| geneid | 316 |
|---|---|
| ensemblid | ENSG00000138356.14 |
| hgncid | 553 |
| symbol | AOX1 |
| name | aldehyde oxidase 1 |
| refseq_nuc | NM_001159.4 |
| refseq_prot | NP_001150.3 |
| ensembl_nuc | ENST00000374700.7 |
| ensembl_prot | ENSP00000363832.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 200586014 |
| end | 200671495 |
| strand | + |
| ver | v1.2 |
| region | chr2:200586014-200671495 |
| region5000 | chr2:200581014-200676495 |
| regionname0 | AOX1_chr2_200586014_200671495 |
| regionname5000 | AOX1_chr2_200581014_200676495 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1338 | 279 | 52 | 54 | 131 | 8 | 33 | 99 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0002 | 0/1 | 1338 | 38 | 1 | 11 | 18 | 2 | 5 | 13 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003 | 0/0 | 1338 | 26 | 21 | 0 | 0 | 2 | 3 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0004 | 0/0 | 1338 | 8 | 0 | 4 | 4 | 0 | 0 | 4 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0005 | 0/0 | 1338 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0006 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0007 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0008 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0009 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0010 | 0/0 | 965 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0011 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0012 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0013 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0014 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0015 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0016 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0017 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0018 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0019 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 4017 | 265 | 42 | 53 | 130 | 7 | 32 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0002 | 0/1 | 4017 | 38 | 1 | 11 | 18 | 2 | 5 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0003 | 0/0 | 4017 | 17 | 13 | 0 | 0 | 2 | 2 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0004 | 0/0 | 4017 | 8 | 0 | 4 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0005 | 0/0 | 4017 | 5 | 5 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0006 | 0/0 | 4017 | 4 | 4 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0007 | 0/0 | 4017 | 4 | 0 | 0 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0008 | 0/0 | 4017 | 3 | 3 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0009 | 0/0 | 4017 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0010 | 0/0 | 4017 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0011 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0012 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0013 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0014 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0015 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0016 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0017 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0018 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0019 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0020 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0021 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0022 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0023 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0024 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0025 | 0/0 | 4017 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0026 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0027 | 0/0 | 4017 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0028 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0029 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0030 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0031 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| c0032 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 912 | 180 | 54 | 25 | 74 | 4 | 23 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0002 | 0/0 | 910 | 141 | 13 | 33 | 75 | 6 | 14 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0003 | 0/1 | 912 | 31 | 0 | 12 | 11 | 2 | 5 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0004 | 0/0 | 910 | 7 | 7 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0005 | 1/0 | 912 | 4 | 3 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0006 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0007 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0008 | 0/0 | 910 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0009 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| t0010 | 0/0 | 910 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4017 | 265 | 42 | 53 | 130 | 7 | 32 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0005 | 0/0 | 4017 | 5 | 5 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0008 | 0/0 | 4017 | 3 | 3 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0014 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0019 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0020 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0027 | 0/0 | 4017 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0029 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0031 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0002c0002 | 0/1 | 4017 | 38 | 1 | 11 | 18 | 2 | 5 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0003 | 0/0 | 4017 | 17 | 13 | 0 | 0 | 2 | 2 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0006 | 0/0 | 4017 | 4 | 4 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0009 | 0/0 | 4017 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0018 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0026 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0030 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0004c0004 | 0/0 | 4017 | 8 | 0 | 4 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0005c0007 | 0/0 | 4017 | 4 | 0 | 0 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0006c0010 | 0/0 | 4017 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0007c0013 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0008c0016 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0009c0028 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0010c0025 | 0/0 | 4017 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0011c0023 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0012c0022 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0013c0021 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0014c0024 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0015c0017 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0016c0015 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0017c0032 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0018c0012 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0019c0011 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4928 | 140 | 31 | 22 | 67 | 2 | 18 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0001t0002 | 0/0 | 4926 | 119 | 8 | 31 | 61 | 5 | 14 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0001t0005 | 1/0 | 4928 | 4 | 3 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0001t0008 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0001t0010 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0005t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0005t0002 | 0/0 | 4926 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0005t0004 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0005t0006 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0008t0001 | 0/0 | 4928 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0008t0002 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0014t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0019t0002 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0020t0001 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0027t0002 | 0/0 | 4926 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0029t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0001c0031t0001 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0002c0002t0002 | 0/0 | 4926 | 7 | 0 | 0 | 7 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0002c0002t0003 | 0/1 | 4928 | 30 | 0 | 11 | 11 | 2 | 5 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0002c0002t0007 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0003t0001 | 0/0 | 4928 | 10 | 6 | 0 | 0 | 2 | 2 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0003t0004 | 0/0 | 4926 | 6 | 6 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0003t0006 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0006t0001 | 0/0 | 4928 | 4 | 4 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0009t0001 | 0/0 | 4928 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0018t0001 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0026t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0003c0030t0002 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0004c0004t0001 | 0/0 | 4928 | 7 | 0 | 3 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0004c0004t0002 | 0/0 | 4926 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0005c0007t0002 | 0/0 | 4926 | 4 | 0 | 0 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0006c0010t0007 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0006c0010t0009 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0007c0013t0002 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0008c0016t0002 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0009c0028t0001 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0010c0025t0003 | 0/0 | 4928 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0011c0023t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0012c0022t0002 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0013c0021t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0014c0024t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0015c0017t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0016c0015t0002 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0017c0032t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0018c0012t0001 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| a0019c0011t0001 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | copy fasta | chr2 | 200581014 | 200676495 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0005g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0008g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0005t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0005t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0005t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0008t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0008t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0008t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0014t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0019t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0020t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0027t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0029t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0001c0031t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0003g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0002c0002t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0003t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0006t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0009t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0009t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0018t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0026t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0003c0030t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0004c0004t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0005c0007t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0005c0007t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0005c0007t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0005c0007t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0006c0010t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0006c0010t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0007c0013t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0008c0016t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0009c0028t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0010c0025t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0011c0023t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0012c0022t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0013c0021t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0014c0024t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0015c0017t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0016c0015t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0017c0032t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0018c0012t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| a0019c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0295 | EUR | GBR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00140 | hp2 | a0001 | c0019 | t0002 | g0149 | EUR | GBR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | FIN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00408 | hp1 | a0005 | c0007 | t0002 | g0223 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00408 | hp2 | a0009 | c0028 | t0001 | g0313 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00423 | hp2 | a0001 | c0001 | t0008 | g0344 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00642 | hp1 | a0004 | c0004 | t0001 | g0302 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0365 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00738 | hp1 | a0001 | c0027 | t0002 | g0029 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0046 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0067 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01255 | hp2 | a0010 | c0025 | t0003 | g0287 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0043 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0065 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0071 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0245 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0045 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0250 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0044 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01884 | hp2 | a0001 | c0005 | t0002 | g0217 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0070 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0201 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01981 | hp1 | a0004 | c0004 | t0002 | g0290 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01993 | hp2 | a0004 | c0004 | t0001 | g0301 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02055 | hp2 | a0003 | c0009 | t0001 | g0097 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02071 | hp1 | a0002 | c0002 | t0003 | g0047 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0066 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02258 | hp1 | a0003 | c0006 | t0001 | g0093 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02258 | hp2 | a0001 | c0005 | t0004 | g0297 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02273 | hp1 | a0004 | c0004 | t0001 | g0300 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0064 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0068 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0219 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02602 | hp1 | a0001 | c0031 | t0001 | g0079 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02622 | hp2 | a0016 | c0015 | t0002 | g0074 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02647 | hp1 | a0003 | c0003 | t0004 | g0276 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0081 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02723 | hp1 | a0003 | c0003 | t0004 | g0214 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02723 | hp2 | a0003 | c0003 | t0004 | g0092 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02809 | hp2 | a0011 | c0023 | t0001 | g0251 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0090 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0096 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02895 | hp1 | a0003 | c0006 | t0001 | g0095 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02965 | hp1 | a0001 | c0008 | t0002 | g0203 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02970 | hp1 | a0001 | c0008 | t0001 | g0050 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02976 | hp1 | a0015 | c0017 | t0001 | g0063 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02976 | hp2 | a0003 | c0006 | t0001 | g0122 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0094 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03041 | hp2 | a0013 | c0021 | t0001 | g0259 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03130 | hp2 | a0003 | c0003 | t0004 | g0209 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03209 | hp1 | a0003 | c0003 | t0004 | g0073 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03209 | hp2 | a0001 | c0029 | t0001 | g0076 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03225 | hp2 | a0003 | c0026 | t0001 | g0213 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0059 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03453 | hp2 | a0006 | c0010 | t0007 | g0280 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03486 | hp2 | a0002 | c0002 | t0007 | g0252 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03491 | hp1 | a0002 | c0002 | t0003 | g0265 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0274 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03540 | hp1 | a0001 | c0005 | t0006 | g0075 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03540 | hp2 | a0014 | c0024 | t0001 | g0215 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0052 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0040 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03704 | hp2 | a0003 | c0018 | t0001 | g0222 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0249 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0364 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03927 | hp1 | a0018 | c0012 | t0001 | g0198 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0352 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0355 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0261 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18522 | hp2 | a0003 | c0030 | t0002 | g0218 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18747 | hp2 | a0012 | c0022 | t0002 | g0108 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18906 | hp1 | a0001 | c0014 | t0001 | g0353 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18906 | hp2 | a0001 | c0005 | t0002 | g0060 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0348 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18950 | hp1 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0152 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18960 | hp1 | a0008 | c0016 | t0002 | g0107 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18960 | hp2 | a0004 | c0004 | t0001 | g0304 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18968 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18977 | hp2 | a0004 | c0004 | t0001 | g0327 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18979 | hp1 | a0005 | c0007 | t0002 | g0242 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19004 | hp1 | a0001 | c0020 | t0001 | g0230 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19007 | hp1 | a0004 | c0004 | t0001 | g0305 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19056 | hp1 | a0005 | c0007 | t0002 | g0210 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19062 | hp1 | a0004 | c0004 | t0001 | g0303 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19070 | hp1 | a0007 | c0013 | t0002 | g0140 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19074 | hp2 | a0019 | c0011 | t0001 | g0202 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19082 | hp1 | a0005 | c0007 | t0002 | g0240 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0151 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19240 | hp1 | a0017 | c0032 | t0001 | g0277 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0289 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0159 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0293 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0367 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02109 | hp1 | a0003 | c0009 | t0001 | g0361 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02109 | hp2 | a0003 | c0003 | t0004 | g0211 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02486 | hp2 | a0001 | c0008 | t0001 | g0362 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03471 | hp1 | a0006 | c0010 | t0009 | g0106 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| HG06807 | hp2 | a0003 | c0006 | t0001 | g0105 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA20300 | hp2 | a0003 | c0003 | t0006 | g0329 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0366 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0248 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0025 | REF | REF | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0053 | REF | REF | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200599627
|
T | C | 1 | a0019 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.317T>C | p.Ile106Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/35 | 412/4928 | 317/4017 | 106/1338 | chr2 | 200599627 | ||
| chr2:200599743
|
G | A | 1 | a0018 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.433G>A | p.Gly145Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/35 | 528/4928 | 433/4017 | 145/1338 | chr2 | 200599743 | ||
| chr2:200609017
|
A | G | 1 | a0017 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.941A>G | p.Gln314Arg | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 11/35 | 1036/4928 | 941/4017 | 314/1338 | chr2 | 200609017 | ||
| chr2:200612631
|
G | A | 1 | a0007 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.1286G>A | p.Arg429Gln | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/35 | 1381/4928 | 1286/4017 | 429/1338 | chr2 | 200612631 | ||
| chr2:200613946
|
T | A | 1 | a0016 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1591T>A | p.Ser531Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/35 | 1686/4928 | 1591/4017 | 531/1338 | chr2 | 200613946 | ||
| chr2:200620738
|
T | A | 1 | a0004 | 8 | HG00642.hp1 HG01981.hp1 HG01993.hp2 others(5): Show |
missense_variant | MODERATE | c.1793T>A | p.Ile598Asn | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/35 | 1888/4928 | 1793/4017 | 598/1338 | chr2 | 200620738 | ||
| chr2:200620761
|
G | A | 1 | a0008 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.1816G>A | p.Val606Met | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/35 | 1911/4928 | 1816/4017 | 606/1338 | chr2 | 200620761 | ||
| chr2:200621220
|
G | A | 1 | a0015 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1975G>A | p.Ala659Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/35 | 2070/4928 | 1975/4017 | 659/1338 | chr2 | 200621220 | ||
| chr2:200634833
|
C | T | 1 | a0005 | 4 | HG00408.hp1 NA18979.hp1 NA19056.hp1 others(1): Show |
missense_variant | MODERATE | c.2264C>T | p.Thr755Ile | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/35 | 2359/4928 | 2264/4017 | 755/1338 | chr2 | 200634833 | ||
| chr2:200634886
|
G | T | 1 | a0009 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.2317G>T | p.Val773Leu | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/35 | 2412/4928 | 2317/4017 | 773/1338 | chr2 | 200634886 | ||
| chr2:200651022
|
C | T | 1 | a0010 | 1 | HG01255.hp2 | stop_gained | HIGH | c.2896C>T | p.Gln966* | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/35 | 2991/4928 | 2896/4017 | 966/1338 | chr2 | 200651022 | ||
| chr2:200659241
|
C | G | 1 | a0014 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.3248C>G | p.Ala1083Gly | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/35 | 3343/4928 | 3248/4017 | 1083/1338 | chr2 | 200659241 | ||
| chr2:200659279
|
G | A | 1 | a0013 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3286G>A | p.Gly1096Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/35 | 3381/4928 | 3286/4017 | 1096/1338 | chr2 | 200659279 | ||
| chr2:200661607
|
A | G | 3 | a0003a0006a0014 | 29 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(26): Show |
missense_variant | MODERATE | c.3404A>G | p.Asn1135Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/35 | 3499/4928 | 3404/4017 | 1135/1338 | chr2 | 200661607 | ||
| chr2:200662889
|
G | A | 1 | a0012 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.3463G>A | p.Glu1155Lys | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/35 | 3558/4928 | 3463/4017 | 1155/1338 | chr2 | 200662889 | ||
| chr2:200668648
|
T | C | 1 | a0011 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.3643T>C | p.Tyr1215His | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/35 | 3738/4928 | 3643/4017 | 1215/1338 | chr2 | 200668648 | ||
| chr2:200669666
|
A | G | 3 | a0002a0006a0010 | 41 | HG00621.hp1 HG00673.hp2 HG01106.hp1 others(38): Show |
missense_variant | MODERATE | c.3890A>G | p.His1297Arg | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/35 | 3985/4928 | 3890/4017 | 1297/1338 | chr2 | 200669666 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200613804
|
G | A | 1 | a0001c0014 | 1 | NA18906.hp1 | splice_region_variant&synonymous_variant | LOW | c.1449G>A | p.Arg483Arg | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/35 | 1544/4928 | 1449/4017 | 483/1338 | chr2 | 200613804 | ||
| chr2:200616016
|
T | C | 1 | a0003c0009 | 2 | HG02055.hp2 HG02109.hp1 |
synonymous_variant | LOW | c.1657T>C | p.Leu553Leu | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/35 | 1752/4928 | 1657/4017 | 553/1338 | chr2 | 200616016 | ||
| chr2:200621192
|
C | T | 1 | a0001c0031 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1947C>T | p.Asp649Asp | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/35 | 2042/4928 | 1947/4017 | 649/1338 | chr2 | 200621192 | ||
| chr2:200627439
|
A | G | 4 | a0001c0005a0001c0029a0003c0030others(1): Show | 8 | HG01884.hp2 HG02258.hp2 HG02976.hp1 others(5): Show |
synonymous_variant | LOW | c.2211A>G | p.Gln737Gln | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/35 | 2306/4928 | 2211/4017 | 737/1338 | chr2 | 200627439 | ||
| chr2:200636928
|
C | G | 1 | a0001c0027 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.2364C>G | p.Thr788Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/35 | 2459/4928 | 2364/4017 | 788/1338 | chr2 | 200636928 | ||
| chr2:200636982
|
G | A | 1 | a0003c0018 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.2418G>A | p.Ala806Ala | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/35 | 2513/4928 | 2418/4017 | 806/1338 | chr2 | 200636982 | ||
| chr2:200641112
|
C | T | 5 | a0001c0005a0001c0008a0003c0009others(2): Show | 12 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
synonymous_variant | LOW | c.2583C>T | p.Asn861Asn | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/35 | 2678/4928 | 2583/4017 | 861/1338 | chr2 | 200641112 | ||
| chr2:200641115
|
T | C | 1 | a0001c0019 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.2586T>C | p.Asp862Asp | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/35 | 2681/4928 | 2586/4017 | 862/1338 | chr2 | 200641115 | ||
| chr2:200651090
|
G | A | 1 | a0001c0020 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.2964G>A | p.Leu988Leu | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/35 | 3059/4928 | 2964/4017 | 988/1338 | chr2 | 200651090 | ||
| chr2:200668740
|
C | T | 1 | a0003c0006 | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.3735C>T | p.Pro1245Pro | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/35 | 3830/4928 | 3735/4017 | 1245/1338 | chr2 | 200668740 | ||
| chr2:200668797
|
A | G | 1 | a0003c0006 | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.3792A>G | p.Ser1264Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/35 | 3887/4928 | 3792/4017 | 1264/1338 | chr2 | 200668797 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200586027
|
G | A | 1 | a0001c0001t0008 | 1 | HG00423.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-82G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/35 | chr2 | 200586027 | ||||||
| chr2:200670851
|
T | C | 2 | a0001c0005t0004a0003c0003t0004 | 7 | HG02109.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*172T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 172 | chr2 | 200670851 | |||||
| chr2:200670923
|
C | T | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(42): Show | 366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 244 | chr2 | 200670923 | |||||
| chr2:200671058
|
T | G | 4 | a0001c0005t0006a0002c0002t0003a0003c0003t0006others(1): Show | 33 | HG01106.hp1 HG01123.hp2 HG01192.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*379T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 379 | chr2 | 200671058 | |||||
| chr2:200671172
|
C | T | 1 | a0001c0001t0010 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*493C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 493 | chr2 | 200671172 | |||||
| chr2:200671207
|
G | A | 2 | a0002c0002t0003a0010c0025t0003 | 31 | HG01106.hp1 HG01123.hp2 HG01192.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 528 | chr2 | 200671207 | |||||
| chr2:200671272
|
CAT | C | 17 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(14): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*598_*599delAT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 598 | INFO_REALIGN_3_PRIME | chr2 | 200671272 | ||||
| chr2:200671290
|
C | A | 2 | a0002c0002t0007a0006c0010t0007 | 2 | HG03453.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*611C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 611 | chr2 | 200671290 | |||||
| chr2:200671384
|
A | C | 1 | a0006c0010t0009 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 705 | chr2 | 200671384 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200586239
|
C | G | 3 | a0001c0001t0002g0365a0001c0001t0002g0366a0002c0002t0003g0367 | 3 | HG00733.hp1 HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.45+86C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586239 | ||||||
| chr2:200586277
|
T | C | 1 | a0001c0001t0002g0004 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.45+124T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586277 | ||||||
| chr2:200586283
|
C | T | 281 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(278): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.45+130C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586283 | ||||||
| chr2:200586291
|
C | G | 1 | a0001c0001t0002g0364 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.45+138C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586291 | ||||||
| chr2:200586545
|
T | G | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+392T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586545 | ||||||
| chr2:200586655
|
C | A | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+502C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586655 | ||||||
| chr2:200586686
|
A | G | 1 | a0001c0001t0002g0363 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.45+533A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586686 | ||||||
| chr2:200586723
|
A | G | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+570A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586723 | ||||||
| chr2:200586868
|
C | G | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+715C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586868 | ||||||
| chr2:200586870
|
G | A | 1 | a0003c0009t0001g0097 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.45+717G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586870 | ||||||
| chr2:200586903
|
C | T | 2 | a0003c0009t0001g0097a0003c0009t0001g0361 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.45+750C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586903 | ||||||
| chr2:200586924
|
A | G | 83 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.45+771A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586924 | ||||||
| chr2:200586931
|
A | G | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+778A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586931 | ||||||
| chr2:200587103
|
C | CA | 11 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0282others(8): Show | 11 | HG02738.hp2 HG04199.hp2 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+960dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200587103 | |||||
| chr2:200587112
|
AACC | A | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+961_45+963delCC others(1): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200587112 | |||||
| chr2:200587114
|
C | A | 2 | a0001c0001t0002g0281a0001c0008t0001g0362 | 2 | HG01361.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.45+961C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587114 | ||||||
| chr2:200587115
|
C | A | 2 | a0001c0008t0001g0362a0006c0010t0009g0106 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.45+962C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587115 | ||||||
| chr2:200587124
|
C | A | 106 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(103): Show | 107 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.45+971C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587124 | ||||||
| chr2:200587126
|
A | C | 2 | a0001c0008t0002g0203a0002c0002t0002g0204 | 2 | HG02965.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.45+973A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587126 | ||||||
| chr2:200587137
|
A | C | 1 | a0019c0011t0001g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.45+984A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587137 | ||||||
| chr2:200587753
|
A | G | 1 | a0001c0001t0002g0360 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.45+1600A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587753 | ||||||
| chr2:200588025
|
G | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 6 | NA18947.hp2 NA18948.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+1872G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588025 | ||||||
| chr2:200588111
|
G | T | 1 | a0003c0006t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.45+1958G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588111 | ||||||
| chr2:200588229
|
C | G | 9 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+2076C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588229 | ||||||
| chr2:200588273
|
A | G | 9 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+2120A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588273 | ||||||
| chr2:200588329
|
T | G | 113 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(110): Show | 114 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.45+2176T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588329 | ||||||
| chr2:200588334
|
T | A | 7 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+2181T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588334 | ||||||
| chr2:200588451
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0002g0013 | 3 | HG02132.hp1 NA18961.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.45+2298T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588451 | ||||||
| chr2:200588726
|
C | CT | 13 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 14 | HG01975.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+2594dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+2588_45+2594dup others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0205 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.45+2583_45+2584ins others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(4): Show |
1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+2584_45+2594dup others(11): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0284 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+2580_45+2594dup others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0285a0001c0001t0002g0286a0003c0030t0002g0218 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.45+2579_45+2594dup others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0220a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG01070.hp2 HG01255.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+2578_45+2594dup others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(11): Show |
36 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.45+2577_45+2594dup others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(12): Show |
46 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0241others(43): Show | 46 | HG00408.hp2 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.45+2576_45+2594dup others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(13): Show |
36 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0260others(33): Show | 36 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.45+2575_45+2594dup others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(14): Show |
14 | a0001c0001t0001g0003a0001c0001t0001g0270a0001c0001t0001g0271others(11): Show | 15 | HG01243.hp2 HG01261.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+2574_45+2594dup others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0104a0001c0001t0001g0358a0001c0001t0002g0278others(2): Show | 5 | HG01106.hp2 HG01358.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+2594_45+2595ins others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0359 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.45+2594_45+2595ins others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
CT | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG00597.hp1 HG02965.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+2594delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588726
|
CTT | C | 105 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(102): Show | 106 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.45+2593_45+2594del others(2): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | |||||
| chr2:200588754
|
G | A | 1 | a0003c0003t0004g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2601G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588754 | ||||||
| chr2:200588905
|
C | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0220a0001c0001t0001g0234others(12): Show | 16 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+2752C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588905 | ||||||
| chr2:200589028
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0220others(104): Show | 108 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.45+2875G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589028 | ||||||
| chr2:200589225
|
C | A | 43 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.45+3072C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589225 | ||||||
| chr2:200589346
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+3193A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589346 | ||||||
| chr2:200589501
|
G | A | 10 | a0001c0001t0002g0091a0001c0005t0002g0217a0003c0003t0001g0090others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+3348G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589501 | ||||||
| chr2:200589520
|
G | A | 10 | a0001c0001t0002g0091a0001c0005t0002g0217a0003c0003t0001g0090others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+3367G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589520 | ||||||
| chr2:200589566
|
C | A | 44 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(41): Show | 44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.45+3413C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589566 | ||||||
| chr2:200589612
|
TAGC | T | 10 | a0001c0001t0002g0091a0001c0005t0002g0217a0003c0003t0001g0090others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+3462_45+3464del others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200589612 | |||||
| chr2:200589620
|
TGG | T | 85 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.45+3469_45+3470del others(2): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200589620 | |||||
| chr2:200589726
|
G | T | 5 | a0001c0001t0001g0104a0001c0001t0001g0263a0001c0001t0002g0264others(2): Show | 5 | HG01934.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3420G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589726 | ||||||
| chr2:200589902
|
G | A | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-3244G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589902 | ||||||
| chr2:200590035
|
C | T | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-3111C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590035 | ||||||
| chr2:200590098
|
C | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-3048C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590098 | ||||||
| chr2:200590417
|
A | C | 2 | a0002c0002t0003g0265a0002c0002t0003g0274 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.46-2729A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590417 | ||||||
| chr2:200590446
|
T | G | 2 | a0003c0003t0001g0212a0003c0003t0004g0211 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.46-2700T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590446 | ||||||
| chr2:200590522
|
C | A | 1 | a0002c0002t0002g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.46-2624C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590522 | ||||||
| chr2:200590585
|
A | C | 1 | a0001c0001t0002g0103 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.46-2561A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590585 | ||||||
| chr2:200590622
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.46-2524G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590622 | ||||||
| chr2:200591000
|
C | T | 44 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(41): Show | 44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.46-2146C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591000 | ||||||
| chr2:200591051
|
A | G | 54 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(51): Show | 54 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-2095A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591051 | ||||||
| chr2:200591113
|
T | C | 8 | a0001c0001t0001g0205a0001c0001t0001g0257a0001c0001t0001g0258others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-2033T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591113 | ||||||
| chr2:200591207
|
C | T | 48 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.46-1939C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591207 | ||||||
| chr2:200591240
|
G | C | 1 | a0001c0001t0002g0017 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.46-1906G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591240 | ||||||
| chr2:200591325
|
G | A | 1 | a0001c0001t0001g0330 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.46-1821G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591325 | ||||||
| chr2:200591361
|
A | T | 48 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.46-1785A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591361 | ||||||
| chr2:200591435
|
G | A | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.46-1711G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591435 | ||||||
| chr2:200591495
|
G | A | 1 | a0008c0016t0002g0107 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.46-1651G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591495 | ||||||
| chr2:200591508
|
T | A | 1 | a0012c0022t0002g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.46-1638T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591508 | ||||||
| chr2:200591522
|
G | A | 48 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.46-1624G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591522 | ||||||
| chr2:200591530
|
T | C | 1 | a0001c0001t0002g0352 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.46-1616T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591530 | ||||||
| chr2:200591555
|
C | T | 1 | a0018c0012t0001g0198 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.46-1591C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591555 | ||||||
| chr2:200591622
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0263a0001c0001t0002g0264others(2): Show | 5 | HG01934.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-1524G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591622 | ||||||
| chr2:200591667
|
A | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0220others(20): Show | 24 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.46-1479A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591667 | ||||||
| chr2:200591671
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0002g0109 | 2 | HG00609.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.46-1475G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591671 | ||||||
| chr2:200591724
|
T | C | 270 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-1422T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591724 | ||||||
| chr2:200591769
|
C | G | 43 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.46-1377C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591769 | ||||||
| chr2:200591786
|
G | A | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-1360G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591786 | ||||||
| chr2:200592549
|
G | GC | 270 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-597_46-596insC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592549 | ||||||
| chr2:200592747
|
G | A | 4 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0308others(1): Show | 4 | HG02486.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-399G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592747 | ||||||
| chr2:200592801
|
C | G | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0002c0002t0002g0098 | 3 | HG00423.hp1 NA18612.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.46-345C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592801 | ||||||
| chr2:200592887
|
T | C | 54 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(51): Show | 54 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-259T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592887 | ||||||
| chr2:200593027
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0271 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.46-119A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200593027 | ||||||
| chr2:200593048
|
G | T | 1 | a0011c0023t0001g0251 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-98G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200593048 | ||||||
| chr2:200593104
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.46-42T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200593104 | ||||||
| chr2:200593204
|
G | A | 1 | a0002c0002t0003g0111 | 1 | NA18968.hp1 | splice_donor_variant&intron_variant | HIGH | c.103+1G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593204 | ||||||
| chr2:200593220
|
T | C | 1 | a0001c0008t0002g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103+17T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593220 | ||||||
| chr2:200593485
|
T | TA | 270 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.103+283dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr2 | 200593485 | |||||
| chr2:200593690
|
G | A | 7 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0112others(4): Show | 7 | HG06807.hp1 NA18960.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+487G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593690 | ||||||
| chr2:200593737
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.103+534A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593737 | ||||||
| chr2:200594040
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.103+837G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594040 | ||||||
| chr2:200594139
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.103+936T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594139 | ||||||
| chr2:200594296
|
G | A | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.104-976G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594296 | ||||||
| chr2:200594305
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.104-967G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594305 | ||||||
| chr2:200594441
|
T | C | 108 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(105): Show | 109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.104-831T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594441 | ||||||
| chr2:200594722
|
A | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 19 | HG00597.hp1 HG00639.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.104-550A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594722 | ||||||
| chr2:200594855
|
C | T | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.104-417C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594855 | ||||||
| chr2:200594889
|
T | A | 3 | a0001c0001t0001g0117a0001c0001t0005g0002a0001c0001t0005g0116 | 4 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-383T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594889 | ||||||
| chr2:200594988
|
C | T | 270 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.104-284C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594988 | ||||||
| chr2:200595048
|
T | C | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.104-224T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200595048 | ||||||
| chr2:200595381
|
A | G | 108 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(105): Show | 109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.200+13A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595381 | ||||||
| chr2:200595539
|
A | G | 2 | a0003c0003t0001g0212a0003c0003t0004g0211 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.200+171A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595539 | ||||||
| chr2:200595553
|
T | A | 2 | a0003c0003t0001g0096a0006c0010t0007g0280 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.200+185T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595553 | ||||||
| chr2:200595584
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.200+216C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595584 | ||||||
| chr2:200595593
|
G | T | 108 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(105): Show | 109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.200+225G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595593 | ||||||
| chr2:200595599
|
T | C | 270 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.200+231T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595599 | ||||||
| chr2:200595828
|
T | C | 1 | a0003c0003t0004g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.200+460T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595828 | ||||||
| chr2:200595965
|
G | T | 1 | a0001c0001t0001g0330 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.200+597G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595965 | ||||||
| chr2:200596118
|
G | C | 305 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(302): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.200+750G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596118 | ||||||
| chr2:200596315
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.200+947T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596315 | ||||||
| chr2:200596368
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 23 | HG00597.hp1 HG00639.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.200+1000C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596368 | ||||||
| chr2:200596515
|
G | A | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201-882G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596515 | ||||||
| chr2:200596659
|
G | T | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-738G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596659 | ||||||
| chr2:200596761
|
GTTTA | G | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-625_201-622del others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr2 | 200596761 | |||||
| chr2:200596981
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.201-416C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596981 | ||||||
| chr2:200597002
|
A | G | 2 | a0003c0003t0001g0096a0006c0010t0007g0280 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.201-395A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597002 | ||||||
| chr2:200597091
|
G | A | 108 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(105): Show | 109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.201-306G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597091 | ||||||
| chr2:200597160
|
C | A | 47 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(44): Show | 47 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.201-237C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597160 | ||||||
| chr2:200597230
|
C | A | 8 | a0001c0001t0001g0205a0001c0001t0001g0257a0001c0001t0001g0258others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-167C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597230 | ||||||
| chr2:200597608
|
C | T | 1 | a0003c0003t0001g0250 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.309+103C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597608 | ||||||
| chr2:200597634
|
C | T | 48 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.309+129C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597634 | ||||||
| chr2:200597926
|
T | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | NA18944.hp2 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+421T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597926 | ||||||
| chr2:200597966
|
G | A | 1 | a0003c0006t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.309+461G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597966 | ||||||
| chr2:200597984
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.309+479A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597984 | ||||||
| chr2:200598099
|
C | T | 2 | a0001c0001t0001g0231a0011c0023t0001g0251 | 2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.309+594C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598099 | ||||||
| chr2:200598295
|
T | G | 44 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(41): Show | 44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.309+790T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598295 | ||||||
| chr2:200598399
|
T | C | 1 | a0003c0003t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.309+894T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598399 | ||||||
| chr2:200598565
|
A | G | 1 | a0013c0021t0001g0259 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.310-1055A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598565 | ||||||
| chr2:200598652
|
GA | G | 133 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(130): Show | 133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.310-966delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr2 | 200598652 | |||||
| chr2:200598655
|
T | G | 133 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(130): Show | 133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.310-965T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598655 | ||||||
| chr2:200598787
|
T | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0220others(22): Show | 26 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.310-833T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598787 | ||||||
| chr2:200599005
|
G | A | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.310-615G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599005 | ||||||
| chr2:200599262
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.310-358C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599262 | ||||||
| chr2:200599372
|
G | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(132): Show | 137 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.310-248G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599372 | ||||||
| chr2:200599441
|
C | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.310-179C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599441 | ||||||
| chr2:200599490
|
C | T | 2 | a0001c0005t0002g0217a0001c0008t0001g0362 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.310-130C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599490 | ||||||
| chr2:200599496
|
G | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0084others(1): Show | 4 | HG00597.hp1 HG03927.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-124G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599496 | ||||||
| chr2:200599537
|
A | G | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.310-83A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599537 | ||||||
| chr2:200599572
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(223): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.310-48T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599572 | ||||||
| chr2:200599807
|
C | A | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+61C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200599807 | ||||||
| chr2:200599842
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0220others(106): Show | 110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.436+96C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200599842 | ||||||
| chr2:200599931
|
C | T | 8 | a0001c0001t0001g0205a0001c0001t0001g0257a0001c0001t0001g0258others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.436+185C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200599931 | ||||||
| chr2:200600042
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.436+296T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600042 | ||||||
| chr2:200600069
|
C | G | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.436+323C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600069 | ||||||
| chr2:200600229
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.436+483A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600229 | ||||||
| chr2:200600245
|
T | C | 1 | a0002c0002t0002g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.436+499T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600245 | ||||||
| chr2:200600475
|
C | CG | 53 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(50): Show | 53 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.436+737dupG | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200600475 | |||||
| chr2:200600475
|
CG | C | 202 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(199): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.436+737delG | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200600475 | |||||
| chr2:200600478
|
G | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.436+732G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600478 | ||||||
| chr2:200600503
|
T | C | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+757T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600503 | ||||||
| chr2:200600568
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0220others(20): Show | 24 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.436+822C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600568 | ||||||
| chr2:200600660
|
G | A | 1 | a0003c0003t0001g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.436+914G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600660 | ||||||
| chr2:200600789
|
T | C | 1 | a0001c0008t0002g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.436+1043T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600789 | ||||||
| chr2:200600834
|
T | A | 43 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+1088T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600834 | ||||||
| chr2:200600949
|
G | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(223): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.436+1203G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600949 | ||||||
| chr2:200600995
|
T | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(223): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.436+1249T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600995 | ||||||
| chr2:200601073
|
C | CTTT | 133 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0121others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.437-1195_437-1193d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | |||||
| chr2:200601073
|
C | CTTTT | 25 | a0001c0001t0001g0003a0001c0001t0001g0188a0001c0001t0001g0189others(22): Show | 26 | HG00621.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.437-1196_437-1193d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | |||||
| chr2:200601073
|
C | CTTTTT | 11 | a0001c0001t0001g0195a0001c0001t0001g0234a0001c0001t0001g0235others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-1197_437-1193d others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | |||||
| chr2:200601073
|
CT | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0084others(7): Show | 10 | HG00597.hp1 HG03225.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1193delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | |||||
| chr2:200601073
|
CTT | C | 87 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.437-1194_437-1193d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | |||||
| chr2:200601118
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0275a0003c0003t0004g0276 | 4 | HG02647.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-1166G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601118 | ||||||
| chr2:200601126
|
C | A | 1 | a0001c0001t0001g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.437-1158C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601126 | ||||||
| chr2:200601373
|
T | C | 108 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(105): Show | 109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.437-911T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601373 | ||||||
| chr2:200601612
|
G | A | 305 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(302): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.437-672G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601612 | ||||||
| chr2:200601632
|
T | A | 1 | a0001c0001t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.437-652T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601632 | ||||||
| chr2:200601632
|
T | TA | 126 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(123): Show | 128 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.437-642dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601632 | |||||
| chr2:200601643
|
T | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.437-641T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601643 | ||||||
| chr2:200601698
|
T | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(277): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.437-586T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601698 | ||||||
| chr2:200601831
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.437-453G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601831 | ||||||
| chr2:200601857
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.437-427C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601857 | ||||||
| chr2:200601898
|
A | G | 1 | a0002c0002t0002g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.437-386A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601898 | ||||||
| chr2:200601913
|
G | A | 2 | a0003c0003t0001g0212a0003c0003t0004g0211 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.437-371G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601913 | ||||||
| chr2:200602009
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(223): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.437-275T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602009 | ||||||
| chr2:200602152
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.437-132T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602152 | ||||||
| chr2:200602176
|
C | G | 1 | a0002c0002t0002g0348 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.437-108C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602176 | ||||||
| chr2:200602200
|
G | A | 1 | a0003c0006t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.437-84G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602200 | ||||||
| chr2:200602231
|
C | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.437-53C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602231 | ||||||
| chr2:200602392
|
C | T | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.498+47C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602392 | ||||||
| chr2:200602417
|
TA | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0002g0013 | 3 | HG02132.hp1 NA18961.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.498+73delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602417 | ||||||
| chr2:200602508
|
A | G | 87 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.498+163A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602508 | ||||||
| chr2:200602601
|
T | C | 9 | a0001c0001t0002g0208a0003c0003t0001g0212a0003c0003t0004g0209others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.498+256T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602601 | ||||||
| chr2:200602783
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.498+438T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602783 | ||||||
| chr2:200602840
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0002g0175 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.499-427A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602840 | ||||||
| chr2:200603156
|
G | T | 8 | a0001c0001t0002g0069a0002c0002t0003g0064a0002c0002t0003g0065others(5): Show | 8 | HG01192.hp2 HG01358.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-111G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200603156 | ||||||
| chr2:200603357
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | splice_donor_variant&intron_variant | HIGH | c.588+1G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603357 | ||||||
| chr2:200603371
|
A | G | 1 | a0015c0017t0001g0063 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.588+15A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603371 | ||||||
| chr2:200603456
|
G | A | 1 | a0003c0003t0004g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.588+100G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603456 | ||||||
| chr2:200603792
|
T | C | 87 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.589-225T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603792 | ||||||
| chr2:200603797
|
G | T | 43 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.589-220G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603797 | ||||||
| chr2:200603798
|
G | T | 43 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.589-219G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603798 | ||||||
| chr2:200603799
|
A | T | 43 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.589-218A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603799 | ||||||
| chr2:200603880
|
G | A | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589-137G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603880 | ||||||
| chr2:200603915
|
G | C | 6 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-102G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603915 | ||||||
| chr2:200604009
|
C | G | 107 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(104): Show | 108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
splice_region_variant&intron_variant | LOW | c.589-8C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200604009 | ||||||
| chr2:200604187
|
T | C | 1 | a0001c0001t0002g0309 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.669+90T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604187 | ||||||
| chr2:200604207
|
C | T | 2 | a0003c0003t0001g0212a0003c0003t0004g0211 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.669+110C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604207 | ||||||
| chr2:200604321
|
T | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+224T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604321 | ||||||
| chr2:200604366
|
T | G | 95 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.669+269T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604366 | ||||||
| chr2:200604415
|
C | T | 1 | a0001c0001t0001g0001 | 2 | NA18947.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.670-281C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604415 | ||||||
| chr2:200604426
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-270A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604426 | ||||||
| chr2:200604528
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0275others(2): Show | 6 | HG02647.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-168T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604528 | ||||||
| chr2:200604661
|
T | C | 1 | a0003c0006t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.670-35T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604661 | ||||||
| chr2:200604902
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(29): Show | 32 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.814+62G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200604902 | ||||||
| chr2:200604958
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.814+118A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200604958 | ||||||
| chr2:200604963
|
T | G | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.814+123T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200604963 | ||||||
| chr2:200605031
|
C | T | 17 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(14): Show | 17 | HG01192.hp1 HG01261.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.814+191C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605031 | ||||||
| chr2:200605068
|
C | G | 95 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.814+228C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605068 | ||||||
| chr2:200605122
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 23 | HG00597.hp1 HG00639.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.814+282C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605122 | ||||||
| chr2:200605225
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0220a0001c0001t0001g0234others(12): Show | 16 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.815-311G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605225 | ||||||
| chr2:200605263
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0188a0001c0001t0002g0206others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-273C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605263 | ||||||
| chr2:200605312
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.815-224A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605312 | ||||||
| chr2:200605510
|
A | AT | 29 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(26): Show | 29 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.815-11dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | |||||
| chr2:200605510
|
AT | A | 28 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0041others(25): Show | 28 | HG01106.hp1 HG01123.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.815-11delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | |||||
| chr2:200605510
|
ATT | A | 19 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(16): Show | 19 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.815-12_815-11delTT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | |||||
| chr2:200605510
|
ATTT | A | 77 | a0001c0001t0001g0117a0001c0001t0001g0165a0001c0001t0001g0283others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.815-13_815-11delTT others(1): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | |||||
| chr2:200605510
|
ATTTT | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0121others(124): Show | 129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.815-14_815-11delTT others(2): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | |||||
| chr2:200605631
|
G | A | 8 | a0001c0001t0001g0205a0001c0001t0001g0257a0001c0001t0001g0258others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.907+3G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200605631 | ||||||
| chr2:200605693
|
C | G | 2 | a0001c0001t0001g0229a0001c0001t0002g0246 | 2 | NA19005.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.907+65C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200605693 | ||||||
| chr2:200605991
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.907+363A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200605991 | ||||||
| chr2:200606420
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.907+792C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606420 | ||||||
| chr2:200606532
|
G | A | 7 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.907+904G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606532 | ||||||
| chr2:200606609
|
C | T | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.907+981C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606609 | ||||||
| chr2:200606821
|
C | G | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.907+1193C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606821 | ||||||
| chr2:200606825
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.907+1197T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606825 | ||||||
| chr2:200606889
|
C | T | 3 | a0001c0001t0002g0289a0001c0001t0002g0299a0001c0001t0002g0366 | 3 | HG01433.hp2 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.907+1261C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606889 | ||||||
| chr2:200606957
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.907+1329A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606957 | ||||||
| chr2:200607152
|
A | G | 228 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(225): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.907+1524A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607152 | ||||||
| chr2:200607342
|
G | A | 1 | a0013c0021t0001g0259 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.908-1642G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607342 | ||||||
| chr2:200607359
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0002g0164 | 3 | HG00642.hp2 HG00733.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.908-1625C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607359 | ||||||
| chr2:200607540
|
G | A | 4 | a0001c0001t0001g0310a0001c0001t0002g0311a0002c0002t0002g0098others(1): Show | 4 | HG00673.hp1 NA18944.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.908-1444G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607540 | ||||||
| chr2:200607568
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.908-1416A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607568 | ||||||
| chr2:200607569
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.908-1415G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607569 | ||||||
| chr2:200607705
|
T | C | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.908-1279T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607705 | ||||||
| chr2:200608023
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.908-961G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608023 | ||||||
| chr2:200608039
|
A | G | 1 | a0003c0018t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.908-945A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608039 | ||||||
| chr2:200608046
|
G | T | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.908-938G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608046 | ||||||
| chr2:200608316
|
G | A | 1 | a0002c0002t0003g0039 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.908-668G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608316 | ||||||
| chr2:200608389
|
C | T | 1 | a0001c0001t0002g0243 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.908-595C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608389 | ||||||
| chr2:200608734
|
A | AC | 271 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.908-246dupC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | INFO_REALIGN_3_PRIME | chr2 | 200608734 | |||||
| chr2:200608802
|
C | A | 1 | a0001c0001t0002g0272 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.908-182C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608802 | ||||||
| chr2:200608876
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.908-108G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608876 | ||||||
| chr2:200608951
|
G | A | 271 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.908-33G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608951 | ||||||
| chr2:200609456
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1153+42C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609456 | ||||||
| chr2:200609511
|
C | T | 20 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(17): Show | 20 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1153+97C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609511 | ||||||
| chr2:200609514
|
A | G | 95 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1153+100A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609514 | ||||||
| chr2:200609601
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1153+187T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609601 | ||||||
| chr2:200609713
|
A | G | 271 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1153+299A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609713 | ||||||
| chr2:200609826
|
A | G | 271 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0117others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1153+412A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609826 | ||||||
| chr2:200609916
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1153+502A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609916 | ||||||
| chr2:200609924
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1153+510G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609924 | ||||||
| chr2:200610076
|
C | CT | 250 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0117others(247): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1153+675dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr2 | 200610076 | |||||
| chr2:200610096
|
G | T | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1153+682G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610096 | ||||||
| chr2:200610202
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1153+788G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610202 | ||||||
| chr2:200610434
|
A | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(22): Show | 25 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1154-950A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610434 | ||||||
| chr2:200610599
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1154-785A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610599 | ||||||
| chr2:200610732
|
C | G | 1 | a0015c0017t0001g0063 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1154-652C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610732 | ||||||
| chr2:200611000
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1154-384C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611000 | ||||||
| chr2:200611045
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1154-339A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611045 | ||||||
| chr2:200611101
|
T | C | 1 | a0003c0003t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1154-283T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611101 | ||||||
| chr2:200611151
|
A | G | 228 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(225): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1154-233A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611151 | ||||||
| chr2:200611552
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1263+59T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611552 | ||||||
| chr2:200611553
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1263+60C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611553 | ||||||
| chr2:200611580
|
G | T | 1 | a0001c0001t0002g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1263+87G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611580 | ||||||
| chr2:200611676
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1263+183C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611676 | ||||||
| chr2:200611701
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1263+208T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611701 | ||||||
| chr2:200611707
|
A | AT | 147 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(144): Show | 148 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1263+229dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr2 | 200611707 | |||||
| chr2:200611707
|
AT | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(72): Show | 75 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1263+229delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr2 | 200611707 | |||||
| chr2:200611731
|
G | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1263+238G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611731 | ||||||
| chr2:200611736
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(131): Show | 136 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1263+243G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611736 | ||||||
| chr2:200611807
|
C | T | 2 | a0001c0001t0002g0166a0002c0002t0002g0204 | 2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1263+314C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611807 | ||||||
| chr2:200611893
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1263+400C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611893 | ||||||
| chr2:200611894
|
G | A | 9 | a0001c0001t0002g0208a0003c0003t0001g0212a0003c0003t0004g0209others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1263+401G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611894 | ||||||
| chr2:200611901
|
C | T | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1263+408C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611901 | ||||||
| chr2:200611947
|
C | T | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1263+454C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611947 | ||||||
| chr2:200612107
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1264-502A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200612107 | ||||||
| chr2:200612442
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1264-167G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200612442 | ||||||
| chr2:200612858
|
C | T | 1 | a0003c0003t0001g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1448+65C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200612858 | ||||||
| chr2:200613003
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1448+226_1448+235d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613003 | |||||
| chr2:200613003
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0002g0171 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1448+224_1448+235d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613003 | |||||
| chr2:200613003
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0002g0161 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1448+222_1448+235d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613003 | |||||
| chr2:200613004
|
G | C | 4 | a0001c0001t0001g0310a0001c0001t0002g0311a0002c0002t0002g0098others(1): Show | 4 | HG00673.hp1 NA18944.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1448+211G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613004 | ||||||
| chr2:200613025
|
T | TGAGAGA | 37 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(34): Show | 37 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1448+233_1448+234i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613025 | |||||
| chr2:200613027
|
T | A | 39 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(36): Show | 39 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1448+234T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613027 | ||||||
| chr2:200613027
|
T | TGAGAGA | 3 | a0001c0001t0001g0273a0001c0001t0002g0278a0001c0001t0002g0279 | 3 | HG01106.hp2 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1448+247_1448+252d others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGAGAGAG others(1): Show |
85 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1448+245_1448+252d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGAGAG others(3): Show |
10 | a0001c0001t0001g0355a0001c0001t0001g0358a0001c0001t0002g0091others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGA | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0165 | 3 | HG01346.hp2 HG02015.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1448+235_1448+236i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGAG others(3): Show |
2 | a0001c0001t0001g0126a0001c0001t0002g0177 | 2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGTG others(3): Show |
12 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0128others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGTG others(5): Show |
2 | a0001c0008t0002g0203a0006c0010t0007g0280 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1448+235_1448+236i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGTG others(3): Show |
64 | a0001c0001t0001g0121a0001c0001t0001g0134a0001c0001t0001g0153others(61): Show | 64 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGTG others(5): Show |
12 | a0001c0001t0001g0205a0001c0001t0001g0254a0001c0001t0001g0257others(9): Show | 12 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGTG others(5): Show |
8 | a0001c0001t0001g0117a0001c0001t0002g0101a0001c0001t0002g0160others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGTG others(7): Show |
11 | a0001c0001t0001g0003a0001c0001t0001g0220a0001c0001t0001g0234others(8): Show | 12 | HG00639.hp2 HG01243.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613027
|
T | TGTGTGTG others(7): Show |
13 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0190others(10): Show | 13 | NA18940.hp2 NA18947.hp1 NA18968.hp2 others(10): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | |||||
| chr2:200613313
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1449-491G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613313 | ||||||
| chr2:200613449
|
T | G | 1 | a0003c0003t0004g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1449-355T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613449 | ||||||
| chr2:200613505
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1449-299A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613505 | ||||||
| chr2:200613541
|
G | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(225): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1449-263G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613541 | ||||||
| chr2:200613559
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1449-245G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613559 | ||||||
| chr2:200613563
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1449-241T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613563 | ||||||
| chr2:200613768
|
C | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1449-36C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613768 | ||||||
| chr2:200613784
|
C | T | 8 | a0001c0001t0001g0205a0001c0001t0001g0257a0001c0001t0001g0258others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1449-20C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613784 | ||||||
| chr2:200613997
|
A | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0002g0164 | 3 | HG00642.hp2 HG00733.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1611+31A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200613997 | ||||||
| chr2:200614043
|
T | A | 1 | a0001c0001t0002g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1611+77T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614043 | ||||||
| chr2:200614055
|
G | C | 1 | a0001c0001t0001g0358 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1611+89G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614055 | ||||||
| chr2:200614131
|
T | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0174 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1611+165T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614131 | ||||||
| chr2:200614173
|
G | A | 253 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(250): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1611+207G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614173 | ||||||
| chr2:200614188
|
C | T | 1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1611+222C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614188 | ||||||
| chr2:200614214
|
T | G | 296 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1611+248T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614214 | ||||||
| chr2:200614370
|
A | G | 296 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1611+404A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614370 | ||||||
| chr2:200614417
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1611+451C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614417 | ||||||
| chr2:200614733
|
C | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(250): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1611+767C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614733 | ||||||
| chr2:200614804
|
C | T | 1 | a0019c0011t0001g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1611+838C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614804 | ||||||
| chr2:200615014
|
AT | A | 292 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(289): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1612-946delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr2 | 200615014 | |||||
| chr2:200615300
|
C | T | 7 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-671C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615300 | ||||||
| chr2:200615386
|
A | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(250): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1612-585A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615386 | ||||||
| chr2:200615399
|
G | A | 5 | a0001c0001t0002g0208a0003c0003t0004g0209a0003c0003t0004g0214others(2): Show | 5 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1612-572G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615399 | ||||||
| chr2:200615426
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(110): Show | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1612-545A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615426 | ||||||
| chr2:200615599
|
G | A | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1612-372G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615599 | ||||||
| chr2:200615741
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1612-230G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615741 | ||||||
| chr2:200615955
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1612-16T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615955 | ||||||
| chr2:200616069
|
C | T | 13 | a0001c0001t0002g0069a0002c0002t0003g0006a0002c0002t0003g0039others(10): Show | 13 | HG01192.hp2 HG01358.hp2 HG01361.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1704+6C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616069 | ||||||
| chr2:200616212
|
A | T | 1 | a0003c0003t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1704+149A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616212 | ||||||
| chr2:200616316
|
C | T | 2 | a0001c0001t0002g0166a0002c0002t0002g0204 | 2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1704+253C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616316 | ||||||
| chr2:200616337
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1704+274G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616337 | ||||||
| chr2:200616422
|
G | A | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1704+359G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616422 | ||||||
| chr2:200616660
|
C | T | 3 | a0001c0001t0002g0325a0001c0001t0002g0346a0001c0001t0002g0347 | 3 | HG02129.hp1 NA18992.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1704+597C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616660 | ||||||
| chr2:200616713
|
C | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1704+650C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616713 | ||||||
| chr2:200616782
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1704+719G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616782 | ||||||
| chr2:200616789
|
A | G | 10 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(7): Show | 10 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1704+726A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616789 | ||||||
| chr2:200616856
|
G | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0332 | 2 | HG00597.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1704+793G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616856 | ||||||
| chr2:200617210
|
GC | G | 9 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(6): Show | 9 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1704+1149delC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617210 | |||||
| chr2:200617235
|
T | A | 1 | a0002c0002t0003g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1704+1172T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617235 | ||||||
| chr2:200617258
|
C | G | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1704+1195C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617258 | ||||||
| chr2:200617325
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0220others(20): Show | 24 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1704+1262G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617325 | ||||||
| chr2:200617479
|
T | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(128): Show | 133 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1704+1416T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617479 | ||||||
| chr2:200617481
|
C | CA | 65 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0018others(62): Show | 65 | HG00609.hp1 HG00639.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1704+1443dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | |||||
| chr2:200617481
|
C | CAA | 8 | a0001c0001t0001g0234a0001c0001t0001g0268a0001c0001t0002g0024others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1704+1442_1704+144 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | |||||
| chr2:200617481
|
CA | C | 82 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0125others(79): Show | 83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1704+1443delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | |||||
| chr2:200617481
|
CAA | C | 10 | a0001c0001t0001g0121a0001c0001t0002g0123a0001c0001t0002g0161others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1704+1442_1704+144 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | |||||
| chr2:200617548
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1704+1485A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617548 | ||||||
| chr2:200617666
|
C | CCATTA | 112 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1704+1606_1704+161 others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617666 | |||||
| chr2:200617744
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 62 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.1704+1681A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617744 | ||||||
| chr2:200617759
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1704+1696T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617759 | ||||||
| chr2:200617864
|
G | A | 1 | a0010c0025t0003g0287 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1704+1801G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617864 | ||||||
| chr2:200617965
|
G | T | 1 | a0001c0001t0002g0366 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1704+1902G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617965 | ||||||
| chr2:200617997
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0188 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1704+1934T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617997 | ||||||
| chr2:200618143
|
G | T | 343 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(340): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1704+2080G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618143 | ||||||
| chr2:200618231
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1704+2168T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618231 | ||||||
| chr2:200618365
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1705-2285A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618365 | ||||||
| chr2:200618393
|
T | C | 43 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.1705-2257T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618393 | ||||||
| chr2:200618497
|
T | G | 9 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0028others(6): Show | 9 | HG00738.hp1 HG01258.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1705-2153T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618497 | ||||||
| chr2:200618514
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1705-2136A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618514 | ||||||
| chr2:200618533
|
G | GT | 7 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1705-2110dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200618533 | |||||
| chr2:200618591
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG00733.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1705-2059C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618591 | ||||||
| chr2:200618648
|
T | C | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-2002T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618648 | ||||||
| chr2:200618660
|
T | C | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-1990T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618660 | ||||||
| chr2:200618711
|
T | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1705-1939T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618711 | ||||||
| chr2:200618958
|
A | G | 358 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(355): Show | 361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1705-1692A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618958 | ||||||
| chr2:200619013
|
T | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(22): Show | 25 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1705-1637T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619013 | ||||||
| chr2:200619048
|
T | G | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1705-1602T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619048 | ||||||
| chr2:200619106
|
T | G | 7 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1705-1544T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619106 | ||||||
| chr2:200619108
|
TC | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0275others(2): Show | 6 | HG02647.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1705-1538delC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200619108 | |||||
| chr2:200619151
|
C | A | 1 | a0003c0026t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1705-1499C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619151 | ||||||
| chr2:200619194
|
G | A | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | HG02056.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1705-1456G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619194 | ||||||
| chr2:200619202
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1705-1448G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619202 | ||||||
| chr2:200619254
|
G | T | 112 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1705-1396G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619254 | ||||||
| chr2:200619307
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1705-1343G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619307 | ||||||
| chr2:200619342
|
C | T | 113 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1705-1308C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619342 | ||||||
| chr2:200619377
|
C | G | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-1273C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619377 | ||||||
| chr2:200619461
|
G | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-1189G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619461 | ||||||
| chr2:200619467
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(223): Show | 227 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1705-1183A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619467 | ||||||
| chr2:200619663
|
C | T | 1 | a0001c0008t0002g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1705-987C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619663 | ||||||
| chr2:200619673
|
G | T | 2 | a0001c0001t0001g0176a0001c0001t0002g0175 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1705-977G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619673 | ||||||
| chr2:200619759
|
T | C | 1 | a0001c0008t0002g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1705-891T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619759 | ||||||
| chr2:200619849
|
A | G | 10 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(7): Show | 10 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1705-801A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619849 | ||||||
| chr2:200619990
|
T | C | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1705-660T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619990 | ||||||
| chr2:200619997
|
G | A | 2 | a0001c0001t0002g0110a0001c0001t0002g0167 | 2 | HG01255.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1705-653G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619997 | ||||||
| chr2:200620054
|
C | G | 1 | a0003c0030t0002g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1705-596C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620054 | ||||||
| chr2:200620198
|
A | AG | 42 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(39): Show | 42 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.1705-452_1705-451i others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620198 | ||||||
| chr2:200620198
|
A | AGT | 3 | a0001c0001t0001g0104a0001c0001t0002g0232a0005c0007t0002g0210 | 3 | HG02083.hp2 HG04199.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1705-452_1705-451i others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620198 | ||||||
| chr2:200620198
|
AC | A | 5 | a0001c0001t0002g0208a0003c0003t0004g0209a0003c0003t0004g0214others(2): Show | 5 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705-451delC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620198 | ||||||
| chr2:200620199
|
C | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 64 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.1705-451C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620199 | ||||||
| chr2:200620199
|
C | T | 45 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(42): Show | 45 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.1705-451C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620199 | ||||||
| chr2:200620199
|
CT | C | 113 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1705-432delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200620199 | |||||
| chr2:200620199
|
CTT | C | 105 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0124others(102): Show | 106 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1705-433_1705-432d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200620199 | |||||
| chr2:200620200
|
T | G | 5 | a0001c0001t0002g0208a0003c0003t0004g0209a0003c0003t0004g0214others(2): Show | 5 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705-450T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620200 | ||||||
| chr2:200620202
|
T | G | 3 | a0001c0005t0006g0075a0001c0029t0001g0076a0016c0015t0002g0074 | 3 | HG02622.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1705-448T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620202 | ||||||
| chr2:200620273
|
G | A | 1 | a0003c0006t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1705-377G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620273 | ||||||
| chr2:200620383
|
T | TG | 113 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1705-267_1705-266i others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620383 | ||||||
| chr2:200620384
|
T | G | 8 | a0001c0001t0001g0269a0001c0001t0002g0028a0001c0001t0002g0136others(5): Show | 8 | HG01884.hp2 HG01993.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1705-266T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620384 | ||||||
| chr2:200620393
|
G | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1705-257G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620393 | ||||||
| chr2:200620397
|
C | T | 87 | a0001c0001t0001g0237a0001c0001t0001g0267a0001c0001t0001g0282others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1705-253C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620397 | ||||||
| chr2:200620411
|
G | A | 1 | a0009c0028t0001g0313 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1705-239G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620411 | ||||||
| chr2:200620550
|
C | T | 1 | a0003c0003t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1705-100C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620550 | ||||||
| chr2:200620849
|
A | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1874+30A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200620849 | ||||||
| chr2:200620862
|
T | A | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1874+43T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200620862 | ||||||
| chr2:200620926
|
T | G | 118 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(115): Show | 118 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1874+107T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200620926 | ||||||
| chr2:200621024
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1875-96G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200621024 | ||||||
| chr2:200621107
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 62 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.1875-13G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200621107 | ||||||
| chr2:200621294
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2001+48G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621294 | ||||||
| chr2:200621461
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2001+215G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621461 | ||||||
| chr2:200621593
|
G | A | 107 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(104): Show | 108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2001+347G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621593 | ||||||
| chr2:200621641
|
C | CT | 11 | a0001c0001t0001g0267a0001c0001t0001g0282a0001c0001t0001g0330others(8): Show | 11 | HG00642.hp1 HG01981.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001+401dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621641 | |||||
| chr2:200621676
|
T | TTCTC | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2001+447_2001+450d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621676 | |||||
| chr2:200621676
|
T | TTCTCTC | 46 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(43): Show | 47 | HG00639.hp2 HG01106.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.2001+445_2001+450d others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621676 | |||||
| chr2:200621676
|
T | TTCTCTCT others(1): Show |
105 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(102): Show | 106 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2001+443_2001+450d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621676 | |||||
| chr2:200621697
|
A | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2001+451A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621697 | ||||||
| chr2:200621698
|
A | C | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2001+452A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621698 | ||||||
| chr2:200621700
|
T | C | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2001+454T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621700 | ||||||
| chr2:200621998
|
C | T | 107 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(104): Show | 108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2001+752C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621998 | ||||||
| chr2:200622180
|
T | C | 2 | a0001c0001t0001g0231a0011c0023t0001g0251 | 2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2001+934T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622180 | ||||||
| chr2:200622232
|
G | C | 44 | a0001c0001t0001g0104a0001c0001t0001g0221a0001c0001t0001g0224others(41): Show | 44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.2001+986G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622232 | ||||||
| chr2:200622393
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(230): Show | 234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.2001+1147A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622393 | ||||||
| chr2:200622401
|
T | G | 1 | a0001c0001t0002g0017 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2001+1155T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622401 | ||||||
| chr2:200622595
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2002-1266C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622595 | ||||||
| chr2:200622634
|
C | G | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2002-1227C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622634 | ||||||
| chr2:200622720
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2002-1141A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622720 | ||||||
| chr2:200622809
|
C | A | 1 | a0003c0026t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2002-1052C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622809 | ||||||
| chr2:200623040
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 71 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.2002-821C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623040 | ||||||
| chr2:200623144
|
A | T | 1 | a0001c0001t0002g0011 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2002-717A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623144 | ||||||
| chr2:200623267
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(230): Show | 234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.2002-594C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623267 | ||||||
| chr2:200623443
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(230): Show | 234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.2002-418T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623443 | ||||||
| chr2:200623460
|
G | T | 1 | a0001c0001t0002g0037 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2002-401G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623460 | ||||||
| chr2:200623500
|
C | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2002-361C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623500 | ||||||
| chr2:200623643
|
G | A | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2002-218G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623643 | ||||||
| chr2:200623690
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(340): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2002-171A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623690 | ||||||
| chr2:200623712
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2002-149T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623712 | ||||||
| chr2:200623794
|
G | A | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2002-67G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623794 | ||||||
| chr2:200624035
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(225): Show | 229 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.2124+52A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624035 | ||||||
| chr2:200624148
|
C | A | 1 | a0001c0001t0002g0299 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2124+165C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624148 | ||||||
| chr2:200624278
|
C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(22): Show | 25 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.2124+295C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624278 | ||||||
| chr2:200624336
|
T | G | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2124+353T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624336 | ||||||
| chr2:200624427
|
T | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.2124+444T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624427 | ||||||
| chr2:200624439
|
G | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG01192.hp1 HG01261.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.2124+456G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624439 | ||||||
| chr2:200624619
|
G | T | 1 | a0001c0001t0001g0343 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2124+636G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624619 | ||||||
| chr2:200624695
|
T | G | 1 | a0003c0006t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2124+712T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624695 | ||||||
| chr2:200624742
|
A | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2124+759A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624742 | ||||||
| chr2:200624767
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(223): Show | 227 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.2124+784A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624767 | ||||||
| chr2:200624829
|
T | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.2124+846T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624829 | ||||||
| chr2:200624935
|
C | T | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2124+952C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624935 | ||||||
| chr2:200624943
|
C | T | 1 | a0001c0008t0002g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2124+960C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624943 | ||||||
| chr2:200625091
|
A | C | 1 | a0002c0002t0002g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2124+1108A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625091 | ||||||
| chr2:200625113
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(230): Show | 236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2124+1130C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625113 | ||||||
| chr2:200625299
|
C | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2124+1316C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625299 | ||||||
| chr2:200625347
|
G | A | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2124+1364G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625347 | ||||||
| chr2:200625626
|
A | G | 107 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(104): Show | 108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2124+1643A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625626 | ||||||
| chr2:200626003
|
C | T | 1 | a0002c0002t0003g0068 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2125-1350C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626003 | ||||||
| chr2:200626004
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2125-1349G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626004 | ||||||
| chr2:200626098
|
T | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0182 | 2 | HG00621.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2125-1255T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626098 | ||||||
| chr2:200626184
|
G | A | 358 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(355): Show | 361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.2125-1169G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626184 | ||||||
| chr2:200626300
|
G | A | 1 | a0001c0001t0002g0360 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2125-1053G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626300 | ||||||
| chr2:200626536
|
T | G | 2 | a0003c0009t0001g0097a0003c0009t0001g0361 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2125-817T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626536 | ||||||
| chr2:200626558
|
T | A | 343 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(340): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2125-795T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626558 | ||||||
| chr2:200626707
|
C | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2125-646C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626707 | ||||||
| chr2:200626727
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(315): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2125-626A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626727 | ||||||
| chr2:200626837
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(90): Show | 94 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2125-516G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626837 | ||||||
| chr2:200627099
|
A | T | 6 | a0001c0001t0001g0359a0001c0001t0002g0325a0001c0001t0002g0345others(3): Show | 6 | HG00423.hp2 HG00544.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2125-254A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200627099 | ||||||
| chr2:200627202
|
C | T | 1 | a0002c0002t0003g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2125-151C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200627202 | ||||||
| chr2:200627562
|
G | T | 1 | a0002c0002t0003g0049 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2221+113G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200627562 | ||||||
| chr2:200627787
|
G | A | 2 | a0001c0001t0002g0157a0003c0003t0001g0096 | 2 | HG02886.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2221+338G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200627787 | ||||||
| chr2:200627801
|
A | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | HG01192.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2221+352A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200627801 | ||||||
| chr2:200628094
|
C | T | 3 | a0001c0001t0002g0208a0003c0003t0004g0214a0003c0026t0001g0213 | 3 | HG02723.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2221+645C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628094 | ||||||
| chr2:200628100
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(225): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.2221+651G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628100 | ||||||
| chr2:200628178
|
TACACACA others(7): Show |
T | 1 | a0010c0025t0003g0287 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2221+741_2221+754d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200628178 | |||||
| chr2:200628312
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2221+863T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628312 | ||||||
| chr2:200628401
|
G | GA | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(246): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.2221+957dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200628401 | |||||
| chr2:200628435
|
A | G | 8 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2221+986A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628435 | ||||||
| chr2:200628579
|
A | T | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2221+1130A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628579 | ||||||
| chr2:200628695
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2221+1246G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628695 | ||||||
| chr2:200628764
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2221+1315A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628764 | ||||||
| chr2:200628788
|
G | A | 2 | a0001c0005t0006g0075a0001c0008t0002g0203 | 2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2221+1339G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628788 | ||||||
| chr2:200628925
|
T | TCAAA | 3 | a0001c0001t0001g0227a0001c0001t0001g0244a0006c0010t0009g0106 | 3 | HG03471.hp1 NA18965.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2221+1501_2221+150 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200628925 | |||||
| chr2:200629019
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2221+1570A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200629019 | ||||||
| chr2:200629183
|
A | C | 1 | a0001c0001t0002g0243 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2221+1734A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200629183 | ||||||
| chr2:200629256
|
C | T | 1 | a0001c0001t0002g0345 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2221+1807C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200629256 | ||||||
| chr2:200629751
|
T | C | 366 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(363): Show | 369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.2221+2302T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200629751 | ||||||
| chr2:200630113
|
C | T | 1 | a0016c0015t0002g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2221+2664C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630113 | ||||||
| chr2:200630189
|
T | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(338): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.2221+2740T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630189 | ||||||
| chr2:200630210
|
T | TA | 34 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0088others(31): Show | 34 | HG01109.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.2221+2788dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
T | TAAAAAAA others(8): Show |
1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2221+2774_2221+278 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
T | TAAAAAAA others(9): Show |
1 | a0003c0003t0004g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2221+2773_2221+278 others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
T | TAAAAAAA others(10): Show |
3 | a0001c0001t0002g0208a0003c0003t0004g0214a0003c0026t0001g0213 | 3 | HG02723.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2221+2772_2221+278 others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
T | TAAAAAAA others(11): Show |
1 | a0003c0003t0004g0276 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2221+2771_2221+278 others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
TAA | T | 13 | a0001c0001t0002g0150a0001c0001t0002g0233a0001c0001t0002g0239others(10): Show | 13 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2221+2787_2221+278 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
TAAA | T | 85 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(82): Show | 85 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2221+2786_2221+278 others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
TAAAAAAA others(3): Show |
T | 13 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0291others(10): Show | 14 | HG00733.hp1 HG01884.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2221+2779_2221+278 others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
TAAAAAAA others(5): Show |
T | 19 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(16): Show | 19 | HG01192.hp1 HG01261.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2221+2777_2221+278 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
TAAAAAAA others(6): Show |
T | 86 | a0001c0001t0001g0001a0001c0001t0001g0117a0001c0001t0001g0121others(83): Show | 88 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.2221+2776_2221+278 others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630210
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0019t0002g0149 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2221+2775_2221+278 others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | |||||
| chr2:200630340
|
T | C | 75 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.2221+2891T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630340 | ||||||
| chr2:200630390
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(232): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2221+2941A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630390 | ||||||
| chr2:200630428
|
C | T | 3 | a0001c0005t0002g0060a0001c0005t0004g0297a0015c0017t0001g0063 | 3 | HG02258.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2221+2979C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630428 | ||||||
| chr2:200630486
|
G | A | 1 | a0001c0001t0002g0360 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2221+3037G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630486 | ||||||
| chr2:200630526
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2221+3077A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630526 | ||||||
| chr2:200630537
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2221+3088T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630537 | ||||||
| chr2:200630548
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2221+3099G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630548 | ||||||
| chr2:200630548
|
G | GAGGA | 46 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0041others(43): Show | 46 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.2221+3148_2221+315 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
G | GAGGAAGG others(1): Show |
52 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 52 | HG00597.hp1 HG00639.hp2 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.2221+3144_2221+315 others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
G | GAGGAAGG others(5): Show |
21 | a0001c0001t0001g0012a0001c0001t0001g0086a0001c0001t0001g0089others(18): Show | 21 | HG00741.hp2 HG01258.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.2221+3140_2221+315 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
G | GAGGAAGG others(9): Show |
4 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0002g0031others(1): Show | 4 | HG02004.hp2 HG03831.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2221+3136_2221+315 others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
G | GAGGAAGG others(13): Show |
2 | a0001c0001t0002g0030a0001c0027t0002g0029 | 2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2221+3132_2221+315 others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGA | G | 5 | a0001c0001t0001g0357a0001c0001t0002g0262a0001c0001t0002g0363others(2): Show | 5 | HG02027.hp1 HG02055.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2221+3148_2221+315 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGAAGG others(1): Show |
G | 3 | a0001c0005t0001g0052a0001c0029t0001g0076a0003c0030t0002g0218 | 3 | HG03209.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2221+3144_2221+315 others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGAAGG others(5): Show |
G | 3 | a0001c0005t0002g0060a0001c0005t0004g0297a0015c0017t0001g0063 | 3 | HG02258.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2221+3140_2221+315 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGAAGG others(9): Show |
G | 19 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0257others(16): Show | 19 | HG00621.hp1 HG00642.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2221+3136_2221+315 others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGAAGG others(13): Show |
G | 93 | a0001c0001t0001g0001a0001c0001t0001g0117a0001c0001t0001g0121others(90): Show | 95 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2221+3132_2221+315 others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGAAGG others(17): Show |
G | 77 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.2221+3128_2221+315 others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGAAGG others(21): Show |
G | 12 | a0001c0001t0001g0003a0001c0001t0001g0275a0001c0001t0001g0291others(9): Show | 13 | HG00733.hp1 HG02280.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2221+3124_2221+315 others(32): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630548
|
GAGGAAGG others(25): Show |
G | 1 | a0001c0001t0002g0148 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2221+3120_2221+315 others(36): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | |||||
| chr2:200630627
|
G | A | 4 | a0001c0008t0001g0362a0003c0003t0001g0212a0003c0003t0004g0211others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2221+3178G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630627 | ||||||
| chr2:200630634
|
G | A | 1 | a0005c0007t0002g0240 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2221+3185G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630634 | ||||||
| chr2:200630648
|
G | A | 1 | a0003c0003t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2221+3199G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630648 | ||||||
| chr2:200630780
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2221+3331T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630780 | ||||||
| chr2:200630951
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2221+3502G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630951 | ||||||
| chr2:200631029
|
T | C | 1 | a0001c0001t0002g0101 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2221+3580T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631029 | ||||||
| chr2:200631388
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(235): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2222-3403A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631388 | ||||||
| chr2:200631742
|
A | C | 2 | a0001c0001t0005g0002a0001c0001t0005g0116 | 3 | HG02451.hp2 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2222-3049A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631742 | ||||||
| chr2:200631796
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2222-2995C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631796 | ||||||
| chr2:200632046
|
T | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(186): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.2222-2745T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632046 | ||||||
| chr2:200632232
|
A | G | 4 | a0001c0008t0001g0362a0003c0003t0001g0212a0003c0003t0004g0211others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2222-2559A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632232 | ||||||
| chr2:200632298
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.2222-2493C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632298 | ||||||
| chr2:200632312
|
TA | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(84): Show | 89 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2222-2478delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632312 | ||||||
| chr2:200632496
|
A | G | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2222-2295A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632496 | ||||||
| chr2:200632591
|
G | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0235 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2222-2200G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632591 | ||||||
| chr2:200632633
|
T | TA | 173 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(170): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2222-2148dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200632633 | |||||
| chr2:200632633
|
T | TAA | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2222-2149_2222-214 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200632633 | |||||
| chr2:200632879
|
CT | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(75): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2222-1902delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200632879 | |||||
| chr2:200633009
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0235 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2222-1782G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633009 | ||||||
| chr2:200633047
|
C | T | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2222-1744C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633047 | ||||||
| chr2:200633081
|
G | A | 1 | a0001c0005t0004g0297 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2222-1710G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633081 | ||||||
| chr2:200633098
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2222-1693C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633098 | ||||||
| chr2:200633099
|
G | A | 1 | a0001c0008t0002g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2222-1692G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633099 | ||||||
| chr2:200633202
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0002g0027a0001c0001t0002g0035 | 3 | NA18939.hp2 NA18940.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2222-1589G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633202 | ||||||
| chr2:200633314
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2222-1477G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633314 | ||||||
| chr2:200633349
|
T | C | 8 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0004g0297others(5): Show | 8 | HG02258.hp2 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2222-1442T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633349 | ||||||
| chr2:200633562
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(170): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2222-1229C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633562 | ||||||
| chr2:200634164
|
A | AT | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0042others(103): Show | 109 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.2222-602dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | |||||
| chr2:200634164
|
A | ATT | 14 | a0001c0001t0001g0134a0001c0001t0001g0197a0001c0001t0002g0051others(11): Show | 14 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2222-603_2222-602d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | |||||
| chr2:200634164
|
AT | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0169others(26): Show | 29 | HG00408.hp1 HG01192.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.2222-602delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | |||||
| chr2:200634164
|
ATTT | A | 6 | a0001c0001t0001g0062a0001c0001t0001g0244a0001c0001t0001g0321others(3): Show | 6 | HG02622.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2222-604_2222-602d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | |||||
| chr2:200634164
|
ATTTT | A | 78 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(75): Show | 78 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2222-605_2222-602d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | |||||
| chr2:200634164
|
ATTTTTTT | A | 7 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0008t0001g0050others(4): Show | 7 | HG02970.hp1 HG02976.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2222-608_2222-602d others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | |||||
| chr2:200634164
|
ATTTTTTT others(1): Show |
A | 14 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0273others(11): Show | 14 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2222-609_2222-602d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | |||||
| chr2:200634255
|
A | AAAC | 9 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0002g0217others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2222-521_2222-519d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634255 | |||||
| chr2:200634268
|
A | C | 3 | a0001c0001t0001g0087a0001c0001t0002g0027a0001c0001t0002g0035 | 3 | NA18939.hp2 NA18940.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2222-523A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634268 | ||||||
| chr2:200634460
|
C | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0235 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2222-331C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634460 | ||||||
| chr2:200634497
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0002g0175a0006c0010t0009g0106 | 3 | HG02280.hp1 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2222-294G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634497 | ||||||
| chr2:200634556
|
A | C | 1 | a0001c0001t0002g0161 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2222-235A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634556 | ||||||
| chr2:200634691
|
G | A | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2222-100G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634691 | ||||||
| chr2:200634737
|
G | T | 1 | a0001c0001t0002g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2222-54G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634737 | ||||||
| chr2:200634789
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG03225.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.2222-2A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634789 | ||||||
| chr2:200635054
|
G | T | 1 | a0002c0002t0003g0071 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2346+139G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635054 | ||||||
| chr2:200635306
|
C | G | 1 | a0001c0001t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2346+391C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635306 | ||||||
| chr2:200635351
|
G | A | 13 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0273others(10): Show | 13 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2346+436G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635351 | ||||||
| chr2:200635421
|
T | G | 2 | a0001c0001t0001g0176a0001c0001t0002g0175 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2346+506T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635421 | ||||||
| chr2:200635460
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(227): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2346+545T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635460 | ||||||
| chr2:200635468
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(20): Show | 24 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2346+553G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635468 | ||||||
| chr2:200635477
|
GGAAA | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(76): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2346+565_2346+568d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200635477 | |||||
| chr2:200635638
|
C | T | 1 | a0001c0001t0002g0354 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2346+723C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635638 | ||||||
| chr2:200635873
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2346+958G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635873 | ||||||
| chr2:200635908
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(195): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2346+993C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635908 | ||||||
| chr2:200635973
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0020t0001g0230 | 3 | NA18942.hp2 NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2347-938C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635973 | ||||||
| chr2:200636046
|
G | C | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2347-865G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636046 | ||||||
| chr2:200636065
|
G | GA | 86 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.2347-843dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636065 | |||||
| chr2:200636117
|
C | CT | 106 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 106 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.2347-765dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | |||||
| chr2:200636117
|
C | CTT | 39 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0042others(36): Show | 39 | HG00597.hp1 HG01123.hp1 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.2347-766_2347-765d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | |||||
| chr2:200636117
|
C | CTTT | 6 | a0002c0002t0003g0066a0002c0002t0003g0071a0003c0003t0004g0209others(3): Show | 6 | HG01361.hp1 HG02109.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2347-767_2347-765d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | |||||
| chr2:200636117
|
CT | C | 16 | a0001c0001t0001g0283a0001c0001t0002g0167a0001c0001t0002g0186others(13): Show | 16 | HG00642.hp1 HG01070.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.2347-765delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | |||||
| chr2:200636117
|
CTT | C | 14 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0357others(11): Show | 14 | HG00408.hp1 HG01106.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2347-766_2347-765d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | |||||
| chr2:200636117
|
CTTT | C | 12 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0273others(9): Show | 12 | HG00280.hp1 HG01099.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2347-767_2347-765d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | |||||
| chr2:200636422
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0054others(139): Show | 145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2347-489T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636422 | ||||||
| chr2:200636450
|
A | G | 1 | a0003c0030t0002g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2347-461A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636450 | ||||||
| chr2:200636491
|
G | A | 1 | a0001c0001t0001g0001 | 2 | NA18947.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2347-420G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636491 | ||||||
| chr2:200636648
|
AT | A | 3 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0003t0004g0092 | 3 | HG02723.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2347-262delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636648 | ||||||
| chr2:200636708
|
A | G | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2347-203A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636708 | ||||||
| chr2:200636845
|
A | G | 35 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0273others(32): Show | 35 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.2347-66A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636845 | ||||||
| chr2:200637121
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2480+77C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637121 | ||||||
| chr2:200637349
|
T | A | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2480+305T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637349 | ||||||
| chr2:200637490
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(20): Show | 24 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2480+446T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637490 | ||||||
| chr2:200637599
|
G | A | 7 | a0001c0001t0001g0117a0001c0001t0001g0205a0001c0001t0001g0257others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2480+555G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637599 | ||||||
| chr2:200637672
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(84): Show | 89 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2481-543T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637672 | ||||||
| chr2:200637789
|
A | G | 4 | a0001c0001t0001g0134a0001c0001t0002g0100a0001c0001t0002g0101others(1): Show | 4 | HG00544.hp1 NA18961.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2481-426A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637789 | ||||||
| chr2:200637912
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(20): Show | 24 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2481-303C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637912 | ||||||
| chr2:200638081
|
T | C | 3 | a0001c0001t0001g0247a0001c0001t0002g0281a0002c0002t0003g0025 | 3 | HG01361.hp2 HG02602.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2481-134T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200638081 | ||||||
| chr2:200638175
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(76): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2481-40G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200638175 | ||||||
| chr2:200638348
|
A | G | 1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2568+46A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638348 | ||||||
| chr2:200638361
|
G | T | 1 | a0002c0002t0003g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2568+59G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638361 | ||||||
| chr2:200638362
|
C | T | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2568+60C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638362 | ||||||
| chr2:200638453
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(115): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2568+151A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638453 | ||||||
| chr2:200638460
|
A | C | 1 | a0001c0001t0002g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2568+158A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638460 | ||||||
| chr2:200638539
|
G | A | 1 | a0003c0003t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2568+237G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638539 | ||||||
| chr2:200638543
|
T | C | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2568+241T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638543 | ||||||
| chr2:200638594
|
G | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(18): Show | 22 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2568+292G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638594 | ||||||
| chr2:200638665
|
GTTATGTG others(9): Show |
G | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2568+368_2568+383d others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200638665 | |||||
| chr2:200638695
|
G | T | 74 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.2568+393G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638695 | ||||||
| chr2:200638849
|
A | G | 1 | a0001c0005t0002g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2568+547A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638849 | ||||||
| chr2:200638892
|
AGCTCAAT others(5): Show |
A | 274 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(271): Show | 277 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2568+603_2568+614d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200638892 | |||||
| chr2:200639101
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2568+799G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639101 | ||||||
| chr2:200639169
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2568+867C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639169 | ||||||
| chr2:200639273
|
G | A | 13 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0273others(10): Show | 13 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2568+971G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639273 | ||||||
| chr2:200639681
|
G | A | 74 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.2568+1379G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639681 | ||||||
| chr2:200639755
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2569-1343C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639755 | ||||||
| chr2:200639762
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2569-1336C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639762 | ||||||
| chr2:200639773
|
G | A | 1 | a0004c0004t0001g0303 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2569-1325G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639773 | ||||||
| chr2:200639775
|
C | G | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2569-1323C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639775 | ||||||
| chr2:200639873
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | HG01192.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2569-1225A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639873 | ||||||
| chr2:200639894
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2569-1204G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639894 | ||||||
| chr2:200639895
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2569-1203G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639895 | ||||||
| chr2:200639896
|
G | A | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-1202G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639896 | ||||||
| chr2:200639977
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG00597.hp1 HG02602.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.2569-1121C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639977 | ||||||
| chr2:200639992
|
G | A | 3 | a0001c0001t0001g0231a0003c0003t0001g0096a0011c0023t0001g0251 | 3 | HG02809.hp2 HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2569-1106G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639992 | ||||||
| chr2:200640005
|
C | G | 1 | a0001c0001t0002g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2569-1093C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640005 | ||||||
| chr2:200640009
|
C | A | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-1089C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640009 | ||||||
| chr2:200640036
|
C | CA | 75 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(72): Show | 75 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2569-1044dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200640036 | |||||
| chr2:200640036
|
CA | C | 32 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0078others(29): Show | 32 | HG01106.hp1 HG01169.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.2569-1044delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200640036 | |||||
| chr2:200640053
|
A | G | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-1045A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640053 | ||||||
| chr2:200640125
|
A | G | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-973A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640125 | ||||||
| chr2:200640276
|
G | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0199 | 2 | NA18968.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2569-822G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640276 | ||||||
| chr2:200640326
|
C | T | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2569-772C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640326 | ||||||
| chr2:200640425
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2569-673A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640425 | ||||||
| chr2:200640546
|
C | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(213): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2569-552C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640546 | ||||||
| chr2:200640549
|
C | T | 1 | a0011c0023t0001g0251 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2569-549C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640549 | ||||||
| chr2:200640965
|
T | C | 2 | a0003c0009t0001g0097a0003c0009t0001g0361 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2569-133T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640965 | ||||||
| chr2:200641006
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0002g0145 | 2 | HG02165.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2569-92G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200641006 | ||||||
| chr2:200641199
|
G | A | 1 | a0003c0003t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2655+15G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641199 | ||||||
| chr2:200641230
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.2655+46C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641230 | ||||||
| chr2:200641245
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2655+61C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641245 | ||||||
| chr2:200641249
|
G | A | 4 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0004g0297others(1): Show | 4 | HG02258.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2655+65G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641249 | ||||||
| chr2:200641333
|
G | A | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2655+149G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641333 | ||||||
| chr2:200641374
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 13 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2655+190G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641374 | ||||||
| chr2:200641535
|
G | A | 11 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0002g0217others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2655+351G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641535 | ||||||
| chr2:200641619
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2655+435G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641619 | ||||||
| chr2:200641694
|
AT | A | 16 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0357others(13): Show | 16 | HG00408.hp1 HG01433.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2655+519delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr2 | 200641694 | |||||
| chr2:200641858
|
C | G | 8 | a0001c0001t0001g0117a0001c0001t0001g0205a0001c0001t0001g0257others(5): Show | 8 | HG01109.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2655+674C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641858 | ||||||
| chr2:200641904
|
A | G | 1 | a0001c0001t0002g0166 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2656-706A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641904 | ||||||
| chr2:200641990
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(213): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2656-620A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641990 | ||||||
| chr2:200642035
|
A | C | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2656-575A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642035 | ||||||
| chr2:200642078
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2656-532G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642078 | ||||||
| chr2:200642086
|
A | G | 1 | a0001c0001t0002g0019 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2656-524A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642086 | ||||||
| chr2:200642128
|
T | TA | 10 | a0001c0001t0001g0267a0001c0001t0001g0282a0001c0001t0001g0330others(7): Show | 10 | HG00642.hp1 HG01993.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.2656-472dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr2 | 200642128 | |||||
| chr2:200642431
|
T | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(213): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2656-179T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642431 | ||||||
| chr2:200642455
|
C | CAAA | 81 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2656-151_2656-149d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr2 | 200642455 | |||||
| chr2:200642837
|
G | T | 1 | a0004c0004t0001g0303 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2847+36G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642837 | ||||||
| chr2:200642849
|
C | T | 5 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0227others(2): Show | 5 | HG02015.hp2 NA18965.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2847+48C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642849 | ||||||
| chr2:200642850
|
G | T | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+49G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642850 | ||||||
| chr2:200642860
|
T | G | 2 | a0003c0009t0001g0097a0003c0009t0001g0361 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2847+59T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642860 | ||||||
| chr2:200642899
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2847+98G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642899 | ||||||
| chr2:200642954
|
C | G | 1 | a0003c0003t0004g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2847+153C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642954 | ||||||
| chr2:200643186
|
CT | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(90): Show | 95 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2847+399delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643186 | |||||
| chr2:200643359
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0366 | 2 | NA18987.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2847+558G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643359 | ||||||
| chr2:200643384
|
T | C | 4 | a0001c0001t0001g0310a0001c0001t0002g0311a0002c0002t0002g0098others(1): Show | 4 | HG00673.hp1 NA18944.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.2847+583T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643384 | ||||||
| chr2:200643386
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2847+585T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643386 | ||||||
| chr2:200643386
|
T | TAC | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2847+597_2847+598d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643386 | |||||
| chr2:200643386
|
T | TACAC | 11 | a0001c0001t0002g0091a0001c0001t0002g0156a0001c0001t0002g0157others(8): Show | 11 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.2847+595_2847+598d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643386 | |||||
| chr2:200643398
|
C | CACAT | 81 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(78): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2847+598_2847+599i others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643398 | |||||
| chr2:200643398
|
C | CAT | 13 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(10): Show | 14 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2847+611_2847+612d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643398 | |||||
| chr2:200643398
|
C | CATAT | 68 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(65): Show | 68 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2847+609_2847+612d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643398 | |||||
| chr2:200643400
|
T | C | 34 | a0001c0001t0001g0056a0001c0001t0001g0225a0001c0001t0001g0228others(31): Show | 34 | HG00280.hp1 HG00408.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.2847+599T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643400 | ||||||
| chr2:200643412
|
T | C | 1 | a0007c0013t0002g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2847+611T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643412 | ||||||
| chr2:200643552
|
G | T | 69 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(66): Show | 69 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2847+751G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643552 | ||||||
| chr2:200643710
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(81): Show | 86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2847+909G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643710 | ||||||
| chr2:200643837
|
G | A | 8 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2847+1036G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643837 | ||||||
| chr2:200644042
|
T | C | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2847+1241T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644042 | ||||||
| chr2:200644131
|
C | G | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+1330C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644131 | ||||||
| chr2:200644335
|
C | T | 1 | a0002c0002t0003g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2847+1534C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644335 | ||||||
| chr2:200644430
|
C | A | 1 | a0001c0001t0002g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2847+1629C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644430 | ||||||
| chr2:200644431
|
T | A | 1 | a0001c0001t0002g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2847+1630T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644431 | ||||||
| chr2:200644435
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2847+1634C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644435 | ||||||
| chr2:200644516
|
T | C | 1 | a0001c0008t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2847+1715T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644516 | ||||||
| chr2:200644544
|
G | A | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+1743G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644544 | ||||||
| chr2:200645151
|
C | CAATATTA others(5): Show |
213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(210): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2847+2354_2847+236 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200645151 | |||||
| chr2:200645151
|
C | CAGTATTA others(5): Show |
1 | a0001c0005t0004g0297 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2847+2351_2847+235 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200645151 | |||||
| chr2:200645265
|
G | C | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2847+2464G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645265 | ||||||
| chr2:200645566
|
G | A | 8 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0002g0217others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2847+2765G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645566 | ||||||
| chr2:200645573
|
G | A | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+2772G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645573 | ||||||
| chr2:200645617
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2847+2816A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645617 | ||||||
| chr2:200645670
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0337 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2847+2869G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645670 | ||||||
| chr2:200645696
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0121others(89): Show | 94 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2847+2895G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645696 | ||||||
| chr2:200645744
|
C | T | 1 | a0003c0030t0002g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2847+2943C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645744 | ||||||
| chr2:200645751
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2847+2950G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645751 | ||||||
| chr2:200645860
|
T | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2847+3059T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645860 | ||||||
| chr2:200645932
|
TAGTG | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 13 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2847+3134_2847+313 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200645932 | |||||
| chr2:200645974
|
C | T | 8 | a0001c0001t0001g0104a0001c0001t0001g0231a0001c0001t0001g0284others(5): Show | 8 | HG02809.hp2 HG02897.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.2847+3173C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645974 | ||||||
| chr2:200645979
|
C | T | 1 | a0003c0018t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2847+3178C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645979 | ||||||
| chr2:200646224
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0188 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2847+3423C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646224 | ||||||
| chr2:200646512
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2847+3711G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646512 | ||||||
| chr2:200646692
|
T | C | 1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2847+3891T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646692 | ||||||
| chr2:200646754
|
T | C | 1 | a0001c0029t0001g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2847+3953T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646754 | ||||||
| chr2:200647035
|
T | C | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2848-3939T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647035 | ||||||
| chr2:200647136
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(213): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2848-3838A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647136 | ||||||
| chr2:200647140
|
T | TTTTG | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(200): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2848-3830_2848-382 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200647140 | |||||
| chr2:200647429
|
C | G | 61 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 61 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.2848-3545C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647429 | ||||||
| chr2:200647433
|
T | C | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2848-3541T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647433 | ||||||
| chr2:200647567
|
G | A | 9 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0002g0217others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2848-3407G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647567 | ||||||
| chr2:200647693
|
A | G | 3 | a0001c0001t0001g0041a0002c0002t0003g0265a0002c0002t0003g0274 | 3 | HG02698.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2848-3281A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647693 | ||||||
| chr2:200647701
|
C | A | 4 | a0001c0001t0001g0134a0001c0001t0002g0100a0001c0001t0002g0101others(1): Show | 4 | HG00544.hp1 NA18961.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-3273C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647701 | ||||||
| chr2:200647944
|
GT | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(210): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2848-3023delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200647944 | |||||
| chr2:200648005
|
T | A | 7 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0004g0297others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2848-2969T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648005 | ||||||
| chr2:200648165
|
T | A | 1 | a0003c0030t0002g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2848-2809T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648165 | ||||||
| chr2:200648384
|
T | G | 31 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0238others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2848-2590T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648384 | ||||||
| chr2:200648450
|
G | A | 1 | a0010c0025t0003g0287 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2848-2524G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648450 | ||||||
| chr2:200648577
|
GGT | G | 4 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0227others(1): Show | 4 | HG02015.hp2 NA18965.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-2395_2848-239 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200648577 | |||||
| chr2:200648581
|
G | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0227others(1): Show | 4 | HG02015.hp2 NA18965.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-2393G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648581 | ||||||
| chr2:200648672
|
T | C | 9 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0002g0217others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2848-2302T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648672 | ||||||
| chr2:200648709
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2848-2265G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648709 | ||||||
| chr2:200648945
|
C | G | 8 | a0001c0001t0002g0091a0003c0003t0001g0090a0003c0003t0001g0094others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2848-2029C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648945 | ||||||
| chr2:200648975
|
C | G | 273 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(270): Show | 274 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.2848-1999C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648975 | ||||||
| chr2:200648993
|
A | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(151): Show | 154 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(151): Show |
intron_variant | MODIFIER | c.2848-1981A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648993 | ||||||
| chr2:200649017
|
G | T | 1 | a0002c0002t0003g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2848-1957G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649017 | ||||||
| chr2:200649048
|
C | T | 1 | a0001c0005t0002g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2848-1926C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649048 | ||||||
| chr2:200649246
|
C | A | 1 | a0001c0001t0001g0356 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2848-1728C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649246 | ||||||
| chr2:200649255
|
G | A | 68 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(65): Show | 68 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2848-1719G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649255 | ||||||
| chr2:200649294
|
T | C | 1 | a0001c0001t0002g0166 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2848-1680T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649294 | ||||||
| chr2:200649346
|
G | A | 1 | a0017c0032t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2848-1628G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649346 | ||||||
| chr2:200649422
|
C | G | 10 | a0001c0001t0001g0318a0001c0001t0001g0333a0001c0001t0001g0339others(7): Show | 10 | NA18939.hp1 NA18950.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.2848-1552C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649422 | ||||||
| chr2:200649475
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2848-1499G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649475 | ||||||
| chr2:200649538
|
G | A | 1 | a0002c0002t0002g0348 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2848-1436G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649538 | ||||||
| chr2:200649555
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2848-1419C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649555 | ||||||
| chr2:200649570
|
A | G | 149 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(146): Show | 149 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.2848-1404A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649570 | ||||||
| chr2:200649750
|
C | T | 1 | a0001c0001t0002g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2848-1224C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649750 | ||||||
| chr2:200649787
|
G | A | 1 | a0003c0030t0002g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2848-1187G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649787 | ||||||
| chr2:200649950
|
C | G | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2848-1024C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649950 | ||||||
| chr2:200650169
|
G | A | 24 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0273others(21): Show | 24 | HG00280.hp1 HG00741.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.2848-805G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650169 | ||||||
| chr2:200650306
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0002g0145 | 2 | HG02165.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2848-668T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650306 | ||||||
| chr2:200650582
|
A | G | 16 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0273others(13): Show | 16 | HG00280.hp1 HG00741.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2848-392A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650582 | ||||||
| chr2:200650684
|
T | C | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2848-290T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650684 | ||||||
| chr2:200650696
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2848-278G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650696 | ||||||
| chr2:200650793
|
T | C | 16 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0357others(13): Show | 16 | HG00408.hp1 HG01433.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2848-181T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650793 | ||||||
| chr2:200650936
|
G | A | 16 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0357others(13): Show | 16 | HG00408.hp1 HG01433.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2848-38G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650936 | ||||||
| chr2:200650940
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2848-34C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650940 | ||||||
| chr2:200651216
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(282): Show | 286 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.3075+15T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651216 | ||||||
| chr2:200651269
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 13 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3075+68G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651269 | ||||||
| chr2:200651304
|
G | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0270others(7): Show | 11 | HG01243.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3075+103G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651304 | ||||||
| chr2:200651574
|
C | T | 1 | a0001c0001t0002g0365 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3075+373C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651574 | ||||||
| chr2:200651617
|
G | T | 8 | a0001c0005t0001g0052a0001c0005t0002g0060a0001c0005t0002g0217others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3075+416G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651617 | ||||||
| chr2:200651741
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3075+540G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651741 | ||||||
| chr2:200651753
|
A | G | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3075+552A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651753 | ||||||
| chr2:200651913
|
C | A | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3075+712C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651913 | ||||||
| chr2:200651917
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3075+716C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651917 | ||||||
| chr2:200651929
|
T | G | 7 | a0001c0001t0001g0120a0001c0001t0001g0275a0001c0001t0001g0320others(4): Show | 7 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3075+728T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651929 | ||||||
| chr2:200651962
|
C | T | 147 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(144): Show | 147 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.3075+761C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651962 | ||||||
| chr2:200652030
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3075+829G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652030 | ||||||
| chr2:200652042
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3075+841G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652042 | ||||||
| chr2:200652062
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3075+861G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652062 | ||||||
| chr2:200652078
|
C | T | 228 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(225): Show | 228 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.3075+877C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652078 | ||||||
| chr2:200652380
|
G | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.3075+1179G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652380 | ||||||
| chr2:200652441
|
G | C | 9 | a0001c0001t0002g0103a0002c0002t0003g0040a0002c0002t0003g0043others(6): Show | 9 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3075+1240G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652441 | ||||||
| chr2:200652671
|
G | A | 1 | a0003c0003t0006g0329 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3075+1470G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652671 | ||||||
| chr2:200652798
|
C | G | 9 | a0001c0001t0002g0103a0002c0002t0003g0040a0002c0002t0003g0043others(6): Show | 9 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3075+1597C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652798 | ||||||
| chr2:200652834
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3075+1633A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652834 | ||||||
| chr2:200652836
|
A | G | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 239 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.3075+1635A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652836 | ||||||
| chr2:200652859
|
G | A | 57 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.3075+1658G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652859 | ||||||
| chr2:200652890
|
C | T | 1 | a0003c0018t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3075+1689C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652890 | ||||||
| chr2:200652943
|
C | A | 6 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0006t0001g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3075+1742C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652943 | ||||||
| chr2:200653089
|
G | A | 3 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0349 | 3 | NA18955.hp2 NA18981.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3075+1888G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653089 | ||||||
| chr2:200653321
|
G | A | 13 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(10): Show | 13 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.3075+2120G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653321 | ||||||
| chr2:200653466
|
A | G | 11 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3075+2265A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653466 | ||||||
| chr2:200653485
|
C | G | 1 | a0001c0001t0002g0288 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3075+2284C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653485 | ||||||
| chr2:200653587
|
G | A | 2 | a0001c0005t0006g0075a0003c0003t0001g0261 | 2 | HG03540.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3075+2386G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653587 | ||||||
| chr2:200653645
|
G | T | 6 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0006t0001g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3075+2444G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653645 | ||||||
| chr2:200653661
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0257others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3075+2460C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653661 | ||||||
| chr2:200653878
|
T | G | 3 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0349 | 3 | NA18955.hp2 NA18981.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3075+2677T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653878 | ||||||
| chr2:200654074
|
C | T | 1 | a0003c0003t0006g0329 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3076-2768C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654074 | ||||||
| chr2:200654179
|
G | C | 1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3076-2663G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654179 | ||||||
| chr2:200654185
|
G | T | 2 | a0001c0001t0001g0324a0001c0001t0001g0326 | 2 | NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3076-2657G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654185 | ||||||
| chr2:200654206
|
C | CA | 22 | a0001c0001t0001g0197a0001c0001t0001g0260a0001c0001t0001g0334others(19): Show | 22 | HG00423.hp1 HG00741.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3076-2609dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | |||||
| chr2:200654206
|
CA | C | 53 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 53 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.3076-2609delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | |||||
| chr2:200654206
|
CAAAAA | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0057others(20): Show | 23 | HG00621.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.3076-2613_3076-260 others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | |||||
| chr2:200654206
|
CAAAAAA | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 129 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.3076-2614_3076-260 others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | |||||
| chr2:200654206
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0364 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3076-2619_3076-260 others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | |||||
| chr2:200654206
|
CAAAAAAA others(7): Show |
C | 10 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.3076-2622_3076-260 others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | |||||
| chr2:200654361
|
T | C | 6 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0006t0001g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076-2481T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654361 | ||||||
| chr2:200654410
|
A | G | 57 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.3076-2432A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654410 | ||||||
| chr2:200654485
|
A | G | 1 | a0003c0003t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3076-2357A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654485 | ||||||
| chr2:200654559
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3076-2283C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654559 | ||||||
| chr2:200654968
|
G | A | 7 | a0001c0001t0001g0117a0001c0001t0001g0129a0001c0001t0001g0231others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3076-1874G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654968 | ||||||
| chr2:200655061
|
C | T | 1 | a0001c0014t0001g0353 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3076-1781C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655061 | ||||||
| chr2:200655230
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3076-1612C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655230 | ||||||
| chr2:200655291
|
G | C | 6 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0006t0001g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076-1551G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655291 | ||||||
| chr2:200655507
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3076-1335T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655507 | ||||||
| chr2:200655548
|
C | T | 4 | a0001c0001t0002g0123a0001c0001t0002g0166a0001c0001t0002g0246others(1): Show | 4 | NA18948.hp1 NA18977.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076-1294C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655548 | ||||||
| chr2:200655875
|
A | G | 161 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 161 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.3076-967A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655875 | ||||||
| chr2:200656130
|
C | T | 9 | a0001c0001t0001g0275a0001c0001t0002g0208a0003c0003t0001g0212others(6): Show | 9 | HG02109.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3076-712C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656130 | ||||||
| chr2:200656171
|
G | A | 1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3076-671G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656171 | ||||||
| chr2:200656199
|
T | C | 1 | a0011c0023t0001g0251 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3076-643T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656199 | ||||||
| chr2:200656286
|
C | T | 6 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0006t0001g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076-556C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656286 | ||||||
| chr2:200656293
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3076-549A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656293 | ||||||
| chr2:200656313
|
T | TA | 163 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.3076-524dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200656313 | |||||
| chr2:200656401
|
G | C | 11 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0002g0150others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.3076-441G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656401 | ||||||
| chr2:200656511
|
C | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(189): Show | 194 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.3076-331C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656511 | ||||||
| chr2:200656660
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(213): Show | 218 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.3076-182T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656660 | ||||||
| chr2:200656679
|
C | T | 1 | a0002c0002t0003g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3076-163C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656679 | ||||||
| chr2:200656732
|
G | C | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3076-110G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656732 | ||||||
| chr2:200656749
|
G | A | 104 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(101): Show | 104 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.3076-93G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656749 | ||||||
| chr2:200656762
|
C | T | 12 | a0003c0003t0001g0226a0003c0003t0001g0245a0003c0003t0001g0248others(9): Show | 12 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3076-80C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656762 | ||||||
| chr2:200656770
|
A | T | 10 | a0001c0001t0002g0103a0002c0002t0003g0025a0002c0002t0003g0040others(7): Show | 10 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.3076-72A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656770 | ||||||
| chr2:200656786
|
C | T | 9 | a0003c0003t0001g0226a0003c0003t0001g0245a0003c0003t0001g0248others(6): Show | 9 | HG01515.hp1 HG01517.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.3076-56C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656786 | ||||||
| chr2:200657008
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0072others(130): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.3171+71A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657008 | ||||||
| chr2:200657062
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3171+125G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657062 | ||||||
| chr2:200657141
|
T | C | 7 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3171+204T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657141 | ||||||
| chr2:200657161
|
C | A | 1 | a0003c0003t0006g0329 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3171+224C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657161 | ||||||
| chr2:200657161
|
C | CAAAAAAA | 11 | a0001c0001t0001g0134a0001c0001t0001g0273a0001c0001t0002g0171others(8): Show | 11 | HG00544.hp1 HG01496.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657161 | |||||
| chr2:200657161
|
C | CAAAAAAA others(2): Show |
68 | a0001c0001t0001g0196a0001c0001t0001g0357a0001c0001t0002g0017others(65): Show | 68 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(11): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657161 | |||||
| chr2:200657161
|
C | CAAAAAAA others(4): Show |
17 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0238others(14): Show | 18 | HG00423.hp2 HG02129.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657161 | |||||
| chr2:200657165
|
A | AAAAAAAA others(19): Show |
1 | a0003c0003t0004g0276 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(23): Show |
3 | a0001c0001t0001g0275a0003c0003t0004g0073a0003c0003t0004g0092 | 3 | HG02723.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(32): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(27): Show |
2 | a0003c0003t0004g0209a0003c0003t0006g0329 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(36): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(17): Show |
1 | a0003c0003t0004g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(26): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0340 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(14): Show |
3 | a0001c0001t0001g0336a0001c0001t0001g0339a0001c0001t0001g0349 | 3 | NA18955.hp2 NA18963.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(23): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(16): Show |
2 | a0001c0001t0002g0328a0001c0001t0002g0341 | 2 | NA18939.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0002g0342 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(31): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(26): Show |
1 | a0003c0003t0004g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(35): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0002g0208 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(39): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0333a0004c0004t0001g0303 | 2 | NA19062.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(15): Show |
1 | a0004c0004t0001g0301 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(17): Show |
2 | a0001c0001t0001g0077a0004c0004t0001g0300 | 2 | HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(26): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(19): Show |
2 | a0004c0004t0001g0305a0004c0004t0001g0327 | 2 | NA18977.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(30): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(6): Show |
5 | a0001c0001t0002g0314a0001c0001t0002g0315a0001c0001t0002g0338others(2): Show | 5 | NA18942.hp1 NA18943.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0359a0001c0001t0002g0115 | 2 | NA19060.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(12): Show |
4 | a0001c0001t0001g0229a0001c0001t0001g0266a0001c0001t0001g0321others(1): Show | 4 | HG02056.hp1 NA18948.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(14): Show |
6 | a0001c0001t0001g0282a0001c0001t0001g0312a0001c0001t0001g0323others(3): Show | 6 | HG03942.hp1 NA18945.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(23): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(16): Show |
7 | a0001c0001t0001g0165a0001c0001t0001g0241a0001c0001t0001g0324others(4): Show | 7 | HG02015.hp1 HG02056.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(18): Show |
10 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(7): Show | 10 | HG00597.hp2 HG00673.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(27): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(20): Show |
3 | a0001c0001t0001g0021a0001c0001t0001g0224a0002c0002t0002g0348 | 3 | HG02015.hp2 NA18944.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(29): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(22): Show |
3 | a0001c0001t0001g0221a0001c0001t0001g0237a0001c0001t0001g0355 | 3 | HG02155.hp1 HG04199.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(31): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0002g0119a0018c0012t0001g0198 | 2 | HG03927.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0317 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(19): Show |
2 | a0004c0004t0001g0302a0009c0028t0001g0313 | 2 | HG00408.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0322 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(30): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(4): Show |
14 | a0001c0001t0001g0173a0001c0001t0002g0011a0001c0001t0002g0026others(11): Show | 14 | HG01943.hp1 HG01975.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0019a0001c0001t0002g0109 | 2 | HG00609.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0197 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0307a0001c0001t0001g0318a0001c0001t0001g0356 | 3 | NA18950.hp2 NA18978.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAATA others(5): Show |
1 | a0003c0006t0001g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAATA others(7): Show |
1 | a0003c0006t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAATA others(9): Show |
1 | a0003c0006t0001g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AAT | 7 | a0001c0001t0001g0192a0001c0001t0001g0200a0001c0001t0002g0150others(4): Show | 7 | HG00738.hp2 HG01255.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3171+253_3171+254d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | AATAT | 4 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0235others(1): Show | 4 | HG03491.hp2 HG03834.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.3171+251_3171+254d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | |||||
| chr2:200657165
|
A | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0216others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.3171+228A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657165 | ||||||
| chr2:200657167
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.3171+230T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657167 | ||||||
| chr2:200657169
|
T | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0244 | 3 | HG00733.hp2 HG02293.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.3171+232T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657169 | ||||||
| chr2:200657171
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+234T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657171 | ||||||
| chr2:200657173
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+236T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657173 | ||||||
| chr2:200657175
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+238T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657175 | ||||||
| chr2:200657177
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+240T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657177 | ||||||
| chr2:200657184
|
A | AT | 4 | a0001c0001t0001g0001a0001c0001t0002g0132a0001c0001t0002g0364others(1): Show | 5 | HG03831.hp2 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.3171+248dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657184 | |||||
| chr2:200657184
|
A | ATTT | 9 | a0001c0001t0002g0024a0001c0001t0002g0030a0001c0001t0002g0031others(6): Show | 9 | HG00738.hp1 HG01081.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3171+248_3171+249i others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657184 | |||||
| chr2:200657184
|
A | T | 3 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0069 | 3 | HG01943.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.3171+247A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657184 | ||||||
| chr2:200657186
|
A | AT | 13 | a0001c0001t0001g0054a0001c0001t0001g0357a0001c0001t0002g0004others(10): Show | 13 | HG00733.hp1 HG01433.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.3171+250dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657186 | |||||
| chr2:200657186
|
A | ATTT | 3 | a0001c0001t0002g0179a0001c0001t0002g0350a0001c0001t0002g0363 | 3 | NA18967.hp1 NA18992.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3171+250_3171+251i others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657186 | |||||
| chr2:200657186
|
A | ATTTTTTT others(5): Show |
1 | a0003c0003t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3171+250_3171+251i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657186 | |||||
| chr2:200657186
|
A | T | 23 | a0001c0001t0001g0001a0001c0001t0002g0024a0001c0001t0002g0026others(20): Show | 24 | HG00738.hp1 HG01081.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.3171+249A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657186 | ||||||
| chr2:200657188
|
A | AT | 14 | a0001c0001t0001g0283a0001c0001t0002g0130a0001c0001t0002g0141others(11): Show | 14 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.3171+252dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657188 | |||||
| chr2:200657188
|
A | ATTT | 19 | a0001c0001t0001g0196a0001c0001t0002g0017a0001c0001t0002g0027others(16): Show | 19 | HG00609.hp1 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.3171+252_3171+253i others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657188 | |||||
| chr2:200657188
|
A | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(58): Show | 62 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.3171+251A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657188 | ||||||
| chr2:200657189
|
TA | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.3171+253delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657189 | ||||||
| chr2:200657190
|
A | AT | 13 | a0001c0001t0001g0165a0001c0001t0001g0221a0001c0001t0001g0224others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.3171+268dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(12): Show |
1 | a0003c0003t0001g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(44): Show |
1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(53): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(21): Show |
1 | a0003c0003t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(30): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(15): Show |
1 | a0003c0003t0001g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(32): Show |
1 | a0003c0009t0001g0097 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(41): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(19): Show |
1 | a0014c0024t0001g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(15): Show |
2 | a0003c0003t0001g0094a0003c0006t0001g0122 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(16): Show |
1 | a0003c0018t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(8): Show |
1 | a0003c0003t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(19): Show |
1 | a0003c0030t0002g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(7): Show |
1 | a0003c0026t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(14): Show |
1 | a0003c0003t0001g0250 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(23): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(6): Show |
1 | a0003c0003t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0257 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0319 | 4 | HG02615.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0269a0001c0001t0001g0320a0001c0014t0001g0353 | 3 | HG02818.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATAT others(10): Show |
1 | a0017c0032t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATTT others(3): Show |
1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATTT others(8): Show |
3 | a0001c0001t0001g0120a0001c0001t0001g0260a0001c0001t0001g0271 | 3 | HG01109.hp1 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATTT others(9): Show |
2 | a0001c0001t0001g0270a0001c0001t0001g0334 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATATTT others(11): Show |
2 | a0001c0001t0001g0258a0013c0021t0001g0259 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATTTTT others(7): Show |
1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0231 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATTT | 39 | a0001c0001t0001g0077a0001c0001t0001g0121a0001c0001t0001g0273others(36): Show | 39 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.3171+266_3171+268d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATTTT | 10 | a0001c0001t0001g0072a0001c0001t0001g0321a0001c0001t0002g0113others(7): Show | 10 | HG02970.hp2 HG03139.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.3171+265_3171+268d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATTTTT | 14 | a0001c0001t0001g0124a0001c0001t0001g0197a0001c0001t0001g0241others(11): Show | 14 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.3171+264_3171+268d others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0002g0208a0003c0003t0004g0211a0003c0006t0001g0095 | 3 | HG02109.hp2 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3171+259_3171+268d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATTTTTTT others(5): Show |
3 | a0003c0003t0004g0092a0003c0003t0004g0214a0003c0003t0006g0329 | 3 | HG02723.hp1 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3171+257_3171+268d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATTTTTTT others(7): Show |
1 | a0003c0009t0001g0361 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3171+255_3171+268d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | ATTTTTTT others(8): Show |
1 | a0003c0003t0004g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3171+254_3171+268d others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657190
|
A | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(127): Show | 131 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.3171+253A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657190 | ||||||
| chr2:200657190
|
AT | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00639.hp2 HG01123.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3171+268delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | |||||
| chr2:200657191
|
T | TA | 4 | a0001c0001t0001g0268a0001c0001t0001g0337a0001c0001t0001g0343others(1): Show | 4 | HG01123.hp2 HG01981.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3171+254_3171+255i others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657191 | ||||||
| chr2:200657192
|
T | A | 28 | a0001c0001t0001g0169a0001c0001t0001g0192a0001c0001t0001g0225others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.3171+255T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657192 | ||||||
| chr2:200657193
|
T | A | 1 | a0001c0001t0001g0343 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3171+256T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657193 | ||||||
| chr2:200657194
|
T | A | 8 | a0001c0001t0002g0175a0001c0001t0002g0233a0001c0001t0002g0253others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.3171+257T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657194 | ||||||
| chr2:200657383
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(184): Show | 188 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3171+446G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657383 | ||||||
| chr2:200657411
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0177 | 2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.3171+474C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657411 | ||||||
| chr2:200657412
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(236): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.3171+475T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657412 | ||||||
| chr2:200657493
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0102 | 3 | NA18939.hp2 NA18940.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.3171+556G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657493 | ||||||
| chr2:200657539
|
C | T | 1 | a0003c0003t0001g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3171+602C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657539 | ||||||
| chr2:200657654
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3171+717C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657654 | ||||||
| chr2:200657669
|
A | G | 60 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3171+732A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657669 | ||||||
| chr2:200657718
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0020t0001g0230 | 3 | NA18942.hp2 NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.3171+781C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657718 | ||||||
| chr2:200657899
|
G | T | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3171+962G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657899 | ||||||
| chr2:200657992
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3171+1055G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657992 | ||||||
| chr2:200658032
|
C | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(233): Show | 237 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.3171+1095C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658032 | ||||||
| chr2:200658098
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3172-1067C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658098 | ||||||
| chr2:200658166
|
T | C | 6 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0006t0001g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172-999T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658166 | ||||||
| chr2:200658230
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3172-935C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658230 | ||||||
| chr2:200658461
|
C | G | 29 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0003t0001g0096others(26): Show | 29 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.3172-704C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658461 | ||||||
| chr2:200658616
|
C | T | 1 | a0001c0001t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3172-549C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658616 | ||||||
| chr2:200658721
|
C | T | 2 | a0003c0009t0001g0097a0003c0009t0001g0361 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3172-444C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658721 | ||||||
| chr2:200658746
|
T | A | 2 | a0003c0009t0001g0097a0003c0009t0001g0361 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3172-419T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658746 | ||||||
| chr2:200658808
|
G | A | 1 | a0003c0003t0006g0329 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3172-357G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658808 | ||||||
| chr2:200659013
|
A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(242): Show | 246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.3172-152A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659013 | ||||||
| chr2:200659027
|
G | A | 2 | a0001c0005t0006g0075a0002c0002t0007g0252 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3172-138G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659027 | ||||||
| chr2:200659033
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3172-132A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659033 | ||||||
| chr2:200659090
|
T | G | 6 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0006t0001g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172-75T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659090 | ||||||
| chr2:200659391
|
A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0188a0001c0008t0001g0362 | 3 | HG02145.hp2 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.3300+98A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659391 | ||||||
| chr2:200659471
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3300+178C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659471 | ||||||
| chr2:200659474
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0120others(19): Show | 23 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3300+181C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659474 | ||||||
| chr2:200659777
|
TTC | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(48): Show | 52 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3301-209_3301-208d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659777 | |||||
| chr2:200659777
|
TTCTC | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0117a0001c0001t0001g0129others(12): Show | 15 | HG02132.hp2 HG02300.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3301-211_3301-208d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659777 | |||||
| chr2:200659782
|
TCTCTCAC others(1): Show |
T | 6 | a0001c0001t0001g0120a0001c0001t0002g0109a0001c0001t0002g0365others(3): Show | 6 | HG00609.hp2 HG00733.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.3301-211_3301-204d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | |||||
| chr2:200659782
|
TCTCTCAC others(3): Show |
T | 29 | a0001c0001t0001g0238a0001c0001t0001g0273a0001c0001t0001g0357others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.3301-211_3301-202d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | |||||
| chr2:200659782
|
TCTCTCAC others(5): Show |
T | 90 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(87): Show | 90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3301-211_3301-200d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | |||||
| chr2:200659782
|
TCTCTCAC others(7): Show |
T | 1 | a0001c0001t0002g0309 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3301-211_3301-198d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | |||||
| chr2:200659784
|
T | A | 9 | a0001c0001t0001g0020a0001c0001t0001g0335a0001c0001t0001g0336others(6): Show | 9 | HG02056.hp2 HG03942.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.3301-211T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659784 | ||||||
| chr2:200659786
|
T | A | 54 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.3301-209T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659786 | ||||||
| chr2:200659786
|
T | TCA | 26 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(23): Show | 27 | HG00639.hp1 HG00639.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.3301-171_3301-170d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | |||||
| chr2:200659786
|
T | TCACA | 11 | a0001c0001t0001g0072a0001c0001t0001g0121a0001c0001t0001g0168others(8): Show | 11 | HG01192.hp1 HG01261.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.3301-173_3301-170d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | |||||
| chr2:200659786
|
T | TCACACAC others(3): Show |
1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3301-179_3301-170d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | |||||
| chr2:200659786
|
T | TCTCACAC others(5): Show |
1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3301-208_3301-207i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | |||||
| chr2:200659786
|
TCA | T | 20 | a0001c0001t0001g0061a0001c0001t0001g0128a0001c0001t0001g0199others(17): Show | 21 | HG01192.hp2 HG01358.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.3301-171_3301-170d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | |||||
| chr2:200659786
|
TCACACAC others(13): Show |
T | 3 | a0003c0009t0001g0097a0003c0009t0001g0361a0006c0010t0009g0106 | 3 | HG02055.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3301-189_3301-170d others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | |||||
| chr2:200659786
|
TCACACAC others(15): Show |
T | 1 | a0003c0026t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3301-191_3301-170d others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | |||||
| chr2:200659790
|
A | T | 1 | a0002c0002t0003g0049 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3301-205A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659790 | ||||||
| chr2:200659791
|
C | CACACAT | 7 | a0003c0003t0001g0212a0003c0003t0001g0245a0003c0003t0001g0250others(4): Show | 7 | HG01515.hp1 HG01517.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3301-199_3301-198i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659791 | |||||
| chr2:200659793
|
C | CACAT | 8 | a0003c0003t0001g0226a0003c0003t0001g0248a0003c0003t0001g0249others(5): Show | 8 | HG02647.hp1 HG03209.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.3301-199_3301-198i others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659793 | |||||
| chr2:200659806
|
ACACACAC others(15): Show |
A | 2 | a0003c0003t0001g0090a0003c0003t0001g0094 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3301-181_3301-160d others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659806 | |||||
| chr2:200659812
|
ACACACAC others(9): Show |
A | 4 | a0003c0006t0001g0093a0003c0006t0001g0095a0003c0006t0001g0105others(1): Show | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3301-175_3301-160d others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659812 | |||||
| chr2:200660269
|
G | T | 1 | a0001c0001t0002g0363 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3375+200G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660269 | ||||||
| chr2:200660380
|
G | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.3375+311G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660380 | ||||||
| chr2:200660504
|
G | T | 2 | a0001c0005t0006g0075a0002c0002t0007g0252 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3375+435G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660504 | ||||||
| chr2:200660523
|
A | G | 1 | a0001c0008t0001g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3375+454A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660523 | ||||||
| chr2:200660534
|
A | G | 10 | a0001c0001t0002g0103a0002c0002t0003g0025a0002c0002t0003g0040others(7): Show | 10 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.3375+465A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660534 | ||||||
| chr2:200660779
|
G | T | 1 | a0001c0001t0002g0069 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3375+710G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660779 | ||||||
| chr2:200660832
|
G | A | 209 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(206): Show | 210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.3376-747G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660832 | ||||||
| chr2:200660945
|
G | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | NA18948.hp2 NA18955.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3376-634G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660945 | ||||||
| chr2:200660985
|
A | G | 7 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0003t0001g0096others(4): Show | 7 | HG02258.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3376-594A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660985 | ||||||
| chr2:200661159
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(73): Show | 77 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.3376-420G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661159 | ||||||
| chr2:200661186
|
A | G | 60 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3376-393A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661186 | ||||||
| chr2:200661197
|
C | G | 125 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3376-382C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661197 | ||||||
| chr2:200661406
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3376-173A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661406 | ||||||
| chr2:200661645
|
C | G | 29 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0003t0001g0096others(26): Show | 29 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.3428+14C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200661645 | ||||||
| chr2:200661829
|
T | C | 7 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0104others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3428+198T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200661829 | ||||||
| chr2:200662023
|
C | T | 33 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0056others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.3428+392C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662023 | ||||||
| chr2:200662041
|
A | G | 1 | a0001c0020t0001g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3428+410A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662041 | ||||||
| chr2:200662049
|
T | C | 1 | a0001c0001t0002g0243 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3428+418T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662049 | ||||||
| chr2:200662056
|
A | C | 1 | a0001c0001t0002g0178 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3428+425A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662056 | ||||||
| chr2:200662382
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3429-473C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662382 | ||||||
| chr2:200662467
|
G | A | 1 | a0010c0025t0003g0287 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3429-388G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662467 | ||||||
| chr2:200662487
|
A | G | 1 | a0002c0002t0003g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3429-368A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662487 | ||||||
| chr2:200662495
|
A | C | 1 | a0001c0001t0001g0269 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3429-360A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662495 | ||||||
| chr2:200662516
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0117others(146): Show | 150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.3429-339G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662516 | ||||||
| chr2:200662615
|
G | A | 71 | a0001c0001t0001g0124a0001c0001t0001g0162a0001c0001t0001g0163others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.3429-240G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662615 | ||||||
| chr2:200662740
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3429-115A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662740 | ||||||
| chr2:200662806
|
C | T | 12 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0028others(9): Show | 12 | HG00738.hp1 HG01081.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3429-49C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662806 | ||||||
| chr2:200663167
|
T | C | 7 | a0003c0003t0001g0090a0003c0003t0001g0094a0003c0003t0001g0096others(4): Show | 7 | HG02258.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+198T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663167 | ||||||
| chr2:200663212
|
G | T | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3543+243G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663212 | ||||||
| chr2:200663254
|
A | G | 60 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3543+285A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663254 | ||||||
| chr2:200663524
|
A | G | 147 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(144): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.3543+555A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663524 | ||||||
| chr2:200663545
|
A | AACAC | 55 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(52): Show | 55 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.3543+601_3543+604d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | |||||
| chr2:200663545
|
A | AACACACA others(1): Show |
14 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0216others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3543+597_3543+604d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | |||||
| chr2:200663545
|
A | AACACACA others(3): Show |
1 | a0001c0001t0001g0269 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3543+595_3543+604d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | |||||
| chr2:200663545
|
AAC | A | 7 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+603_3543+604d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | |||||
| chr2:200663545
|
AACAC | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0285others(3): Show | 6 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3543+601_3543+604d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | |||||
| chr2:200663561
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3543+592C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663561 | ||||||
| chr2:200663570
|
A | T | 19 | a0001c0001t0001g0238a0001c0001t0001g0357a0001c0001t0002g0130others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.3543+601A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663570 | ||||||
| chr2:200663572
|
A | ACACACAC others(13): Show |
1 | a0003c0026t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3543+604_3543+605i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | |||||
| chr2:200663572
|
A | ACACACT | 3 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0244 | 3 | HG02015.hp2 NA18965.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3543+604_3543+605i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | |||||
| chr2:200663572
|
A | ACACACTC others(3): Show |
2 | a0001c0001t0002g0133a0001c0001t0002g0143 | 2 | HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.3543+604_3543+605i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | |||||
| chr2:200663572
|
A | ACACACTC others(5): Show |
10 | a0003c0003t0001g0226a0003c0003t0001g0245a0003c0003t0001g0250others(7): Show | 10 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.3543+604_3543+605i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | |||||
| chr2:200663572
|
A | ACACTCTC others(3): Show |
7 | a0003c0003t0001g0212a0003c0003t0001g0248a0003c0003t0004g0073others(4): Show | 7 | HG02647.hp1 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+604_3543+605i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | |||||
| chr2:200663572
|
A | T | 38 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0238others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.3543+603A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663572 | ||||||
| chr2:200663574
|
T | A | 4 | a0001c0001t0002g0033a0001c0001t0002g0181a0001c0008t0002g0203others(1): Show | 4 | HG01975.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3543+605T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663574 | ||||||
| chr2:200663575
|
C | G | 18 | a0003c0003t0001g0212a0003c0003t0001g0226a0003c0003t0001g0245others(15): Show | 18 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.3543+606C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663575 | ||||||
| chr2:200663577
|
C | G | 3 | a0001c0001t0002g0133a0001c0001t0002g0143a0003c0030t0002g0218 | 3 | HG02071.hp2 HG02083.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3543+608C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663577 | ||||||
| chr2:200663579
|
C | G | 17 | a0001c0001t0001g0238a0001c0001t0001g0357a0001c0001t0002g0130others(14): Show | 17 | HG00140.hp2 HG00280.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.3543+610C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663579 | ||||||
| chr2:200663581
|
C | G | 6 | a0001c0001t0001g0273a0001c0001t0002g0272a0001c0001t0002g0278others(3): Show | 6 | HG00741.hp1 HG01106.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3543+612C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663581 | ||||||
| chr2:200663583
|
C | G | 96 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(93): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.3543+614C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663583 | ||||||
| chr2:200663585
|
C | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0181a0001c0008t0002g0203 | 3 | HG01975.hp1 HG02965.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.3543+616C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663585 | ||||||
| chr2:200663596
|
T | C | 21 | a0003c0003t0001g0212a0003c0003t0001g0226a0003c0003t0001g0245others(18): Show | 21 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.3543+627T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663596 | ||||||
| chr2:200663596
|
T | TCTCCC | 17 | a0001c0001t0001g0238a0001c0001t0001g0357a0001c0001t0002g0130others(14): Show | 17 | HG00140.hp2 HG00280.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.3543+628_3543+629i others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | |||||
| chr2:200663596
|
T | TCTCTCCC | 6 | a0001c0001t0001g0273a0001c0001t0002g0272a0001c0001t0002g0278others(3): Show | 6 | HG00741.hp1 HG01106.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3543+628_3543+629i others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | |||||
| chr2:200663596
|
T | TCTCTCTC others(2): Show |
96 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(93): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.3543+628_3543+629i others(11): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | |||||
| chr2:200663596
|
T | TCTCTCTC others(4): Show |
3 | a0001c0001t0002g0033a0001c0001t0002g0181a0001c0008t0002g0203 | 3 | HG01975.hp1 HG02965.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.3543+628_3543+629i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | |||||
| chr2:200663603
|
C | T | 1 | a0011c0023t0001g0251 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3543+634C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663603 | ||||||
| chr2:200663604
|
T | C | 1 | a0003c0026t0001g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3543+635T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663604 | ||||||
| chr2:200663618
|
G | A | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3543+649G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663618 | ||||||
| chr2:200663704
|
A | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3543+735A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663704 | ||||||
| chr2:200663777
|
GA | G | 7 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+809delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663777 | ||||||
| chr2:200664022
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(72): Show | 76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3543+1053G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664022 | ||||||
| chr2:200664038
|
G | A | 231 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3543+1069G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664038 | ||||||
| chr2:200664119
|
CTGTT | C | 231 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3543+1168_3543+117 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200664119 | |||||
| chr2:200664271
|
G | A | 7 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0129others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+1302G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664271 | ||||||
| chr2:200664364
|
A | G | 231 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3543+1395A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664364 | ||||||
| chr2:200664380
|
C | T | 4 | a0003c0006t0001g0093a0003c0006t0001g0095a0003c0006t0001g0105others(1): Show | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3543+1411C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664380 | ||||||
| chr2:200664485
|
T | C | 2 | a0003c0003t0001g0248a0003c0003t0001g0249 | 2 | HG03831.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3543+1516T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664485 | ||||||
| chr2:200664719
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3543+1750A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664719 | ||||||
| chr2:200664723
|
G | T | 125 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3543+1754G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664723 | ||||||
| chr2:200664727
|
G | A | 125 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3543+1758G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664727 | ||||||
| chr2:200664743
|
C | G | 1 | a0002c0002t0002g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3543+1774C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664743 | ||||||
| chr2:200664755
|
C | A | 238 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3543+1786C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664755 | ||||||
| chr2:200664901
|
C | T | 1 | a0006c0010t0009g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3544-1786C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664901 | ||||||
| chr2:200664998
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3544-1689T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664998 | ||||||
| chr2:200665017
|
G | A | 1 | a0001c0005t0006g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3544-1670G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665017 | ||||||
| chr2:200665175
|
T | C | 3 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0148 | 3 | NA18961.hp1 NA18980.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3544-1512T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665175 | ||||||
| chr2:200665177
|
C | T | 238 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3544-1510C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665177 | ||||||
| chr2:200665556
|
T | C | 185 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(182): Show | 185 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3544-1131T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665556 | ||||||
| chr2:200665785
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3544-902T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665785 | ||||||
| chr2:200666007
|
T | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3544-680T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666007 | ||||||
| chr2:200666017
|
A | T | 238 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3544-670A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666017 | ||||||
| chr2:200666042
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(79): Show | 83 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.3544-645C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666042 | ||||||
| chr2:200666113
|
C | G | 125 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0162others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3544-574C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666113 | ||||||
| chr2:200666243
|
C | T | 1 | a0003c0003t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3544-444C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666243 | ||||||
| chr2:200666361
|
T | G | 1 | a0002c0002t0007g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3544-326T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666361 | ||||||
| chr2:200666471
|
A | C | 8 | a0003c0003t0001g0226a0003c0003t0001g0245a0003c0003t0001g0248others(5): Show | 8 | HG01515.hp1 HG01517.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.3544-216A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666471 | ||||||
| chr2:200666504
|
T | C | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3544-183T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666504 | ||||||
| chr2:200666537
|
C | A | 244 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(241): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.3544-150C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666537 | ||||||
| chr2:200666911
|
T | C | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3609+159T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200666911 | ||||||
| chr2:200666934
|
G | A | 1 | a0003c0003t0001g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3609+182G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200666934 | ||||||
| chr2:200667042
|
A | G | 250 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(247): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.3609+290A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667042 | ||||||
| chr2:200667059
|
T | C | 61 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 61 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.3609+307T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667059 | ||||||
| chr2:200667077
|
C | T | 1 | a0003c0003t0006g0329 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3609+325C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667077 | ||||||
| chr2:200667121
|
C | T | 255 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(252): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.3609+369C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667121 | ||||||
| chr2:200667172
|
G | A | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG01070.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.3609+420G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667172 | ||||||
| chr2:200667369
|
C | G | 2 | a0003c0003t0006g0329a0003c0026t0001g0213 | 2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3609+617C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667369 | ||||||
| chr2:200667377
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0117others(146): Show | 150 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.3609+625G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667377 | ||||||
| chr2:200667451
|
A | C | 1 | a0001c0001t0002g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3609+699A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667451 | ||||||
| chr2:200667480
|
A | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(245): Show | 249 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.3609+728A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667480 | ||||||
| chr2:200667721
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3610-894A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667721 | ||||||
| chr2:200667740
|
G | A | 2 | a0006c0010t0007g0280a0006c0010t0009g0106 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3610-875G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667740 | ||||||
| chr2:200667757
|
G | C | 3 | a0002c0002t0007g0252a0003c0003t0001g0096a0003c0026t0001g0213 | 3 | HG02886.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3610-858G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667757 | ||||||
| chr2:200667762
|
T | C | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3610-853T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667762 | ||||||
| chr2:200667765
|
A | C | 1 | a0001c0001t0002g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3610-850A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667765 | ||||||
| chr2:200667845
|
A | G | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3610-770A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667845 | ||||||
| chr2:200667902
|
A | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(222): Show | 227 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.3610-713A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667902 | ||||||
| chr2:200667959
|
T | C | 1 | a0003c0003t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3610-656T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667959 | ||||||
| chr2:200667968
|
A | G | 1 | a0001c0005t0002g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3610-647A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667968 | ||||||
| chr2:200667975
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0168a0001c0001t0001g0205others(28): Show | 32 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.3610-640G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667975 | ||||||
| chr2:200668109
|
TA | T | 6 | a0001c0001t0001g0270a0001c0001t0001g0334a0003c0006t0001g0093others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3610-505delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668109 | ||||||
| chr2:200668110
|
A | T | 8 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0153others(5): Show | 8 | HG01496.hp1 HG02129.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3610-505A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668110 | ||||||
| chr2:200668110
|
AT | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0129others(30): Show | 34 | HG01109.hp1 HG01261.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3610-493delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr2 | 200668110 | |||||
| chr2:200668113
|
T | A | 1 | a0003c0003t0001g0250 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3610-502T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668113 | ||||||
| chr2:200668125
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(216): Show | 221 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.3610-490G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668125 | ||||||
| chr2:200668183
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3610-432G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668183 | ||||||
| chr2:200668191
|
C | T | 1 | a0006c0010t0007g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3610-424C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668191 | ||||||
| chr2:200668209
|
G | A | 1 | a0018c0012t0001g0198 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3610-406G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668209 | ||||||
| chr2:200668248
|
G | A | 1 | a0001c0001t0001g0351 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3610-367G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668248 | ||||||
| chr2:200668329
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3610-286A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668329 | ||||||
| chr2:200668393
|
G | C | 1 | a0001c0001t0001g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3610-222G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668393 | ||||||
| chr2:200668401
|
G | T | 1 | a0001c0001t0001g0337 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3610-214G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668401 | ||||||
| chr2:200668440
|
C | A | 2 | a0002c0002t0007g0252a0006c0010t0007g0280 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3610-175C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668440 | ||||||
| chr2:200668488
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3610-127A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668488 | ||||||
| chr2:200668490
|
G | A | 2 | a0001c0001t0002g0365a0001c0001t0002g0366 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3610-125G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668490 | ||||||
| chr2:200668492
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 141 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.3610-123C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668492 | ||||||
| chr2:200669006
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3798+203G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669006 | ||||||
| chr2:200669165
|
C | T | 4 | a0003c0006t0001g0093a0003c0006t0001g0095a0003c0006t0001g0105others(1): Show | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798+362C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669165 | ||||||
| chr2:200669182
|
G | A | 4 | a0003c0006t0001g0093a0003c0006t0001g0095a0003c0006t0001g0105others(1): Show | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798+379G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669182 | ||||||
| chr2:200669192
|
C | G | 1 | a0001c0001t0002g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3799-383C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669192 | ||||||
| chr2:200669260
|
C | G | 1 | a0001c0001t0002g0139 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3799-315C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669260 | ||||||
| chr2:200669262
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(187): Show | 192 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.3799-313A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669262 | ||||||
| chr2:200669293
|
A | G | 1 | a0019c0011t0001g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3799-282A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669293 | ||||||
| chr2:200669316
|
A | T | 1 | a0001c0001t0002g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3799-259A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669316 | ||||||
| chr2:200669413
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(136): Show | 140 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.3799-162C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669413 | ||||||
| chr2:200669450
|
C | CA | 9 | a0001c0001t0001g0120a0001c0001t0001g0129a0001c0001t0001g0231others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3799-112dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr2 | 200669450 | |||||
| chr2:200669461
|
A | C | 11 | a0002c0002t0003g0025a0002c0002t0003g0040a0002c0002t0003g0043others(8): Show | 11 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.3799-114A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669461 | ||||||
| chr2:200669464
|
T | G | 4 | a0003c0006t0001g0093a0003c0006t0001g0095a0003c0006t0001g0105others(1): Show | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3799-111T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669464 | ||||||
| chr2:200669860
|
C | T | 7 | a0001c0005t0004g0297a0003c0003t0004g0073a0003c0003t0004g0092others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3966+118C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200669860 | ||||||
| chr2:200670066
|
A | G | 1 | a0003c0003t0006g0329 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3966+324A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200670066 | ||||||
| chr2:200670352
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(136): Show | 140 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.3967-277G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200670352 | ||||||
| chr2:200670553
|
C | A | 1 | a0019c0011t0001g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3967-76C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200670553 |