chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	48464562	48464563	G	A	18	GENIC	homozygous	113440745
4	48464704	48464705	A	G	24	GENIC	homozygous	113440747
4	48464830	48464831	T	C	37	GENIC	homozygous	113440749
4	48464853	48464854	G	T	41	GENIC	homozygous	113440751
4	48464914	48464915	A	C	33	GENIC	homozygous	113440753
4	48466218	48466219	C	A	25	GENIC	homozygous	112638147
4	48466378	48466379	T	A	15	GENIC	homozygous	113440755
4	48466472	48466473	A	G	17	GENIC	homozygous	112638149
4	48466682	48466683	T	C	15	GENIC	homozygous	112638151
4	48467567	48467568	T	C	22	GENIC	homozygous	113440762
4	48467581	48467582	A	T	24	GENIC	homozygous	112638155
4	48468026	48468027	A	G	39	GENIC	homozygous	113440764
4	48469446	48469447	A	G	21	GENIC	homozygous	112638161
4	48469512	48469513	T	C	17	GENIC	homozygous	112638163
4	48469794	48469795	T	G	12	GENIC	homozygous	112638165
4	48469997	48469998	C	T	27	GENIC	homozygous	112638167
4	48470003	48470004	T	C	31	GENIC	homozygous	112638169
4	48470070	48470071	C	A	39	GENIC	homozygous	112638171
4	48470617	48470618	A	T	19	GENIC	homozygous	112638175
4	48470693	48470694	T	C	21	GENIC	homozygous	112638177
4	48470715	48470716	T	C	24	GENIC	homozygous	112638179
4	48470763	48470764	G	A	25	GENIC	homozygous	112638181
4	48470898	48470899	C	T	16	GENIC	homozygous	112638183
4	48471073	48471074	T	A	26	GENIC	homozygous	112638185
4	48471097	48471098	T	C	29	GENIC	homozygous	112638187
4	48471164	48471165	C	G	36	GENIC	homozygous	112638189
4	48471192	48471193	T	C	26	GENIC	homozygous	112638191
4	48471193	48471194	G	A	25	GENIC	homozygous	112638193
4	48471221	48471222	C	G	23	GENIC	homozygous	112638195