chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	31758342	31758343	T	C	19	GENIC	homozygous	108251305
X	31761062	31761063	C	T	14	GENIC	homozygous	108251307
X	31761478	31761479	A	G	18	GENIC	homozygous	108251309
X	31761662	31761663	G	A	21	GENIC	homozygous	108251311
X	31763324	31763325	T	G	11	GENIC	homozygous	108251313
X	31763891	31763892	A	G	12	GENIC	homozygous	108251315
X	31764540	31764541	T	C	27	GENIC	homozygous	108251317
X	31766133	31766134	T	C	25	GENIC	homozygous	108251319
X	31769277	31769278	C	T	23	GENIC	homozygous	108251322
X	31769515	31769516	A	G	21	GENIC	homozygous	108251324
X	31769601	31769602	T	C	21	GENIC	homozygous	108251326
X	31770123	31770124	G	T	7	GENIC	homozygous	108251328
X	31770131	31770132	G	A	7	GENIC	homozygous	108251330
X	31770768	31770769	A	G	27	GENIC	heterozygous	108744140
X	31770953	31770954	G	T	22	GENIC	homozygous	108251332
X	31771097	31771098	C	G	26	GENIC	homozygous	108251334
X	31775097	31775098	T	C	12	GENIC	homozygous	108251336
X	31775320	31775321	A	C	23	GENIC	homozygous	108251338
X	31775376	31775377	A	T	21	GENIC	homozygous	108251340
X	31776274	31776275	G	A	30	GENIC	homozygous	108251342
X	31780416	31780417	C	T	31	GENIC	homozygous	108251344
X	31772778	31772779	T	G	15	GENIC	homozygous	108665387
X	31778632	31778633	C	A	12	GENIC	homozygous	108478712
X	31778670	31778671	C	T	19	GENIC	homozygous	108478714