homozygous	108416418
X	110799574	110799575	G	A	10	GENIC	homozygous	108416420
X	110800421	110800422	T	G	9	GENIC	homozygous	108416422
X	110802250	110802251	A	G	10	GENIC	homozygous	108308735
X	110802251	110802252	A	C	11	GENIC	homozygous	108308737
X	110803193	110803194	A	G	13	GENIC	homozygous	108416424
X	110804601	110804602	C	A	7	GENIC	homozygous	108416426
X	110807336	110807337	G	A	8	GENIC	homozygous	108416428
X	110808068	110808069	G	A	4	GENIC	homozygous	108416430
X	110808159	110808160	C	A	9	GENIC	homozygous	108416432
X	110808725	110808726	T	C	9	GENIC	homozygous	108416434
X	110808747	110808748	A	G	8	GENIC	homozygous	108416436
X	110811742	110811743	A	G	6	GENIC	homozygous	108416438
X	110811766	110811767	A	G	6	GENIC	homozygous	108416440
X	110811769	110811770	A	G	6	GENIC	homozygous	108416442
X	110812337	110812338	A	G	13	GENIC	homozygous	108416444
X	110812673	110812674	G	A	10	GENIC	homozygous	108416446
X	110813762	110813763	A	G	14	GENIC	homozygous	108416448
X	110816087	110816088	C	T	15	GENIC	homozygous	108416450
X	110817167	110817168	A	G	12	GENIC	homozygous	108416452
X	110817422	110817423	T	C	7	GENIC	homozygous	108416454
X	110817507	110817508	A	G	10	GENIC	homozygous	108416456
X	110817670	110817671	A	G	13	GENIC	homozygous	108416458
X	110817830	110817831	A	T	8	GENIC	homozygous	108416460
X	110818096	110818097	C	G	10	GENIC	homozygous	108416462
X	110821498	110821499	C	T	8	GENIC	homozygous	108416464
X	110830220	110830221	C	T	6	GENIC	homozygous	108416466
X	110855061	110855062	A	T	4	GENIC	homozygous	108308743
X	110863782	110863783	A	G	5	GENIC	homozygous	108308745
X	110864123	110864124	G	T	8	GENIC	homozygous	108308748
X	110872628	110872629	G	C	4	GENIC	homozygous	108308752