chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	15713534	15713535	C	T	12	GENIC	homozygous	108472335
X	15714637	15714638	C	T	17	GENIC	homozygous	108472337
X	15715657	15715658	T	C	13	GENIC	homozygous	108369997
X	15716319	15716320	G	A	11	GENIC	possibly homozygous	108671666
X	15717269	15717270	T	C	6	GENIC	homozygous	108370001
X	15719294	15719295	A	G	10	GENIC	homozygous	108472339
X	15723072	15723073	G	A	10	GENIC	homozygous	108472341
X	15725476	15725477	A	G	12	GENIC	homozygous	108370013
X	15726376	15726377	G	A	11	GENIC	homozygous	108370015
X	15727463	15727464	T	C	8	GENIC	homozygous	108370019
X	15730869	15730870	C	T	14	GENIC	homozygous	108370023
X	15733944	15733945	G	C	11	GENIC	homozygous	108472344
X	15734825	15734826	C	T	6	GENIC	homozygous	108472346
X	15734856	15734857	T	C	8	GENIC	homozygous	108472348
X	15737104	15737105	G	A	12	GENIC	homozygous	108370025
X	15738775	15738776	C	G	5	GENIC	homozygous	108671669
X	15717436	15717437	C	G	73	GENIC	heterozygous	120023057
X	15717821	15717822	C	G	244	GENIC	heterozygous	120023058
X	15719191	15719192	G	T	7	GENIC	homozygous	120023059
X	15739073	15739074	G	A	6	GENIC	homozygous	108563003
X	15739119	15739120	C	T	9	GENIC	homozygous	108563005
X	15739586	15739587	C	T	16	GENIC	homozygous	108472354
X	15739854	15739855	G	C	9	GENIC	homozygous	108563007
X	15739875	15739876	C	T	10	GENIC	homozygous	108563009
X	15740219	15740220	A	T	9	GENIC	homozygous	108563011
X	15740240	15740241	A	G	9	GENIC	homozygous	108370031
X	15740308	15740309	T	A	7	GENIC	homozygous	108472357
X	15740380	15740381	C	T	9	GENIC	homozygous	108472359