chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	31758342	31758343	T	C	15	GENIC	homozygous	108251305
X	31761478	31761479	A	G	6	GENIC	homozygous	108251309
X	31761643	31761644	G	T	9	GENIC	homozygous	108791895
X	31762926	31762927	C	T	20	GENIC	homozygous	108791897
X	31763249	31763250	A	G	9	GENIC	homozygous	108791899
X	31763298	31763299	G	A	11	GENIC	homozygous	108791901
X	31763891	31763892	A	G	12	GENIC	homozygous	108251315
X	31764540	31764541	T	C	16	GENIC	homozygous	108251317
X	31765498	31765499	C	T	21	GENIC	homozygous	108550295
X	31766133	31766134	T	C	16	GENIC	homozygous	108251319
X	31767131	31767132	C	A	11	GENIC	homozygous	108791903
X	31767233	31767234	A	G	15	GENIC	homozygous	108791905
X	31768215	31768216	G	A	15	GENIC	homozygous	108791907
X	31769601	31769602	T	C	10	GENIC	homozygous	108251326
X	31770123	31770124	G	T	19	GENIC	homozygous	108251328
X	31770131	31770132	G	A	21	GENIC	homozygous	108251330
X	31770953	31770954	G	T	9	GENIC	homozygous	108251332
X	31771682	31771683	G	A	6	GENIC	homozygous	108791911
X	31772655	31772656	G	T	8	GENIC	homozygous	108791913
X	31772720	31772721	G	A	10	GENIC	homozygous	108791915
X	31772779	31772780	T	G	8	GENIC	homozygous	108791917
X	31772811	31772812	G	A	8	GENIC	homozygous	108791919
X	31772837	31772838	G	A	7	GENIC	homozygous	108791921
X	31775097	31775098	T	C	12	GENIC	homozygous	108251336
X	31775376	31775377	A	T	7	GENIC	homozygous	108251340
X	31776274	31776275	G	A	11	GENIC	possibly homozygous	108251342
X	31777308	31777309	A	G	16	GENIC	homozygous	108791925