chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	81714770	81714771	C	T	24	GENIC	homozygous	112749131
4	81715015	81715016	T	C	31	GENIC	homozygous	112749135
4	81715130	81715131	T	C	21	GENIC	homozygous	112749137
4	81715612	81715613	C	A	36	GENIC	homozygous	112749139
4	81715689	81715690	A	G	28	GENIC	homozygous	112749141
4	81715798	81715799	A	C	27	GENIC	homozygous	112749143
4	81716837	81716838	A	T	17	GENIC	homozygous	112749145
4	81716904	81716905	A	G	16	GENIC	homozygous	112749147
4	81717167	81717168	C	T	33	GENIC	homozygous	112749149
4	81717181	81717182	C	G	30	GENIC	homozygous	112749151
4	81717480	81717481	C	T	28	GENIC	homozygous	112749153
4	81717602	81717603	G	C	26	GENIC	homozygous	112749155
4	81717813	81717814	A	G	43	GENIC	homozygous	112749157
4	81718138	81718139	A	T	18	GENIC	homozygous	112749159
4	81718346	81718347	A	G	27	GENIC	homozygous	112749163
4	81718525	81718526	C	T	25	GENIC	homozygous	112749165
4	81718706	81718707	C	T	37	GENIC	homozygous	112749167
4	81718900	81718901	C	T	34	GENIC	homozygous	112749169
4	81719201	81719202	A	G	18	GENIC	homozygous	112749173
4	81719571	81719572	C	T	12	GENIC	possibly homozygous	112749175
4	81719776	81719777	A	G	23	GENIC	homozygous	112749177
4	81719898	81719899	C	T	27	GENIC	homozygous	112749179
4	81720189	81720190	C	T	22	GENIC	homozygous	112749181
4	81720319	81720320	T	C	27	GENIC	homozygous	112749183
4	81720416	81720417	G	A	29	GENIC	homozygous	112749185
4	81720635	81720636	A	C	30	GENIC	homozygous	112749187
4	81720641	81720642	A	G	31	GENIC	homozygous	112749189
4	81720849	81720850	C	T	26	GENIC	homozygous	112749191
4	81722736	81722737	T	C	22	GENIC	homozygous	112749205
4	81722853	81722854	A	C	20	GENIC	homozygous	112749207
4	81723984	81723985	T	C	18	GENIC	homozygous	112749211
4	81723989	81723990	A	G	18	GENIC	homozygous	112749213
4	81725996	81725997	A	T	32	GENIC	homozygous	112749217