Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 130340 |
|---|---|
| ensemblid | ENSG00000152056.18 |
| hgncid | 18971 |
| symbol | AP1S3 |
| name | adaptor related protein complex 1 subunit sigma 3 |
| refseq_nuc | NM_001039569.2 |
| refseq_prot | NP_001034658.1 |
| ensembl_nuc | ENST00000396654.7 |
| ensembl_prot | ENSP00000379891.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 223755326 |
| end | 223837582 |
| strand | - |
| ver | v1.2 |
| region | chr2:223755326-223837582 |
| region5000 | chr2:223750326-223842582 |
| regionname0 | AP1S3_chr2_223755326_223837582 |
| regionname5000 | AP1S3_chr2_223750326_223842582 |
| 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 | 1/1 | 154 | 334 | 82 | 52 | 156 | 6 | 36 | 122 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0002 | 0/0 | 154 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0003 | 0/0 | 154 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0004 | 0/0 | 154 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0005 | 0/0 | 154 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| 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 | 1/1 | 465 | 332 | 81 | 52 | 155 | 6 | 36 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| c0002 | 0/0 | 465 | 3 | 3 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| c0003 | 0/0 | 465 | 2 | 1 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| c0004 | 0/0 | 465 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| c0005 | 0/0 | 465 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| c0006 | 0/0 | 465 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| 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 | 0/1 | 3521 | 68 | 7 | 11 | 35 | 2 | 12 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0002 | 0/0 | 3536 | 45 | 19 | 1 | 20 | 0 | 5 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0003 | 0/0 | 3535 | 32 | 1 | 4 | 23 | 0 | 4 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0004 | 0/0 | 3524 | 23 | 0 | 9 | 8 | 1 | 5 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0005 | 0/0 | 3524 | 20 | 1 | 6 | 12 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0006 | 0/0 | 3548 | 13 | 0 | 1 | 12 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0007 | 0/0 | 3523 | 12 | 3 | 1 | 5 | 0 | 3 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0008 | 0/0 | 3538 | 7 | 7 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0009 | 0/0 | 3527 | 7 | 7 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0010 | 0/0 | 3543 | 6 | 0 | 0 | 6 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0011 | 0/0 | 3536 | 6 | 0 | 0 | 6 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0012 | 0/0 | 3526 | 5 | 5 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0013 | 0/0 | 3521 | 4 | 3 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0014 | 0/0 | 3521 | 4 | 0 | 3 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0015 | 0/0 | 3537 | 4 | 2 | 1 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0016 | 0/0 | 3537 | 4 | 0 | 0 | 4 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0017 | 0/0 | 3535 | 4 | 4 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0018 | 0/0 | 3522 | 3 | 0 | 1 | 1 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0019 | 0/0 | 3522 | 3 | 1 | 0 | 1 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0020 | 0/0 | 3524 | 3 | 3 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0021 | 0/0 | 3527 | 3 | 3 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0022 | 0/0 | 3522 | 3 | 0 | 2 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0023 | 0/0 | 3525 | 3 | 0 | 3 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0024 | 0/0 | 3538 | 2 | 0 | 0 | 2 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0025 | 0/0 | 3522 | 2 | 0 | 2 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0026 | 0/0 | 3523 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0027 | 0/0 | 3535 | 2 | 0 | 0 | 2 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0028 | 0/0 | 3536 | 2 | 1 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0029 | 0/0 | 3525 | 2 | 0 | 1 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0030 | 0/0 | 3524 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0031 | 0/0 | 3524 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0032 | 0/0 | 3522 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0033 | 0/0 | 3535 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0034 | 0/0 | 3521 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0035 | 0/0 | 3521 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0036 | 0/0 | 3521 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0037 | 0/0 | 3527 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0038 | 0/0 | 3523 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0039 | 0/0 | 3521 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0040 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0041 | 0/0 | 3521 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0042 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0043 | 0/0 | 3523 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0044 | 0/0 | 3521 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0045 | 0/0 | 3536 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0046 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0047 | 0/0 | 3538 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0048 | 0/0 | 3553 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0049 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0050 | 0/0 | 3553 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0051 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0052 | 0/0 | 3536 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0053 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0054 | 0/0 | 3533 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0055 | 0/0 | 3534 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0056 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0057 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0058 | 0/0 | 3523 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0059 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0060 | 0/0 | 3535 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0061 | 0/0 | 3522 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0062 | 0/0 | 3504 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0063 | 0/0 | 3524 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0064 | 1/0 | 3522 | 1 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0065 | 0/0 | 3523 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0066 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0067 | 0/0 | 3522 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0068 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0069 | 0/0 | 3535 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0070 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0071 | 0/0 | 3536 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| t0072 | 0/0 | 3536 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| 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 | 0 | 0 | 2 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| 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 | 1/1 | 465 | 332 | 81 | 52 | 155 | 6 | 36 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0003 | 0/0 | 465 | 2 | 1 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0002c0002 | 0/0 | 465 | 3 | 3 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0003c0004 | 0/0 | 465 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0004c0006 | 0/0 | 465 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0005c0005 | 0/0 | 465 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3985 | 68 | 7 | 11 | 35 | 2 | 12 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0002 | 0/0 | 4000 | 42 | 16 | 1 | 20 | 0 | 5 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0003 | 0/0 | 3999 | 32 | 1 | 4 | 23 | 0 | 4 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0004 | 0/0 | 3988 | 23 | 0 | 9 | 8 | 1 | 5 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0005 | 0/0 | 3988 | 19 | 1 | 5 | 12 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0006 | 0/0 | 4012 | 13 | 0 | 1 | 12 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0007 | 0/0 | 3987 | 12 | 3 | 1 | 5 | 0 | 3 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0008 | 0/0 | 4002 | 7 | 7 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0009 | 0/0 | 3991 | 7 | 7 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0010 | 0/0 | 4007 | 6 | 0 | 0 | 6 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0011 | 0/0 | 4000 | 6 | 0 | 0 | 6 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0012 | 0/0 | 3990 | 5 | 5 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0013 | 0/0 | 3985 | 4 | 3 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0014 | 0/0 | 3985 | 4 | 0 | 3 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0015 | 0/0 | 4001 | 4 | 2 | 1 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0016 | 0/0 | 4001 | 4 | 0 | 0 | 4 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0017 | 0/0 | 3999 | 4 | 4 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0018 | 0/0 | 3986 | 3 | 0 | 1 | 1 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0019 | 0/0 | 3986 | 3 | 1 | 0 | 1 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0020 | 0/0 | 3988 | 3 | 3 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0021 | 0/0 | 3991 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0022 | 0/0 | 3986 | 3 | 0 | 2 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0023 | 0/0 | 3989 | 2 | 0 | 2 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0024 | 0/0 | 4002 | 2 | 0 | 0 | 2 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0025 | 0/0 | 3986 | 2 | 0 | 2 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0026 | 0/0 | 3987 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0027 | 0/0 | 3999 | 2 | 0 | 0 | 2 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0028 | 0/0 | 4000 | 2 | 1 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0029 | 0/0 | 3989 | 2 | 0 | 1 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0030 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0031 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0032 | 0/0 | 3986 | 2 | 2 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0033 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0035 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0036 | 0/0 | 3985 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0037 | 0/0 | 3991 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0038 | 0/0 | 3987 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0039 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0040 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0041 | 0/0 | 3985 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0042 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0043 | 0/0 | 3987 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0044 | 0/0 | 3985 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0045 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0047 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0048 | 0/0 | 4017 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0049 | 0/0 | 4013 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0050 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0051 | 0/0 | 3984 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0052 | 0/0 | 4000 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0053 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0054 | 0/0 | 3997 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0055 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0056 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0057 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0058 | 0/0 | 3987 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0059 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0060 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0061 | 0/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0062 | 0/0 | 3968 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0063 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0064 | 1/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0065 | 0/0 | 3987 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0066 | 0/0 | 3989 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0067 | 0/0 | 3986 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0068 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0069 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0070 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0071 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0001t0072 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0003t0021 | 0/0 | 3991 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0001c0003t0034 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0002c0002t0002 | 0/0 | 4000 | 3 | 3 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0003c0004t0005 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0004c0006t0023 | 0/0 | 3989 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| a0005c0005t0046 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | copy fasta | chr2 | 223750326 | 223842582 |
| 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 | 0 | 0 | 2 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0010g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0010g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0011g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0011g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0012g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0013g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0013g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0013g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0014g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0014g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0014g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0015g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0015g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0015g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0016g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0016g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0016g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0016g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0017g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0017g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0017g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0017g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0018g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0018g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0018g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0019g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0019g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0020g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0020g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0021g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0021g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0022g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0022g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0022g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0023g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0023g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0024g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0024g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0025g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0025g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0026g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0026g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0027g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0027g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0028g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0028g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0029g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0029g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0030g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0030g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0031g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0031g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0032g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0032g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0033g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0035g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0036g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0037g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0038g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0039g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0040g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0041g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0042g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0043g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0044g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0045g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0047g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0048g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0049g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0050g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0051g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0052g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0053g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0054g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0055g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0056g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0057g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0058g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0059g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0060g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0061g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0062g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0063g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0064g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0065g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0066g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0067g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0068g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0069g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0070g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0071g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0001t0072g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0003t0021g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0001c0003t0034g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0002c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0002c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0003c0004t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0004c0006t0023g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| a0005c0005t0046g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0022 | g0130 | EUR | GBR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0300 | EUR | GBR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00140 | hp1 | a0001 | c0001 | t0043 | g0259 | EUR | GBR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0107 | EUR | GBR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00408 | hp1 | a0001 | c0001 | t0010 | g0325 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00408 | hp2 | a0001 | c0001 | t0024 | g0054 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00609 | hp1 | a0001 | c0001 | t0019 | g0086 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00609 | hp2 | a0001 | c0001 | t0024 | g0042 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00639 | hp1 | a0001 | c0001 | t0015 | g0217 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0286 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00735 | hp2 | a0001 | c0001 | t0029 | g0123 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00741 | hp1 | a0001 | c0001 | t0038 | g0278 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG00741 | hp2 | a0001 | c0001 | t0022 | g0279 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0219 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01071 | hp2 | a0001 | c0001 | t0022 | g0101 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0112 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01106 | hp2 | a0003 | c0004 | t0005 | g0277 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0220 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01109 | hp2 | a0001 | c0001 | t0058 | g0100 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0268 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01175 | hp1 | a0001 | c0001 | t0018 | g0149 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0299 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01192 | hp1 | a0004 | c0006 | t0023 | g0208 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01192 | hp2 | a0001 | c0001 | t0036 | g0311 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01243 | hp1 | a0001 | c0001 | t0062 | g0102 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0165 | AMR | PUR | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01255 | hp2 | a0001 | c0001 | t0065 | g0127 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0329 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0158 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01433 | hp2 | a0001 | c0001 | t0063 | g0145 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0210 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0143 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01891 | hp1 | a0001 | c0001 | t0042 | g0152 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01891 | hp2 | a0001 | c0003 | t0021 | g0320 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01978 | hp1 | a0001 | c0001 | t0023 | g0293 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01978 | hp2 | a0001 | c0001 | t0014 | g0015 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0067 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01993 | hp2 | a0001 | c0001 | t0025 | g0079 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0235 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02027 | hp2 | a0001 | c0001 | t0010 | g0262 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0180 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0207 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02056 | hp1 | a0001 | c0001 | t0027 | g0335 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02056 | hp2 | a0001 | c0001 | t0069 | g0059 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02071 | hp1 | a0001 | c0001 | t0045 | g0227 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0251 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02074 | hp2 | a0001 | c0001 | t0016 | g0089 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02080 | hp1 | a0001 | c0001 | t0027 | g0332 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0176 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02148 | hp1 | a0001 | c0001 | t0014 | g0030 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | CDX | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02155 | hp2 | a0001 | c0001 | t0050 | g0077 | EAS | CDX | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0159 | EAS | CDX | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02258 | hp2 | a0001 | c0001 | t0031 | g0246 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02273 | hp1 | a0001 | c0001 | t0014 | g0033 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0064 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02280 | hp2 | a0001 | c0001 | t0015 | g0186 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0083 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02300 | hp1 | a0001 | c0001 | t0025 | g0048 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02300 | hp2 | a0001 | c0001 | t0023 | g0280 | AMR | PEL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02451 | hp1 | a0001 | c0001 | t0047 | g0322 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0337 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | KHV | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02572 | hp1 | a0001 | c0001 | t0026 | g0241 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02615 | hp2 | a0001 | c0001 | t0031 | g0215 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0188 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0142 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0167 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0146 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02698 | hp2 | a0001 | c0001 | t0019 | g0265 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0243 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0182 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02723 | hp1 | a0001 | c0001 | t0054 | g0005 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0231 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0166 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02818 | hp2 | a0001 | c0001 | t0053 | g0321 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0177 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02896 | hp1 | a0001 | c0001 | t0032 | g0225 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02965 | hp2 | a0001 | c0001 | t0060 | g0190 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0140 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0061 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0169 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03098 | hp2 | a0001 | c0001 | t0017 | g0212 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0040 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0106 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0096 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0170 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0292 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03225 | hp2 | a0001 | c0001 | t0070 | g0308 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0099 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03453 | hp2 | a0001 | c0001 | t0021 | g0336 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0291 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0244 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03491 | hp2 | a0001 | c0001 | t0041 | g0260 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0245 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0181 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0187 | AFR | ESN | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03540 | hp2 | a0001 | c0001 | t0032 | g0216 | AFR | GWD | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0230 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0129 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0253 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03831 | hp2 | a0001 | c0001 | t0061 | g0120 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03927 | hp2 | a0001 | c0001 | t0051 | g0256 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03942 | hp2 | a0001 | c0001 | t0052 | g0254 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04184 | hp1 | a0001 | c0001 | t0048 | g0074 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04184 | hp2 | a0001 | c0001 | t0018 | g0068 | SAS | BEB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0281 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18522 | hp1 | a0001 | c0001 | t0068 | g0173 | AFR | YRI | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0137 | AFR | YRI | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | CHB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18747 | hp2 | a0001 | c0001 | t0055 | g0172 | EAS | CHB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18906 | hp1 | a0001 | c0001 | t0026 | g0319 | AFR | YRI | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0183 | AFR | YRI | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0266 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18953 | hp2 | a0001 | c0001 | t0039 | g0090 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18954 | hp2 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18964 | hp2 | a0001 | c0001 | t0010 | g0237 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0317 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0228 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18973 | hp1 | a0001 | c0001 | t0067 | g0221 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18973 | hp2 | a0001 | c0001 | t0014 | g0307 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18974 | hp1 | a0001 | c0001 | t0007 | g0316 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18978 | hp1 | a0001 | c0001 | t0059 | g0082 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18978 | hp2 | a0001 | c0001 | t0015 | g0069 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0315 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18982 | hp2 | a0001 | c0001 | t0007 | g0314 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18983 | hp2 | a0001 | c0003 | t0034 | g0164 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0289 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18984 | hp2 | a0001 | c0001 | t0011 | g0238 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18985 | hp2 | a0001 | c0001 | t0016 | g0047 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18986 | hp2 | a0001 | c0001 | t0029 | g0303 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18991 | hp1 | a0001 | c0001 | t0066 | g0161 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18994 | hp1 | a0001 | c0001 | t0016 | g0045 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0022 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0283 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19001 | hp1 | a0001 | c0001 | t0010 | g0274 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19003 | hp2 | a0001 | c0001 | t0040 | g0236 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19009 | hp1 | a0001 | c0001 | t0049 | g0255 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | LWK | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | LWK | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0313 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19062 | hp1 | a0001 | c0001 | t0033 | g0093 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19068 | hp1 | a0001 | c0001 | t0010 | g0275 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19074 | hp1 | a0001 | c0001 | t0035 | g0025 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19074 | hp2 | a0001 | c0001 | t0011 | g0214 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19079 | hp1 | a0001 | c0001 | t0071 | g0338 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19079 | hp2 | a0001 | c0001 | t0011 | g0036 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19087 | hp1 | a0001 | c0001 | t0028 | g0117 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19087 | hp2 | a0001 | c0001 | t0016 | g0288 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19089 | hp1 | a0001 | c0001 | t0011 | g0200 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19089 | hp2 | a0001 | c0001 | t0018 | g0104 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19090 | hp2 | a0001 | c0001 | t0072 | g0339 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19091 | hp2 | a0001 | c0001 | t0010 | g0331 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19240 | hp1 | a0001 | c0001 | t0015 | g0095 | AFR | YRI | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA19240 | hp2 | a0001 | c0001 | t0057 | g0118 | AFR | YRI | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | ASW | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA20129 | hp2 | a0001 | c0001 | t0030 | g0242 | AFR | ASW | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0157 | SAS | GIH | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | GIH | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG01123 | hp2 | a0001 | c0001 | t0044 | g0150 | AMR | CLM | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02109 | hp2 | a0001 | c0001 | t0028 | g0178 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02486 | hp2 | a0001 | c0001 | t0021 | g0323 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02559 | hp1 | a0001 | c0001 | t0030 | g0240 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0223 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| HG03471 | hp2 | a0001 | c0001 | t0019 | g0139 | AFR | MSL | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA20300 | hp1 | a0005 | c0005 | t0046 | g0065 | AFR | USA | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA20300 | hp2 | a0001 | c0001 | t0037 | g0105 | AFR | USA | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA21309 | hp1 | a0001 | c0001 | t0056 | g0003 | AFR | LWK | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| NA21309 | hp2 | a0001 | c0001 | t0017 | g0185 | AFR | LWK | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0271 | REF | REF | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0064 | g0264 | REF | REF | AP1S3_chr2_223750326_223842582 | AP1S3 | chr2 | 223750326 | 223842582 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:223765288
|
T | C | 1 | a0002 | 3 | HG02257.hp1 HG03209.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.354A>G | p.Ile118Met | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/5 | 486/3986 | 354/465 | 118/154 | chr2 | 223765288 | ||
| chr2:223775957
|
A | C | 1 | a0005 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.235T>G | p.Leu79Val | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/5 | 367/3986 | 235/465 | 79/154 | chr2 | 223775957 | ||
| chr2:223777809
|
T | C | 1 | a0004 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.64A>G | p.Thr22Ala | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/5 | 196/3986 | 64/465 | 22/154 | chr2 | 223777809 | ||
| chr2:223777862
|
A | C | 1 | a0003 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.11T>G | p.Phe4Cys | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/5 | 143/3986 | 11/465 | 4/154 | chr2 | 223777862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:223765297
|
G | A | 1 | a0001c0003 | 2 | HG01891.hp2 NA18983.hp2 |
synonymous_variant | LOW | c.345C>T | p.Asp115Asp | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/5 | 477/3986 | 345/465 | 115/154 | chr2 | 223765297 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:223755464
|
G | T | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | 256 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*3251C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3251 | chr2 | 223755464 | |||||
| chr2:223755505
|
A | G | 8 | a0001c0001t0004a0001c0001t0023a0001c0001t0030others(5): Show | 32 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3210T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3210 | chr2 | 223755505 | |||||
| chr2:223755529
|
A | AT | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(21): Show | 120 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*3185dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3185 | chr2 | 223755529 | |||||
| chr2:223755529
|
A | ATT | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(14): Show | 71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3184_*3185dupAA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3185 | chr2 | 223755529 | |||||
| chr2:223755529
|
A | ATTT | 6 | a0001c0001t0023a0001c0001t0029a0001c0001t0056others(3): Show | 8 | HG00735.hp2 HG01192.hp1 HG01978.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3183_*3185dupAAA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3185 | chr2 | 223755529 | |||||
| chr2:223755529
|
AT | A | 18 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(15): Show | 106 | HG00099.hp1 HG00639.hp2 HG00673.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3185delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3185 | chr2 | 223755529 | |||||
| chr2:223755573
|
C | T | 20 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(17): Show | 110 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*3142G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3142 | chr2 | 223755573 | |||||
| chr2:223755677
|
T | C | 1 | a0001c0001t0030 | 2 | HG02559.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3038A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3038 | chr2 | 223755677 | |||||
| chr2:223755679
|
T | C | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*3036A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3036 | chr2 | 223755679 | |||||
| chr2:223755683
|
A | G | 1 | a0001c0001t0063 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3032T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 3032 | chr2 | 223755683 | |||||
| chr2:223755750
|
C | T | 19 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(16): Show | 103 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2965G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2965 | chr2 | 223755750 | |||||
| chr2:223755877
|
C | T | 1 | a0001c0001t0036 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2838G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2838 | chr2 | 223755877 | |||||
| chr2:223755891
|
A | G | 1 | a0001c0001t0035 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2824T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2824 | chr2 | 223755891 | |||||
| chr2:223755952
|
T | G | 1 | a0001c0001t0047 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2763A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2763 | chr2 | 223755952 | |||||
| chr2:223756017
|
G | A | 1 | a0001c0001t0060 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2698C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2698 | chr2 | 223756017 | |||||
| chr2:223756111
|
G | A | 7 | a0001c0001t0006a0001c0001t0010a0001c0001t0024others(4): Show | 25 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2604C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2604 | chr2 | 223756111 | |||||
| chr2:223756146
|
T | G | 1 | a0001c0001t0031 | 2 | HG02258.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2569A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2569 | chr2 | 223756146 | |||||
| chr2:223756167
|
A | C | 20 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(17): Show | 106 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2548T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2548 | chr2 | 223756167 | |||||
| chr2:223756185
|
A | G | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(23): Show | 122 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2530T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2530 | chr2 | 223756185 | |||||
| chr2:223756206
|
G | A | 3 | a0001c0001t0056a0001c0001t0057a0001c0001t0058 | 3 | HG01109.hp2 NA19240.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2509C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2509 | chr2 | 223756206 | |||||
| chr2:223756251
|
C | T | 1 | a0001c0001t0052 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2464 | chr2 | 223756251 | |||||
| chr2:223756276
|
GCAGTGAC others(9): Show |
G | 1 | a0001c0001t0051 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2423_*2438delTGAT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2423 | chr2 | 223756276 | |||||
| chr2:223756295
|
C | T | 7 | a0001c0001t0006a0001c0001t0010a0001c0001t0024others(4): Show | 25 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2420G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2420 | chr2 | 223756295 | |||||
| chr2:223756338
|
G | GAAAGA | 3 | a0001c0001t0009a0001c0001t0012a0001c0001t0037 | 13 | HG02055.hp1 HG02055.hp2 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2372_*2376dupTCTT others(1): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2376 | chr2 | 223756338 | |||||
| chr2:223756338
|
G | GGAAGAAA others(8): Show |
2 | a0001c0001t0024a0001c0001t0047 | 3 | HG00408.hp2 HG00609.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2376_*2377insTCTT others(11): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2376 | chr2 | 223756338 | |||||
| chr2:223756338
|
G | GGAAGAAA others(13): Show |
1 | a0001c0001t0010 | 6 | HG00408.hp1 HG02027.hp2 NA18964.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2376_*2377insTCTT others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2376 | chr2 | 223756338 | |||||
| chr2:223756338
|
G | GGAAGAAA others(18): Show |
2 | a0001c0001t0006a0001c0001t0049 | 14 | HG00673.hp1 HG01261.hp2 HG02015.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2376_*2377insTCTT others(21): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2376 | chr2 | 223756338 | |||||
| chr2:223756338
|
G | GGAAGAAA others(23): Show |
1 | a0001c0001t0050 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2376_*2377insTCTT others(26): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2376 | chr2 | 223756338 | |||||
| chr2:223756338
|
G | GGAAGAAA others(23): Show |
1 | a0001c0001t0048 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2376_*2377insTCTT others(26): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2376 | chr2 | 223756338 | |||||
| chr2:223756353
|
A | G | 8 | a0001c0001t0003a0001c0001t0011a0001c0001t0028others(5): Show | 45 | HG00423.hp1 HG00544.hp2 HG01433.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2362T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2362 | chr2 | 223756353 | |||||
| chr2:223756403
|
A | AAGGG | 6 | a0001c0001t0006a0001c0001t0010a0001c0001t0024others(3): Show | 24 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2308_*2311dupCCCT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2311 | chr2 | 223756403 | |||||
| chr2:223756427
|
A | AG | 27 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(24): Show | 137 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2287dupC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2287 | chr2 | 223756427 | |||||
| chr2:223756439
|
G | A | 1 | a0001c0001t0017 | 4 | HG01884.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2276C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2276 | chr2 | 223756439 | |||||
| chr2:223756447
|
GGAAAAGA others(10): Show |
G | 1 | a0001c0001t0062 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2251_*2267delTTTC others(13): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2251 | chr2 | 223756447 | |||||
| chr2:223756449
|
A | AAAAG | 2 | a0001c0001t0021a0001c0003t0021 | 3 | HG01891.hp2 HG02486.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2262_*2265dupCTTT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2265 | chr2 | 223756449 | |||||
| chr2:223756453
|
G | GAAAGAAA others(6): Show |
21 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(18): Show | 117 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2249_*2261dupTCTT others(9): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2261 | chr2 | 223756453 | |||||
| chr2:223756462
|
A | G | 1 | a0001c0003t0034 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2253T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2253 | chr2 | 223756462 | |||||
| chr2:223756470
|
G | GAAAGAAA others(3): Show |
1 | a0001c0001t0054 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235_*2244dupTTCT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2244 | chr2 | 223756470 | |||||
| chr2:223756480
|
A | AAAGAAAG others(4): Show |
1 | a0001c0001t0055 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2234_*2235insCTTT others(7): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2234 | chr2 | 223756480 | |||||
| chr2:223756482
|
G | A | 1 | a0001c0001t0055 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2233C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2233 | chr2 | 223756482 | |||||
| chr2:223756486
|
AAAAG | A | 6 | a0001c0001t0006a0001c0001t0010a0001c0001t0024others(3): Show | 24 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2225_*2228delCTTT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2225 | chr2 | 223756486 | |||||
| chr2:223756600
|
G | C | 1 | a0001c0001t0039 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2115C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2115 | chr2 | 223756600 | |||||
| chr2:223756710
|
A | G | 1 | a0001c0001t0013 | 4 | HG01243.hp2 HG01884.hp2 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2005T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 2005 | chr2 | 223756710 | |||||
| chr2:223756988
|
C | CT | 3 | a0001c0001t0008a0001c0001t0015a0001c0001t0018 | 14 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1726dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1726 | chr2 | 223756988 | |||||
| chr2:223756988
|
CT | C | 13 | a0001c0001t0003a0001c0001t0028a0001c0001t0032others(10): Show | 46 | HG00423.hp1 HG00544.hp2 HG01109.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1726delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1726 | chr2 | 223756988 | |||||
| chr2:223756992
|
T | C | 1 | a0001c0001t0014 | 4 | HG01978.hp2 HG02148.hp1 HG02273.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1723A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1723 | chr2 | 223756992 | |||||
| chr2:223757034
|
G | C | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(26): Show | 127 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1681C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1681 | chr2 | 223757034 | |||||
| chr2:223757146
|
T | C | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(25): Show | 126 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1569A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1569 | chr2 | 223757146 | |||||
| chr2:223757170
|
T | C | 19 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(16): Show | 108 | HG00609.hp1 HG00639.hp2 HG00673.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1545A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1545 | chr2 | 223757170 | |||||
| chr2:223757256
|
C | T | 7 | a0001c0001t0006a0001c0001t0010a0001c0001t0024others(4): Show | 25 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1459G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1459 | chr2 | 223757256 | |||||
| chr2:223757395
|
G | A | 1 | a0001c0001t0041 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1320C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1320 | chr2 | 223757395 | |||||
| chr2:223757422
|
A | G | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | 258 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1293T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1293 | chr2 | 223757422 | |||||
| chr2:223757530
|
C | A | 1 | a0001c0001t0068 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1185G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1185 | chr2 | 223757530 | |||||
| chr2:223757584
|
G | A | 1 | a0001c0001t0044 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1131C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 1131 | chr2 | 223757584 | |||||
| chr2:223757815
|
G | A | 1 | a0001c0001t0069 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*900C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 900 | chr2 | 223757815 | |||||
| chr2:223757953
|
A | C | 1 | a0005c0005t0046 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*762T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 762 | chr2 | 223757953 | |||||
| chr2:223757964
|
C | T | 1 | a0001c0001t0045 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 751 | chr2 | 223757964 | |||||
| chr2:223758143
|
TA | T | 18 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(15): Show | 101 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*571delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 571 | chr2 | 223758143 | |||||
| chr2:223758524
|
T | A | 1 | a0001c0001t0070 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 191 | chr2 | 223758524 | |||||
| chr2:223758657
|
C | T | 1 | a0001c0001t0033 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*58G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 5/5 | 58 | chr2 | 223758657 | |||||
| chr2:223837504
|
G | A | 2 | a0001c0001t0071a0001c0001t0072 | 2 | NA19079.hp1 NA19090.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/5 | chr2 | 223837504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:223759027
|
C | A | 2 | a0001c0001t0031g0215a0001c0001t0031g0246 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.430-277G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759027 | ||||||
| chr2:223759032
|
G | A | 1 | a0001c0001t0001g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.430-282C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759032 | ||||||
| chr2:223759064
|
T | C | 1 | a0001c0001t0019g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.430-314A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759064 | ||||||
| chr2:223759137
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.430-387C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759137 | ||||||
| chr2:223759145
|
T | G | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430-395A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759145 | ||||||
| chr2:223759173
|
G | A | 67 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(64): Show | 67 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.430-423C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759173 | ||||||
| chr2:223759211
|
G | A | 2 | a0001c0001t0032g0216a0001c0001t0032g0225 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.430-461C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759211 | ||||||
| chr2:223759217
|
T | C | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430-467A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759217 | ||||||
| chr2:223759266
|
G | A | 2 | a0001c0001t0021g0336a0001c0003t0021g0320 | 2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.430-516C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759266 | ||||||
| chr2:223759273
|
C | T | 1 | a0001c0001t0026g0241 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.430-523G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759273 | ||||||
| chr2:223759274
|
G | A | 45 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(42): Show | 45 | HG00423.hp1 HG00544.hp2 HG01433.hp1 others(42): Show |
intron_variant | MODIFIER | c.430-524C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759274 | ||||||
| chr2:223759295
|
A | G | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.430-545T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759295 | ||||||
| chr2:223759296
|
AG | A | 85 | a0001c0001t0002g0004a0001c0001t0002g0039a0001c0001t0002g0051others(82): Show | 85 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.430-547delC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759296 | ||||||
| chr2:223759296
|
AGAGAG | A | 39 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(36): Show | 39 | HG00423.hp2 HG00544.hp1 HG01993.hp2 others(36): Show |
intron_variant | MODIFIER | c.430-551_430-547del others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759296 | ||||||
| chr2:223759404
|
G | A | 121 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(118): Show | 121 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.430-654C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759404 | ||||||
| chr2:223759435
|
T | A | 121 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(118): Show | 121 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.430-685A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759435 | ||||||
| chr2:223759498
|
A | G | 3 | a0001c0001t0056g0003a0001c0001t0057g0118a0001c0001t0058g0100 | 3 | HG01109.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.430-748T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759498 | ||||||
| chr2:223759601
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.430-851T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759601 | ||||||
| chr2:223759815
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0222 | 2 | HG02165.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.430-1065A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759815 | ||||||
| chr2:223759833
|
T | C | 24 | a0001c0001t0006g0023a0001c0001t0006g0026a0001c0001t0006g0072others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.430-1083A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759833 | ||||||
| chr2:223759878
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(104): Show | 108 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.430-1128A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759878 | ||||||
| chr2:223759995
|
C | T | 2 | a0001c0001t0032g0216a0001c0001t0032g0225 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.430-1245G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223759995 | ||||||
| chr2:223760102
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.430-1352A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760102 | ||||||
| chr2:223760197
|
C | T | 67 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(64): Show | 67 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.430-1447G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760197 | ||||||
| chr2:223760238
|
G | A | 37 | a0001c0001t0004g0009a0001c0001t0004g0073a0001c0001t0004g0091others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-1488C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760238 | ||||||
| chr2:223760290
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.430-1540C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760290 | ||||||
| chr2:223760364
|
G | A | 2 | a0001c0001t0032g0216a0001c0001t0032g0225 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.430-1614C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760364 | ||||||
| chr2:223760387
|
T | G | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.430-1637A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760387 | ||||||
| chr2:223760520
|
C | T | 3 | a0001c0001t0056g0003a0001c0001t0057g0118a0001c0001t0058g0100 | 3 | HG01109.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.430-1770G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760520 | ||||||
| chr2:223760616
|
G | T | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.430-1866C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760616 | ||||||
| chr2:223760848
|
G | A | 5 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-2098C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760848 | ||||||
| chr2:223760938
|
C | T | 1 | a0001c0001t0022g0101 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.430-2188G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760938 | ||||||
| chr2:223760939
|
G | A | 127 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(124): Show | 127 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.430-2189C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223760939 | ||||||
| chr2:223761154
|
T | C | 3 | a0001c0001t0020g0137a0001c0001t0020g0140a0001c0001t0020g0177 | 3 | HG02886.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.430-2404A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761154 | ||||||
| chr2:223761196
|
G | C | 1 | a0001c0001t0001g0002 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.430-2446C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761196 | ||||||
| chr2:223761321
|
G | A | 2 | a0001c0001t0009g0181a0001c0001t0009g0183 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.430-2571C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761321 | ||||||
| chr2:223761487
|
C | T | 2 | a0001c0001t0032g0216a0001c0001t0032g0225 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.430-2737G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761487 | ||||||
| chr2:223761519
|
G | A | 3 | a0001c0001t0020g0137a0001c0001t0020g0140a0001c0001t0020g0177 | 3 | HG02886.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.430-2769C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761519 | ||||||
| chr2:223761549
|
C | T | 5 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0171others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-2799G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761549 | ||||||
| chr2:223761764
|
A | G | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-3014T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761764 | ||||||
| chr2:223761771
|
C | A | 1 | a0001c0001t0070g0308 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430-3021G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761771 | ||||||
| chr2:223761907
|
T | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0337a0001c0001t0068g0173 | 3 | HG02451.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.430-3157A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761907 | ||||||
| chr2:223761981
|
T | C | 4 | a0001c0001t0006g0072a0001c0001t0006g0078a0001c0001t0006g0286others(1): Show | 4 | HG00408.hp1 HG00673.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-3231A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761981 | ||||||
| chr2:223761995
|
CAG | C | 24 | a0001c0001t0006g0023a0001c0001t0006g0026a0001c0001t0006g0072others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.429+3216_429+3217d others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223761995 | ||||||
| chr2:223762021
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(289): Show | 293 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.429+3192T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762021 | ||||||
| chr2:223762123
|
C | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0337a0001c0001t0068g0173 | 3 | HG02451.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.429+3090G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762123 | ||||||
| chr2:223762256
|
T | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(286): Show | 290 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.429+2957A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762256 | ||||||
| chr2:223762268
|
A | AT | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(91): Show | 95 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.429+2944dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762268 | ||||||
| chr2:223762268
|
A | ATT | 29 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0135others(26): Show | 29 | HG00673.hp2 HG00741.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.429+2943_429+2944d others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762268 | ||||||
| chr2:223762268
|
AT | A | 61 | a0001c0001t0002g0179a0001c0001t0002g0309a0001c0001t0002g0310others(58): Show | 61 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.429+2944delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762268 | ||||||
| chr2:223762268
|
ATT | A | 16 | a0001c0001t0005g0088a0001c0001t0005g0199a0001c0001t0005g0211others(13): Show | 16 | HG01361.hp2 HG02165.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.429+2943_429+2944d others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762268 | ||||||
| chr2:223762268
|
ATTT | A | 13 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(10): Show | 13 | HG00438.hp1 HG01175.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+2942_429+2944d others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762268 | ||||||
| chr2:223762342
|
GGCTCACT | G | 123 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(120): Show | 123 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.429+2864_429+2870d others(9): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762342 | ||||||
| chr2:223762452
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.429+2761A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762452 | ||||||
| chr2:223762515
|
C | T | 1 | a0001c0001t0050g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.429+2698G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762515 | ||||||
| chr2:223762525
|
G | A | 2 | a0001c0001t0032g0216a0001c0001t0032g0225 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.429+2688C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762525 | ||||||
| chr2:223762543
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.429+2670C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762543 | ||||||
| chr2:223762702
|
C | A | 123 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(120): Show | 123 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.429+2511G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762702 | ||||||
| chr2:223762755
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.429+2458G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762755 | ||||||
| chr2:223762934
|
GA | G | 18 | a0001c0001t0003g0063a0001c0001t0006g0072a0001c0001t0006g0078others(15): Show | 18 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+2278delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762934 | ||||||
| chr2:223762946
|
A | G | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.429+2267T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223762946 | ||||||
| chr2:223763014
|
C | T | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+2199G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763014 | ||||||
| chr2:223763058
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(261): Show | 265 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(262): Show |
intron_variant | MODIFIER | c.429+2155A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763058 | ||||||
| chr2:223763131
|
G | T | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.429+2082C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763131 | ||||||
| chr2:223763245
|
A | G | 2 | a0001c0001t0008g0187a0001c0001t0015g0186 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.429+1968T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763245 | ||||||
| chr2:223763451
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.429+1762C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763451 | ||||||
| chr2:223763463
|
C | T | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+1750G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763463 | ||||||
| chr2:223763491
|
TA | T | 130 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(127): Show | 130 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.429+1721delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763491 | ||||||
| chr2:223763613
|
G | A | 32 | a0001c0001t0004g0009a0001c0001t0004g0073a0001c0001t0004g0091others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.429+1600C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763613 | ||||||
| chr2:223763712
|
G | A | 34 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(31): Show | 34 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.429+1501C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763712 | ||||||
| chr2:223763723
|
C | A | 1 | a0001c0001t0005g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.429+1490G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763723 | ||||||
| chr2:223763804
|
A | G | 2 | a0001c0001t0009g0181a0001c0001t0009g0183 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.429+1409T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763804 | ||||||
| chr2:223763859
|
T | C | 1 | a0001c0001t0005g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.429+1354A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763859 | ||||||
| chr2:223763895
|
G | A | 130 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(127): Show | 130 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.429+1318C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763895 | ||||||
| chr2:223763916
|
CTTAT | C | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+1293_429+1296d others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223763916 | ||||||
| chr2:223764004
|
C | T | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+1209G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764004 | ||||||
| chr2:223764073
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.429+1140G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764073 | ||||||
| chr2:223764075
|
T | C | 1 | a0001c0001t0069g0059 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.429+1138A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764075 | ||||||
| chr2:223764121
|
A | G | 1 | a0001c0001t0057g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.429+1092T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764121 | ||||||
| chr2:223764206
|
AC | A | 120 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(117): Show | 120 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.429+1006delG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764206 | ||||||
| chr2:223764208
|
C | A | 2 | a0001c0001t0009g0181a0001c0001t0009g0183 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.429+1005G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764208 | ||||||
| chr2:223764208
|
C | G | 5 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+1005G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764208 | ||||||
| chr2:223764209
|
G | A | 1 | a0001c0001t0002g0330 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.429+1004C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764209 | ||||||
| chr2:223764300
|
C | G | 4 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0012g0207others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+913G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764300 | ||||||
| chr2:223764421
|
C | T | 1 | a0001c0001t0048g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.429+792G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764421 | ||||||
| chr2:223764605
|
T | G | 1 | a0001c0001t0044g0150 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.429+608A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764605 | ||||||
| chr2:223764616
|
G | A | 130 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(127): Show | 130 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.429+597C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764616 | ||||||
| chr2:223764751
|
A | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(286): Show | 290 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.429+462T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764751 | ||||||
| chr2:223764904
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.429+309A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764904 | ||||||
| chr2:223764910
|
G | A | 1 | a0001c0001t0004g0009 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.429+303C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223764910 | ||||||
| chr2:223765075
|
G | A | 1 | a0001c0001t0035g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.429+138C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223765075 | ||||||
| chr2:223765134
|
C | CT | 130 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(127): Show | 130 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.429+78dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223765134 | ||||||
| chr2:223765150
|
T | A | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+63A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223765150 | ||||||
| chr2:223765159
|
C | CCAT | 135 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(132): Show | 135 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.429+51_429+53dupAT others(1): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223765159 | ||||||
| chr2:223765159
|
C | CCATCAT | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(97): Show | 101 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.429+48_429+53dupAT others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 4/4 | chr2 | 223765159 | ||||||
| chr2:223765419
|
C | A | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-69G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223765419 | ||||||
| chr2:223765505
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.292-155A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223765505 | ||||||
| chr2:223765608
|
G | A | 2 | a0001c0001t0026g0241a0001c0001t0026g0319 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.292-258C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223765608 | ||||||
| chr2:223765837
|
G | A | 34 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(31): Show | 34 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.292-487C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223765837 | ||||||
| chr2:223765949
|
C | T | 3 | a0001c0001t0011g0214a0001c0001t0011g0228a0001c0001t0011g0238 | 3 | NA18971.hp1 NA18984.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.292-599G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223765949 | ||||||
| chr2:223765959
|
C | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(261): Show | 265 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(262): Show |
intron_variant | MODIFIER | c.292-609G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223765959 | ||||||
| chr2:223765986
|
G | A | 122 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(119): Show | 122 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.292-636C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223765986 | ||||||
| chr2:223766222
|
A | G | 1 | a0001c0001t0028g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292-872T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766222 | ||||||
| chr2:223766240
|
C | G | 1 | a0001c0001t0011g0200 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.292-890G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766240 | ||||||
| chr2:223766241
|
G | C | 1 | a0001c0001t0011g0200 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.292-891C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766241 | ||||||
| chr2:223766443
|
T | C | 1 | a0001c0001t0005g0199 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.292-1093A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766443 | ||||||
| chr2:223766542
|
A | C | 1 | a0001c0001t0008g0230 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292-1192T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766542 | ||||||
| chr2:223766648
|
G | C | 1 | a0001c0001t0008g0230 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292-1298C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766648 | ||||||
| chr2:223766698
|
T | G | 2 | a0001c0001t0032g0216a0001c0001t0032g0225 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.292-1348A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766698 | ||||||
| chr2:223766919
|
A | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(261): Show | 265 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(262): Show |
intron_variant | MODIFIER | c.292-1569T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766919 | ||||||
| chr2:223766969
|
C | A | 34 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(31): Show | 34 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.292-1619G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223766969 | ||||||
| chr2:223767043
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(100): Show | 104 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.292-1693C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767043 | ||||||
| chr2:223767097
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(254): Show | 258 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.292-1747T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767097 | ||||||
| chr2:223767175
|
G | C | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.292-1825C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767175 | ||||||
| chr2:223767192
|
G | C | 3 | a0001c0001t0056g0003a0001c0001t0057g0118a0001c0001t0058g0100 | 3 | HG01109.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.292-1842C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767192 | ||||||
| chr2:223767236
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(94): Show | 98 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.292-1886G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767236 | ||||||
| chr2:223767472
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(285): Show | 289 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.292-2122T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767472 | ||||||
| chr2:223767594
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(97): Show | 101 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.292-2244C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767594 | ||||||
| chr2:223767673
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0271 | 3 | HG03491.hp1 HG03492.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.292-2323G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223767673 | ||||||
| chr2:223768172
|
T | A | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.292-2822A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768172 | ||||||
| chr2:223768232
|
A | T | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.292-2882T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768232 | ||||||
| chr2:223768248
|
A | G | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.292-2898T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768248 | ||||||
| chr2:223768449
|
C | T | 127 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(124): Show | 127 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.292-3099G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768449 | ||||||
| chr2:223768582
|
T | C | 1 | a0001c0001t0004g0009 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.292-3232A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768582 | ||||||
| chr2:223768636
|
C | G | 32 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(29): Show | 32 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.292-3286G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768636 | ||||||
| chr2:223768728
|
G | A | 1 | a0001c0001t0003g0270 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.292-3378C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768728 | ||||||
| chr2:223768927
|
C | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0302a0001c0001t0001g0318 | 3 | NA19060.hp1 NA19066.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.292-3577G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223768927 | ||||||
| chr2:223769110
|
C | T | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.292-3760G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769110 | ||||||
| chr2:223769125
|
C | T | 120 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(117): Show | 120 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.292-3775G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769125 | ||||||
| chr2:223769192
|
A | C | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-3842T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769192 | ||||||
| chr2:223769568
|
G | C | 45 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(42): Show | 45 | HG00423.hp1 HG00544.hp2 HG01433.hp1 others(42): Show |
intron_variant | MODIFIER | c.292-4218C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769568 | ||||||
| chr2:223769611
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(254): Show | 258 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.292-4261A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769611 | ||||||
| chr2:223769613
|
A | AAGCGTTT | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(254): Show | 258 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.292-4264_292-4263i others(9): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769613 | ||||||
| chr2:223769614
|
G | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(254): Show | 258 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.292-4264C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769614 | ||||||
| chr2:223769656
|
A | G | 6 | a0001c0001t0002g0179a0001c0001t0002g0309a0001c0001t0002g0310others(3): Show | 6 | HG02257.hp1 HG02630.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-4306T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769656 | ||||||
| chr2:223769736
|
A | AT | 77 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0057others(74): Show | 78 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.292-4387dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769736 | ||||||
| chr2:223769736
|
A | ATT | 31 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0055others(28): Show | 31 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.292-4388_292-4387d others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769736 | ||||||
| chr2:223769736
|
A | ATTT | 7 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0202others(4): Show | 7 | NA18965.hp1 NA18995.hp2 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-4389_292-4387d others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769736 | ||||||
| chr2:223769736
|
AT | A | 79 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0053others(76): Show | 79 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.292-4387delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769736 | ||||||
| chr2:223769736
|
ATT | A | 69 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0035others(66): Show | 69 | HG00639.hp1 HG01496.hp1 HG01993.hp2 others(66): Show |
intron_variant | MODIFIER | c.292-4388_292-4387d others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769736 | ||||||
| chr2:223769736
|
ATTT | A | 26 | a0001c0001t0002g0004a0001c0001t0006g0026a0001c0001t0006g0072others(23): Show | 26 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.292-4389_292-4387d others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769736 | ||||||
| chr2:223769783
|
G | A | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.292-4433C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769783 | ||||||
| chr2:223769831
|
C | T | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.292-4481G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769831 | ||||||
| chr2:223769834
|
C | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(96): Show | 100 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.292-4484G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769834 | ||||||
| chr2:223769861
|
C | T | 1 | a0001c0001t0016g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.292-4511G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769861 | ||||||
| chr2:223769919
|
T | C | 29 | a0001c0001t0006g0023a0001c0001t0006g0026a0001c0001t0006g0072others(26): Show | 29 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.292-4569A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223769919 | ||||||
| chr2:223770044
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0012g0207others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-4694C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770044 | ||||||
| chr2:223770046
|
G | A | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(327): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.292-4696C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770046 | ||||||
| chr2:223770067
|
A | G | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.292-4717T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770067 | ||||||
| chr2:223770497
|
T | TAC | 48 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(45): Show | 48 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.292-5149_292-5148d others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACAC | 15 | a0001c0001t0005g0269a0001c0001t0005g0298a0001c0001t0007g0061others(12): Show | 15 | HG00609.hp1 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.292-5151_292-5148d others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACACAC | 21 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0160others(18): Show | 22 | HG01168.hp1 HG01261.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.292-5153_292-5148d others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACACACA others(1): Show |
115 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.292-5155_292-5148d others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACACACA others(3): Show |
75 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0125others(72): Show | 75 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.292-5157_292-5148d others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACACACA others(5): Show |
23 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0097others(20): Show | 23 | HG01123.hp1 HG01993.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.292-5159_292-5148d others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACACACA others(7): Show |
26 | a0001c0001t0001g0070a0001c0001t0001g0110a0001c0001t0002g0007others(23): Show | 26 | HG00544.hp2 HG01433.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.292-5161_292-5148d others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACACACA others(9): Show |
1 | a0001c0001t0002g0309 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292-5163_292-5148d others(18): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770497
|
T | TACACACA others(11): Show |
2 | a0001c0001t0003g0021a0001c0001t0003g0056 | 2 | NA18957.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.292-5165_292-5148d others(20): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770497 | ||||||
| chr2:223770532
|
C | A | 155 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(152): Show | 155 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.292-5182G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770532 | ||||||
| chr2:223770613
|
C | G | 1 | a0001c0001t0023g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.292-5263G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770613 | ||||||
| chr2:223770640
|
A | T | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.291+5261T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770640 | ||||||
| chr2:223770726
|
C | CTTT | 13 | a0001c0001t0001g0162a0001c0001t0001g0257a0001c0001t0001g0290others(10): Show | 13 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.291+5174_291+5175i others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770726 | ||||||
| chr2:223770727
|
A | AT | 8 | a0001c0001t0007g0156a0001c0001t0007g0170a0001c0001t0007g0337others(5): Show | 8 | HG02451.hp1 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+5173dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770727 | ||||||
| chr2:223770727
|
A | ATTT | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(112): Show | 116 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.291+5171_291+5173d others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770727 | ||||||
| chr2:223770727
|
A | ATTTT | 38 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0037others(35): Show | 38 | HG00438.hp1 HG00544.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.291+5170_291+5173d others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770727 | ||||||
| chr2:223770727
|
A | ATTTTT | 106 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(103): Show | 106 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.291+5169_291+5173d others(7): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770727 | ||||||
| chr2:223770727
|
A | ATTTTTT | 11 | a0001c0001t0002g0008a0001c0001t0002g0098a0001c0001t0003g0013others(8): Show | 11 | HG01433.hp1 HG01496.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+5168_291+5173d others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770727 | ||||||
| chr2:223770727
|
A | T | 13 | a0001c0001t0001g0162a0001c0001t0001g0257a0001c0001t0001g0290others(10): Show | 13 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.291+5174T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770727 | ||||||
| chr2:223770767
|
A | G | 156 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(153): Show | 156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.291+5134T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770767 | ||||||
| chr2:223770926
|
G | T | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.291+4975C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770926 | ||||||
| chr2:223770927
|
A | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(157): Show | 160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.291+4974T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223770927 | ||||||
| chr2:223771039
|
G | A | 1 | a0003c0004t0005g0277 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.291+4862C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771039 | ||||||
| chr2:223771107
|
G | A | 1 | a0003c0004t0005g0277 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.291+4794C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771107 | ||||||
| chr2:223771127
|
A | C | 1 | a0001c0001t0002g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.291+4774T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771127 | ||||||
| chr2:223771146
|
G | A | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.291+4755C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771146 | ||||||
| chr2:223771173
|
T | C | 2 | a0001c0001t0021g0323a0001c0001t0021g0336 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+4728A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771173 | ||||||
| chr2:223771217
|
A | G | 3 | a0001c0001t0020g0137a0001c0001t0020g0140a0001c0001t0020g0177 | 3 | HG02886.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+4684T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771217 | ||||||
| chr2:223771245
|
G | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.291+4656C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771245 | ||||||
| chr2:223771253
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(282): Show | 286 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.291+4648A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771253 | ||||||
| chr2:223771459
|
C | G | 2 | a0001c0001t0032g0216a0001c0001t0032g0225 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.291+4442G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771459 | ||||||
| chr2:223771493
|
T | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.291+4408A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771493 | ||||||
| chr2:223771773
|
A | C | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.291+4128T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771773 | ||||||
| chr2:223771817
|
T | C | 1 | a0001c0001t0025g0048 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.291+4084A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771817 | ||||||
| chr2:223771829
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.291+4072C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771829 | ||||||
| chr2:223771839
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.291+4062C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223771839 | ||||||
| chr2:223772103
|
G | A | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.291+3798C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223772103 | ||||||
| chr2:223772121
|
A | G | 159 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(156): Show | 159 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.291+3780T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223772121 | ||||||
| chr2:223772198
|
C | T | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.291+3703G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223772198 | ||||||
| chr2:223772362
|
C | T | 156 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(153): Show | 156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.291+3539G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223772362 | ||||||
| chr2:223772654
|
T | TA | 15 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(12): Show | 15 | HG00438.hp1 HG01175.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.291+3246dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223772654 | ||||||
| chr2:223772681
|
T | G | 1 | a0001c0001t0003g0021 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.291+3220A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223772681 | ||||||
| chr2:223773250
|
A | G | 157 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.291+2651T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773250 | ||||||
| chr2:223773264
|
C | T | 2 | a0001c0001t0031g0215a0001c0001t0031g0246 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.291+2637G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773264 | ||||||
| chr2:223773313
|
C | A | 5 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+2588G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773313 | ||||||
| chr2:223773494
|
G | C | 1 | a0001c0001t0004g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.291+2407C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773494 | ||||||
| chr2:223773499
|
G | T | 156 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(153): Show | 156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.291+2402C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773499 | ||||||
| chr2:223773591
|
ATT | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0337a0001c0001t0068g0173 | 3 | HG02451.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.291+2308_291+2309d others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773591 | ||||||
| chr2:223773601
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.291+2300C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773601 | ||||||
| chr2:223773735
|
CAAG | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+2163_291+2165d others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773735 | ||||||
| chr2:223773738
|
G | C | 32 | a0001c0001t0006g0023a0001c0001t0006g0026a0001c0001t0006g0072others(29): Show | 32 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.291+2163C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773738 | ||||||
| chr2:223773755
|
G | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+2146C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773755 | ||||||
| chr2:223773771
|
C | G | 1 | a0001c0001t0007g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.291+2130G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773771 | ||||||
| chr2:223773803
|
G | A | 3 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0016g0045 | 3 | NA18983.hp1 NA18994.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.291+2098C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773803 | ||||||
| chr2:223773814
|
G | A | 1 | a0001c0001t0048g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.291+2087C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773814 | ||||||
| chr2:223773850
|
A | G | 2 | a0001c0001t0004g0124a0001c0001t0066g0161 | 2 | NA18991.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.291+2051T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773850 | ||||||
| chr2:223773942
|
G | C | 29 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(26): Show | 29 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.291+1959C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773942 | ||||||
| chr2:223773947
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.291+1954C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773947 | ||||||
| chr2:223773968
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1933G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223773968 | ||||||
| chr2:223774120
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1781C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774120 | ||||||
| chr2:223774148
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1753G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774148 | ||||||
| chr2:223774149
|
G | A | 2 | a0001c0001t0030g0240a0001c0001t0030g0242 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.291+1752C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774149 | ||||||
| chr2:223774165
|
G | A | 29 | a0001c0001t0006g0023a0001c0001t0006g0026a0001c0001t0006g0072others(26): Show | 29 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.291+1736C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774165 | ||||||
| chr2:223774246
|
A | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1655T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774246 | ||||||
| chr2:223774259
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0110a0001c0001t0018g0068 | 3 | HG03688.hp2 HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.291+1642C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774259 | ||||||
| chr2:223774279
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1622G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774279 | ||||||
| chr2:223774289
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1612G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774289 | ||||||
| chr2:223774361
|
G | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+1540C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774361 | ||||||
| chr2:223774372
|
T | TAATA | 63 | a0001c0001t0004g0009a0001c0001t0004g0073a0001c0001t0004g0091others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.291+1525_291+1528d others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774372 | ||||||
| chr2:223774372
|
T | TAATAAAT others(1): Show |
10 | a0001c0001t0004g0253a0001c0001t0005g0269a0001c0001t0006g0329others(7): Show | 10 | HG00099.hp1 HG01071.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.291+1521_291+1528d others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774372 | ||||||
| chr2:223774372
|
TAATA | T | 14 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0003g0029others(11): Show | 14 | HG00738.hp1 HG01981.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.291+1525_291+1528d others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774372 | ||||||
| chr2:223774372
|
TAATAAAT others(1): Show |
T | 56 | a0001c0001t0001g0001a0001c0001t0003g0010a0001c0001t0003g0011others(53): Show | 57 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.291+1521_291+1528d others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774372 | ||||||
| chr2:223774372
|
TAATAAAT others(5): Show |
T | 191 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(188): Show | 191 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.291+1517_291+1528d others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774372 | ||||||
| chr2:223774426
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(95): Show | 99 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.291+1475T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774426 | ||||||
| chr2:223774668
|
T | C | 3 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0003g0029 | 3 | HG01981.hp2 HG01993.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.291+1233A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774668 | ||||||
| chr2:223774697
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.291+1204T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774697 | ||||||
| chr2:223774745
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(283): Show | 287 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.291+1156C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774745 | ||||||
| chr2:223774765
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1136C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774765 | ||||||
| chr2:223774772
|
T | C | 1 | a0001c0001t0004g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.291+1129A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774772 | ||||||
| chr2:223774798
|
A | C | 2 | a0001c0001t0024g0042a0001c0001t0024g0054 | 2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.291+1103T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774798 | ||||||
| chr2:223774821
|
G | A | 3 | a0001c0001t0007g0170a0001c0001t0013g0142a0001c0001t0070g0308 | 3 | HG02622.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.291+1080C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774821 | ||||||
| chr2:223774831
|
T | C | 73 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(70): Show | 73 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.291+1070A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774831 | ||||||
| chr2:223774900
|
C | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+1001G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774900 | ||||||
| chr2:223774922
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+979T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774922 | ||||||
| chr2:223774927
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+974C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774927 | ||||||
| chr2:223774983
|
G | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0337a0001c0001t0068g0173 | 3 | HG02451.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.291+918C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223774983 | ||||||
| chr2:223775001
|
C | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+900G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775001 | ||||||
| chr2:223775013
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+888A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775013 | ||||||
| chr2:223775014
|
T | TTCAGAAA others(18): Show |
254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(251): Show | 255 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.291+886_291+887ins others(25): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775014 | ||||||
| chr2:223775147
|
C | T | 1 | a0001c0001t0016g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.291+754G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775147 | ||||||
| chr2:223775154
|
G | C | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.291+747C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775154 | ||||||
| chr2:223775548
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(254): Show | 258 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.291+353T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775548 | ||||||
| chr2:223775562
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(254): Show | 258 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.291+339A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775562 | ||||||
| chr2:223775662
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(253): Show | 257 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(254): Show |
intron_variant | MODIFIER | c.291+239T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775662 | ||||||
| chr2:223775780
|
G | A | 27 | a0001c0001t0005g0064a0001c0001t0005g0067a0001c0001t0005g0083others(24): Show | 27 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.291+121C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775780 | ||||||
| chr2:223775784
|
C | G | 1 | a0001c0001t0012g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.291+117G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 3/4 | chr2 | 223775784 | ||||||
| chr2:223776086
|
C | CAA | 78 | a0001c0001t0004g0009a0001c0001t0004g0073a0001c0001t0004g0091others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.183-78_183-77insTT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776086 | ||||||
| chr2:223776146
|
C | T | 73 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(70): Show | 73 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.183-137G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776146 | ||||||
| chr2:223776179
|
T | C | 73 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(70): Show | 73 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.183-170A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776179 | ||||||
| chr2:223776330
|
T | C | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.183-321A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776330 | ||||||
| chr2:223776380
|
C | T | 115 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(112): Show | 115 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.183-371G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776380 | ||||||
| chr2:223776445
|
C | T | 33 | a0001c0001t0002g0039a0001c0001t0002g0051a0001c0001t0005g0064others(30): Show | 33 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.183-436G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776445 | ||||||
| chr2:223776547
|
C | T | 159 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(156): Show | 159 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.183-538G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776547 | ||||||
| chr2:223776593
|
C | A | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.183-584G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776593 | ||||||
| chr2:223776852
|
C | T | 76 | a0001c0001t0001g0058a0001c0001t0002g0004a0001c0001t0002g0006others(73): Show | 76 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.182+839G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223776852 | ||||||
| chr2:223777001
|
T | C | 2 | a0001c0001t0008g0187a0001c0001t0015g0186 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182+690A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223777001 | ||||||
| chr2:223777309
|
C | T | 1 | a0001c0001t0021g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+382G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223777309 | ||||||
| chr2:223777332
|
T | C | 164 | a0001c0001t0001g0058a0001c0001t0002g0004a0001c0001t0002g0006others(161): Show | 164 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.182+359A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223777332 | ||||||
| chr2:223777381
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(68): Show | 71 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.182+310G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223777381 | ||||||
| chr2:223777389
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0147 | 2 | HG00639.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.182+302G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 2/4 | chr2 | 223777389 | ||||||
| chr2:223777891
|
A | C | 2 | a0001c0001t0007g0170a0001c0001t0070g0308 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4-22T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223777891 | ||||||
| chr2:223777898
|
C | A | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-29G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223777898 | ||||||
| chr2:223778102
|
T | G | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0032g0216others(3): Show | 6 | HG02630.hp2 HG02896.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-233A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778102 | ||||||
| chr2:223778111
|
G | GT | 9 | a0001c0001t0005g0064a0001c0001t0008g0176a0001c0001t0008g0188others(6): Show | 9 | HG00639.hp1 HG02145.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.4-243dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778111 | ||||||
| chr2:223778111
|
G | T | 1 | a0001c0001t0027g0332 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4-242C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778111 | ||||||
| chr2:223778116
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4-247A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778116 | ||||||
| chr2:223778116
|
TTTTG | T | 4 | a0001c0001t0006g0072a0001c0001t0006g0078a0001c0001t0006g0286others(1): Show | 4 | HG00673.hp1 HG01261.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-251_4-248delCAAA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778116 | ||||||
| chr2:223778120
|
G | T | 154 | a0001c0001t0001g0058a0001c0001t0001g0144a0001c0001t0002g0004others(151): Show | 154 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.4-251C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778120 | ||||||
| chr2:223778133
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4-264A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778133 | ||||||
| chr2:223778171
|
G | C | 40 | a0001c0001t0002g0039a0001c0001t0002g0051a0001c0001t0002g0179others(37): Show | 40 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.4-302C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778171 | ||||||
| chr2:223778175
|
GAGTGCAG others(10): Show |
G | 40 | a0001c0001t0002g0039a0001c0001t0002g0051a0001c0001t0002g0179others(37): Show | 40 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.4-323_4-307delGACC others(13): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778175 | ||||||
| chr2:223778193
|
T | G | 40 | a0001c0001t0002g0039a0001c0001t0002g0051a0001c0001t0002g0179others(37): Show | 40 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.4-324A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778193 | ||||||
| chr2:223778228
|
C | T | 10 | a0001c0001t0001g0271a0001c0001t0005g0268a0001c0001t0005g0269others(7): Show | 10 | HG00099.hp2 HG00741.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-359G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778228 | ||||||
| chr2:223778276
|
C | T | 35 | a0001c0001t0002g0039a0001c0001t0002g0051a0001c0001t0002g0179others(32): Show | 35 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.4-407G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778276 | ||||||
| chr2:223778606
|
C | T | 1 | a0001c0001t0058g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4-737G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778606 | ||||||
| chr2:223778658
|
C | G | 1 | a0001c0001t0002g0263 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4-789G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778658 | ||||||
| chr2:223778674
|
A | G | 194 | a0001c0001t0001g0058a0001c0001t0001g0144a0001c0001t0002g0004others(191): Show | 194 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.4-805T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778674 | ||||||
| chr2:223778698
|
C | CT | 42 | a0001c0001t0001g0195a0001c0001t0002g0039a0001c0001t0002g0051others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.4-830dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778698 | ||||||
| chr2:223778709
|
TC | T | 7 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0003g0028others(4): Show | 7 | HG00544.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-841delG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778709 | ||||||
| chr2:223778710
|
C | T | 156 | a0001c0001t0001g0058a0001c0001t0002g0004a0001c0001t0002g0006others(153): Show | 156 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.4-841G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778710 | ||||||
| chr2:223778785
|
C | T | 35 | a0001c0001t0004g0009a0001c0001t0004g0073a0001c0001t0004g0091others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.4-916G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778785 | ||||||
| chr2:223778830
|
G | C | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-961C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778830 | ||||||
| chr2:223778835
|
T | C | 3 | a0001c0001t0020g0137a0001c0001t0020g0140a0001c0001t0020g0177 | 3 | HG02886.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4-966A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778835 | ||||||
| chr2:223778941
|
C | T | 16 | a0001c0001t0003g0017a0001c0001t0003g0020a0001c0001t0003g0021others(13): Show | 16 | HG02056.hp2 HG02074.hp1 HG03490.hp2 others(13): Show |
intron_variant | MODIFIER | c.4-1072G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778941 | ||||||
| chr2:223778972
|
T | C | 1 | a0001c0001t0035g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4-1103A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223778972 | ||||||
| chr2:223779074
|
T | C | 8 | a0001c0001t0005g0211a0001c0001t0005g0298a0001c0001t0007g0159others(5): Show | 8 | HG02165.hp1 NA18961.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-1205A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779074 | ||||||
| chr2:223779214
|
G | A | 4 | a0001c0001t0007g0156a0001c0001t0007g0337a0001c0001t0021g0336others(1): Show | 4 | HG02451.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-1345C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779214 | ||||||
| chr2:223779254
|
T | G | 1 | a0001c0001t0003g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4-1385A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779254 | ||||||
| chr2:223779268
|
A | G | 34 | a0001c0001t0002g0039a0001c0001t0002g0051a0001c0001t0005g0064others(31): Show | 34 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.4-1399T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779268 | ||||||
| chr2:223779354
|
G | A | 3 | a0001c0001t0032g0216a0001c0001t0032g0225a0001c0001t0056g0003 | 3 | HG02896.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4-1485C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779354 | ||||||
| chr2:223779376
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4-1507A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779376 | ||||||
| chr2:223779433
|
T | C | 1 | a0001c0001t0058g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4-1564A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779433 | ||||||
| chr2:223779623
|
T | C | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-1754A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779623 | ||||||
| chr2:223779658
|
C | T | 37 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(34): Show | 37 | HG00544.hp2 HG01433.hp1 HG01978.hp2 others(34): Show |
intron_variant | MODIFIER | c.4-1789G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779658 | ||||||
| chr2:223779705
|
C | T | 2 | a0001c0001t0007g0337a0001c0001t0068g0173 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4-1836G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779705 | ||||||
| chr2:223779725
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4-1856A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779725 | ||||||
| chr2:223779733
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(76): Show | 79 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.4-1864G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779733 | ||||||
| chr2:223779734
|
G | A | 21 | a0001c0001t0002g0263a0001c0001t0006g0023a0001c0001t0006g0026others(18): Show | 21 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.4-1865C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779734 | ||||||
| chr2:223779825
|
C | T | 1 | a0001c0001t0061g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4-1956G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779825 | ||||||
| chr2:223779868
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.4-1999C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779868 | ||||||
| chr2:223779870
|
G | A | 1 | a0001c0001t0002g0234 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4-2001C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779870 | ||||||
| chr2:223779908
|
A | G | 1 | a0001c0001t0039g0090 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4-2039T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779908 | ||||||
| chr2:223779924
|
G | A | 5 | a0001c0001t0012g0099a0001c0001t0012g0106a0001c0001t0012g0180others(2): Show | 5 | HG02055.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-2055C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223779924 | ||||||
| chr2:223780174
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4-2305A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780174 | ||||||
| chr2:223780276
|
A | AAT | 8 | a0001c0001t0001g0250a0001c0001t0002g0085a0001c0001t0008g0233others(5): Show | 8 | HG01106.hp2 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-2409_4-2408dupAT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
A | AATAT | 13 | a0001c0001t0001g0132a0001c0001t0001g0148a0001c0001t0001g0151others(10): Show | 13 | HG00544.hp1 HG01496.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2411_4-2408dupAT others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
A | AATATAT | 10 | a0001c0001t0001g0121a0001c0001t0002g0196a0001c0001t0002g0234others(7): Show | 10 | HG01070.hp1 HG01192.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.4-2413_4-2408dupAT others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
A | AATATATA others(1): Show |
8 | a0001c0001t0001g0126a0001c0001t0001g0133a0001c0001t0002g0051others(5): Show | 8 | HG00423.hp2 HG01258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-2415_4-2408dupAT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0160a0001c0001t0002g0066a0001c0001t0042g0152 | 3 | HG01261.hp1 HG01891.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.4-2417_4-2408dupAT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
A | AATATATA others(5): Show |
2 | a0001c0001t0002g0039a0001c0001t0007g0061 | 2 | HG02572.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.4-2419_4-2408dupAT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
A | AATATATA others(7): Show |
1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4-2421_4-2408dupAT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
A | AATATATA others(11): Show |
1 | a0001c0001t0005g0266 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4-2425_4-2408dupAT others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
AAT | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0094a0001c0001t0001g0192others(9): Show | 12 | HG01243.hp2 HG01515.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.4-2409_4-2408delAT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
AATAT | A | 15 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0247others(12): Show | 15 | HG00140.hp1 HG00609.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.4-2411_4-2408delAT others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
AATATAT | A | 13 | a0001c0001t0001g0202a0001c0001t0001g0271a0001c0001t0001g0304others(10): Show | 13 | HG00544.hp2 HG00673.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2413_4-2408delAT others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
AATATATA others(1): Show |
A | 8 | a0001c0001t0001g0055a0001c0001t0001g0084a0001c0001t0001g0282others(5): Show | 8 | HG01071.hp2 HG01243.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-2415_4-2408delAT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780276
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0001g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4-2417_4-2408delAT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780276 | ||||||
| chr2:223780286
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0005g0326 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.4-2443_4-2418delCT others(24): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780286 | ||||||
| chr2:223780288
|
TATATATA others(25): Show |
T | 1 | a0001c0001t0022g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4-2451_4-2420delCT others(30): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780288 | ||||||
| chr2:223780290
|
TATATATA others(23): Show |
T | 1 | a0001c0001t0004g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4-2451_4-2422delCT others(28): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780290 | ||||||
| chr2:223780290
|
TATATATA others(25): Show |
T | 3 | a0001c0001t0004g0107a0001c0001t0004g0128a0001c0001t0065g0127 | 3 | HG00140.hp2 HG01255.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.4-2453_4-2422delCT others(30): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780290 | ||||||
| chr2:223780294
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0010g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4-2449_4-2426delCT others(22): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780294 | ||||||
| chr2:223780296
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0068g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4-2443_4-2428delCT others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780296 | ||||||
| chr2:223780296
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0019g0139 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4-2449_4-2428delCT others(20): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780296 | ||||||
| chr2:223780296
|
TATATATA others(23): Show |
T | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4-2457_4-2428delCT others(28): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780296 | ||||||
| chr2:223780298
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0023g0280 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4-2441_4-2430delCT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780298 | ||||||
| chr2:223780298
|
TATATATA others(13): Show |
T | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4-2449_4-2430delCT others(18): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780298 | ||||||
| chr2:223780300
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0022g0279 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4-2441_4-2432delCT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780300 | ||||||
| chr2:223780300
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0005g0300 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4-2443_4-2432delCT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780300 | ||||||
| chr2:223780300
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0006g0026a0001c0001t0007g0337 | 2 | HG02451.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.4-2445_4-2432delCT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780300 | ||||||
| chr2:223780302
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0002g0041a0001c0001t0019g0265 | 3 | HG00738.hp2 HG02698.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.4-2433A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(1): Show |
T | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0003g0052others(4): Show | 7 | HG02165.hp1 NA18946.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-2441_4-2434delCT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0003g0037a0001c0001t0047g0322 | 2 | HG02451.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.4-2443_4-2434delCT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0006g0023 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4-2447_4-2434delCT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0050g0077a0001c0001t0058g0100 | 2 | HG01109.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.4-2449_4-2434delCT others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(11): Show |
T | 3 | a0001c0001t0010g0331a0002c0002t0002g0291a0002c0002t0002g0292 | 3 | HG03209.hp2 HG03486.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4-2451_4-2434delCT others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4-2453_4-2434delCT others(18): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0005g0269 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4-2455_4-2434delCT others(20): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780302
|
TATATATA others(21): Show |
T | 4 | a0001c0001t0012g0099a0001c0001t0012g0106a0001c0001t0012g0182others(1): Show | 4 | HG02717.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2461_4-2434delCT others(26): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780302 | ||||||
| chr2:223780304
|
T | G | 17 | a0001c0001t0001g0162a0001c0001t0001g0192a0001c0001t0001g0248others(14): Show | 17 | HG00738.hp2 HG01168.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.4-2435A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAG | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0193a0001c0001t0001g0201others(7): Show | 10 | HG00735.hp1 HG00741.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-2441_4-2436delCT others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAGA others(1): Show |
T | 7 | a0001c0001t0001g0205a0001c0001t0002g0038a0001c0001t0002g0153others(4): Show | 7 | HG03130.hp2 HG03490.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-2443_4-2436delCT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAGA others(3): Show |
T | 7 | a0001c0001t0001g0290a0001c0001t0001g0295a0001c0001t0002g0163others(4): Show | 7 | HG02886.hp1 HG02897.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-2445_4-2436delCT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAGA others(5): Show |
T | 1 | a0001c0001t0003g0029 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4-2447_4-2436delCT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAGA others(7): Show |
T | 4 | a0001c0001t0001g0070a0001c0001t0003g0270a0001c0001t0006g0251others(1): Show | 4 | HG02071.hp2 HG02723.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-2449_4-2436delCT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAGA others(9): Show |
T | 2 | a0001c0001t0002g0310a0001c0001t0049g0255 | 2 | NA19009.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4-2451_4-2436delCT others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAGA others(11): Show |
T | 4 | a0001c0001t0002g0309a0001c0001t0006g0272a0001c0001t0024g0042others(1): Show | 4 | HG00408.hp2 HG00609.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-2453_4-2436delCT others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780304
|
TATATAGA others(25): Show |
T | 1 | a0001c0001t0012g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4-2467_4-2436delCT others(30): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780304 | ||||||
| chr2:223780306
|
T | G | 31 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0162others(28): Show | 31 | HG00140.hp1 HG00738.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.4-2437A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780306 | ||||||
| chr2:223780306
|
TATAG | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0110others(3): Show | 6 | HG03710.hp1 NA18906.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-2441_4-2438delCT others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780306 | ||||||
| chr2:223780306
|
TATAGAG | T | 8 | a0001c0001t0001g0191a0001c0001t0001g0203a0001c0001t0001g0239others(5): Show | 8 | HG01993.hp1 NA18971.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-2443_4-2438delCT others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780306 | ||||||
| chr2:223780306
|
TATAGAGA others(3): Show |
T | 5 | a0001c0001t0001g0122a0001c0001t0003g0018a0001c0001t0003g0062others(2): Show | 5 | HG00639.hp2 HG02683.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-2447_4-2438delCT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780306 | ||||||
| chr2:223780306
|
TATAGAGA others(7): Show |
T | 1 | a0001c0001t0014g0015 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4-2451_4-2438delCT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780306 | ||||||
| chr2:223780306
|
TATAGAGA others(9): Show |
T | 1 | a0001c0001t0006g0235 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4-2453_4-2438delCT others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780306 | ||||||
| chr2:223780306
|
TATAGAGA others(11): Show |
T | 2 | a0001c0001t0006g0317a0001c0001t0010g0237 | 2 | NA18964.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.4-2455_4-2438delCT others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780306 | ||||||
| chr2:223780308
|
T | G | 54 | a0001c0001t0001g0043a0001c0001t0001g0058a0001c0001t0001g0084others(51): Show | 54 | HG00140.hp1 HG00738.hp2 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.4-2439A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
T | TATATAGA others(3): Show |
1 | a0001c0001t0067g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4-2440_4-2439insCT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
T | TATATATA others(5): Show |
1 | a0001c0001t0027g0335 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4-2440_4-2439insCT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0252a0001c0001t0005g0328 | 2 | NA18980.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.4-2440_4-2439insCT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
TAG | T | 10 | a0001c0001t0001g0001a0001c0001t0002g0060a0001c0001t0002g0076others(7): Show | 11 | HG00735.hp2 HG01175.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.4-2441_4-2440delCT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
TAGAG | T | 11 | a0001c0001t0001g0057a0001c0001t0003g0031a0001c0001t0004g0108others(8): Show | 11 | HG00639.hp1 HG01074.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.4-2443_4-2440delCT others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
TAGAGAG | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0305a0001c0001t0003g0020others(4): Show | 7 | HG01074.hp2 HG02074.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-2445_4-2440delCT others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
TAGAGAGA others(1): Show |
T | 8 | a0001c0001t0001g0138a0001c0001t0003g0024a0001c0001t0004g0009others(5): Show | 8 | HG00438.hp2 HG01981.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.4-2447_4-2440delCT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
TAGAGAGA others(3): Show |
T | 5 | a0001c0001t0003g0021a0001c0001t0004g0073a0001c0001t0004g0091others(2): Show | 5 | HG01123.hp1 HG02148.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-2449_4-2440delCT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
TAGAGAGA others(5): Show |
T | 3 | a0001c0001t0004g0113a0001c0001t0004g0124a0001c0001t0004g0253 | 3 | HG03688.hp1 NA18981.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4-2451_4-2440delCT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780308
|
TAGAGAGA others(7): Show |
T | 6 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-2453_4-2440delCT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780308 | ||||||
| chr2:223780310
|
G | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.4-2441C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780310 | ||||||
| chr2:223780312
|
G | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0131a0001c0001t0001g0132others(45): Show | 48 | HG00408.hp1 HG00423.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.4-2443C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780312 | ||||||
| chr2:223780314
|
G | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0131a0001c0001t0001g0134others(33): Show | 36 | HG00423.hp2 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.4-2445C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780314 | ||||||
| chr2:223780316
|
G | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0134a0001c0001t0001g0135others(23): Show | 26 | HG00423.hp2 HG01074.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.4-2447C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780316 | ||||||
| chr2:223780318
|
G | T | 21 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00438.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.4-2449C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780318 | ||||||
| chr2:223780320
|
G | T | 14 | a0001c0001t0001g0136a0001c0001t0002g0098a0001c0001t0002g0179others(11): Show | 14 | HG00438.hp2 HG01123.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.4-2451C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780320 | ||||||
| chr2:223780322
|
G | T | 11 | a0001c0001t0001g0136a0001c0001t0002g0179a0001c0001t0003g0021others(8): Show | 11 | HG01123.hp1 HG02148.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.4-2453C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780322 | ||||||
| chr2:223780324
|
G | T | 7 | a0001c0001t0002g0179a0001c0001t0003g0021a0001c0001t0004g0091others(4): Show | 7 | HG01123.hp1 HG03130.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-2455C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780324 | ||||||
| chr2:223780326
|
G | T | 5 | a0001c0001t0004g0091a0001c0001t0004g0113a0001c0001t0004g0124others(2): Show | 5 | HG01123.hp1 HG03130.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-2457C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780326 | ||||||
| chr2:223780328
|
G | T | 2 | a0001c0001t0004g0113a0001c0001t0004g0253 | 2 | HG03688.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.4-2459C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780328 | ||||||
| chr2:223780330
|
G | T | 1 | a0001c0001t0004g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4-2461C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780330 | ||||||
| chr2:223780339
|
A | T | 1 | a0001c0001t0001g0248 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4-2470T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780339 | ||||||
| chr2:223780341
|
A | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0197a0001c0001t0001g0248others(3): Show | 6 | HG01978.hp1 NA18747.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-2472T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780341 | ||||||
| chr2:223780341
|
AGAGAGAG others(11): Show |
A | 5 | a0001c0001t0002g0263a0001c0001t0006g0289a0001c0001t0006g0301others(2): Show | 5 | NA18953.hp1 NA18975.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-2490_4-2473delAC others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780341 | ||||||
| chr2:223780343
|
A | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0162others(12): Show | 15 | HG00544.hp1 HG00673.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.4-2474T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780343 | ||||||
| chr2:223780343
|
AGAGAGAG others(9): Show |
A | 2 | a0001c0001t0006g0078a0001c0001t0006g0286 | 2 | HG00673.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.4-2490_4-2475delAC others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780343 | ||||||
| chr2:223780345
|
A | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0046others(32): Show | 35 | HG00544.hp1 HG00673.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.4-2476T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780345 | ||||||
| chr2:223780345
|
AGAGAGAG others(7): Show |
A | 1 | a0001c0001t0006g0072 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4-2490_4-2477delAC others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780345 | ||||||
| chr2:223780347
|
A | AGTGT | 5 | a0001c0001t0003g0019a0001c0001t0008g0243a0001c0001t0016g0047others(2): Show | 5 | HG01993.hp2 HG02300.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-2479_4-2478insAC others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780347 | ||||||
| chr2:223780347
|
A | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(65): Show | 68 | HG00544.hp1 HG00639.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.4-2478T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780347 | ||||||
| chr2:223780347
|
AGAGAGAG others(5): Show |
A | 1 | a0001c0001t0030g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4-2490_4-2479delAC others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780347 | ||||||
| chr2:223780349
|
A | AGT | 4 | a0001c0001t0003g0284a0001c0001t0007g0156a0001c0001t0017g0096others(1): Show | 4 | HG02965.hp1 HG03195.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-2481_4-2480insAC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780349 | ||||||
| chr2:223780349
|
A | AGTGT | 4 | a0001c0001t0002g0039a0001c0001t0002g0080a0001c0001t0002g0081others(1): Show | 4 | HG02572.hp2 NA18947.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2481_4-2480insAC others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780349 | ||||||
| chr2:223780349
|
A | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.4-2480T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780349 | ||||||
| chr2:223780349
|
AGAGAGAG others(3): Show |
A | 2 | a0001c0001t0030g0242a0001c0001t0057g0118 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4-2490_4-2481delAC others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780349 | ||||||
| chr2:223780351
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0005g0299 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4-2483_4-2482insAC others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780351 | ||||||
| chr2:223780351
|
A | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.4-2482T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780351 | ||||||
| chr2:223780353
|
A | AGTGT | 3 | a0001c0001t0002g0051a0001c0001t0002g0097a0001c0001t0005g0334 | 3 | HG00438.hp1 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.4-2485_4-2484insAC others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780353 | ||||||
| chr2:223780353
|
A | AGTGTGT | 4 | a0001c0001t0003g0224a0001c0001t0005g0211a0001c0001t0031g0246others(1): Show | 4 | HG00423.hp1 HG02258.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2485_4-2484insAC others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780353 | ||||||
| chr2:223780353
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0031g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4-2485_4-2484insAC others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780353 | ||||||
| chr2:223780353
|
A | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.4-2484T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780353 | ||||||
| chr2:223780353
|
AGAGAGT | A | 6 | a0001c0001t0004g0141a0001c0001t0004g0155a0001c0001t0004g0218others(3): Show | 6 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-2490_4-2485delAC others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780353 | ||||||
| chr2:223780353
|
AGAGAGTG others(7): Show |
A | 1 | a0001c0001t0060g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4-2498_4-2485delAC others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780353 | ||||||
| chr2:223780355
|
A | AGTGTGT | 3 | a0001c0001t0005g0088a0001c0001t0005g0333a0001c0001t0016g0288 | 3 | HG02523.hp2 NA18995.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4-2487_4-2486insAC others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780355 | ||||||
| chr2:223780355
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0016g0045 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4-2487_4-2486insAC others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780355 | ||||||
| chr2:223780355
|
A | AGTGTGTG others(9): Show |
2 | a0001c0001t0002g0229a0001c0001t0002g0232 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4-2487_4-2486insAC others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780355 | ||||||
| chr2:223780355
|
A | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(223): Show | 226 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.4-2486T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780355 | ||||||
| chr2:223780357
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0002g0154a0001c0001t0067g0221 | 2 | HG03540.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.4-2498_4-2489dupAC others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780357 | ||||||
| chr2:223780357
|
A | AGTGTGTG others(15): Show |
1 | a0001c0001t0002g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4-2510_4-2489dupAC others(20): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780357 | ||||||
| chr2:223780357
|
A | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4-2488T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780357 | ||||||
| chr2:223780357
|
AGTGTGT | A | 6 | a0001c0001t0012g0099a0001c0001t0012g0106a0001c0001t0012g0182others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-2494_4-2489delAC others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780357 | ||||||
| chr2:223780359
|
T | A | 15 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0160others(12): Show | 15 | HG00408.hp2 HG00609.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.4-2490A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780359 | ||||||
| chr2:223780361
|
T | A | 4 | a0001c0001t0005g0326a0001c0001t0010g0262a0001c0001t0012g0180others(1): Show | 4 | HG02027.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2492A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780361 | ||||||
| chr2:223780395
|
TG | T | 7 | a0001c0001t0004g0124a0001c0001t0009g0040a0001c0001t0009g0166others(4): Show | 7 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-2527delC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780395 | ||||||
| chr2:223780397
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0002g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4-2529_4-2528insCA others(11): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780397 | ||||||
| chr2:223780408
|
C | T | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4-2539G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780408 | ||||||
| chr2:223780437
|
C | T | 32 | a0001c0001t0001g0252a0001c0001t0002g0039a0001c0001t0002g0051others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.4-2568G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780437 | ||||||
| chr2:223780537
|
C | A | 1 | a0001c0001t0058g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4-2668G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780537 | ||||||
| chr2:223780563
|
A | ATT | 5 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0058g0100others(2): Show | 5 | HG01109.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-2696_4-2695dupAA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780563 | ||||||
| chr2:223780632
|
T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.4-2763A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780632 | ||||||
| chr2:223780655
|
T | C | 21 | a0001c0001t0002g0263a0001c0001t0006g0023a0001c0001t0006g0026others(18): Show | 21 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.4-2786A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780655 | ||||||
| chr2:223780751
|
CT | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.4-2883delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780751 | ||||||
| chr2:223780819
|
G | A | 1 | a0001c0001t0005g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4-2950C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223780819 | ||||||
| chr2:223781019
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4-3150C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781019 | ||||||
| chr2:223781054
|
CTGTGT | C | 36 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(33): Show | 36 | HG00544.hp2 HG01433.hp1 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.4-3190_4-3186delAC others(3): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781054 | ||||||
| chr2:223781199
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4-3330C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781199 | ||||||
| chr2:223781415
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4-3546C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781415 | ||||||
| chr2:223781461
|
T | C | 2 | a0001c0001t0022g0101a0001c0001t0062g0102 | 2 | HG01071.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.4-3592A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781461 | ||||||
| chr2:223781568
|
T | C | 2 | a0001c0001t0018g0149a0001c0001t0044g0150 | 2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.4-3699A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781568 | ||||||
| chr2:223781724
|
A | T | 1 | a0001c0001t0002g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4-3855T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781724 | ||||||
| chr2:223781962
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0007g0337a0001c0001t0068g0173 | 3 | HG01168.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4-4093T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781962 | ||||||
| chr2:223781999
|
T | C | 36 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(33): Show | 36 | HG00544.hp2 HG01433.hp1 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.4-4130A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223781999 | ||||||
| chr2:223782011
|
C | CT | 81 | a0001c0001t0001g0160a0001c0001t0001g0252a0001c0001t0001g0290others(78): Show | 81 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.4-4143dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782011 | ||||||
| chr2:223782011
|
C | CTT | 13 | a0001c0001t0002g0273a0001c0001t0003g0016a0001c0001t0003g0020others(10): Show | 13 | HG00423.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.4-4144_4-4143dupAA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782011 | ||||||
| chr2:223782085
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(268): Show | 271 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.4-4216A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782085 | ||||||
| chr2:223782089
|
G | A | 1 | a0001c0001t0002g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-4220C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782089 | ||||||
| chr2:223782090
|
C | A | 1 | a0001c0001t0002g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-4221G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782090 | ||||||
| chr2:223782183
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0146 | 2 | HG01074.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.4-4314A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782183 | ||||||
| chr2:223782310
|
G | C | 27 | a0001c0001t0002g0263a0001c0001t0006g0023a0001c0001t0006g0026others(24): Show | 27 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.4-4441C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782310 | ||||||
| chr2:223782419
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.4-4550A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782419 | ||||||
| chr2:223782946
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4-5077T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223782946 | ||||||
| chr2:223783243
|
G | A | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4-5374C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783243 | ||||||
| chr2:223783303
|
C | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(76): Show | 79 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.4-5434G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783303 | ||||||
| chr2:223783306
|
C | T | 37 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(34): Show | 37 | HG00408.hp1 HG00544.hp2 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.4-5437G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783306 | ||||||
| chr2:223783394
|
A | G | 1 | a0005c0005t0046g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4-5525T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783394 | ||||||
| chr2:223783448
|
G | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0043others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.4-5579C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783448 | ||||||
| chr2:223783573
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4-5704C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783573 | ||||||
| chr2:223783609
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4-5740C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783609 | ||||||
| chr2:223783640
|
A | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0192a0001c0001t0001g0297others(1): Show | 4 | HG02080.hp2 NA18947.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-5771T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783640 | ||||||
| chr2:223783758
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4-5889G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783758 | ||||||
| chr2:223783829
|
C | T | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4-5960G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783829 | ||||||
| chr2:223783848
|
T | C | 55 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0257others(52): Show | 55 | HG00423.hp1 HG00423.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.4-5979A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783848 | ||||||
| chr2:223783887
|
G | A | 1 | a0001c0001t0045g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4-6018C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783887 | ||||||
| chr2:223783969
|
G | T | 6 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-6100C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223783969 | ||||||
| chr2:223784001
|
C | T | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0165others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-6132G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784001 | ||||||
| chr2:223784064
|
GCA | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.4-6197_4-6196delTG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784064 | ||||||
| chr2:223784211
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0020g0177 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.4-6342G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784211 | ||||||
| chr2:223784242
|
C | T | 52 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0304others(49): Show | 52 | HG00423.hp1 HG00423.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.4-6373G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784242 | ||||||
| chr2:223784289
|
C | G | 1 | a0001c0001t0020g0177 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4-6420G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784289 | ||||||
| chr2:223784291
|
C | T | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4-6422G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784291 | ||||||
| chr2:223784454
|
A | G | 72 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(69): Show | 72 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.4-6585T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784454 | ||||||
| chr2:223784507
|
C | T | 21 | a0001c0001t0002g0097a0001c0001t0002g0109a0001c0001t0002g0153others(18): Show | 21 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4-6638G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784507 | ||||||
| chr2:223784597
|
A | C | 1 | a0003c0004t0005g0277 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4-6728T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784597 | ||||||
| chr2:223784617
|
C | T | 52 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(49): Show | 52 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.4-6748G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784617 | ||||||
| chr2:223784622
|
A | T | 1 | a0003c0004t0005g0277 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4-6753T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784622 | ||||||
| chr2:223784660
|
G | A | 9 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(6): Show | 9 | HG00639.hp1 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.4-6791C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784660 | ||||||
| chr2:223784728
|
G | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-6859C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784728 | ||||||
| chr2:223784823
|
A | C | 81 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0191others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.4-6954T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223784823 | ||||||
| chr2:223785002
|
A | T | 1 | a0001c0001t0003g0284 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4-7133T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785002 | ||||||
| chr2:223785072
|
C | T | 7 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(4): Show | 7 | HG00639.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-7203G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785072 | ||||||
| chr2:223785215
|
G | A | 8 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(5): Show | 8 | HG00639.hp1 HG01109.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.4-7346C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785215 | ||||||
| chr2:223785274
|
G | A | 7 | a0001c0001t0009g0040a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG02257.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-7405C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785274 | ||||||
| chr2:223785292
|
A | G | 1 | a0001c0001t0012g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4-7423T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785292 | ||||||
| chr2:223785377
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4-7508A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785377 | ||||||
| chr2:223785591
|
A | C | 2 | a0001c0001t0007g0170a0001c0001t0070g0308 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4-7722T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785591 | ||||||
| chr2:223785614
|
G | A | 55 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(52): Show | 55 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.4-7745C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785614 | ||||||
| chr2:223785966
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4-8097G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223785966 | ||||||
| chr2:223786018
|
A | G | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4-8149T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786018 | ||||||
| chr2:223786025
|
G | A | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4-8156C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786025 | ||||||
| chr2:223786122
|
A | T | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4-8253T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786122 | ||||||
| chr2:223786224
|
G | A | 53 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(50): Show | 53 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.4-8355C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786224 | ||||||
| chr2:223786359
|
C | T | 3 | a0001c0001t0021g0336a0001c0001t0031g0215a0001c0001t0031g0246 | 3 | HG02258.hp2 HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4-8490G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786359 | ||||||
| chr2:223786546
|
G | T | 1 | a0001c0001t0008g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4-8677C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786546 | ||||||
| chr2:223786561
|
C | G | 2 | a0001c0001t0026g0319a0001c0001t0054g0005 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4-8692G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786561 | ||||||
| chr2:223786592
|
C | CA | 56 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0136others(53): Show | 56 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.4-8724dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786592 | ||||||
| chr2:223786627
|
A | G | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4-8758T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786627 | ||||||
| chr2:223786666
|
C | A | 2 | a0001c0001t0002g0004a0001c0003t0021g0320 | 2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.4-8797G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786666 | ||||||
| chr2:223786791
|
A | G | 25 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(22): Show | 25 | HG01496.hp1 HG01884.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4-8922T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786791 | ||||||
| chr2:223786916
|
A | C | 1 | a0001c0001t0010g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4-9047T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223786916 | ||||||
| chr2:223787122
|
T | G | 2 | a0001c0001t0012g0106a0001c0001t0037g0105 | 2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4-9253A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787122 | ||||||
| chr2:223787170
|
A | G | 61 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.4-9301T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787170 | ||||||
| chr2:223787179
|
C | G | 2 | a0001c0001t0026g0319a0001c0001t0054g0005 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4-9310G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787179 | ||||||
| chr2:223787294
|
A | T | 2 | a0001c0001t0007g0170a0001c0001t0070g0308 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4-9425T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787294 | ||||||
| chr2:223787306
|
C | T | 4 | a0001c0001t0008g0176a0001c0001t0012g0099a0001c0001t0012g0180others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-9437G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787306 | ||||||
| chr2:223787529
|
T | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(323): Show | 327 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.4-9660A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787529 | ||||||
| chr2:223787568
|
A | G | 1 | a0001c0001t0010g0325 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4-9699T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787568 | ||||||
| chr2:223787581
|
G | C | 1 | a0001c0001t0026g0241 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4-9712C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787581 | ||||||
| chr2:223787644
|
C | A | 1 | a0001c0001t0014g0015 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4-9775G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787644 | ||||||
| chr2:223787749
|
A | AAC | 12 | a0001c0001t0001g0162a0001c0001t0001g0290a0001c0001t0001g0295others(9): Show | 12 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.4-9882_4-9881dupGT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787749 | ||||||
| chr2:223787846
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.4-9977G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787846 | ||||||
| chr2:223787966
|
C | CT | 61 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.4-10098dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787966 | ||||||
| chr2:223787996
|
A | G | 61 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.4-10127T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223787996 | ||||||
| chr2:223788138
|
A | G | 61 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.4-10269T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788138 | ||||||
| chr2:223788239
|
G | A | 1 | a0001c0001t0003g0284 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4-10370C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788239 | ||||||
| chr2:223788290
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4-10421G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788290 | ||||||
| chr2:223788384
|
G | C | 1 | a0001c0001t0063g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4-10515C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788384 | ||||||
| chr2:223788469
|
T | C | 2 | a0001c0001t0008g0187a0001c0001t0015g0186 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4-10600A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788469 | ||||||
| chr2:223788534
|
A | G | 2 | a0001c0001t0012g0207a0001c0001t0015g0217 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.4-10665T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788534 | ||||||
| chr2:223788597
|
C | CA | 82 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0125others(79): Show | 82 | HG00423.hp1 HG00544.hp2 HG01106.hp2 others(79): Show |
intron_variant | MODIFIER | c.4-10729dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788597 | ||||||
| chr2:223788597
|
C | CAA | 7 | a0001c0001t0001g0126a0001c0001t0002g0066a0001c0001t0002g0175others(4): Show | 7 | HG01981.hp1 HG02723.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-10730_4-10729dup others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788597 | ||||||
| chr2:223788604
|
A | G | 1 | a0001c0001t0022g0101 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4-10735T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788604 | ||||||
| chr2:223788719
|
G | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.4-10850C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788719 | ||||||
| chr2:223788762
|
T | TA | 35 | a0001c0001t0001g0239a0001c0001t0002g0097a0001c0001t0002g0098others(32): Show | 35 | HG01496.hp1 HG01884.hp1 HG01978.hp2 others(32): Show |
intron_variant | MODIFIER | c.4-10894dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788762 | ||||||
| chr2:223788762
|
TA | T | 11 | a0001c0001t0001g0121a0001c0001t0001g0138a0001c0001t0001g0144others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.4-10894delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788762 | ||||||
| chr2:223788779
|
A | G | 59 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(56): Show | 59 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.4-10910T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788779 | ||||||
| chr2:223788788
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.4-10919C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788788 | ||||||
| chr2:223788806
|
G | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(263): Show | 267 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.4-10937C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788806 | ||||||
| chr2:223788808
|
A | T | 3 | a0001c0001t0010g0237a0001c0001t0010g0274a0001c0001t0010g0275 | 3 | NA18964.hp2 NA19001.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4-10939T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788808 | ||||||
| chr2:223788876
|
T | G | 1 | a0001c0001t0002g0007 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4-11007A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788876 | ||||||
| chr2:223788940
|
T | C | 80 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0191others(77): Show | 80 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.4-11071A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223788940 | ||||||
| chr2:223789049
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0160a0001c0001t0001g0250 | 3 | HG01070.hp1 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.4-11180G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789049 | ||||||
| chr2:223789136
|
G | GA | 197 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4-11268dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789136 | ||||||
| chr2:223789213
|
C | T | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11344G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789213 | ||||||
| chr2:223789250
|
C | T | 1 | a0001c0001t0007g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4-11381G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789250 | ||||||
| chr2:223789346
|
A | G | 25 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(22): Show | 25 | HG01496.hp1 HG01884.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4-11477T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789346 | ||||||
| chr2:223789376
|
C | A | 59 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(56): Show | 59 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.4-11507G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789376 | ||||||
| chr2:223789382
|
A | G | 1 | a0001c0001t0019g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4-11513T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789382 | ||||||
| chr2:223789384
|
T | C | 1 | a0001c0001t0026g0241 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4-11515A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789384 | ||||||
| chr2:223789400
|
G | A | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11531C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789400 | ||||||
| chr2:223789674
|
C | CA | 10 | a0001c0001t0001g0136a0001c0001t0001g0160a0001c0001t0001g0191others(7): Show | 10 | HG00735.hp1 HG00741.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.4-11806dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789674 | ||||||
| chr2:223789674
|
C | CAAA | 48 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(45): Show | 48 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.4-11808_4-11806dup others(3): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789674 | ||||||
| chr2:223789674
|
C | CAAAA | 11 | a0001c0001t0002g0007a0001c0001t0002g0038a0001c0001t0002g0060others(8): Show | 11 | HG01109.hp2 HG01981.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.4-11809_4-11806dup others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789674 | ||||||
| chr2:223789699
|
G | A | 13 | a0001c0001t0001g0252a0001c0001t0002g0039a0001c0001t0002g0051others(10): Show | 13 | HG00438.hp1 HG01361.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.4-11830C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789699 | ||||||
| chr2:223789793
|
A | G | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11924T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789793 | ||||||
| chr2:223789794
|
T | C | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11925A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789794 | ||||||
| chr2:223789801
|
C | G | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11932G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789801 | ||||||
| chr2:223789813
|
C | G | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11944G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789813 | ||||||
| chr2:223789816
|
T | C | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11947A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789816 | ||||||
| chr2:223789819
|
T | C | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11950A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789819 | ||||||
| chr2:223789821
|
G | GAGCGAGA others(31): Show |
3 | a0001c0001t0002g0310a0001c0001t0015g0217a0002c0002t0002g0291 | 3 | HG00639.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4-11953_4-11952ins others(38): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789821 | ||||||
| chr2:223789821
|
G | GAGCGAGA others(32): Show |
3 | a0001c0001t0002g0309a0001c0001t0012g0207a0002c0002t0002g0292 | 3 | HG02055.hp2 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4-11953_4-11952ins others(39): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789821 | ||||||
| chr2:223789822
|
T | A | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11953A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789822 | ||||||
| chr2:223789824
|
C | A | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-11955G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789824 | ||||||
| chr2:223789835
|
C | CA | 72 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.4-11967dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789835 | ||||||
| chr2:223789835
|
CA | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0119a0001c0001t0001g0121others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.4-11967delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789835 | ||||||
| chr2:223789941
|
A | G | 1 | a0001c0001t0020g0177 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4-12072T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223789941 | ||||||
| chr2:223790036
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4-12167G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790036 | ||||||
| chr2:223790200
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4-12331G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790200 | ||||||
| chr2:223790233
|
C | CT | 72 | a0001c0001t0001g0001a0001c0001t0001g0119a0001c0001t0001g0121others(69): Show | 73 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.4-12365dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790233 | ||||||
| chr2:223790367
|
G | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(175): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.4-12498C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790367 | ||||||
| chr2:223790427
|
G | T | 5 | a0001c0001t0003g0016a0001c0001t0003g0018a0001c0001t0003g0028others(2): Show | 5 | HG00544.hp2 HG03927.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-12558C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790427 | ||||||
| chr2:223790478
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.4-12609G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790478 | ||||||
| chr2:223790486
|
G | A | 1 | a0001c0001t0006g0329 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4-12617C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790486 | ||||||
| chr2:223790514
|
G | A | 1 | a0001c0001t0005g0326 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.4-12645C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790514 | ||||||
| chr2:223790553
|
T | G | 4 | a0001c0001t0013g0142a0001c0001t0013g0143a0001c0001t0013g0165others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-12684A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790553 | ||||||
| chr2:223790630
|
A | G | 61 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(58): Show | 61 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.4-12761T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790630 | ||||||
| chr2:223790695
|
T | C | 60 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(57): Show | 60 | HG00423.hp1 HG00639.hp1 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.4-12826A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790695 | ||||||
| chr2:223790708
|
T | G | 28 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(25): Show | 28 | HG01496.hp1 HG01884.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4-12839A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790708 | ||||||
| chr2:223790763
|
G | T | 7 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(4): Show | 7 | HG00639.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-12894C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790763 | ||||||
| chr2:223790831
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0206 | 2 | NA18970.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4-12962C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790831 | ||||||
| chr2:223790831
|
G | C | 1 | a0001c0001t0045g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4-12962C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790831 | ||||||
| chr2:223790888
|
C | T | 6 | a0001c0001t0009g0181a0001c0001t0009g0183a0001c0001t0012g0099others(3): Show | 6 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-13019G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790888 | ||||||
| chr2:223790914
|
T | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-13045A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223790914 | ||||||
| chr2:223791117
|
A | G | 1 | a0001c0001t0026g0241 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4-13248T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791117 | ||||||
| chr2:223791232
|
C | A | 4 | a0001c0001t0002g0179a0001c0001t0007g0337a0001c0001t0047g0322others(1): Show | 4 | HG02451.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-13363G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791232 | ||||||
| chr2:223791257
|
C | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0032others(333): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.4-13388G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791257 | ||||||
| chr2:223791270
|
T | G | 26 | a0001c0001t0001g0318a0001c0001t0002g0209a0001c0001t0002g0263others(23): Show | 26 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.4-13401A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791270 | ||||||
| chr2:223791299
|
A | G | 1 | a0001c0001t0003g0027 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4-13430T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791299 | ||||||
| chr2:223791409
|
A | G | 52 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(49): Show | 52 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.4-13540T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791409 | ||||||
| chr2:223791484
|
C | G | 1 | a0001c0001t0058g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4-13615G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791484 | ||||||
| chr2:223791562
|
C | A | 4 | a0001c0001t0011g0200a0001c0001t0011g0214a0001c0001t0011g0228others(1): Show | 4 | NA18971.hp1 NA18984.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-13693G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791562 | ||||||
| chr2:223791609
|
T | C | 1 | a0001c0001t0017g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4-13740A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791609 | ||||||
| chr2:223791641
|
T | C | 52 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(49): Show | 52 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.4-13772A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223791641 | ||||||
| chr2:223792048
|
C | A | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4-14179G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223792048 | ||||||
| chr2:223792071
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.4-14202C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223792071 | ||||||
| chr2:223792293
|
CA | C | 7 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(4): Show | 7 | HG00639.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-14425delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223792293 | ||||||
| chr2:223792465
|
T | C | 3 | a0001c0001t0005g0213a0001c0001t0005g0333a0001c0001t0005g0334 | 3 | HG00438.hp1 NA18962.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.4-14596A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223792465 | ||||||
| chr2:223792674
|
T | C | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-14805A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223792674 | ||||||
| chr2:223792896
|
C | T | 1 | a0001c0001t0017g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4-15027G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223792896 | ||||||
| chr2:223792904
|
G | C | 4 | a0001c0001t0007g0061a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 4 | HG00408.hp1 HG03017.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-15035C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223792904 | ||||||
| chr2:223793047
|
G | C | 1 | a0001c0001t0002g0051 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4-15178C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793047 | ||||||
| chr2:223793049
|
CCATT | C | 53 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(50): Show | 53 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.4-15184_4-15181del others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793049 | ||||||
| chr2:223793170
|
C | G | 7 | a0001c0001t0001g0119a0001c0001t0004g0108a0001c0001t0004g0114others(4): Show | 7 | NA18975.hp1 NA18980.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-15301G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793170 | ||||||
| chr2:223793176
|
G | A | 1 | a0001c0001t0004g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4-15307C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793176 | ||||||
| chr2:223793297
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4-15428G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793297 | ||||||
| chr2:223793355
|
G | A | 53 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(50): Show | 53 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.4-15486C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793355 | ||||||
| chr2:223793509
|
G | T | 1 | a0001c0001t0026g0319 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-15640C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793509 | ||||||
| chr2:223793519
|
T | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(195): Show | 199 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.4-15650A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793519 | ||||||
| chr2:223793708
|
A | T | 1 | a0001c0001t0020g0177 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4-15839T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793708 | ||||||
| chr2:223793759
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4-15890C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793759 | ||||||
| chr2:223793805
|
G | GT | 6 | a0001c0001t0001g0162a0001c0001t0004g0253a0001c0001t0005g0211others(3): Show | 6 | HG00738.hp2 HG03688.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-15937dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793805 | ||||||
| chr2:223793836
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4-15967C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223793836 | ||||||
| chr2:223794016
|
C | A | 52 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(49): Show | 52 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.4-16147G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794016 | ||||||
| chr2:223794191
|
T | C | 1 | a0001c0001t0016g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4-16322A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794191 | ||||||
| chr2:223794289
|
C | T | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4-16420G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794289 | ||||||
| chr2:223794310
|
G | A | 3 | a0001c0001t0003g0184a0001c0001t0028g0178a0001c0001t0060g0190 | 3 | HG02109.hp2 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4-16441C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794310 | ||||||
| chr2:223794322
|
C | T | 1 | a0001c0001t0058g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4-16453G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794322 | ||||||
| chr2:223794864
|
T | A | 84 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0191others(81): Show | 84 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.4-16995A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794864 | ||||||
| chr2:223794890
|
T | C | 1 | a0001c0001t0002g0309 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4-17021A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794890 | ||||||
| chr2:223794984
|
C | CAGTG | 3 | a0001c0001t0010g0237a0001c0001t0010g0274a0001c0001t0010g0275 | 3 | NA18964.hp2 NA19001.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4-17119_4-17116dup others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223794984 | ||||||
| chr2:223795087
|
T | C | 1 | a0001c0001t0003g0287 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4-17218A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795087 | ||||||
| chr2:223795110
|
G | A | 1 | a0001c0001t0027g0335 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4-17241C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795110 | ||||||
| chr2:223795190
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4-17321C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795190 | ||||||
| chr2:223795266
|
T | A | 16 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0001t0003g0198others(13): Show | 16 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.4-17397A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795266 | ||||||
| chr2:223795390
|
A | C | 1 | a0001c0001t0005g0299 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4-17521T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795390 | ||||||
| chr2:223795464
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4-17595T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795464 | ||||||
| chr2:223795544
|
G | A | 7 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(4): Show | 7 | HG00639.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-17675C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795544 | ||||||
| chr2:223795586
|
GCAGAAGG others(3): Show |
G | 1 | a0001c0001t0002g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-17727_4-17718del others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795586 | ||||||
| chr2:223795590
|
AAGGGGCC others(3): Show |
A | 270 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(267): Show | 271 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.4-17731_4-17722del others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795590 | ||||||
| chr2:223795603
|
G | A | 1 | a0001c0001t0007g0159 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4-17734C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795603 | ||||||
| chr2:223795604
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(267): Show | 271 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.4-17735G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795604 | ||||||
| chr2:223795769
|
T | A | 1 | a0001c0001t0002g0053 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4-17900A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795769 | ||||||
| chr2:223795993
|
C | A | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-18124G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795993 | ||||||
| chr2:223795994
|
G | A | 2 | a0001c0001t0008g0187a0001c0001t0015g0186 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4-18125C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223795994 | ||||||
| chr2:223796035
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4-18166G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796035 | ||||||
| chr2:223796156
|
CAG | C | 16 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0001t0003g0198others(13): Show | 16 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.4-18289_4-18288del others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796156 | ||||||
| chr2:223796248
|
A | G | 2 | a0001c0001t0004g0281a0001c0001t0023g0280 | 2 | HG02300.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4-18379T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796248 | ||||||
| chr2:223796255
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(194): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4-18386G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796255 | ||||||
| chr2:223796262
|
A | T | 7 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(4): Show | 7 | HG00639.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-18393T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796262 | ||||||
| chr2:223796509
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4-18640T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796509 | ||||||
| chr2:223796602
|
C | T | 2 | a0001c0001t0003g0092a0001c0001t0033g0093 | 2 | NA18999.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.4-18733G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796602 | ||||||
| chr2:223796654
|
T | A | 53 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0144others(50): Show | 53 | HG00423.hp1 HG01106.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.4-18785A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796654 | ||||||
| chr2:223796723
|
G | C | 1 | a0001c0001t0007g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4-18854C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796723 | ||||||
| chr2:223796776
|
G | A | 1 | a0001c0001t0050g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4-18907C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796776 | ||||||
| chr2:223796915
|
C | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0055others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.4-19046G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223796915 | ||||||
| chr2:223797113
|
T | C | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-19244A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797113 | ||||||
| chr2:223797116
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4-19247G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797116 | ||||||
| chr2:223797246
|
G | A | 3 | a0001c0001t0003g0184a0001c0001t0028g0178a0001c0001t0060g0190 | 3 | HG02109.hp2 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4-19377C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797246 | ||||||
| chr2:223797587
|
C | T | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-19718G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797587 | ||||||
| chr2:223797619
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4-19750C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797619 | ||||||
| chr2:223797619
|
G | T | 3 | a0001c0001t0002g0209a0001c0001t0006g0272a0001c0001t0049g0255 | 3 | NA18954.hp2 NA19002.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.4-19750C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797619 | ||||||
| chr2:223797661
|
G | A | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0012g0207others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-19792C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797661 | ||||||
| chr2:223797858
|
G | A | 7 | a0001c0001t0001g0144a0001c0001t0002g0189a0001c0001t0008g0230others(4): Show | 7 | HG01168.hp1 HG01884.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-19989C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797858 | ||||||
| chr2:223797987
|
T | C | 1 | a0001c0001t0017g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4-20118A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223797987 | ||||||
| chr2:223798009
|
C | T | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4-20140G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798009 | ||||||
| chr2:223798096
|
T | G | 1 | a0001c0001t0020g0137 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4-20227A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798096 | ||||||
| chr2:223798131
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0058others(202): Show | 206 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.4-20262G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798131 | ||||||
| chr2:223798177
|
A | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(209): Show | 213 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.4-20308T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798177 | ||||||
| chr2:223798277
|
G | A | 16 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0009g0040others(13): Show | 16 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.4-20408C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798277 | ||||||
| chr2:223798667
|
G | C | 4 | a0001c0001t0002g0189a0001c0001t0007g0337a0001c0001t0008g0187others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-20798C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798667 | ||||||
| chr2:223798745
|
C | G | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-20876G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798745 | ||||||
| chr2:223798747
|
C | G | 1 | a0001c0001t0019g0139 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4-20878G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798747 | ||||||
| chr2:223798773
|
T | C | 1 | a0001c0001t0052g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4-20904A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798773 | ||||||
| chr2:223798813
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0119others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.4-20944A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798813 | ||||||
| chr2:223798874
|
C | T | 1 | a0001c0001t0017g0212 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4-21005G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798874 | ||||||
| chr2:223798951
|
A | G | 1 | a0003c0004t0005g0277 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4-21082T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223798951 | ||||||
| chr2:223799003
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.4-21134G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799003 | ||||||
| chr2:223799027
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.4-21158G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799027 | ||||||
| chr2:223799028
|
G | A | 7 | a0001c0001t0001g0055a0001c0001t0001g0194a0001c0001t0001g0195others(4): Show | 7 | NA18946.hp2 NA18962.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-21159C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799028 | ||||||
| chr2:223799091
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(133): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.4-21222C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799091 | ||||||
| chr2:223799201
|
G | A | 3 | a0001c0001t0002g0196a0001c0001t0006g0286a0001c0001t0016g0288 | 3 | HG00673.hp1 NA18612.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4-21332C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799201 | ||||||
| chr2:223799208
|
G | GAC | 24 | a0001c0001t0001g0055a0001c0001t0001g0191a0001c0001t0001g0193others(21): Show | 24 | HG00140.hp1 HG01168.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.4-21341_4-21340dup others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
G | GACAC | 9 | a0001c0001t0001g0204a0001c0001t0005g0266a0001c0001t0005g0269others(6): Show | 9 | HG00099.hp2 HG00673.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.4-21343_4-21340dup others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
G | GACACAC | 58 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0162others(55): Show | 58 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.4-21345_4-21340dup others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
G | GACACACA others(1): Show |
9 | a0001c0001t0001g0084a0001c0001t0001g0250a0001c0001t0001g0302others(6): Show | 9 | HG01255.hp1 HG02698.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.4-21347_4-21340dup others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
G | GACACACA others(3): Show |
3 | a0001c0001t0006g0235a0001c0001t0014g0307a0001c0001t0055g0172 | 3 | HG02015.hp2 NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.4-21349_4-21340dup others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
GAC | G | 12 | a0001c0001t0002g0060a0001c0001t0002g0174a0001c0001t0003g0184others(9): Show | 12 | HG00639.hp1 HG02055.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.4-21341_4-21340del others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
GACAC | G | 41 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0222others(38): Show | 41 | HG00423.hp1 HG01891.hp2 HG01981.hp1 others(38): Show |
intron_variant | MODIFIER | c.4-21343_4-21340del others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
GACACAC | G | 8 | a0001c0001t0002g0004a0001c0001t0002g0085a0001c0001t0002g0087others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.4-21345_4-21340del others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
GACACACA others(5): Show |
G | 2 | a0001c0001t0047g0322a0001c0001t0056g0003 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4-21351_4-21340del others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
GACACACA others(7): Show |
G | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-21353_4-21340del others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
GACACACA others(9): Show |
G | 65 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(62): Show | 65 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.4-21355_4-21340del others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799208
|
GACACACA others(11): Show |
G | 68 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.4-21357_4-21340del others(18): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799208 | ||||||
| chr2:223799236
|
CACACACA others(8): Show |
C | 1 | a0001c0001t0003g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4-21382_4-21368del others(15): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799236 | ||||||
| chr2:223799333
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.4-21464G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799333 | ||||||
| chr2:223799690
|
T | C | 1 | a0001c0001t0068g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4-21821A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799690 | ||||||
| chr2:223799756
|
C | T | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0008g0176others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-21887G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799756 | ||||||
| chr2:223799790
|
A | C | 1 | a0001c0001t0068g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4-21921T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799790 | ||||||
| chr2:223799917
|
CAATT | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-22052_4-22049del others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223799917 | ||||||
| chr2:223800026
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-22157A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800026 | ||||||
| chr2:223800035
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-22166G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800035 | ||||||
| chr2:223800036
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-22167T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800036 | ||||||
| chr2:223800086
|
A | G | 1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4-22217T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800086 | ||||||
| chr2:223800112
|
TG | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.4-22244delC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800112 | ||||||
| chr2:223800213
|
TA | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.4-22345delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800213 | ||||||
| chr2:223800216
|
A | G | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-22347T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800216 | ||||||
| chr2:223800217
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.4-22348T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800217 | ||||||
| chr2:223800295
|
G | C | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | NA18747.hp1 NA18950.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-22426C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800295 | ||||||
| chr2:223800354
|
G | C | 56 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(53): Show | 56 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.4-22485C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800354 | ||||||
| chr2:223800400
|
C | T | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4-22531G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800400 | ||||||
| chr2:223800481
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4-22612C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800481 | ||||||
| chr2:223800531
|
T | TA | 137 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.4-22663dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800531 | ||||||
| chr2:223800641
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.4-22772A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800641 | ||||||
| chr2:223800669
|
G | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0034others(1): Show | 4 | HG02074.hp1 NA18957.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-22800C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800669 | ||||||
| chr2:223800852
|
G | A | 1 | a0001c0001t0014g0030 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4-22983C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800852 | ||||||
| chr2:223800862
|
G | T | 2 | a0001c0001t0007g0170a0001c0001t0007g0337 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4-22993C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800862 | ||||||
| chr2:223800940
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0002g0226a0001c0001t0003g0224 | 3 | HG00423.hp1 HG02165.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.4-23071A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800940 | ||||||
| chr2:223800977
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-23108T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223800977 | ||||||
| chr2:223801031
|
CCCTACTG others(42): Show |
C | 1 | a0001c0001t0029g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4-23211_4-23163del others(49): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801031 | ||||||
| chr2:223801246
|
G | A | 2 | a0001c0001t0003g0037a0001c0001t0011g0036 | 2 | NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.4-23377C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801246 | ||||||
| chr2:223801270
|
G | C | 1 | a0001c0001t0006g0329 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4-23401C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801270 | ||||||
| chr2:223801282
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4-23413G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801282 | ||||||
| chr2:223801318
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4-23449C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801318 | ||||||
| chr2:223801387
|
C | T | 1 | a0001c0001t0021g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4-23518G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801387 | ||||||
| chr2:223801664
|
G | A | 1 | a0001c0001t0029g0303 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4-23795C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801664 | ||||||
| chr2:223801683
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-23814C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801683 | ||||||
| chr2:223801731
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-23862T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801731 | ||||||
| chr2:223801740
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0002g0226a0001c0001t0003g0224 | 3 | HG00423.hp1 HG02165.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.4-23871C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801740 | ||||||
| chr2:223801991
|
A | G | 1 | a0001c0001t0072g0339 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4-24122T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223801991 | ||||||
| chr2:223802003
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4-24134T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802003 | ||||||
| chr2:223802105
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-24236G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802105 | ||||||
| chr2:223802109
|
G | T | 1 | a0001c0001t0020g0137 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4-24240C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802109 | ||||||
| chr2:223802113
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.4-24244G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802113 | ||||||
| chr2:223802269
|
G | A | 3 | a0001c0001t0004g0218a0001c0001t0004g0219a0001c0001t0004g0220 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.4-24400C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802269 | ||||||
| chr2:223802298
|
T | C | 1 | a0001c0001t0004g0009 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4-24429A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802298 | ||||||
| chr2:223802302
|
AT | A | 52 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(49): Show | 52 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.4-24434delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802302 | ||||||
| chr2:223802306
|
T | A | 2 | a0001c0001t0001g0267a0001c0001t0002g0004 | 2 | HG02257.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.4-24437A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802306 | ||||||
| chr2:223802306
|
TA | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(78): Show | 82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.4-24438delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802306 | ||||||
| chr2:223802307
|
A | T | 12 | a0001c0001t0001g0267a0001c0001t0002g0004a0001c0001t0004g0155others(9): Show | 12 | HG00738.hp1 HG01433.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.4-24438T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802307 | ||||||
| chr2:223802308
|
T | A | 1 | a0001c0001t0007g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4-24439A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802308 | ||||||
| chr2:223802446
|
G | T | 51 | a0001c0001t0001g0055a0001c0001t0001g0191a0001c0001t0001g0192others(48): Show | 51 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.4-24577C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802446 | ||||||
| chr2:223802447
|
C | T | 51 | a0001c0001t0001g0055a0001c0001t0001g0191a0001c0001t0001g0192others(48): Show | 51 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.4-24578G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802447 | ||||||
| chr2:223802719
|
T | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0050others(2): Show | 5 | NA18965.hp1 NA18985.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-24850A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802719 | ||||||
| chr2:223802975
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4-25106C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223802975 | ||||||
| chr2:223803091
|
T | C | 1 | a0001c0001t0015g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4-25222A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803091 | ||||||
| chr2:223803318
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.4-25449C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803318 | ||||||
| chr2:223803363
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4-25494C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803363 | ||||||
| chr2:223803582
|
A | G | 1 | a0001c0001t0005g0266 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4-25713T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803582 | ||||||
| chr2:223803650
|
T | C | 3 | a0001c0001t0003g0184a0001c0001t0028g0178a0001c0001t0060g0190 | 3 | HG02109.hp2 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4-25781A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803650 | ||||||
| chr2:223803785
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0204a0001c0001t0001g0239 | 3 | NA18942.hp2 NA18964.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.4-25916G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803785 | ||||||
| chr2:223803850
|
A | G | 7 | a0001c0001t0002g0004a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-25981T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803850 | ||||||
| chr2:223803866
|
C | T | 1 | a0001c0001t0005g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4-25997G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803866 | ||||||
| chr2:223803879
|
C | CA | 10 | a0001c0001t0001g0192a0001c0001t0002g0041a0001c0001t0002g0097others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-26011dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803879 | ||||||
| chr2:223803879
|
CA | C | 78 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.4-26011delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803879 | ||||||
| chr2:223803898
|
T | A | 1 | a0001c0001t0017g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4-26029A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803898 | ||||||
| chr2:223803950
|
G | A | 1 | a0001c0001t0022g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4-26081C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223803950 | ||||||
| chr2:223804433
|
T | G | 1 | a0001c0001t0041g0260 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4-26564A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804433 | ||||||
| chr2:223804434
|
C | T | 1 | a0001c0001t0005g0199 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4-26565G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804434 | ||||||
| chr2:223804712
|
T | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(76): Show | 80 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.4-26843A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804712 | ||||||
| chr2:223804717
|
C | CA | 14 | a0001c0001t0002g0004a0001c0001t0002g0309a0001c0001t0002g0310others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4-26849dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804717 | ||||||
| chr2:223804717
|
CA | C | 6 | a0001c0001t0002g0007a0001c0001t0002g0163a0001c0001t0002g0196others(3): Show | 6 | HG02523.hp1 HG02897.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-26849delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804717 | ||||||
| chr2:223804821
|
TTA | T | 5 | a0001c0001t0009g0166a0001c0001t0009g0167a0001c0001t0009g0168others(2): Show | 5 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-26954_4-26953del others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804821 | ||||||
| chr2:223804833
|
G | A | 7 | a0001c0001t0006g0026a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-26964C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804833 | ||||||
| chr2:223804953
|
G | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.4-27084C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223804953 | ||||||
| chr2:223805113
|
T | G | 1 | a0001c0001t0004g0108 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4-27244A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805113 | ||||||
| chr2:223805168
|
G | A | 5 | a0001c0001t0009g0166a0001c0001t0009g0167a0001c0001t0009g0168others(2): Show | 5 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-27299C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805168 | ||||||
| chr2:223805175
|
A | ACGC | 5 | a0001c0001t0009g0166a0001c0001t0009g0167a0001c0001t0009g0168others(2): Show | 5 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-27309_4-27307dup others(3): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805175 | ||||||
| chr2:223805237
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0050others(3): Show | 6 | NA18965.hp1 NA18985.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-27368C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805237 | ||||||
| chr2:223805335
|
C | T | 1 | a0001c0001t0003g0287 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4-27466G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805335 | ||||||
| chr2:223805367
|
A | G | 7 | a0001c0001t0002g0004a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-27498T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805367 | ||||||
| chr2:223805519
|
A | G | 2 | a0001c0001t0007g0170a0001c0001t0007g0337 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4-27650T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805519 | ||||||
| chr2:223805631
|
A | G | 1 | a0001c0001t0017g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4-27762T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805631 | ||||||
| chr2:223805681
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.4-27812G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805681 | ||||||
| chr2:223805695
|
T | C | 1 | a0001c0001t0016g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4-27826A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805695 | ||||||
| chr2:223805784
|
A | T | 40 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0222others(37): Show | 40 | HG00423.hp1 HG01106.hp2 HG01981.hp1 others(37): Show |
intron_variant | MODIFIER | c.4-27915T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805784 | ||||||
| chr2:223805869
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4-28000T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223805869 | ||||||
| chr2:223806277
|
A | AT | 26 | a0001c0001t0001g0296a0001c0001t0002g0014a0001c0001t0002g0041others(23): Show | 26 | HG00735.hp1 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.4-28409dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806277 | ||||||
| chr2:223806277
|
A | ATT | 47 | a0001c0001t0001g0055a0001c0001t0001g0191a0001c0001t0001g0192others(44): Show | 47 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.4-28410_4-28409dup others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806277 | ||||||
| chr2:223806277
|
AT | A | 12 | a0001c0001t0001g0094a0001c0001t0001g0271a0001c0001t0003g0016others(9): Show | 12 | HG02080.hp1 HG02148.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.4-28409delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806277 | ||||||
| chr2:223806277
|
ATT | A | 52 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0327others(49): Show | 52 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.4-28410_4-28409del others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806277 | ||||||
| chr2:223806277
|
ATTTT | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(67): Show | 71 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.4-28412_4-28409del others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806277 | ||||||
| chr2:223806277
|
ATTTTT | A | 11 | a0001c0001t0002g0004a0001c0001t0004g0113a0001c0001t0008g0187others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.4-28413_4-28409del others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806277 | ||||||
| chr2:223806409
|
G | A | 1 | a0001c0001t0007g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4-28540C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806409 | ||||||
| chr2:223806879
|
G | GT | 9 | a0001c0001t0008g0233a0001c0001t0012g0207a0001c0001t0015g0217others(6): Show | 9 | HG00639.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.4-29011dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806879 | ||||||
| chr2:223806935
|
G | A | 1 | a0001c0001t0022g0101 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4-29066C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223806935 | ||||||
| chr2:223807087
|
G | A | 1 | a0001c0001t0002g0309 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4-29218C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807087 | ||||||
| chr2:223807253
|
T | C | 7 | a0001c0001t0002g0004a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-29384A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807253 | ||||||
| chr2:223807283
|
G | C | 1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4-29414C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807283 | ||||||
| chr2:223807429
|
T | C | 1 | a0001c0001t0026g0319 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-29560A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807429 | ||||||
| chr2:223807519
|
T | C | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0008g0176others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-29650A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807519 | ||||||
| chr2:223807718
|
T | C | 21 | a0001c0001t0001g0032a0001c0001t0002g0007a0001c0001t0003g0010others(18): Show | 21 | HG00544.hp2 HG01978.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.3+29730A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807718 | ||||||
| chr2:223807838
|
T | C | 1 | a0001c0001t0003g0019 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3+29610A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807838 | ||||||
| chr2:223807867
|
C | CT | 16 | a0001c0001t0001g0194a0001c0001t0001g0201a0001c0001t0001g0203others(13): Show | 16 | HG01192.hp2 HG02027.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.3+29580dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223807867
|
C | CTTT | 26 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(23): Show | 26 | HG01109.hp2 HG01168.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.3+29578_3+29580dup others(3): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223807867
|
C | CTTTT | 40 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(37): Show | 41 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.3+29577_3+29580dup others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223807867
|
C | CTTTTT | 13 | a0001c0001t0001g0257a0001c0001t0002g0309a0001c0001t0003g0018others(10): Show | 13 | HG01255.hp2 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3+29576_3+29580dup others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223807867
|
C | CTTTTTT | 27 | a0001c0001t0001g0032a0001c0001t0002g0007a0001c0001t0002g0310others(24): Show | 27 | HG00544.hp2 HG00609.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.3+29575_3+29580dup others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223807867
|
C | CTTTTTTT | 20 | a0001c0001t0001g0043a0001c0001t0003g0011a0001c0001t0003g0020others(17): Show | 20 | HG01261.hp2 HG01978.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.3+29574_3+29580dup others(7): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223807867
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0002g0330a0001c0001t0003g0056a0001c0001t0005g0328others(5): Show | 8 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+29573_3+29580dup others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223807867
|
CT | C | 46 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0058others(43): Show | 46 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.3+29580delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223807867 | ||||||
| chr2:223808017
|
G | A | 2 | a0001c0001t0003g0037a0001c0001t0011g0036 | 2 | NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3+29431C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808017 | ||||||
| chr2:223808269
|
A | G | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3+29179T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808269 | ||||||
| chr2:223808277
|
C | T | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+29171G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808277 | ||||||
| chr2:223808283
|
T | C | 1 | a0001c0001t0026g0241 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3+29165A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808283 | ||||||
| chr2:223808298
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(80): Show | 84 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.3+29150A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808298 | ||||||
| chr2:223808530
|
C | T | 6 | a0001c0001t0002g0189a0001c0001t0008g0187a0001c0001t0011g0200others(3): Show | 6 | HG02280.hp2 HG02559.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+28918G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808530 | ||||||
| chr2:223808666
|
T | G | 1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3+28782A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808666 | ||||||
| chr2:223808685
|
T | C | 3 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0016g0045 | 3 | NA18983.hp1 NA18994.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.3+28763A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808685 | ||||||
| chr2:223808743
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3+28705G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808743 | ||||||
| chr2:223808862
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(70): Show | 74 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.3+28586C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223808862 | ||||||
| chr2:223809160
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3+28288T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809160 | ||||||
| chr2:223809186
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0017g0185 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3+28262G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809186 | ||||||
| chr2:223809218
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3+28230C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809218 | ||||||
| chr2:223809269
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3+28179A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809269 | ||||||
| chr2:223809537
|
C | T | 6 | a0001c0001t0009g0166a0001c0001t0009g0167a0001c0001t0009g0168others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+27911G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809537 | ||||||
| chr2:223809566
|
C | A | 2 | a0001c0001t0004g0124a0001c0001t0066g0161 | 2 | NA18991.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3+27882G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809566 | ||||||
| chr2:223809569
|
G | A | 1 | a0001c0001t0007g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3+27879C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809569 | ||||||
| chr2:223809600
|
C | T | 6 | a0001c0001t0009g0166a0001c0001t0009g0167a0001c0001t0009g0168others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+27848G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809600 | ||||||
| chr2:223809623
|
G | C | 1 | a0001c0001t0003g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3+27825C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809623 | ||||||
| chr2:223809717
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3+27731C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809717 | ||||||
| chr2:223809732
|
AT | A | 11 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0085others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+27715delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809732 | ||||||
| chr2:223809735
|
T | TA | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0017g0096others(3): Show | 6 | HG02630.hp2 HG02965.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+27712_3+27713ins others(1): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809735 | ||||||
| chr2:223809736
|
T | A | 60 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(57): Show | 60 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3+27712A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809736 | ||||||
| chr2:223809737
|
T | A | 8 | a0001c0001t0002g0004a0001c0001t0009g0166a0001c0001t0009g0167others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+27711A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809737 | ||||||
| chr2:223809792
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.3+27656C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809792 | ||||||
| chr2:223809819
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.3+27629G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809819 | ||||||
| chr2:223809843
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0017g0185 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3+27605G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809843 | ||||||
| chr2:223809885
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(70): Show | 74 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.3+27563G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809885 | ||||||
| chr2:223809918
|
A | G | 1 | a0001c0001t0048g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3+27530T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809918 | ||||||
| chr2:223809954
|
C | T | 2 | a0001c0001t0004g0281a0001c0001t0023g0280 | 2 | HG02300.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3+27494G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809954 | ||||||
| chr2:223809990
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3+27458C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223809990 | ||||||
| chr2:223810021
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+27427G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810021 | ||||||
| chr2:223810098
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+27350G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810098 | ||||||
| chr2:223810151
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+27297C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810151 | ||||||
| chr2:223810189
|
A | G | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+27259T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810189 | ||||||
| chr2:223810411
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0017g0185 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3+27037G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810411 | ||||||
| chr2:223810444
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3+27004C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810444 | ||||||
| chr2:223810472
|
C | A | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+26976G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810472 | ||||||
| chr2:223810483
|
A | G | 1 | a0001c0001t0058g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3+26965T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810483 | ||||||
| chr2:223810591
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+26857C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810591 | ||||||
| chr2:223810737
|
T | C | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+26711A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810737 | ||||||
| chr2:223810739
|
CA | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.3+26708delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810739 | ||||||
| chr2:223810778
|
G | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.3+26670C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810778 | ||||||
| chr2:223810831
|
A | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+26617T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810831 | ||||||
| chr2:223810963
|
A | T | 2 | a0001c0001t0002g0179a0001c0001t0017g0185 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3+26485T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223810963 | ||||||
| chr2:223811001
|
A | G | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+26447T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811001 | ||||||
| chr2:223811036
|
G | T | 3 | a0001c0001t0002g0098a0001c0001t0002g0154a0001c0001t0012g0099 | 3 | HG01496.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3+26412C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811036 | ||||||
| chr2:223811096
|
CT | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.3+26351delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811096 | ||||||
| chr2:223811183
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3+26265C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811183 | ||||||
| chr2:223811183
|
G | T | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+26265C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811183 | ||||||
| chr2:223811295
|
C | T | 1 | a0001c0001t0017g0212 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3+26153G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811295 | ||||||
| chr2:223811321
|
A | T | 1 | a0001c0001t0022g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3+26127T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811321 | ||||||
| chr2:223811436
|
G | A | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+26012C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811436 | ||||||
| chr2:223811568
|
C | CA | 86 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.3+25879dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811568 | ||||||
| chr2:223811680
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+25768C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811680 | ||||||
| chr2:223811711
|
C | A | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+25737G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811711 | ||||||
| chr2:223811870
|
A | G | 1 | a0001c0001t0004g0009 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3+25578T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811870 | ||||||
| chr2:223811970
|
C | T | 2 | a0001c0001t0021g0336a0001c0001t0070g0308 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3+25478G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223811970 | ||||||
| chr2:223812054
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+25394T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812054 | ||||||
| chr2:223812149
|
T | C | 1 | a0001c0001t0003g0029 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3+25299A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812149 | ||||||
| chr2:223812155
|
A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+25293T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812155 | ||||||
| chr2:223812341
|
C | G | 1 | a0001c0001t0010g0325 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3+25107G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812341 | ||||||
| chr2:223812368
|
C | T | 1 | a0001c0001t0068g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3+25080G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812368 | ||||||
| chr2:223812456
|
A | G | 1 | a0001c0001t0051g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3+24992T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812456 | ||||||
| chr2:223812468
|
C | T | 6 | a0001c0001t0003g0017a0001c0001t0003g0019a0001c0001t0003g0020others(3): Show | 6 | HG02074.hp1 NA18957.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+24980G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812468 | ||||||
| chr2:223812498
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+24950T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812498 | ||||||
| chr2:223812595
|
T | C | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+24853A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812595 | ||||||
| chr2:223812610
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0002g0049others(2): Show | 5 | NA18955.hp2 NA18985.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+24838C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812610 | ||||||
| chr2:223812637
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.3+24811A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812637 | ||||||
| chr2:223812651
|
T | G | 1 | a0001c0001t0026g0319 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+24797A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812651 | ||||||
| chr2:223812707
|
A | G | 4 | a0001c0001t0002g0097a0001c0001t0002g0109a0001c0001t0002g0153others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+24741T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812707 | ||||||
| chr2:223812912
|
A | G | 1 | a0001c0001t0038g0278 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3+24536T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812912 | ||||||
| chr2:223812921
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+24527C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223812921 | ||||||
| chr2:223813073
|
C | T | 9 | a0001c0001t0002g0004a0001c0001t0007g0170a0001c0001t0009g0166others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+24375G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813073 | ||||||
| chr2:223813087
|
C | A | 9 | a0001c0001t0002g0004a0001c0001t0007g0170a0001c0001t0009g0166others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+24361G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813087 | ||||||
| chr2:223813210
|
G | A | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+24238C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813210 | ||||||
| chr2:223813278
|
A | C | 2 | a0001c0001t0017g0096a0001c0001t0060g0190 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3+24170T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813278 | ||||||
| chr2:223813300
|
G | A | 11 | a0001c0001t0002g0004a0001c0001t0007g0170a0001c0001t0009g0166others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+24148C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813300 | ||||||
| chr2:223813408
|
G | A | 7 | a0001c0001t0007g0170a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+24040C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813408 | ||||||
| chr2:223813625
|
G | A | 1 | a0001c0001t0057g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3+23823C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813625 | ||||||
| chr2:223813637
|
T | C | 4 | a0001c0001t0009g0181a0001c0001t0009g0183a0001c0001t0012g0180others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+23811A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813637 | ||||||
| chr2:223813788
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3+23660C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813788 | ||||||
| chr2:223813907
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3+23541A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223813907 | ||||||
| chr2:223814548
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(78): Show | 82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3+22900A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814548 | ||||||
| chr2:223814549
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+22899C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814549 | ||||||
| chr2:223814593
|
C | T | 57 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(54): Show | 57 | HG00423.hp1 HG00639.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.3+22855G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814593 | ||||||
| chr2:223814607
|
G | A | 1 | a0001c0001t0005g0269 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3+22841C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814607 | ||||||
| chr2:223814622
|
A | G | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+22826T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814622 | ||||||
| chr2:223814713
|
A | G | 8 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0008g0176others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+22735T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814713 | ||||||
| chr2:223814718
|
C | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(190): Show | 194 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.3+22730G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814718 | ||||||
| chr2:223814790
|
A | C | 1 | a0001c0001t0004g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3+22658T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814790 | ||||||
| chr2:223814803
|
G | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0258a0001c0001t0001g0267others(2): Show | 5 | HG00423.hp2 HG02015.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+22645C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814803 | ||||||
| chr2:223814865
|
C | A | 1 | a0001c0001t0021g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3+22583G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814865 | ||||||
| chr2:223814930
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.3+22518A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223814930 | ||||||
| chr2:223815106
|
A | G | 2 | a0001c0001t0007g0337a0001c0001t0026g0319 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3+22342T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815106 | ||||||
| chr2:223815122
|
C | A | 7 | a0001c0001t0007g0170a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+22326G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815122 | ||||||
| chr2:223815210
|
G | GA | 5 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0002g0049others(2): Show | 5 | NA18955.hp2 NA18985.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+22237dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815210 | ||||||
| chr2:223815233
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0006g0235 | 2 | HG02015.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3+22215C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815233 | ||||||
| chr2:223815234
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+22214G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815234 | ||||||
| chr2:223815258
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+22190T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815258 | ||||||
| chr2:223815417
|
G | GC | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+22030dupG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815417 | ||||||
| chr2:223815451
|
C | T | 7 | a0001c0001t0007g0170a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+21997G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815451 | ||||||
| chr2:223815657
|
T | C | 1 | a0001c0001t0004g0009 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3+21791A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815657 | ||||||
| chr2:223815867
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+21581G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815867 | ||||||
| chr2:223815875
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(191): Show | 195 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.3+21573A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815875 | ||||||
| chr2:223815918
|
T | A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+21530A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223815918 | ||||||
| chr2:223816143
|
C | T | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+21305G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816143 | ||||||
| chr2:223816225
|
C | T | 1 | a0001c0001t0037g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3+21223G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816225 | ||||||
| chr2:223816330
|
C | T | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+21118G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816330 | ||||||
| chr2:223816340
|
GA | G | 122 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(119): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3+21107delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816340 | ||||||
| chr2:223816340
|
GAAA | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+21105_3+21107del others(3): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816340 | ||||||
| chr2:223816397
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+21051G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816397 | ||||||
| chr2:223816500
|
A | G | 1 | a0001c0001t0021g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3+20948T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816500 | ||||||
| chr2:223816529
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3+20919G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816529 | ||||||
| chr2:223816743
|
C | G | 1 | a0001c0001t0003g0019 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3+20705G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816743 | ||||||
| chr2:223816860
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3+20588C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816860 | ||||||
| chr2:223816910
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.3+20538G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816910 | ||||||
| chr2:223816993
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(78): Show | 82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3+20455A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223816993 | ||||||
| chr2:223817015
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+20433G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817015 | ||||||
| chr2:223817016
|
G | A | 1 | a0001c0001t0033g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+20432C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817016 | ||||||
| chr2:223817088
|
G | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+20360C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817088 | ||||||
| chr2:223817345
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+20103T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817345 | ||||||
| chr2:223817410
|
A | G | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+20038T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817410 | ||||||
| chr2:223817438
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3+20010C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817438 | ||||||
| chr2:223817477
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19971T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817477 | ||||||
| chr2:223817479
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19969T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817479 | ||||||
| chr2:223817480
|
T | C | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19968A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817480 | ||||||
| chr2:223817488
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19960T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817488 | ||||||
| chr2:223817494
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19954T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817494 | ||||||
| chr2:223817501
|
G | A | 7 | a0001c0001t0007g0170a0001c0001t0009g0166a0001c0001t0009g0167others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+19947C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817501 | ||||||
| chr2:223817514
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19934T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817514 | ||||||
| chr2:223817522
|
T | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19926A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817522 | ||||||
| chr2:223817525
|
T | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19923A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817525 | ||||||
| chr2:223817539
|
T | C | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19909A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817539 | ||||||
| chr2:223817544
|
G | C | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19904C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817544 | ||||||
| chr2:223817557
|
G | A | 2 | a0001c0001t0006g0289a0001c0001t0006g0301 | 2 | NA18953.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3+19891C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817557 | ||||||
| chr2:223817562
|
C | T | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19886G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817562 | ||||||
| chr2:223817565
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19883T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817565 | ||||||
| chr2:223817569
|
T | C | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19879A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817569 | ||||||
| chr2:223817583
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19865T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817583 | ||||||
| chr2:223817594
|
A | T | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19854T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817594 | ||||||
| chr2:223817595
|
C | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19853G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817595 | ||||||
| chr2:223817603
|
G | A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19845C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817603 | ||||||
| chr2:223817607
|
C | CA | 6 | a0001c0001t0001g0250a0001c0001t0009g0181a0001c0001t0009g0183others(3): Show | 6 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+19840dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817607 | ||||||
| chr2:223817607
|
C | CAAAAA | 6 | a0001c0001t0002g0179a0001c0001t0003g0018a0001c0001t0005g0088others(3): Show | 6 | HG02451.hp2 HG02523.hp2 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+19836_3+19840dup others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817607 | ||||||
| chr2:223817607
|
C | CAAAAAA | 99 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0050others(96): Show | 99 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.3+19835_3+19840dup others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817607 | ||||||
| chr2:223817621
|
A | AG | 71 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(68): Show | 72 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.3+19826_3+19827ins others(1): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817621 | ||||||
| chr2:223817623
|
AAGAAAAG others(491): Show |
A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19327_3+19824del | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817623 | ||||||
| chr2:223817649
|
T | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+19799A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817649 | ||||||
| chr2:223817675
|
G | A | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0008g0176others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+19773C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817675 | ||||||
| chr2:223817701
|
G | A | 1 | a0001c0001t0002g0330 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+19747C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817701 | ||||||
| chr2:223817768
|
A | G | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+19680T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817768 | ||||||
| chr2:223817849
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3+19599G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817849 | ||||||
| chr2:223817950
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+19498A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817950 | ||||||
| chr2:223817960
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+19488C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817960 | ||||||
| chr2:223817991
|
C | A | 5 | a0001c0001t0001g0261a0001c0001t0002g0209a0001c0001t0005g0266others(2): Show | 5 | NA18951.hp2 NA18954.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+19457G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223817991 | ||||||
| chr2:223818042
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+19406C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818042 | ||||||
| chr2:223818123
|
T | A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19325A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818123 | ||||||
| chr2:223818144
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+19304G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818144 | ||||||
| chr2:223818377
|
A | G | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+19071T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818377 | ||||||
| chr2:223818396
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+19052T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818396 | ||||||
| chr2:223818422
|
C | CAA | 181 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3+19024_3+19025dup others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818422 | ||||||
| chr2:223818436
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+19012C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818436 | ||||||
| chr2:223818450
|
G | C | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+18998C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818450 | ||||||
| chr2:223818488
|
G | A | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3+18960C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818488 | ||||||
| chr2:223818524
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(186): Show | 190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3+18924A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818524 | ||||||
| chr2:223818637
|
C | T | 115 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(112): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3+18811G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818637 | ||||||
| chr2:223818645
|
T | A | 2 | a0001c0001t0008g0187a0001c0001t0015g0186 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3+18803A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818645 | ||||||
| chr2:223818755
|
T | C | 101 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(98): Show | 101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.3+18693A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223818755 | ||||||
| chr2:223819439
|
G | A | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3+18009C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819439 | ||||||
| chr2:223819518
|
T | G | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3+17930A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819518 | ||||||
| chr2:223819598
|
T | TA | 106 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(103): Show | 106 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.3+17849dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819598 | ||||||
| chr2:223819598
|
TA | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(85): Show | 89 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.3+17849delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819598 | ||||||
| chr2:223819621
|
C | CCTA | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+17824_3+17826dup others(3): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819621 | ||||||
| chr2:223819675
|
C | T | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+17773G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819675 | ||||||
| chr2:223819683
|
C | T | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+17765G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819683 | ||||||
| chr2:223819778
|
A | G | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+17670T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819778 | ||||||
| chr2:223819812
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+17636A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819812 | ||||||
| chr2:223819904
|
T | A | 110 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(107): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.3+17544A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819904 | ||||||
| chr2:223819931
|
TA | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.3+17516delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819931 | ||||||
| chr2:223819931
|
TAA | T | 116 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.3+17515_3+17516del others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819931 | ||||||
| chr2:223819973
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+17475C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819973 | ||||||
| chr2:223819985
|
A | ATCAGTG | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+17462_3+17463ins others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223819985 | ||||||
| chr2:223820168
|
GT | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+17279delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820168 | ||||||
| chr2:223820169
|
T | C | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+17279A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820169 | ||||||
| chr2:223820251
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+17197G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820251 | ||||||
| chr2:223820267
|
G | A | 45 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0057others(42): Show | 45 | HG00609.hp1 HG01106.hp2 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.3+17181C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820267 | ||||||
| chr2:223820327
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(186): Show | 190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3+17121A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820327 | ||||||
| chr2:223820399
|
G | A | 6 | a0001c0001t0007g0170a0001c0001t0009g0166a0001c0001t0009g0167others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+17049C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820399 | ||||||
| chr2:223820549
|
C | CA | 63 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.3+16898dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820549 | ||||||
| chr2:223820556
|
A | C | 1 | a0001c0001t0001g0304 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3+16892T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820556 | ||||||
| chr2:223820617
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+16831A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820617 | ||||||
| chr2:223820620
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(186): Show | 190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3+16828T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820620 | ||||||
| chr2:223820644
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+16804A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820644 | ||||||
| chr2:223820668
|
G | GA | 8 | a0001c0001t0001g0070a0001c0001t0001g0119a0001c0001t0002g0041others(5): Show | 8 | HG02293.hp1 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+16779dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820668 | ||||||
| chr2:223820668
|
G | GAA | 71 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0121others(68): Show | 72 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.3+16778_3+16779dup others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820668 | ||||||
| chr2:223820669
|
A | G | 3 | a0001c0001t0009g0167a0001c0001t0009g0169a0001c0001t0054g0005 | 3 | HG02630.hp1 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3+16779T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820669 | ||||||
| chr2:223820797
|
G | A | 2 | a0001c0001t0012g0207a0001c0001t0015g0217 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.3+16651C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820797 | ||||||
| chr2:223820836
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(186): Show | 190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3+16612A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820836 | ||||||
| chr2:223820837
|
C | T | 110 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(107): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.3+16611G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820837 | ||||||
| chr2:223820876
|
C | A | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+16572G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223820876 | ||||||
| chr2:223821006
|
C | T | 103 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(100): Show | 103 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.3+16442G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821006 | ||||||
| chr2:223821103
|
T | C | 2 | a0001c0001t0021g0336a0001c0001t0070g0308 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3+16345A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821103 | ||||||
| chr2:223821192
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3+16256G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821192 | ||||||
| chr2:223821193
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0017g0185 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3+16255C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821193 | ||||||
| chr2:223821372
|
G | C | 1 | a0001c0001t0001g0327 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3+16076C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821372 | ||||||
| chr2:223821483
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+15965T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821483 | ||||||
| chr2:223821515
|
T | C | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+15933A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821515 | ||||||
| chr2:223821520
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+15928G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821520 | ||||||
| chr2:223821685
|
C | T | 103 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(100): Show | 103 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.3+15763G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821685 | ||||||
| chr2:223821692
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+15756C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821692 | ||||||
| chr2:223821697
|
C | T | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+15751G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821697 | ||||||
| chr2:223821797
|
C | T | 3 | a0001c0001t0002g0196a0001c0001t0006g0286a0001c0001t0016g0288 | 3 | HG00673.hp1 NA18612.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3+15651G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821797 | ||||||
| chr2:223821811
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+15637T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821811 | ||||||
| chr2:223821831
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3+15617C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821831 | ||||||
| chr2:223821932
|
GA | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+15515delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821932 | ||||||
| chr2:223821971
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3+15477C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821971 | ||||||
| chr2:223821978
|
C | A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+15470G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223821978 | ||||||
| chr2:223822001
|
A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+15447T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822001 | ||||||
| chr2:223822174
|
G | A | 2 | a0001c0001t0012g0207a0001c0001t0015g0217 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.3+15274C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822174 | ||||||
| chr2:223822177
|
C | G | 115 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(112): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3+15271G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822177 | ||||||
| chr2:223822244
|
T | A | 115 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(112): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3+15204A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822244 | ||||||
| chr2:223822261
|
C | T | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+15187G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822261 | ||||||
| chr2:223822283
|
T | C | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+15165A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822283 | ||||||
| chr2:223822377
|
T | C | 1 | a0001c0001t0057g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3+15071A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822377 | ||||||
| chr2:223822412
|
C | T | 115 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(112): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3+15036G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822412 | ||||||
| chr2:223822512
|
T | C | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+14936A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822512 | ||||||
| chr2:223822587
|
G | A | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3+14861C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822587 | ||||||
| chr2:223822632
|
C | T | 39 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(36): Show | 39 | HG00423.hp1 HG01192.hp1 HG02071.hp1 others(36): Show |
intron_variant | MODIFIER | c.3+14816G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822632 | ||||||
| chr2:223822700
|
G | A | 2 | a0001c0001t0012g0207a0001c0001t0015g0217 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.3+14748C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822700 | ||||||
| chr2:223822829
|
T | C | 1 | a0001c0001t0009g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3+14619A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822829 | ||||||
| chr2:223822916
|
A | C | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3+14532T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822916 | ||||||
| chr2:223822916
|
A | T | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+14532T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822916 | ||||||
| chr2:223822922
|
A | G | 10 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0138others(7): Show | 10 | HG01168.hp1 HG01243.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+14526T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822922 | ||||||
| chr2:223822925
|
G | T | 6 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0007g0337others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+14523C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822925 | ||||||
| chr2:223822984
|
A | G | 49 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0057others(46): Show | 49 | HG00609.hp1 HG01106.hp2 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.3+14464T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223822984 | ||||||
| chr2:223823349
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.3+14099C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823349 | ||||||
| chr2:223823350
|
T | C | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+14098A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823350 | ||||||
| chr2:223823382
|
T | C | 1 | a0001c0001t0002g0330 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+14066A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823382 | ||||||
| chr2:223823399
|
T | C | 10 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(7): Show | 10 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+14049A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823399 | ||||||
| chr2:223823459
|
C | T | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+13989G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823459 | ||||||
| chr2:223823535
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.3+13913A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823535 | ||||||
| chr2:223823581
|
C | A | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3+13867G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823581 | ||||||
| chr2:223823648
|
C | G | 113 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(110): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3+13800G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823648 | ||||||
| chr2:223823691
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3+13757A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823691 | ||||||
| chr2:223823850
|
C | T | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+13598G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823850 | ||||||
| chr2:223823933
|
A | C | 6 | a0001c0001t0017g0210a0001c0001t0017g0212a0001c0001t0031g0215others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+13515T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823933 | ||||||
| chr2:223823993
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+13455G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223823993 | ||||||
| chr2:223824015
|
G | A | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+13433C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824015 | ||||||
| chr2:223824027
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+13421C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824027 | ||||||
| chr2:223824176
|
T | G | 1 | a0001c0001t0052g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3+13272A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824176 | ||||||
| chr2:223824195
|
G | GT | 113 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(110): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3+13252dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824195 | ||||||
| chr2:223824219
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3+13229G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824219 | ||||||
| chr2:223824222
|
C | T | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+13226G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824222 | ||||||
| chr2:223824288
|
C | G | 9 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(6): Show | 9 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+13160G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824288 | ||||||
| chr2:223824326
|
C | T | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+13122G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824326 | ||||||
| chr2:223824342
|
T | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3+13106A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824342 | ||||||
| chr2:223824506
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3+12942T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824506 | ||||||
| chr2:223824522
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3+12926T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824522 | ||||||
| chr2:223824548
|
G | A | 2 | a0001c0001t0019g0139a0001c0001t0020g0140 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3+12900C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824548 | ||||||
| chr2:223824550
|
GTT | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3+12896_3+12897del others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824550 | ||||||
| chr2:223824603
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+12845A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824603 | ||||||
| chr2:223824721
|
G | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(185): Show | 189 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3+12727C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824721 | ||||||
| chr2:223824780
|
C | G | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+12668G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824780 | ||||||
| chr2:223824782
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.3+12666C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824782 | ||||||
| chr2:223824851
|
C | A | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3+12597G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824851 | ||||||
| chr2:223824943
|
C | A | 113 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(110): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3+12505G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223824943 | ||||||
| chr2:223825024
|
C | T | 107 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(104): Show | 107 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.3+12424G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825024 | ||||||
| chr2:223825028
|
G | C | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+12420C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825028 | ||||||
| chr2:223825034
|
G | A | 1 | a0001c0001t0003g0270 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3+12414C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825034 | ||||||
| chr2:223825046
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.3+12402T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825046 | ||||||
| chr2:223825088
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(183): Show | 187 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3+12360C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825088 | ||||||
| chr2:223825095
|
G | A | 6 | a0001c0001t0007g0170a0001c0001t0009g0166a0001c0001t0009g0167others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+12353C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825095 | ||||||
| chr2:223825206
|
C | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(189): Show | 193 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.3+12242G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825206 | ||||||
| chr2:223825230
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+12218C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825230 | ||||||
| chr2:223825235
|
C | T | 4 | a0001c0001t0008g0243a0001c0001t0026g0241a0001c0001t0030g0240others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+12213G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825235 | ||||||
| chr2:223825270
|
G | C | 101 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(98): Show | 101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.3+12178C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825270 | ||||||
| chr2:223825291
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(183): Show | 187 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3+12157A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825291 | ||||||
| chr2:223825299
|
G | C | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3+12149C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825299 | ||||||
| chr2:223825312
|
C | CAA | 110 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(107): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.3+12134_3+12135dup others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825312 | ||||||
| chr2:223825312
|
C | CAAA | 13 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(10): Show | 13 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3+12133_3+12135dup others(3): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825312 | ||||||
| chr2:223825312
|
C | CAAAA | 63 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.3+12132_3+12135dup others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825312 | ||||||
| chr2:223825378
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0003g0052a0001c0001t0003g0056others(1): Show | 4 | HG03490.hp2 NA18970.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+12070A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825378 | ||||||
| chr2:223825551
|
C | T | 3 | a0001c0001t0004g0218a0001c0001t0004g0219a0001c0001t0004g0220 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.3+11897G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825551 | ||||||
| chr2:223825687
|
G | GT | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+11760dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825687 | ||||||
| chr2:223825687
|
G | T | 1 | a0001c0001t0057g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3+11761C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825687 | ||||||
| chr2:223825743
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+11705T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825743 | ||||||
| chr2:223825877
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+11571A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825877 | ||||||
| chr2:223825926
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+11522C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825926 | ||||||
| chr2:223825965
|
G | A | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+11483C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223825965 | ||||||
| chr2:223826033
|
G | C | 13 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0179others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3+11415C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826033 | ||||||
| chr2:223826058
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+11390T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826058 | ||||||
| chr2:223826109
|
A | C | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+11339T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826109 | ||||||
| chr2:223826310
|
G | T | 5 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(2): Show | 5 | NA18975.hp1 NA18980.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+11138C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826310 | ||||||
| chr2:223826311
|
C | T | 1 | a0001c0001t0008g0230 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3+11137G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826311 | ||||||
| chr2:223826314
|
C | CT | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+11133_3+11134ins others(1): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826314 | ||||||
| chr2:223826325
|
G | A | 101 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(98): Show | 101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.3+11123C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826325 | ||||||
| chr2:223826399
|
C | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+11049G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826399 | ||||||
| chr2:223826404
|
C | G | 1 | a0001c0001t0012g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3+11044G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826404 | ||||||
| chr2:223826544
|
G | A | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+10904C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826544 | ||||||
| chr2:223826593
|
A | G | 109 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3+10855T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826593 | ||||||
| chr2:223826595
|
A | AAACAT | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+10852_3+10853ins others(5): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826595 | ||||||
| chr2:223826647
|
G | A | 1 | a0001c0001t0017g0212 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3+10801C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826647 | ||||||
| chr2:223826716
|
C | T | 101 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(98): Show | 101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.3+10732G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826716 | ||||||
| chr2:223826798
|
C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+10650G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826798 | ||||||
| chr2:223826850
|
A | C | 1 | a0001c0001t0023g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3+10598T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826850 | ||||||
| chr2:223826950
|
A | C | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+10498T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223826950 | ||||||
| chr2:223827012
|
TG | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+10435delC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827012 | ||||||
| chr2:223827040
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0017g0185 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3+10408G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827040 | ||||||
| chr2:223827178
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0016g0089 | 2 | HG02074.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3+10270G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827178 | ||||||
| chr2:223827179
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+10269C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827179 | ||||||
| chr2:223827198
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+10250C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827198 | ||||||
| chr2:223827268
|
T | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+10180A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827268 | ||||||
| chr2:223827286
|
T | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.3+10162A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827286 | ||||||
| chr2:223827302
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+10146C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827302 | ||||||
| chr2:223827337
|
T | C | 1 | a0001c0001t0009g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3+10111A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827337 | ||||||
| chr2:223827342
|
G | A | 1 | a0001c0001t0013g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3+10106C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827342 | ||||||
| chr2:223827446
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+10002C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827446 | ||||||
| chr2:223827461
|
C | G | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+9987G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827461 | ||||||
| chr2:223827465
|
C | T | 1 | a0001c0001t0070g0308 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3+9983G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827465 | ||||||
| chr2:223827573
|
A | T | 2 | a0001c0001t0027g0332a0001c0001t0027g0335 | 2 | HG02056.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.3+9875T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827573 | ||||||
| chr2:223827575
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.3+9873C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827575 | ||||||
| chr2:223827606
|
G | A | 109 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3+9842C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827606 | ||||||
| chr2:223827635
|
C | A | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+9813G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827635 | ||||||
| chr2:223827638
|
A | T | 109 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3+9810T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827638 | ||||||
| chr2:223827701
|
A | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+9747T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827701 | ||||||
| chr2:223827774
|
AG | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+9673delC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827774 | ||||||
| chr2:223827891
|
C | A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+9557G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827891 | ||||||
| chr2:223827936
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+9512T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827936 | ||||||
| chr2:223827942
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+9506A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827942 | ||||||
| chr2:223827954
|
G | T | 109 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3+9494C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223827954 | ||||||
| chr2:223828008
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+9440T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828008 | ||||||
| chr2:223828047
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+9401T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828047 | ||||||
| chr2:223828058
|
T | TA | 15 | a0001c0001t0001g0257a0001c0001t0001g0267a0001c0001t0001g0295others(12): Show | 15 | HG01168.hp2 HG01192.hp2 HG03579.hp2 others(12): Show |
intron_variant | MODIFIER | c.3+9389dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
T | TAA | 7 | a0001c0001t0001g0271a0001c0001t0004g0281a0001c0001t0006g0317others(4): Show | 7 | HG02717.hp2 HG02886.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+9388_3+9389dupTT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TA | T | 25 | a0001c0001t0001g0250a0001c0001t0001g0258a0001c0001t0001g0261others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.3+9389delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAA | T | 23 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0239others(20): Show | 23 | HG00423.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.3+9388_3+9389delTT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAAA | T | 35 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(32): Show | 35 | HG00639.hp1 HG01884.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.3+9387_3+9389delTT others(1): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+9380_3+9389delTT others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0003g0184a0001c0001t0028g0178 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3+9379_3+9389delTT others(9): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0023g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3+9378_3+9389delTT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0234 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3+9375_3+9389delTT others(13): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAAAAAAA others(15): Show |
T | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+9368_3+9389delTT others(20): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828058
|
TAAAAAAA others(16): Show |
T | 181 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3+9367_3+9389delTT others(21): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828058 | ||||||
| chr2:223828068
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0026g0319 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+9354_3+9379delCT others(24): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828068 | ||||||
| chr2:223828091
|
A | G | 6 | a0001c0001t0007g0170a0001c0001t0009g0166a0001c0001t0009g0167others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+9357T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828091 | ||||||
| chr2:223828114
|
G | T | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+9334C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828114 | ||||||
| chr2:223828269
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3+9179A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828269 | ||||||
| chr2:223828290
|
T | TCA | 10 | a0001c0001t0001g0046a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02300.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+9157_3+9158insTG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828290 | ||||||
| chr2:223828292
|
T | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(170): Show | 174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.3+9156A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828292 | ||||||
| chr2:223828295
|
C | CT | 105 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0050others(102): Show | 105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.3+9152dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828295 | ||||||
| chr2:223828295
|
C | T | 10 | a0001c0001t0001g0046a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02300.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+9153G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828295 | ||||||
| chr2:223828297
|
T | C | 1 | a0001c0001t0002g0209 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3+9151A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828297 | ||||||
| chr2:223828421
|
C | T | 3 | a0001c0001t0004g0112a0001c0001t0022g0101a0001c0001t0062g0102 | 3 | HG01071.hp2 HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.3+9027G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828421 | ||||||
| chr2:223828699
|
C | T | 109 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3+8749G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828699 | ||||||
| chr2:223828702
|
GAC | G | 7 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0007g0337others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+8744_3+8745delGT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828702 | ||||||
| chr2:223828773
|
T | C | 1 | a0001c0001t0052g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3+8675A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828773 | ||||||
| chr2:223828810
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+8638A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828810 | ||||||
| chr2:223828811
|
G | A | 2 | a0001c0001t0018g0149a0001c0001t0044g0150 | 2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.3+8637C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828811 | ||||||
| chr2:223828852
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3+8596A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828852 | ||||||
| chr2:223828875
|
C | T | 10 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0179others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+8573G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828875 | ||||||
| chr2:223828936
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+8512C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828936 | ||||||
| chr2:223828980
|
C | T | 1 | a0001c0001t0006g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3+8468G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223828980 | ||||||
| chr2:223829082
|
C | G | 1 | a0001c0001t0002g0294 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3+8366G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829082 | ||||||
| chr2:223829124
|
G | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+8324C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829124 | ||||||
| chr2:223829125
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+8323G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829125 | ||||||
| chr2:223829242
|
A | G | 2 | a0001c0001t0007g0244a0001c0001t0007g0245 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3+8206T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829242 | ||||||
| chr2:223829265
|
G | T | 1 | a0001c0001t0031g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3+8183C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829265 | ||||||
| chr2:223829271
|
T | C | 109 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3+8177A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829271 | ||||||
| chr2:223829328
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+8120A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829328 | ||||||
| chr2:223829441
|
A | G | 109 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3+8007T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829441 | ||||||
| chr2:223829544
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3+7904T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829544 | ||||||
| chr2:223829572
|
G | A | 9 | a0001c0001t0001g0290a0001c0001t0001g0295a0001c0001t0001g0296others(6): Show | 9 | HG00735.hp1 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+7876C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829572 | ||||||
| chr2:223829792
|
A | C | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+7656T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829792 | ||||||
| chr2:223829836
|
C | A | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+7612G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829836 | ||||||
| chr2:223829846
|
C | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+7602G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829846 | ||||||
| chr2:223829846
|
C | CA | 8 | a0001c0001t0002g0004a0001c0001t0002g0309a0001c0001t0002g0310others(5): Show | 8 | HG02148.hp1 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+7601dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829846 | ||||||
| chr2:223829847
|
A | G | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+7601T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829847 | ||||||
| chr2:223829855
|
A | AAC | 63 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.3+7591_3+7592dupGT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829855 | ||||||
| chr2:223829855
|
A | AC | 11 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(8): Show | 11 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3+7592_3+7593insG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829855 | ||||||
| chr2:223829894
|
T | C | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+7554A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829894 | ||||||
| chr2:223829905
|
C | T | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+7543G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829905 | ||||||
| chr2:223829937
|
G | C | 25 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(22): Show | 25 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.3+7511C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829937 | ||||||
| chr2:223829985
|
G | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0296a0001c0001t0001g0305others(1): Show | 4 | HG00735.hp1 HG01074.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+7463C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223829985 | ||||||
| chr2:223830086
|
A | T | 1 | a0001c0001t0018g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3+7362T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830086 | ||||||
| chr2:223830478
|
C | CA | 10 | a0001c0001t0001g0297a0001c0001t0002g0004a0001c0001t0007g0170others(7): Show | 10 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+6969dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830478 | ||||||
| chr2:223830478
|
CA | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(181): Show | 185 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3+6969delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830478 | ||||||
| chr2:223830482
|
A | T | 1 | a0001c0001t0003g0013 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3+6966T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830482 | ||||||
| chr2:223830515
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+6933T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830515 | ||||||
| chr2:223830921
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+6527A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830921 | ||||||
| chr2:223830924
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+6524G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830924 | ||||||
| chr2:223830936
|
A | G | 1 | a0001c0001t0005g0064 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3+6512T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223830936 | ||||||
| chr2:223831008
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+6440G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831008 | ||||||
| chr2:223831101
|
T | C | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+6347A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831101 | ||||||
| chr2:223831127
|
A | T | 5 | a0001c0001t0004g0107a0001c0001t0004g0128a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp1 HG00140.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+6321T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831127 | ||||||
| chr2:223831188
|
T | G | 49 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0057others(46): Show | 49 | HG00609.hp1 HG01106.hp2 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.3+6260A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831188 | ||||||
| chr2:223831287
|
C | T | 4 | a0001c0001t0002g0309a0001c0001t0002g0310a0002c0002t0002g0291others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+6161G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831287 | ||||||
| chr2:223831384
|
T | C | 1 | a0001c0001t0033g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+6064A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831384 | ||||||
| chr2:223831421
|
A | C | 1 | a0001c0001t0053g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3+6027T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831421 | ||||||
| chr2:223831424
|
G | A | 2 | a0001c0001t0027g0332a0001c0001t0027g0335 | 2 | HG02056.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.3+6024C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831424 | ||||||
| chr2:223831550
|
G | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+5898C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831550 | ||||||
| chr2:223831733
|
G | A | 4 | a0001c0001t0008g0243a0001c0001t0026g0241a0001c0001t0030g0240others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+5715C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831733 | ||||||
| chr2:223831805
|
G | C | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+5643C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831805 | ||||||
| chr2:223831848
|
G | A | 1 | a0001c0001t0006g0272 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3+5600C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831848 | ||||||
| chr2:223831904
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+5544T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831904 | ||||||
| chr2:223831926
|
A | T | 1 | a0001c0001t0033g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+5522T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223831926 | ||||||
| chr2:223832032
|
G | A | 1 | a0001c0001t0015g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3+5416C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832032 | ||||||
| chr2:223832076
|
CA | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(172): Show | 176 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.3+5371delT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832076 | ||||||
| chr2:223832090
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(175): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.3+5358A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832090 | ||||||
| chr2:223832091
|
C | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(175): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.3+5357G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832091 | ||||||
| chr2:223832129
|
TTC | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0002g0008others(7): Show | 10 | HG02027.hp1 HG02273.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+5317_3+5318delGA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832129 | ||||||
| chr2:223832129
|
TTCTC | T | 13 | a0001c0001t0001g0327a0001c0001t0002g0035a0001c0001t0002g0041others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3+5315_3+5318delGA others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832129 | ||||||
| chr2:223832131
|
C | CTG | 9 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0002g0014others(6): Show | 9 | HG01978.hp2 HG02300.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+5316_3+5317insCA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTG | C | 36 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0057others(33): Show | 36 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.3+5311_3+5316delCA others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTGT others(1): Show |
C | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0005g0083others(1): Show | 4 | HG02145.hp2 HG02293.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+5309_3+5316delCA others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTGT others(3): Show |
C | 6 | a0001c0001t0001g0084a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 6 | HG01258.hp1 HG02735.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+5307_3+5316delCA others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTGT others(5): Show |
C | 9 | a0001c0001t0001g0110a0001c0001t0001g0136a0001c0001t0001g0138others(6): Show | 9 | HG01106.hp1 HG02970.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+5305_3+5316delCA others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTGT others(7): Show |
C | 43 | a0001c0001t0001g0001a0001c0001t0001g0119a0001c0001t0001g0121others(40): Show | 44 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.3+5303_3+5316delCA others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTGT others(9): Show |
C | 7 | a0001c0001t0001g0151a0001c0001t0004g0107a0001c0001t0004g0128others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+5301_3+5316delCA others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTGT others(11): Show |
C | 10 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(7): Show | 10 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+5299_3+5316delCA others(16): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832131
|
CTCTCTGT others(19): Show |
C | 1 | a0001c0001t0006g0329 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3+5291_3+5316delCA others(24): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832131 | ||||||
| chr2:223832133
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0002g0196 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+5314_3+5315insCA others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832133 | ||||||
| chr2:223832133
|
C | G | 36 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0002g0007others(33): Show | 36 | HG00408.hp1 HG00544.hp2 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.3+5315G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832133 | ||||||
| chr2:223832133
|
CTCTGTGT others(3): Show |
C | 1 | a0001c0001t0054g0005 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3+5305_3+5314delCA others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832133 | ||||||
| chr2:223832135
|
C | CTCTGTGT others(1): Show |
3 | a0001c0001t0001g0195a0001c0001t0002g0174a0001c0001t0002g0175 | 3 | HG02723.hp2 HG02970.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.3+5312_3+5313insCA others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | CTG | 19 | a0001c0001t0001g0002a0001c0001t0001g0222a0001c0001t0001g0252others(16): Show | 19 | HG00423.hp1 HG01175.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.3+5311_3+5312dupCA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | CTGTG | 14 | a0001c0001t0001g0249a0001c0001t0001g0295a0001c0001t0001g0296others(11): Show | 14 | HG00639.hp1 HG00735.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.3+5309_3+5312dupCA others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | CTGTGTG | 12 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0002g0232others(9): Show | 12 | HG01884.hp1 HG02071.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+5307_3+5312dupCA others(4): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | CTGTGTGT others(1): Show |
18 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(15): Show | 18 | HG01192.hp1 HG01255.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.3+5305_3+5312dupCA others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | CTGTGTGT others(3): Show |
10 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(7): Show | 10 | HG00544.hp1 HG02258.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+5303_3+5312dupCA others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0011g0228 | 3 | NA18971.hp1 NA18985.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3+5301_3+5312dupCA others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | CTGTGTGT others(15): Show |
1 | a0001c0001t0045g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3+5291_3+5312dupCA others(20): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
C | G | 46 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0050others(43): Show | 46 | HG00408.hp1 HG00544.hp2 HG01978.hp2 others(43): Show |
intron_variant | MODIFIER | c.3+5313G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
CTG | C | 15 | a0001c0001t0001g0276a0001c0001t0002g0273a0001c0001t0003g0287others(12): Show | 15 | HG00423.hp2 HG00673.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.3+5311_3+5312delCA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
CTGTG | C | 3 | a0001c0001t0001g0282a0001c0001t0007g0170a0001c0001t0047g0322 | 3 | HG02451.hp1 HG03209.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3+5309_3+5312delCA others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832135
|
CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0005g0283a0001c0001t0008g0243a0001c0001t0026g0241others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+5305_3+5312delCA others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832135 | ||||||
| chr2:223832137
|
G | C | 7 | a0001c0001t0001g0194a0001c0001t0004g0281a0001c0001t0020g0177others(4): Show | 7 | HG00741.hp1 HG00741.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+5311C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832137 | ||||||
| chr2:223832141
|
G | C | 1 | a0001c0001t0047g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3+5307C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832141 | ||||||
| chr2:223832143
|
G | C | 2 | a0001c0001t0021g0336a0001c0001t0047g0322 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3+5305C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832143 | ||||||
| chr2:223832145
|
G | C | 4 | a0001c0001t0008g0243a0001c0001t0026g0241a0001c0001t0030g0240others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+5303C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832145 | ||||||
| chr2:223832234
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.3+5214C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832234 | ||||||
| chr2:223832352
|
C | CACAAACA others(1): Show |
178 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(175): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.3+5088_3+5095dupTT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832352 | ||||||
| chr2:223832352
|
C | CACAAACA others(5): Show |
1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+5084_3+5095dupTT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832352 | ||||||
| chr2:223832363
|
A | AAACAAAC others(14): Show |
1 | a0001c0001t0055g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3+5064_3+5084dupCT others(19): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832363 | ||||||
| chr2:223832390
|
C | G | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+5058G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832390 | ||||||
| chr2:223832393
|
T | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(174): Show | 178 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.3+5055A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832393 | ||||||
| chr2:223832400
|
A | G | 11 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0109others(8): Show | 11 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3+5048T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832400 | ||||||
| chr2:223832492
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(180): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3+4956T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832492 | ||||||
| chr2:223832607
|
C | A | 1 | a0001c0001t0001g0318 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3+4841G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832607 | ||||||
| chr2:223832666
|
A | C | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+4782T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832666 | ||||||
| chr2:223832780
|
T | G | 100 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.3+4668A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832780 | ||||||
| chr2:223832784
|
C | T | 4 | a0001c0001t0008g0243a0001c0001t0026g0241a0001c0001t0030g0240others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+4664G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832784 | ||||||
| chr2:223832807
|
C | CT | 7 | a0001c0001t0003g0184a0001c0001t0009g0181a0001c0001t0009g0183others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+4640dupA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832807 | ||||||
| chr2:223832807
|
CT | C | 6 | a0001c0001t0001g0046a0001c0001t0003g0062a0001c0001t0016g0047others(3): Show | 6 | HG02071.hp1 HG02451.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+4640delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832807 | ||||||
| chr2:223832807
|
CTT | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(170): Show | 174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.3+4639_3+4640delAA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832807 | ||||||
| chr2:223832809
|
T | TG | 4 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0007g0244others(1): Show | 4 | HG03490.hp1 HG03492.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+4638_3+4639insC | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832809 | ||||||
| chr2:223832810
|
T | G | 49 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(46): Show | 49 | HG00423.hp1 HG00639.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.3+4638A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832810 | ||||||
| chr2:223832811
|
T | G | 1 | a0001c0001t0045g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3+4637A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832811 | ||||||
| chr2:223832813
|
T | TC | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0008g0176others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+4634_3+4635insG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832813 | ||||||
| chr2:223832865
|
C | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(177): Show | 181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.3+4583G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832865 | ||||||
| chr2:223832870
|
G | T | 1 | a0001c0001t0033g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+4578C>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832870 | ||||||
| chr2:223832871
|
A | G | 1 | a0001c0001t0033g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+4577T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832871 | ||||||
| chr2:223832929
|
G | A | 1 | a0001c0001t0068g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3+4519C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832929 | ||||||
| chr2:223832935
|
C | G | 1 | a0001c0001t0033g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+4513G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832935 | ||||||
| chr2:223832951
|
AT | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(171): Show | 175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.3+4496delA | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832951 | ||||||
| chr2:223832994
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(174): Show | 178 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.3+4454A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223832994 | ||||||
| chr2:223833093
|
T | C | 1 | a0001c0001t0022g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3+4355A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833093 | ||||||
| chr2:223833176
|
A | G | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+4272T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833176 | ||||||
| chr2:223833181
|
AC | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(179): Show | 183 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.3+4266delG | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833181 | ||||||
| chr2:223833239
|
A | AAAAT | 25 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(22): Show | 25 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.3+4205_3+4208dupAT others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833239 | ||||||
| chr2:223833239
|
A | T | 1 | a0001c0001t0003g0312 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3+4209T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833239 | ||||||
| chr2:223833241
|
A | AATAAATA others(9): Show |
1 | a0001c0001t0016g0045 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3+4206_3+4207insGT others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | AATAAATA others(1): Show |
89 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0070others(86): Show | 90 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.3+4206_3+4207insGT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | AATAAATA others(5): Show |
45 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0055others(42): Show | 45 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.3+4206_3+4207insGT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | AATAAATA others(9): Show |
15 | a0001c0001t0001g0043a0001c0001t0001g0094a0001c0001t0001g0327others(12): Show | 15 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.3+4206_3+4207insGT others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | AATAC | 30 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(27): Show | 30 | HG01978.hp1 HG02055.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.3+4203_3+4206dupGT others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | AATACATA others(1): Show |
49 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0201others(46): Show | 49 | HG00423.hp1 HG00639.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.3+4199_3+4206dupGT others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | AATACATA others(5): Show |
5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | NA18947.hp1 NA18964.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+4195_3+4206dupGT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | AATACATA others(9): Show |
1 | a0001c0001t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3+4191_3+4206dupGT others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
A | C | 1 | a0001c0001t0003g0312 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3+4207T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833241
|
AATACATA others(5): Show |
A | 6 | a0001c0001t0002g0234a0001c0001t0003g0284a0001c0001t0003g0285others(3): Show | 6 | HG00673.hp1 HG02155.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+4195_3+4206delGT others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833241 | ||||||
| chr2:223833245
|
C | A | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+4203G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833245 | ||||||
| chr2:223833283
|
T | TAC | 3 | a0001c0001t0006g0289a0001c0001t0010g0237a0001c0001t0011g0238 | 3 | NA18964.hp2 NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.3+4164_3+4165insGT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833283 | ||||||
| chr2:223833285
|
A | T | 3 | a0001c0001t0006g0289a0001c0001t0010g0237a0001c0001t0011g0238 | 3 | NA18964.hp2 NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.3+4163T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833285 | ||||||
| chr2:223833286
|
A | T | 1 | a0001c0001t0040g0236 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3+4162T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833286 | ||||||
| chr2:223833350
|
A | G | 1 | a0001c0001t0060g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3+4098T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833350 | ||||||
| chr2:223833513
|
C | T | 2 | a0001c0001t0006g0235a0001c0001t0007g0337 | 2 | HG02015.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3+3935G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833513 | ||||||
| chr2:223833574
|
G | C | 1 | a0001c0001t0056g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+3874C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833574 | ||||||
| chr2:223833592
|
T | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(76): Show | 80 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.3+3856A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833592 | ||||||
| chr2:223833604
|
A | T | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+3844T>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833604 | ||||||
| chr2:223833635
|
G | C | 4 | a0001c0001t0009g0181a0001c0001t0009g0183a0001c0001t0012g0180others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+3813C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833635 | ||||||
| chr2:223833720
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(78): Show | 82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3+3728T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833720 | ||||||
| chr2:223833783
|
T | C | 2 | a0001c0001t0021g0323a0001c0001t0026g0319 | 2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3+3665A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833783 | ||||||
| chr2:223833795
|
T | C | 1 | a0001c0001t0042g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3+3653A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833795 | ||||||
| chr2:223833800
|
G | C | 1 | a0001c0001t0060g0190 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3+3648C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833800 | ||||||
| chr2:223833840
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(75): Show | 79 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.3+3608G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833840 | ||||||
| chr2:223833874
|
T | C | 100 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.3+3574A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833874 | ||||||
| chr2:223833882
|
T | TTTATTTA others(4): Show |
1 | a0001c0001t0033g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+3565_3+3566insTA others(9): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833882 | ||||||
| chr2:223833882
|
T | TTTTA | 92 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0050others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.3+3562_3+3565dupTA others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833882 | ||||||
| chr2:223833882
|
T | TTTTATTT others(1): Show |
13 | a0001c0001t0002g0087a0001c0001t0002g0309a0001c0001t0002g0310others(10): Show | 13 | HG00438.hp1 HG00609.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.3+3558_3+3565dupTA others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833882 | ||||||
| chr2:223833882
|
T | TTTTATTT others(5): Show |
3 | a0001c0001t0003g0092a0001c0001t0026g0319a0001c0001t0036g0311 | 3 | HG01192.hp2 NA18906.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3+3554_3+3565dupTA others(10): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833882 | ||||||
| chr2:223833882
|
TTTTA | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(112): Show | 116 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.3+3562_3+3565delTA others(2): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833882 | ||||||
| chr2:223833882
|
TTTTATTT others(1): Show |
T | 7 | a0001c0001t0002g0189a0001c0001t0008g0187a0001c0001t0008g0188others(4): Show | 7 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+3558_3+3565delTA others(6): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223833882 | ||||||
| chr2:223834087
|
T | A | 1 | a0001c0001t0026g0319 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+3361A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834087 | ||||||
| chr2:223834225
|
G | GA | 102 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.3+3222dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834225 | ||||||
| chr2:223834342
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3+3106C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834342 | ||||||
| chr2:223834496
|
A | G | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+2952T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834496 | ||||||
| chr2:223834645
|
TACTCAAG others(6): Show |
T | 102 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.3+2790_3+2802delCA others(11): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834645 | ||||||
| chr2:223834849
|
C | CA | 7 | a0001c0001t0001g0318a0001c0001t0003g0312a0001c0001t0006g0317others(4): Show | 7 | NA18965.hp2 NA18974.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+2598dupT | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834849 | ||||||
| chr2:223834887
|
A | G | 102 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.3+2561T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834887 | ||||||
| chr2:223834907
|
T | C | 1 | a0001c0001t0013g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3+2541A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834907 | ||||||
| chr2:223834908
|
G | C | 2 | a0001c0001t0002g0004a0001c0001t0054g0005 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3+2540C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834908 | ||||||
| chr2:223834992
|
G | A | 102 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.3+2456C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223834992 | ||||||
| chr2:223835071
|
G | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+2377C>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835071 | ||||||
| chr2:223835072
|
A | ATAATATT others(7): Show |
80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+2375_3+2376insAT others(12): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835072 | ||||||
| chr2:223835073
|
C | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+2375G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835073 | ||||||
| chr2:223835075
|
T | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+2373A>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835075 | ||||||
| chr2:223835077
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+2371C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835077 | ||||||
| chr2:223835080
|
G | GTAAAAGT others(9): Show |
80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+2367_3+2368insAA others(14): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835080 | ||||||
| chr2:223835122
|
T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+2326A>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835122 | ||||||
| chr2:223835125
|
C | T | 13 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0179others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3+2323G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835125 | ||||||
| chr2:223835227
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0119others(75): Show | 79 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.3+2221G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835227 | ||||||
| chr2:223835275
|
C | T | 1 | a0001c0001t0005g0324 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3+2173G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835275 | ||||||
| chr2:223835299
|
GAATGAGA others(12): Show |
G | 1 | a0001c0001t0055g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3+2130_3+2148delTT others(17): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835299 | ||||||
| chr2:223835309
|
G | A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+2139C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835309 | ||||||
| chr2:223835319
|
A | G | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+2129T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223835319 | ||||||
| chr2:223836072
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(185): Show | 189 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3+1376T>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836072 | ||||||
| chr2:223836141
|
T | G | 1 | a0001c0003t0021g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+1307A>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836141 | ||||||
| chr2:223836526
|
G | A | 2 | a0001c0001t0047g0322a0001c0001t0053g0321 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+922C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836526 | ||||||
| chr2:223836654
|
C | T | 1 | a0001c0001t0015g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3+794G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836654 | ||||||
| chr2:223836715
|
C | A | 1 | a0001c0001t0021g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3+733G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836715 | ||||||
| chr2:223836723
|
G | A | 1 | a0001c0001t0021g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3+725C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836723 | ||||||
| chr2:223836733
|
A | C | 1 | a0001c0001t0071g0338 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3+715T>G | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836733 | ||||||
| chr2:223836854
|
C | A | 1 | a0001c0001t0027g0335 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3+594G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836854 | ||||||
| chr2:223836906
|
C | T | 105 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0046others(102): Show | 105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.3+542G>A | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836906 | ||||||
| chr2:223836978
|
C | A | 12 | a0001c0001t0001g0327a0001c0001t0002g0330a0001c0001t0005g0324others(9): Show | 12 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+470G>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223836978 | ||||||
| chr2:223837155
|
G | A | 1 | a0001c0001t0021g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3+293C>T | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223837155 | ||||||
| chr2:223837161
|
AGCACCGA others(5): Show |
A | 1 | a0001c0001t0007g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3+275_3+286delCGGG others(8): Show |
AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223837161 | ||||||
| chr2:223837439
|
C | G | 1 | a0001c0001t0001g0002 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3+9G>C | AP1S3 | ENSG00000152056.18 | transcript | ENST00000396654.7 | protein_coding | 1/4 | chr2 | 223837439 |