chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	121054277	121054278	T	A	8	GENIC	homozygous	108421929
X	121054859	121054860	G	A	29	GENIC	homozygous	108320945
X	121057930	121057931	A	G	9	GENIC	homozygous	108320948
X	121058118	121058119	T	G	19	GENIC	homozygous	108421931
X	121058358	121058359	G	A	19	GENIC	homozygous	108421933
X	121058804	121058805	C	T	26	GENIC	homozygous	108421935
X	121060021	121060022	C	T	29	GENIC	homozygous	108421937
X	121060320	121060321	A	G	25	GENIC	homozygous	108320950
X	121060580	121060581	T	G	12	GENIC	homozygous	108421939
X	121062272	121062273	A	G	17	GENIC	homozygous	108421941
X	121062759	121062760	T	C	16	GENIC	homozygous	108421943
X	121063891	121063892	G	T	32	GENIC	homozygous	108421945
X	121063973	121063974	T	C	14	GENIC	homozygous	108421947
X	121064461	121064462	C	T	15	GENIC	homozygous	108421949
X	121064512	121064513	G	T	14	GENIC	homozygous	108421951
X	121064763	121064764	T	C	25	GENIC	homozygous	108421953
X	121064776	121064777	T	C	24	GENIC	homozygous	108320954
X	121065193	121065194	C	T	22	GENIC	homozygous	108421955
X	121065399	121065400	A	G	22	GENIC	homozygous	108320956
X	121065616	121065617	C	T	17	GENIC	homozygous	108421957
X	121066144	121066145	C	T	17	GENIC	homozygous	108320958
X	121066216	121066217	G	A	27	GENIC	homozygous	108421959
X	121066307	121066308	T	C	32	GENIC	homozygous	108320960
X	121066518	121066519	A	G	24	GENIC	homozygous	108320964
X	121066524	121066525	C	T	23	GENIC	homozygous	108421961
X	121066621	121066622	G	T	19	GENIC	homozygous	108421963
X	121066672	121066673	C	A	16	GENIC	homozygous	108421965