chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	127666389	127666390	A	G	18	GENIC	homozygous	60848102
1	127666599	127666600	T	C	11	GENIC	homozygous	60848103
1	127667791	127667792	T	G	18	GENIC	possibly homozygous	60848106
1	127667993	127667994	T	C	17	GENIC	possibly homozygous	60848107
1	127668136	127668137	C	T	18	GENIC	possibly homozygous	60848108
1	127668195	127668196	A	T	5	GENIC	homozygous	60848109
1	127668287	127668288	G	GA	9	GENIC	possibly homozygous	60848110
1	127668674	127668675	G	T	11	GENIC	heterozygous	61517408
1	127668692	127668693	G	T	12	GENIC	homozygous	60848111
1	127668780	127668781	T	C	13	GENIC	possibly homozygous	60848112
1	127668926	127668927	T	C	23	GENIC	homozygous	60848113
1	127669014	127669015	G	A	13	GENIC	possibly homozygous	61517409
1	127669093	127669094	A	G	7	GENIC	homozygous	60848114
1	127670267	127670268	A	G	8	GENIC	homozygous	60848116
1	127670293	127670294	T	C	11	GENIC	homozygous	60848117
1	127670556	127670557	T	G	9	GENIC	possibly homozygous	60848118
1	127670567	127670568	T	C	7	GENIC	homozygous	60848119
1	127671158	127671159	G	GCACATCC	8	GENIC	possibly homozygous	61517410
1	127672096	127672097	A	ACGAGG	1	GENIC	homozygous	60848121
1	127673107	127673108	G	A	13	GENIC	homozygous	62350920
1	127677806	127677807	A	G	6	GENIC	homozygous	62350922
1	127677854	127677855	T	C	11	GENIC	homozygous	61517413
1	127679034	127679035	T	C	20	GENIC	possibly homozygous	60848128
1	127670086	127670087	C	T	19	GENIC	homozygous	62296178
1	127672132	127672133	C	T	5	GENIC	homozygous	62296179