chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	48464562	48464563	G	A	26	GENIC	homozygous	113440745
4	48464830	48464831	T	C	20	GENIC	homozygous	113440749
4	48464853	48464854	G	T	22	GENIC	homozygous	113440751
4	48464914	48464915	A	C	31	GENIC	homozygous	113440753
4	48464993	48464994	T	A	5	GENIC	homozygous	119461557
4	48464995	48464996	T	G	5	GENIC	homozygous	119510911
4	48464997	48464998	T	G	1	GENIC	homozygous	119461558
4	48465715	48465716	C	T	3	GENIC	homozygous	112638143
4	48466218	48466219	C	A	34	GENIC	homozygous	112638147
4	48466472	48466473	A	G	22	GENIC	homozygous	112638149
4	48466682	48466683	T	C	24	GENIC	homozygous	112638151
4	48467567	48467568	T	C	24	GENIC	homozygous	113440762
4	48467581	48467582	A	T	26	GENIC	homozygous	112638155
4	48468026	48468027	A	G	28	GENIC	homozygous	113440764
4	48469446	48469447	A	G	26	GENIC	homozygous	112638161
4	48469512	48469513	T	C	19	GENIC	homozygous	112638163
4	48469794	48469795	T	G	32	GENIC	homozygous	112638165
4	48469997	48469998	C	T	22	GENIC	possibly homozygous	112638167
4	48470003	48470004	T	C	24	GENIC	possibly homozygous	112638169
4	48470070	48470071	C	A	28	GENIC	homozygous	112638171
4	48470617	48470618	A	T	30	GENIC	homozygous	112638175
4	48470693	48470694	T	C	35	GENIC	homozygous	112638177
4	48470715	48470716	T	C	43	GENIC	homozygous	112638179
4	48470763	48470764	G	A	45	GENIC	homozygous	112638181
4	48470898	48470899	C	T	29	GENIC	homozygous	112638183
4	48471073	48471074	T	A	40	GENIC	homozygous	112638185
4	48471097	48471098	T	C	44	GENIC	homozygous	112638187
4	48471164	48471165	C	G	29	GENIC	homozygous	112638189
4	48471192	48471193	T	C	25	GENIC	homozygous	112638191
4	48471193	48471194	G	A	25	GENIC	homozygous	112638193
4	48471221	48471222	C	G	26	GENIC	homozygous	112638195