chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	165520848	165520849	G	A	27	GENIC	possibly homozygous	112193129
3	165524264	165524265	A	G	38	GENIC	homozygous	112193130
3	165524659	165524660	A	G	32	GENIC	homozygous	111809056
3	165524983	165524984	T	C	43	GENIC	homozygous	111809058
3	165525934	165525935	C	T	20	GENIC	homozygous	111809060
3	165526166	165526167	T	C	36	GENIC	homozygous	112193131
3	165526362	165526363	G	A	31	GENIC	homozygous	112193132
3	165526396	165526397	C	A	29	GENIC	homozygous	112193133
3	165528989	165528990	G	C	20	GENIC	homozygous	112193134
3	165532400	165532401	T	C	14	GENIC	homozygous	112193135
3	165532461	165532462	C	T	28	GENIC	homozygous	112193136
3	165532884	165532885	C	G	21	GENIC	possibly homozygous	112193137
3	165533220	165533221	T	C	25	GENIC	homozygous	112193138
3	165534595	165534596	G	A	24	GENIC	homozygous	111809068
3	165535343	165535344	T	C	30	GENIC	homozygous	111809072
3	165535384	165535385	A	T	29	GENIC	homozygous	112193139
3	165535779	165535780	T	A	17	GENIC	homozygous	111809074
3	165535963	165535964	C	G	23	GENIC	homozygous	112193140
3	165536392	165536393	C	G	22	GENIC	homozygous	112193141