Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1361 |
| ensemblid | ENSG00000080618.17 |
| hgncid | 2300 |
| symbol | CPB2 |
| name | carboxypeptidase B2 |
| refseq_nuc | NM_001872.5 |
| refseq_prot | NP_001863.3 |
| ensembl_nuc | ENST00000181383.10 |
| ensembl_prot | ENSP00000181383.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 46053186 |
| end | 46105033 |
| strand | - |
| ver | v1.2 |
| region | chr13:46053186-46105033 |
| region5000 | chr13:46048186-46110033 |
| regionname0 | CPB2_chr13_46053186_46105033 |
| regionname5000 | CPB2_chr13_46048186_46110033 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 423 | 156 | 39 | 29 | 71 | 3 | 14 | 52 | CPB2_chr13_46048186_46110033 | CPB2 | MKLCS others(418): Show |
chr13 | 46048186 | 46110033 |
| a0002 | 0/0 | 423 | 103 | 31 | 20 | 45 | 2 | 5 | 35 | CPB2_chr13_46048186_46110033 | CPB2 | MKLCS others(418): Show |
chr13 | 46048186 | 46110033 |
| a0003 | 1/1 | 423 | 66 | 8 | 16 | 25 | 4 | 11 | 18 | CPB2_chr13_46048186_46110033 | CPB2 | MKLCS others(418): Show |
chr13 | 46048186 | 46110033 |
| a0004 | 0/0 | 323 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | MKLCS others(318): Show |
chr13 | 46048186 | 46110033 |
| a0005 | 0/0 | 423 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | MKLCS others(418): Show |
chr13 | 46048186 | 46110033 |
| a0006 | 0/0 | 423 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | MKLCS others(418): Show |
chr13 | 46048186 | 46110033 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1269 | 105 | 29 | 25 | 38 | 3 | 10 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0001c0004 | 0/0 | 1269 | 50 | 10 | 4 | 32 | 0 | 4 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0001c0009 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0002c0002 | 0/0 | 1269 | 100 | 28 | 20 | 45 | 2 | 5 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0002c0007 | 0/0 | 1269 | 3 | 3 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0003c0003 | 1/0 | 1269 | 59 | 8 | 15 | 23 | 3 | 9 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0003c0005 | 0/1 | 1269 | 7 | 0 | 1 | 2 | 1 | 2 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0004c0006 | 0/0 | 1269 | 3 | 0 | 3 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0005c0010 | 0/0 | 1269 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 | ||
| a0006c0008 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | ATGAA others(1264): Show |
chr13 | 46048186 | 46110033 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1724 | 103 | 28 | 25 | 37 | 3 | 10 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0001c0001t0002 | 0/0 | 1724 | 2 | 1 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0001c0004t0001 | 0/0 | 1724 | 45 | 6 | 4 | 31 | 0 | 4 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0001c0004t0002 | 0/0 | 1724 | 5 | 4 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0001c0009t0001 | 0/0 | 1724 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0002c0002t0001 | 0/0 | 1724 | 14 | 10 | 3 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0002c0002t0002 | 0/0 | 1724 | 86 | 18 | 17 | 44 | 2 | 5 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0002c0007t0001 | 0/0 | 1724 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0002c0007t0005 | 0/0 | 1724 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0003c0003t0003 | 0/0 | 1724 | 51 | 8 | 9 | 23 | 2 | 9 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0003c0003t0004 | 1/0 | 1724 | 8 | 0 | 6 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0003c0005t0001 | 0/1 | 1724 | 5 | 0 | 1 | 0 | 1 | 2 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0003c0005t0003 | 0/0 | 1724 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0004c0006t0001 | 0/0 | 1724 | 3 | 0 | 3 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0005c0010t0003 | 0/0 | 1724 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| a0006c0008t0001 | 0/0 | 1724 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | GTTGT others(1719): Show |
chr13 | 46048186 | 46110033 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0001c0009t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0007t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0002c0007t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0001 | 0/0 | 15 | 0 | 0 | 13 | 0 | 2 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0004g0006 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0003t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0005t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0005t0001g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0005t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0005t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0003c0005t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0004c0006t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0004c0006t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0004c0006t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0005c0010t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| a0006c0008t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00140 | hp1 | a0003 | c0005 | t0001 | g0027 | EUR | GBR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00140 | hp2 | a0003 | c0003 | t0003 | g0068 | EUR | GBR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00280 | hp2 | a0005 | c0010 | t0003 | g0065 | EUR | FIN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0225 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00544 | hp1 | a0001 | c0004 | t0001 | g0249 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00544 | hp2 | a0003 | c0003 | t0003 | g0088 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00558 | hp2 | a0003 | c0003 | t0003 | g0071 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0175 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00642 | hp1 | a0004 | c0006 | t0001 | g0193 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | CHS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00733 | hp1 | a0003 | c0003 | t0003 | g0066 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00735 | hp1 | a0003 | c0003 | t0003 | g0180 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00738 | hp2 | a0003 | c0003 | t0004 | g0079 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00741 | hp1 | a0003 | c0003 | t0003 | g0069 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01069 | hp1 | a0003 | c0003 | t0003 | g0081 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0111 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01070 | hp2 | a0003 | c0003 | t0004 | g0006 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01074 | hp1 | a0001 | c0004 | t0001 | g0172 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01099 | hp1 | a0003 | c0003 | t0003 | g0067 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0229 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01106 | hp2 | a0003 | c0005 | t0001 | g0155 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01255 | hp1 | a0003 | c0003 | t0004 | g0089 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01257 | hp2 | a0003 | c0003 | t0004 | g0015 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01258 | hp2 | a0003 | c0003 | t0004 | g0015 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0046 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01346 | hp2 | a0003 | c0003 | t0003 | g0072 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0244 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01433 | hp2 | a0003 | c0003 | t0003 | g0014 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0099 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0108 | EUR | IBS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01515 | hp2 | a0003 | c0003 | t0004 | g0075 | EUR | IBS | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0113 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01934 | hp2 | a0004 | c0006 | t0001 | g0194 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01978 | hp2 | a0004 | c0006 | t0001 | g0212 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01981 | hp1 | a0003 | c0003 | t0003 | g0011 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01981 | hp2 | a0001 | c0004 | t0001 | g0192 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02015 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02027 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02040 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0231 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02056 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0252 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0250 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02080 | hp1 | a0003 | c0003 | t0003 | g0074 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02129 | hp1 | a0001 | c0004 | t0001 | g0243 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0022 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0190 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0101 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02451 | hp2 | a0003 | c0003 | t0003 | g0012 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | KHV | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02622 | hp2 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02630 | hp1 | a0003 | c0003 | t0003 | g0085 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02683 | hp2 | a0003 | c0005 | t0001 | g0027 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02698 | hp2 | a0003 | c0003 | t0003 | g0178 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0184 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02809 | hp2 | a0003 | c0003 | t0003 | g0055 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02818 | hp1 | a0003 | c0003 | t0003 | g0056 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02895 | hp2 | a0002 | c0007 | t0005 | g0124 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02897 | hp2 | a0002 | c0007 | t0005 | g0123 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02922 | hp2 | a0003 | c0003 | t0003 | g0050 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02970 | hp2 | a0002 | c0007 | t0001 | g0054 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03017 | hp2 | a0003 | c0003 | t0003 | g0076 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0119 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03209 | hp1 | a0003 | c0003 | t0003 | g0057 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0171 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03239 | hp1 | a0003 | c0003 | t0003 | g0084 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0023 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0145 | AFR | ESN | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0126 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0170 | AFR | GWD | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0060 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03654 | hp1 | a0003 | c0003 | t0003 | g0077 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0134 | SAS | STU | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03688 | hp2 | a0003 | c0003 | t0003 | g0001 | SAS | STU | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0164 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03704 | hp2 | a0003 | c0003 | t0003 | g0078 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0122 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0146 | SAS | BEB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0218 | SAS | BEB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG04228 | hp1 | a0003 | c0003 | t0003 | g0090 | SAS | STU | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG04228 | hp2 | a0003 | c0005 | t0001 | g0150 | SAS | STU | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18747 | hp1 | a0001 | c0004 | t0001 | g0198 | EAS | CHB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | CHB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0258 | AFR | YRI | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18947 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18950 | hp2 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18951 | hp2 | a0001 | c0004 | t0002 | g0210 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0240 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18956 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18957 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18959 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18966 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0224 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18970 | hp2 | a0003 | c0003 | t0003 | g0080 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18974 | hp1 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18980 | hp1 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18980 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18982 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18984 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18984 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18985 | hp2 | a0001 | c0004 | t0001 | g0236 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18990 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18993 | hp1 | a0001 | c0004 | t0001 | g0251 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18995 | hp1 | a0001 | c0004 | t0001 | g0216 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18995 | hp2 | a0003 | c0003 | t0003 | g0102 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18999 | hp1 | a0003 | c0005 | t0003 | g0239 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19006 | hp2 | a0001 | c0009 | t0001 | g0083 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0241 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0260 | AFR | LWK | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0161 | AFR | LWK | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19058 | hp2 | a0006 | c0008 | t0001 | g0203 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19062 | hp2 | a0003 | c0003 | t0003 | g0082 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19065 | hp1 | a0003 | c0003 | t0003 | g0064 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19066 | hp2 | a0001 | c0004 | t0001 | g0199 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19068 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0235 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19070 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19070 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19076 | hp1 | a0003 | c0005 | t0003 | g0168 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19079 | hp1 | a0003 | c0003 | t0003 | g0063 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19079 | hp2 | a0001 | c0004 | t0001 | g0237 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19082 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19083 | hp2 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19087 | hp1 | a0001 | c0004 | t0001 | g0181 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | YRI | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0059 | AFR | YRI | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | ASW | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0149 | EUR | TSI | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20805 | hp2 | a0003 | c0003 | t0003 | g0011 | EUR | TSI | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0213 | SAS | GIH | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20905 | hp2 | a0003 | c0003 | t0003 | g0014 | SAS | GIH | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01123 | hp1 | a0003 | c0003 | t0004 | g0006 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02109 | hp2 | a0001 | c0004 | t0002 | g0031 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02486 | hp1 | a0003 | c0003 | t0003 | g0073 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0031 | AFR | ACB | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0169 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | USA | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | USA | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| homoSapiens | chm13v2 | a0003 | c0005 | t0001 | g0151 | REF | REF | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0004 | g0006 | REF | REF | CPB2_chr13_46048186_46110033 | CPB2 | chr13 | 46048186 | 46110033 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46053627 | A | T | 1 | a0006 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1259T>A | p.Ile420Asn | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 11/11 | 1283/1724 | 1259/1272 | 420/423 | chr13 | 46053627 | |||
| chr13:46055809 | A | G | 4 | a0001 a0002 a0004 others(1): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
missense_variant | MODERATE | c.1040T>C | p.Ile347Thr | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/11 | 1064/1724 | 1040/1272 | 347/423 | chr13 | 46055809 | |||
| chr13:46058208 | G | A | 1 | a0004 | 3 | HG00642.hp1 HG01934.hp2 HG01978.hp2 |
stop_gained | HIGH | c.970C>T | p.Arg324* | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/11 | 994/1724 | 970/1272 | 324/423 | chr13 | 46058208 | |||
| chr13:46073934 | T | C | 1 | a0005 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.530A>G | p.Asp177Gly | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/11 | 554/1724 | 530/1272 | 177/423 | chr13 | 46073934 | |||
| chr13:46073959 | C | T | 1 | a0002 | 103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
missense_variant | MODERATE | c.505G>A | p.Ala169Thr | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/11 | 529/1724 | 505/1272 | 169/423 | chr13 | 46073959 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46064691 | G | A | 2 | a0001c0004 a0004c0006 |
53 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(50): Show |
synonymous_variant | LOW | c.753C>T | p.Ile251Ile | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/11 | 777/1724 | 753/1272 | 251/423 | chr13 | 46064691 | |||
| chr13:46067331 | A | G | 2 | a0002c0002 a0002c0007 |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
synonymous_variant | LOW | c.678T>C | p.Asp226Asp | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/11 | 702/1724 | 678/1272 | 226/423 | chr13 | 46067331 | |||
| chr13:46067346 | T | C | 8 | a0001c0001 a0001c0004 a0001c0009 others(5): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
synonymous_variant | LOW | c.663A>G | p.Pro221Pro | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/11 | 687/1724 | 663/1272 | 221/423 | chr13 | 46067346 | |||
| chr13:46078860 | A | G | 1 | a0002c0007 | 3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.426T>C | p.Asp142Asp | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/11 | 450/1724 | 426/1272 | 142/423 | chr13 | 46078860 | |||
| chr13:46082534 | A | G | 6 | a0001c0001 a0001c0004 a0002c0002 others(3): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
synonymous_variant | LOW | c.291T>C | p.Asp97Asp | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/11 | 315/1724 | 291/1272 | 97/423 | chr13 | 46082534 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46053304 | A | T | 3 | a0001c0001t0002 a0001c0004t0002 a0002c0002t0002 |
93 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*310T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 11/11 | 310 | chr13 | 46053304 | ||||||
| chr13:46053345 | C | G | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 others(9): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*269G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 11/11 | 269 | chr13 | 46053345 | ||||||
| chr13:46053377 | T | A | 1 | a0002c0007t0005 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*237A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 11/11 | 237 | chr13 | 46053377 | ||||||
| chr13:46053542 | T | C | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 others(12): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*72A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 11/11 | 72 | chr13 | 46053542 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:46053864 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1088-66C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46053864 | |||||||
| chr13:46054155 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1088-357T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054155 | |||||||
| chr13:46054454 | T | C | 1 | a0001c0004t0001g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1088-656A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054454 | |||||||
| chr13:46054773 | T | C | 1 | a0002c0002t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1088-975A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054773 | |||||||
| chr13:46054847 | T | TTCAAGTA others(317): Show |
1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1087+914_1087+915i others(326): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(321): Show |
2 | a0001c0004t0001g0218 a0001c0004t0001g0232 |
2 | HG04184.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1087+914_1087+915i others(330): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(322): Show |
1 | a0001c0004t0001g0251 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1087+914_1087+915i others(331): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(329): Show |
1 | a0002c0002t0001g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1087+914_1087+915i others(338): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(330): Show |
3 | a0001c0001t0001g0039 a0002c0002t0001g0048 a0002c0002t0001g0117 |
3 | HG02055.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1087+914_1087+915i others(339): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(331): Show |
15 | a0001c0001t0001g0044 a0001c0004t0001g0004 a0001c0004t0001g0013 others(12): Show |
21 | HG00609.hp1 HG01934.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.1087+914_1087+915i others(340): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(332): Show |
17 | a0001c0004t0001g0009 a0001c0004t0001g0030 a0001c0004t0001g0060 others(14): Show |
20 | HG00408.hp1 HG00642.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1087+914_1087+915i others(341): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(333): Show |
7 | a0001c0004t0001g0175 a0001c0004t0001g0224 a0001c0004t0001g0229 others(4): Show |
7 | HG00544.hp1 HG00621.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+914_1087+915i others(342): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(334): Show |
1 | a0001c0004t0001g0252 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1087+914_1087+915i others(343): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054847 | T | TTCAAGTA others(330): Show |
2 | a0001c0004t0001g0216 a0001c0004t0001g0217 |
2 | NA18980.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1087+914_1087+915i others(339): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054847 | |||||||
| chr13:46054866 | T | C | 1 | a0001c0004t0001g0252 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1087+896A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054866 | |||||||
| chr13:46054895 | C | T | 2 | a0003c0003t0003g0050 a0003c0003t0003g0056 |
2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1087+867G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46054895 | |||||||
| chr13:46055074 | TA | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(208): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1087+687delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46055074 | |||||||
| chr13:46055090 | A | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(213): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1087+672T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 10/10 | chr13 | 46055090 | |||||||
| chr13:46055860 | C | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(213): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1000-11G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46055860 | |||||||
| chr13:46056039 | T | C | 2 | a0003c0003t0003g0050 a0003c0003t0003g0056 |
2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1000-190A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46056039 | |||||||
| chr13:46056095 | ATATAT | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0087 |
3 | HG02886.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1000-251_1000-247d others(7): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46056095 | |||||||
| chr13:46056506 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1000-657G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46056506 | |||||||
| chr13:46056540 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG02602.hp2 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-691C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46056540 | |||||||
| chr13:46056814 | A | G | 1 | a0003c0005t0001g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1000-965T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46056814 | |||||||
| chr13:46056832 | C | A | 3 | a0001c0001t0001g0196 a0001c0001t0001g0205 a0001c0001t0001g0233 |
3 | HG00408.hp2 HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1000-983G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46056832 | |||||||
| chr13:46056990 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1000-1141C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46056990 | |||||||
| chr13:46057525 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.999+654C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46057525 | |||||||
| chr13:46057734 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.999+445C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46057734 | |||||||
| chr13:46057964 | G | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0173 a0001c0001t0001g0182 others(7): Show |
11 | HG00099.hp2 HG01192.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.999+215C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46057964 | |||||||
| chr13:46057966 | T | TA | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.999+212_999+213ins others(1): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46057966 | |||||||
| chr13:46058091 | A | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.999+88T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 9/10 | chr13 | 46058091 | |||||||
| chr13:46058657 | C | T | 1 | a0002c0002t0002g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.797-276G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46058657 | |||||||
| chr13:46058701 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-320G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46058701 | |||||||
| chr13:46058705 | C | T | 2 | a0003c0003t0004g0015 a0003c0003t0004g0079 |
3 | HG00738.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.797-324G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46058705 | |||||||
| chr13:46058917 | A | G | 49 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0165 others(46): Show |
58 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.797-536T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46058917 | |||||||
| chr13:46058963 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.797-582T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46058963 | |||||||
| chr13:46059013 | C | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-632G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059013 | |||||||
| chr13:46059061 | T | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-680A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059061 | |||||||
| chr13:46059168 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0133 |
2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.797-787T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059168 | |||||||
| chr13:46059259 | C | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-878G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059259 | |||||||
| chr13:46059315 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.797-934A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059315 | |||||||
| chr13:46059324 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-943G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059324 | |||||||
| chr13:46059394 | A | G | 1 | a0002c0002t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.797-1013T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059394 | |||||||
| chr13:46059427 | A | T | 1 | a0003c0003t0004g0075 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.797-1046T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059427 | |||||||
| chr13:46059548 | G | A | 3 | a0002c0002t0002g0103 a0002c0002t0002g0138 a0002c0002t0002g0141 |
3 | NA18968.hp1 NA18985.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.797-1167C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059548 | |||||||
| chr13:46059577 | TATC | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0162 a0001c0004t0001g0243 others(1): Show |
4 | HG01109.hp2 HG02129.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-1199_797-1197d others(5): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059577 | |||||||
| chr13:46059577 | TATCATC | T | 85 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0087 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.797-1202_797-1197d others(8): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059577 | |||||||
| chr13:46059577 | TATCATCA others(2): Show |
T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(122): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.797-1205_797-1197d others(11): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059577 | |||||||
| chr13:46059577 | TATCATCA others(5): Show |
T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0158 others(1): Show |
4 | HG01891.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-1208_797-1197d others(14): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059577 | |||||||
| chr13:46059922 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.797-1541A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059922 | |||||||
| chr13:46059995 | G | A | 2 | a0002c0002t0002g0258 a0002c0002t0002g0260 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.797-1614C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059995 | |||||||
| chr13:46059996 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-1615T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46059996 | |||||||
| chr13:46060190 | C | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0026 others(61): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.797-1809G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060190 | |||||||
| chr13:46060260 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-1879G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060260 | |||||||
| chr13:46060338 | T | C | 2 | a0001c0004t0001g0224 a0001c0004t0001g0225 |
2 | HG00408.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.797-1957A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060338 | |||||||
| chr13:46060458 | CCA | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(215): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.797-2079_797-2078d others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060458 | |||||||
| chr13:46060759 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0254 |
2 | NA19000.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.797-2378T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060759 | |||||||
| chr13:46060804 | C | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0026 others(61): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.797-2423G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060804 | |||||||
| chr13:46060887 | A | C | 1 | a0003c0003t0003g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.797-2506T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060887 | |||||||
| chr13:46060960 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0173 others(13): Show |
20 | HG00099.hp2 HG00639.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.797-2579G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060960 | |||||||
| chr13:46060966 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.797-2585T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46060966 | |||||||
| chr13:46061016 | C | T | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.797-2635G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46061016 | |||||||
| chr13:46061187 | A | G | 4 | a0001c0001t0001g0188 a0001c0001t0001g0196 a0001c0001t0001g0205 others(1): Show |
4 | HG00408.hp2 HG00642.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-2806T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46061187 | |||||||
| chr13:46061792 | C | A | 49 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0004t0001g0004 others(46): Show |
58 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.796+2856G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46061792 | |||||||
| chr13:46061942 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.796+2706G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46061942 | |||||||
| chr13:46062025 | G | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.796+2623C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062025 | |||||||
| chr13:46062025 | GT | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0026 others(139): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.796+2622delA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062025 | |||||||
| chr13:46062025 | GTT | G | 68 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0039 others(65): Show |
81 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.796+2621_796+2622d others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062025 | |||||||
| chr13:46062044 | T | A | 1 | a0003c0003t0003g0076 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.796+2604A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062044 | |||||||
| chr13:46062100 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.796+2548T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062100 | |||||||
| chr13:46062517 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.796+2131T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062517 | |||||||
| chr13:46062692 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0087 |
3 | HG02886.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.796+1956T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062692 | |||||||
| chr13:46062746 | T | G | 1 | a0003c0003t0003g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.796+1902A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46062746 | |||||||
| chr13:46063063 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.796+1585G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46063063 | |||||||
| chr13:46063083 | G | A | 1 | a0002c0002t0002g0149 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.796+1565C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46063083 | |||||||
| chr13:46063210 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.796+1438A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46063210 | |||||||
| chr13:46063375 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0044 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.796+1273C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46063375 | |||||||
| chr13:46063604 | T | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.796+1044A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46063604 | |||||||
| chr13:46063996 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.796+652G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46063996 | |||||||
| chr13:46064221 | C | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.796+427G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46064221 | |||||||
| chr13:46064512 | C | G | 1 | a0001c0004t0002g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.796+136G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 8/10 | chr13 | 46064512 | |||||||
| chr13:46064782 | G | A | 1 | a0002c0002t0002g0059 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.703-41C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46064782 | |||||||
| chr13:46064896 | C | T | 1 | a0001c0004t0001g0030 | 2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.703-155G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46064896 | |||||||
| chr13:46064901 | G | T | 1 | a0001c0009t0001g0083 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.703-160C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46064901 | |||||||
| chr13:46065488 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0087 |
3 | HG02886.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.703-747C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065488 | |||||||
| chr13:46065496 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703-755C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065496 | |||||||
| chr13:46065513 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.703-772C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065513 | |||||||
| chr13:46065572 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.703-831T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065572 | |||||||
| chr13:46065626 | CA | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(122): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.703-886delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065626 | |||||||
| chr13:46065626 | CAA | C | 74 | a0001c0001t0001g0173 a0001c0001t0001g0206 a0001c0004t0001g0232 others(71): Show |
92 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.703-887_703-886del others(2): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065626 | |||||||
| chr13:46065626 | CAAA | C | 10 | a0001c0001t0001g0125 a0002c0002t0001g0257 a0002c0002t0002g0104 others(7): Show |
10 | HG00639.hp1 HG02080.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.703-888_703-886del others(3): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065626 | |||||||
| chr13:46065920 | C | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.703-1179G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46065920 | |||||||
| chr13:46066007 | G | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.703-1266C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066007 | |||||||
| chr13:46066108 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0044 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.702+1199T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066108 | |||||||
| chr13:46066140 | C | CAT | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+1165_702+1166d others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066140 | |||||||
| chr13:46066150 | A | G | 1 | a0003c0003t0003g0070 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.702+1157T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066150 | |||||||
| chr13:46066467 | G | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+840C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066467 | |||||||
| chr13:46066566 | C | T | 1 | a0003c0003t0003g0072 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.702+741G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066566 | |||||||
| chr13:46066599 | C | T | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.702+708G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066599 | |||||||
| chr13:46066611 | G | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+696C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066611 | |||||||
| chr13:46066629 | G | A | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.702+678C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066629 | |||||||
| chr13:46066630 | G | T | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.702+677C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066630 | |||||||
| chr13:46066702 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.702+605T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066702 | |||||||
| chr13:46066713 | C | A | 2 | a0003c0005t0001g0027 a0003c0005t0001g0150 |
3 | HG00140.hp1 HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.702+594G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066713 | |||||||
| chr13:46066722 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.702+585C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066722 | |||||||
| chr13:46066770 | G | A | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.702+537C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066770 | |||||||
| chr13:46066796 | G | C | 1 | a0001c0004t0001g0240 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.702+511C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066796 | |||||||
| chr13:46066823 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.702+484G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066823 | |||||||
| chr13:46066824 | G | A | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.702+483C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066824 | |||||||
| chr13:46066832 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+475T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066832 | |||||||
| chr13:46066844 | C | CA | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0032 others(23): Show |
32 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.702+462dupT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066844 | |||||||
| chr13:46066844 | CA | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0087 others(3): Show |
7 | HG00558.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+462delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066844 | |||||||
| chr13:46066844 | CAAAA | C | 81 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(78): Show |
99 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.702+459_702+462del others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066844 | |||||||
| chr13:46066946 | T | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+361A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066946 | |||||||
| chr13:46066972 | T | C | 1 | a0001c0009t0001g0083 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.702+335A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46066972 | |||||||
| chr13:46067012 | G | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+295C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067012 | |||||||
| chr13:46067093 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(1): Show |
6 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+214C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067093 | |||||||
| chr13:46067114 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+193T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067114 | |||||||
| chr13:46067128 | G | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+179C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067128 | |||||||
| chr13:46067146 | A | T | 1 | a0001c0004t0001g0236 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.702+161T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067146 | |||||||
| chr13:46067153 | C | G | 1 | a0002c0002t0002g0219 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.702+154G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067153 | |||||||
| chr13:46067189 | T | TA | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(132): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.702+117dupT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067189 | |||||||
| chr13:46067189 | TA | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.702+117delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 7/10 | chr13 | 46067189 | |||||||
| chr13:46067511 | T | C | 1 | a0001c0001t0001g0036 | 2 | NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.592-94A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46067511 | |||||||
| chr13:46067550 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-133T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46067550 | |||||||
| chr13:46067590 | G | A | 2 | a0003c0003t0003g0012 a0003c0003t0003g0055 |
3 | HG02451.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.592-173C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46067590 | |||||||
| chr13:46067606 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.592-189C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46067606 | |||||||
| chr13:46067750 | G | A | 1 | a0002c0002t0002g0098 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.592-333C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46067750 | |||||||
| chr13:46068021 | G | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-604C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068021 | |||||||
| chr13:46068115 | T | C | 1 | a0002c0002t0002g0220 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.592-698A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068115 | |||||||
| chr13:46068533 | G | A | 4 | a0002c0002t0002g0021 a0002c0002t0002g0092 a0002c0002t0002g0139 others(1): Show |
5 | HG01243.hp1 HG01934.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1116C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068533 | |||||||
| chr13:46068624 | C | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1207G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068624 | |||||||
| chr13:46068632 | A | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1215T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068632 | |||||||
| chr13:46068650 | G | A | 1 | a0002c0002t0002g0137 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.592-1233C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068650 | |||||||
| chr13:46068699 | C | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1282G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068699 | |||||||
| chr13:46068729 | C | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1312G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068729 | |||||||
| chr13:46068762 | G | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1345C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068762 | |||||||
| chr13:46068857 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1440A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068857 | |||||||
| chr13:46068889 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1472A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068889 | |||||||
| chr13:46068979 | AAAATAAT others(5): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.592-1574_592-1563d others(14): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46068979 | |||||||
| chr13:46069049 | T | G | 3 | a0002c0002t0002g0105 a0002c0002t0002g0130 a0002c0002t0002g0163 |
3 | NA18959.hp2 NA19063.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.592-1632A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069049 | |||||||
| chr13:46069100 | C | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.592-1683G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069100 | |||||||
| chr13:46069154 | T | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1737A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069154 | |||||||
| chr13:46069238 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-1821T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069238 | |||||||
| chr13:46069297 | G | A | 1 | a0003c0003t0004g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.592-1880C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069297 | |||||||
| chr13:46069333 | T | G | 2 | a0001c0004t0001g0216 a0001c0004t0001g0217 |
2 | NA18980.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.592-1916A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069333 | |||||||
| chr13:46069353 | C | T | 3 | a0002c0002t0001g0259 a0002c0002t0002g0258 a0002c0002t0002g0260 |
3 | HG02280.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.592-1936G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069353 | |||||||
| chr13:46069426 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2009T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069426 | |||||||
| chr13:46069471 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2054T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069471 | |||||||
| chr13:46069673 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2256A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069673 | |||||||
| chr13:46069783 | A | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.592-2366T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069783 | |||||||
| chr13:46069875 | T | A | 1 | a0001c0004t0001g0218 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.592-2458A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069875 | |||||||
| chr13:46069921 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2504T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069921 | |||||||
| chr13:46069995 | C | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2578G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46069995 | |||||||
| chr13:46070017 | T | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2600A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070017 | |||||||
| chr13:46070038 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.592-2621G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070038 | |||||||
| chr13:46070070 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.592-2653C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070070 | |||||||
| chr13:46070270 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2853A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070270 | |||||||
| chr13:46070358 | C | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.592-2941G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070358 | |||||||
| chr13:46070485 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
7 | HG01192.hp1 HG01243.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-3068T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070485 | |||||||
| chr13:46070689 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0205 |
2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.591+3184T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070689 | |||||||
| chr13:46070725 | A | G | 2 | a0003c0003t0003g0011 a0003c0003t0003g0046 |
3 | HG01261.hp1 HG01981.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.591+3148T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070725 | |||||||
| chr13:46070739 | C | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.591+3134G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070739 | |||||||
| chr13:46070740 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0044 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.591+3133C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070740 | |||||||
| chr13:46070980 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.591+2893G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46070980 | |||||||
| chr13:46071251 | T | C | 3 | a0003c0003t0003g0012 a0003c0003t0003g0055 a0003c0003t0003g0057 |
4 | HG02451.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+2622A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071251 | |||||||
| chr13:46071410 | A | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.591+2463T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071410 | |||||||
| chr13:46071605 | G | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.591+2268C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071605 | |||||||
| chr13:46071672 | A | T | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.591+2201T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071672 | |||||||
| chr13:46071692 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.591+2181A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071692 | |||||||
| chr13:46071726 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.591+2147A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071726 | |||||||
| chr13:46071929 | A | T | 1 | a0001c0004t0001g0251 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.591+1944T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071929 | |||||||
| chr13:46071932 | A | T | 1 | a0003c0003t0003g0014 | 2 | HG01433.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.591+1941T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071932 | |||||||
| chr13:46071933 | G | A | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.591+1940C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071933 | |||||||
| chr13:46071943 | G | A | 1 | a0001c0004t0001g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.591+1930C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46071943 | |||||||
| chr13:46072032 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0086 others(1): Show |
4 | HG01891.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+1841C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072032 | |||||||
| chr13:46072292 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.591+1581A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072292 | |||||||
| chr13:46072309 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.591+1564T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072309 | |||||||
| chr13:46072437 | A | G | 1 | a0003c0003t0003g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.591+1436T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072437 | |||||||
| chr13:46072576 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.591+1297G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072576 | |||||||
| chr13:46072707 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0044 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.591+1166G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072707 | |||||||
| chr13:46072756 | C | A | 1 | a0001c0004t0001g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.591+1117G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072756 | |||||||
| chr13:46072986 | T | C | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.591+887A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46072986 | |||||||
| chr13:46073055 | C | T | 1 | a0001c0004t0001g0250 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.591+818G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073055 | |||||||
| chr13:46073327 | G | A | 2 | a0003c0003t0003g0063 a0003c0003t0003g0080 |
2 | NA18970.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.591+546C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073327 | |||||||
| chr13:46073402 | C | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.591+471G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073402 | |||||||
| chr13:46073582 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.591+291C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073582 | |||||||
| chr13:46073597 | T | TCAATGTA others(297): Show |
1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.591+275_591+276ins others(304): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(298): Show |
2 | a0002c0002t0001g0042 a0002c0002t0002g0143 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.591+275_591+276ins others(305): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(301): Show |
1 | a0002c0002t0002g0220 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.591+275_591+276ins others(308): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(306): Show |
1 | a0002c0002t0002g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.591+275_591+276ins others(313): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(307): Show |
1 | a0002c0002t0002g0059 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.591+275_591+276ins others(314): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(308): Show |
14 | a0002c0002t0001g0106 a0002c0002t0002g0008 a0002c0002t0002g0034 others(11): Show |
17 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.591+275_591+276ins others(315): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(308): Show |
2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.591+275_591+276ins others(315): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(309): Show |
33 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0048 others(30): Show |
42 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.591+275_591+276ins others(316): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(310): Show |
18 | a0002c0002t0001g0115 a0002c0002t0001g0259 a0002c0002t0002g0007 others(15): Show |
23 | HG00423.hp2 HG00621.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.591+275_591+276ins others(317): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(310): Show |
1 | a0002c0002t0002g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.591+275_591+276ins others(317): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(311): Show |
8 | a0002c0002t0002g0017 a0002c0002t0002g0092 a0002c0002t0002g0094 others(5): Show |
9 | HG02148.hp1 HG02300.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.591+275_591+276ins others(318): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(312): Show |
1 | a0002c0002t0002g0141 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.591+275_591+276ins others(319): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46073597 | T | TCAATGTA others(313): Show |
2 | a0002c0002t0002g0163 a0002c0002t0002g0201 |
2 | NA19058.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.591+275_591+276ins others(320): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 6/10 | chr13 | 46073597 | |||||||
| chr13:46074234 | T | TC | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-258dupG | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074234 | |||||||
| chr13:46074388 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-411T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074388 | |||||||
| chr13:46074424 | ATTT | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-450_487-448del others(3): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074424 | |||||||
| chr13:46074472 | C | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-495G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074472 | |||||||
| chr13:46074474 | C | T | 1 | a0002c0002t0002g0059 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.487-497G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074474 | |||||||
| chr13:46074718 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-741A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074718 | |||||||
| chr13:46074840 | C | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-863G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074840 | |||||||
| chr13:46074984 | C | T | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.487-1007G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074984 | |||||||
| chr13:46074991 | G | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.487-1014C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46074991 | |||||||
| chr13:46075213 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.487-1236T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075213 | |||||||
| chr13:46075263 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-1286T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075263 | |||||||
| chr13:46075318 | C | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-1341G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075318 | |||||||
| chr13:46075319 | G | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.487-1342C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075319 | |||||||
| chr13:46075378 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0116 a0001c0001t0001g0125 others(1): Show |
4 | HG02572.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1401G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075378 | |||||||
| chr13:46075412 | T | A | 12 | a0002c0002t0001g0110 a0002c0002t0002g0002 a0002c0002t0002g0020 others(9): Show |
18 | HG00609.hp2 HG01069.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.487-1435A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075412 | |||||||
| chr13:46075433 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-1456T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075433 | |||||||
| chr13:46075451 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0044 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.487-1474A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075451 | |||||||
| chr13:46075586 | G | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-1609C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075586 | |||||||
| chr13:46075588 | G | A | 82 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
100 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.487-1611C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075588 | |||||||
| chr13:46075712 | C | T | 1 | a0002c0002t0002g0169 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.487-1735G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075712 | |||||||
| chr13:46075809 | TA | T | 5 | a0001c0004t0001g0171 a0001c0004t0001g0172 a0001c0004t0002g0031 others(2): Show |
6 | HG01074.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-1833delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075809 | |||||||
| chr13:46075827 | A | G | 1 | a0001c0004t0001g0171 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.487-1850T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075827 | |||||||
| chr13:46075949 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
7 | HG01192.hp1 HG01243.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.487-1972T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075949 | |||||||
| chr13:46075986 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-2009T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46075986 | |||||||
| chr13:46076069 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.487-2092G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076069 | |||||||
| chr13:46076084 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.487-2107A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076084 | |||||||
| chr13:46076218 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.487-2241A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076218 | |||||||
| chr13:46076228 | G | A | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.487-2251C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076228 | |||||||
| chr13:46076260 | A | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0044 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.487-2283T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076260 | |||||||
| chr13:46076396 | C | CA | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(133): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.486+2403dupT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076396 | |||||||
| chr13:46076411 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+2389T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076411 | |||||||
| chr13:46076551 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(196): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.486+2249C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076551 | |||||||
| chr13:46076559 | G | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+2241C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076559 | |||||||
| chr13:46076653 | A | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+2147T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076653 | |||||||
| chr13:46076671 | A | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+2129T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076671 | |||||||
| chr13:46076945 | A | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1855T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076945 | |||||||
| chr13:46076956 | T | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1844A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076956 | |||||||
| chr13:46076973 | C | G | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1827G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46076973 | |||||||
| chr13:46077025 | A | AT | 4 | a0002c0002t0001g0118 a0002c0002t0002g0022 a0002c0002t0002g0126 others(1): Show |
5 | HG02145.hp1 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1774dupA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077025 | |||||||
| chr13:46077130 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0044 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.486+1670G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077130 | |||||||
| chr13:46077173 | G | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1627C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077173 | |||||||
| chr13:46077209 | C | T | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1591G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077209 | |||||||
| chr13:46077386 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1414A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077386 | |||||||
| chr13:46077491 | T | A | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1309A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077491 | |||||||
| chr13:46077628 | T | C | 85 | a0002c0002t0001g0019 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.486+1172A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077628 | |||||||
| chr13:46077696 | T | TG | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.486+1103dupC | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077696 | |||||||
| chr13:46077853 | A | G | 1 | a0002c0002t0002g0258 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.486+947T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46077853 | |||||||
| chr13:46078098 | T | C | 1 | a0003c0003t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.486+702A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46078098 | |||||||
| chr13:46078261 | T | A | 1 | a0001c0001t0001g0029 | 2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.486+539A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46078261 | |||||||
| chr13:46078555 | G | T | 83 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0045 others(80): Show |
101 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.486+245C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46078555 | |||||||
| chr13:46078566 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0204 |
2 | NA18955.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.486+234T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 5/10 | chr13 | 46078566 | |||||||
| chr13:46079086 | A | G | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.385-185T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079086 | |||||||
| chr13:46079154 | A | G | 3 | a0003c0003t0003g0067 a0003c0003t0003g0069 a0003c0003t0003g0180 |
3 | HG00735.hp1 HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.385-253T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079154 | |||||||
| chr13:46079368 | A | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(217): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.385-467T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079368 | |||||||
| chr13:46079445 | C | T | 1 | a0002c0002t0001g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385-544G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079445 | |||||||
| chr13:46079476 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.385-575G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079476 | |||||||
| chr13:46079535 | CA | C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0177 others(9): Show |
14 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.385-635delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079535 | |||||||
| chr13:46079535 | CAA | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(116): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.385-636_385-635del others(2): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079535 | |||||||
| chr13:46079551 | A | AAAG | 78 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0039 others(75): Show |
98 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.385-651_385-650ins others(3): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46079551 | |||||||
| chr13:46080027 | C | T | 1 | a0001c0004t0001g0237 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.385-1126G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080027 | |||||||
| chr13:46080047 | T | G | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.385-1146A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080047 | |||||||
| chr13:46080421 | A | G | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.385-1520T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080421 | |||||||
| chr13:46080477 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.385-1576G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080477 | |||||||
| chr13:46080595 | G | A | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.385-1694C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080595 | |||||||
| chr13:46080675 | A | G | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.384+1766T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080675 | |||||||
| chr13:46080709 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(217): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.384+1732T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080709 | |||||||
| chr13:46080832 | C | A | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1609G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080832 | |||||||
| chr13:46080860 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.384+1581A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080860 | |||||||
| chr13:46080971 | C | CA | 194 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0026 others(191): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.384+1469dupT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080971 | |||||||
| chr13:46080971 | C | CAA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0176 others(7): Show |
14 | HG01192.hp1 HG01243.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.384+1468_384+1469d others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080971 | |||||||
| chr13:46080985 | A | AAG | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(2): Show |
7 | HG01070.hp1 HG01496.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+1455_384+1456i others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46080985 | |||||||
| chr13:46081013 | A | C | 1 | a0001c0004t0001g0249 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.384+1428T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081013 | |||||||
| chr13:46081029 | G | A | 1 | a0001c0004t0001g0243 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.384+1412C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081029 | |||||||
| chr13:46081033 | C | A | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1408G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081033 | |||||||
| chr13:46081224 | C | G | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1217G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081224 | |||||||
| chr13:46081240 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.384+1201C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081240 | |||||||
| chr13:46081314 | T | C | 77 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0121 others(74): Show |
95 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.384+1127A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081314 | |||||||
| chr13:46081366 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(217): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.384+1075A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081366 | |||||||
| chr13:46081368 | A | G | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1073T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081368 | |||||||
| chr13:46081369 | TG | T | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1071delC | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081369 | |||||||
| chr13:46081372 | A | T | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1069T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081372 | |||||||
| chr13:46081373 | G | T | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1068C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081373 | |||||||
| chr13:46081374 | G | T | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1067C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081374 | |||||||
| chr13:46081376 | G | GC | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+1064_384+1065i others(3): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081376 | |||||||
| chr13:46081458 | T | C | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.384+983A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081458 | |||||||
| chr13:46081943 | C | A | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+498G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46081943 | |||||||
| chr13:46082000 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.384+441T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082000 | |||||||
| chr13:46082134 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.384+307A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082134 | |||||||
| chr13:46082157 | A | T | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+284T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082157 | |||||||
| chr13:46082196 | T | C | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+245A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082196 | |||||||
| chr13:46082277 | T | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(123): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.384+164A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082277 | |||||||
| chr13:46082317 | A | G | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.384+124T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082317 | |||||||
| chr13:46082327 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.384+114A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082327 | |||||||
| chr13:46082378 | G | C | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.384+63C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 4/10 | chr13 | 46082378 | |||||||
| chr13:46082715 | G | A | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.276-166C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46082715 | |||||||
| chr13:46082780 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(217): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.276-231G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46082780 | |||||||
| chr13:46082806 | G | C | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.276-257C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46082806 | |||||||
| chr13:46082895 | A | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.276-346T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46082895 | |||||||
| chr13:46083014 | G | A | 1 | a0002c0002t0002g0143 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.276-465C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46083014 | |||||||
| chr13:46083409 | C | T | 1 | a0003c0003t0003g0102 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.275+810G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46083409 | |||||||
| chr13:46083658 | G | T | 3 | a0002c0007t0001g0054 a0002c0007t0005g0123 a0002c0007t0005g0124 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.275+561C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46083658 | |||||||
| chr13:46083696 | G | A | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.275+523C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46083696 | |||||||
| chr13:46083726 | T | C | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.275+493A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46083726 | |||||||
| chr13:46083762 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(5): Show |
10 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.275+457C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46083762 | |||||||
| chr13:46083903 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.275+316G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46083903 | |||||||
| chr13:46084044 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.275+175T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 3/10 | chr13 | 46084044 | |||||||
| chr13:46084577 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(123): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.151-234T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46084577 | |||||||
| chr13:46084768 | T | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(217): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.151-425A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46084768 | |||||||
| chr13:46084846 | A | T | 2 | a0002c0002t0002g0195 a0002c0002t0002g0201 |
2 | NA19058.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.151-503T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46084846 | |||||||
| chr13:46084860 | A | AT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(7): Show |
12 | HG01070.hp1 HG01496.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.151-518dupA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46084860 | |||||||
| chr13:46084860 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.151-517T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46084860 | |||||||
| chr13:46085000 | G | A | 1 | a0003c0003t0003g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.151-657C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085000 | |||||||
| chr13:46085201 | T | C | 2 | a0002c0002t0002g0113 a0002c0002t0002g0114 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.151-858A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085201 | |||||||
| chr13:46085718 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(217): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.151-1375T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085718 | |||||||
| chr13:46085724 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.151-1381A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085724 | |||||||
| chr13:46085799 | G | T | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.151-1456C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085799 | |||||||
| chr13:46085832 | G | A | 1 | a0002c0002t0002g0092 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.151-1489C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085832 | |||||||
| chr13:46085893 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151-1550G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085893 | |||||||
| chr13:46085978 | T | C | 2 | a0001c0004t0001g0224 a0001c0004t0001g0225 |
2 | HG00408.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.151-1635A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46085978 | |||||||
| chr13:46086059 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.150+1686G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086059 | |||||||
| chr13:46086257 | T | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(214): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.150+1488A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086257 | |||||||
| chr13:46086441 | C | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(205): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.150+1304G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086441 | |||||||
| chr13:46086559 | G | A | 6 | a0001c0004t0001g0030 a0001c0004t0001g0171 a0001c0004t0001g0172 others(3): Show |
8 | HG01074.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+1186C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086559 | |||||||
| chr13:46086592 | T | C | 1 | a0003c0005t0001g0155 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.150+1153A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086592 | |||||||
| chr13:46086688 | C | A | 1 | a0002c0002t0002g0139 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.150+1057G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086688 | |||||||
| chr13:46086721 | G | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(7): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.150+1024C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086721 | |||||||
| chr13:46086815 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.150+930G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086815 | |||||||
| chr13:46086994 | G | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(214): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.150+751C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46086994 | |||||||
| chr13:46087036 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.150+709T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46087036 | |||||||
| chr13:46087115 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.150+630A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46087115 | |||||||
| chr13:46087216 | G | A | 2 | a0002c0007t0005g0123 a0002c0007t0005g0124 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.150+529C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46087216 | |||||||
| chr13:46087306 | T | A | 1 | a0002c0002t0001g0115 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.150+439A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 2/10 | chr13 | 46087306 | |||||||
| chr13:46087852 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(4): Show |
9 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-32A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46087852 | |||||||
| chr13:46087882 | T | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
8 | HG02602.hp2 HG02683.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-62A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46087882 | |||||||
| chr13:46087947 | G | A | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-127C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46087947 | |||||||
| chr13:46088151 | T | C | 1 | a0003c0003t0003g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.75-331A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088151 | |||||||
| chr13:46088254 | C | T | 1 | a0003c0003t0003g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75-434G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088254 | |||||||
| chr13:46088418 | T | C | 1 | a0001c0004t0001g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.75-598A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088418 | |||||||
| chr13:46088449 | G | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.75-629C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088449 | |||||||
| chr13:46088455 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(122): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.75-635C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088455 | |||||||
| chr13:46088495 | T | C | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0039 others(84): Show |
106 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.75-675A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088495 | |||||||
| chr13:46088505 | G | A | 86 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0039 others(83): Show |
105 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.75-685C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088505 | |||||||
| chr13:46088638 | C | G | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-818G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088638 | |||||||
| chr13:46088710 | A | G | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-890T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088710 | |||||||
| chr13:46088784 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(218): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.75-964G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088784 | |||||||
| chr13:46088931 | A | G | 10 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0173 others(7): Show |
12 | HG00099.hp2 HG01192.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.75-1111T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46088931 | |||||||
| chr13:46089150 | C | CT | 68 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0133 others(65): Show |
85 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.75-1331dupA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46089150 | |||||||
| chr13:46089660 | G | A | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-1840C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46089660 | |||||||
| chr13:46089846 | GC | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(211): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.75-2027delG | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46089846 | |||||||
| chr13:46089873 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(211): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.75-2053C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46089873 | |||||||
| chr13:46089928 | A | C | 1 | a0002c0002t0002g0141 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.75-2108T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46089928 | |||||||
| chr13:46090044 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.75-2224A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090044 | |||||||
| chr13:46090102 | T | C | 1 | a0002c0002t0002g0101 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75-2282A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090102 | |||||||
| chr13:46090309 | T | C | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0039 others(84): Show |
106 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.75-2489A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090309 | |||||||
| chr13:46090362 | C | CT | 84 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(81): Show |
102 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.75-2543dupA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090362 | |||||||
| chr13:46090439 | T | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(211): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.75-2619A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090439 | |||||||
| chr13:46090448 | C | T | 1 | a0001c0004t0001g0236 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.75-2628G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090448 | |||||||
| chr13:46090578 | G | A | 3 | a0002c0002t0002g0021 a0002c0002t0002g0092 a0002c0002t0002g0139 |
4 | HG01243.hp1 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-2758C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090578 | |||||||
| chr13:46090682 | C | T | 1 | a0005c0010t0003g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.75-2862G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090682 | |||||||
| chr13:46090724 | C | CT | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(120): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.75-2905dupA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090724 | |||||||
| chr13:46090724 | C | CTT | 88 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(85): Show |
108 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.75-2906_75-2905dup others(2): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090724 | |||||||
| chr13:46090724 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75-2904G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090724 | |||||||
| chr13:46090746 | C | T | 80 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(77): Show |
97 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.75-2926G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090746 | |||||||
| chr13:46090793 | G | A | 1 | a0002c0002t0002g0140 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.75-2973C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090793 | |||||||
| chr13:46090925 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(211): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.75-3105A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090925 | |||||||
| chr13:46090959 | C | T | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-3139G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46090959 | |||||||
| chr13:46091127 | A | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(4): Show |
9 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-3307T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46091127 | |||||||
| chr13:46091437 | A | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(202): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.75-3617T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46091437 | |||||||
| chr13:46091516 | T | A | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-3696A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46091516 | |||||||
| chr13:46091679 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(210): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.75-3859A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46091679 | |||||||
| chr13:46091814 | G | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(4): Show |
9 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-3994C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46091814 | |||||||
| chr13:46091953 | A | G | 1 | a0002c0002t0002g0149 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.75-4133T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46091953 | |||||||
| chr13:46092073 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(4): Show |
9 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-4253G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46092073 | |||||||
| chr13:46092100 | C | T | 1 | a0002c0002t0002g0094 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.75-4280G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46092100 | |||||||
| chr13:46092142 | T | G | 8 | a0002c0002t0001g0118 a0002c0002t0002g0022 a0002c0002t0002g0119 others(5): Show |
9 | HG02145.hp1 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-4322A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46092142 | |||||||
| chr13:46092157 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.75-4337G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46092157 | |||||||
| chr13:46092219 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(2): Show |
7 | HG01070.hp1 HG01496.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.75-4399T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46092219 | |||||||
| chr13:46092669 | A | G | 1 | a0002c0002t0002g0101 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75-4849T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46092669 | |||||||
| chr13:46093004 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75-5184G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093004 | |||||||
| chr13:46093155 | C | T | 1 | a0005c0010t0003g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.75-5335G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093155 | |||||||
| chr13:46093226 | C | A | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-5406G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093226 | |||||||
| chr13:46093282 | G | C | 1 | a0001c0004t0001g0232 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.75-5462C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093282 | |||||||
| chr13:46093369 | T | C | 1 | a0002c0002t0002g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.75-5549A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093369 | |||||||
| chr13:46093386 | C | T | 4 | a0001c0001t0001g0191 a0001c0004t0001g0192 a0004c0006t0001g0193 others(1): Show |
4 | HG00642.hp1 HG01934.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-5566G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093386 | |||||||
| chr13:46093638 | GA | G | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(203): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.75-5819delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093638 | |||||||
| chr13:46093774 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.75-5954C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093774 | |||||||
| chr13:46093849 | C | A | 1 | a0001c0004t0002g0031 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.75-6029G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093849 | |||||||
| chr13:46093942 | G | A | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75-6122C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093942 | |||||||
| chr13:46093976 | A | G | 204 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(201): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.75-6156T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46093976 | |||||||
| chr13:46094167 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(210): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.75-6347C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46094167 | |||||||
| chr13:46094219 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.75-6399G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46094219 | |||||||
| chr13:46094250 | C | T | 1 | a0002c0002t0002g0100 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75-6430G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46094250 | |||||||
| chr13:46094687 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75-6867A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46094687 | |||||||
| chr13:46094897 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(210): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.75-7077T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46094897 | |||||||
| chr13:46095145 | T | C | 1 | a0001c0004t0001g0234 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.75-7325A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095145 | |||||||
| chr13:46095321 | TA | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(194): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.75-7502delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095321 | |||||||
| chr13:46095321 | TAA | T | 8 | a0001c0004t0001g0030 a0001c0004t0001g0171 a0001c0004t0001g0172 others(5): Show |
10 | HG01074.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.75-7503_75-7502del others(2): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095321 | |||||||
| chr13:46095323 | A | T | 1 | a0002c0002t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.75-7503T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095323 | |||||||
| chr13:46095415 | T | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(188): Show |
232 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.75-7595A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095415 | |||||||
| chr13:46095567 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75-7747T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095567 | |||||||
| chr13:46095637 | A | G | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.75-7817T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095637 | |||||||
| chr13:46095650 | T | C | 1 | a0001c0001t0001g0038 | 2 | NA19062.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.75-7830A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095650 | |||||||
| chr13:46095867 | G | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(188): Show |
232 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.75-8047C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095867 | |||||||
| chr13:46095876 | C | CT | 54 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(51): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.75-8057dupA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095876 | |||||||
| chr13:46095876 | C | CTT | 62 | a0001c0001t0001g0040 a0001c0001t0001g0116 a0001c0001t0001g0133 others(59): Show |
79 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.75-8058_75-8057dup others(2): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46095876 | |||||||
| chr13:46096022 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.75-8202T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096022 | |||||||
| chr13:46096212 | T | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(4): Show |
9 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.75-8392A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096212 | |||||||
| chr13:46096226 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.75-8406G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096226 | |||||||
| chr13:46096575 | C | T | 76 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(73): Show |
93 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.74+8361G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096575 | |||||||
| chr13:46096594 | A | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(10): Show |
17 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.74+8342T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096594 | |||||||
| chr13:46096607 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.74+8329T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096607 | |||||||
| chr13:46096652 | A | G | 1 | a0001c0004t0001g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.74+8284T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096652 | |||||||
| chr13:46096757 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0183 |
2 | HG02572.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.74+8179G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096757 | |||||||
| chr13:46096833 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.74+8103G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096833 | |||||||
| chr13:46096856 | C | G | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.74+8080G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096856 | |||||||
| chr13:46096868 | G | A | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.74+8068C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46096868 | |||||||
| chr13:46097767 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.74+7169T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46097767 | |||||||
| chr13:46097805 | G | A | 1 | a0001c0004t0001g0235 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.74+7131C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46097805 | |||||||
| chr13:46097825 | C | T | 2 | a0002c0007t0001g0054 a0003c0003t0003g0050 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.74+7111G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46097825 | |||||||
| chr13:46098458 | T | C | 7 | a0001c0001t0002g0238 a0001c0004t0001g0004 a0001c0004t0001g0236 others(4): Show |
11 | HG00609.hp1 NA18954.hp1 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+6478A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098458 | |||||||
| chr13:46098548 | G | A | 1 | a0002c0002t0002g0130 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.74+6388C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098548 | |||||||
| chr13:46098735 | A | T | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.74+6201T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098735 | |||||||
| chr13:46098739 | C | A | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.74+6197G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098739 | |||||||
| chr13:46098759 | C | T | 1 | a0002c0002t0002g0098 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.74+6177G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098759 | |||||||
| chr13:46098765 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.74+6171C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098765 | |||||||
| chr13:46098773 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0182 a0001c0001t0001g0245 others(1): Show |
5 | NA18981.hp2 NA19010.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+6163G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098773 | |||||||
| chr13:46098786 | G | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.74+6150C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098786 | |||||||
| chr13:46098804 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.74+6132T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098804 | |||||||
| chr13:46098870 | G | T | 1 | a0001c0004t0001g0244 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.74+6066C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098870 | |||||||
| chr13:46098929 | G | A | 1 | a0003c0003t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.74+6007C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098929 | |||||||
| chr13:46098991 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.74+5945G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46098991 | |||||||
| chr13:46099182 | G | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(188): Show |
232 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.74+5754C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46099182 | |||||||
| chr13:46099702 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.74+5234G>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46099702 | |||||||
| chr13:46099762 | C | A | 1 | a0002c0002t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74+5174G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46099762 | |||||||
| chr13:46099762 | C | T | 6 | a0002c0002t0002g0016 a0002c0002t0002g0094 a0002c0002t0002g0095 others(3): Show |
7 | HG00621.hp2 HG02523.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+5174G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46099762 | |||||||
| chr13:46099790 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(210): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.74+5146A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46099790 | |||||||
| chr13:46099791 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(4): Show |
9 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+5145C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46099791 | |||||||
| chr13:46099997 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.74+4939G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46099997 | |||||||
| chr13:46100484 | AT | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(111): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.74+4451delA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46100484 | |||||||
| chr13:46100774 | G | A | 78 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(75): Show |
95 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.74+4162C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46100774 | |||||||
| chr13:46100819 | G | A | 1 | a0002c0007t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.74+4117C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46100819 | |||||||
| chr13:46101145 | C | T | 7 | a0001c0001t0001g0086 a0001c0004t0002g0161 a0003c0003t0003g0012 others(4): Show |
8 | HG02451.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.74+3791G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101145 | |||||||
| chr13:46101160 | T | G | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.74+3776A>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101160 | |||||||
| chr13:46101196 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.74+3740T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101196 | |||||||
| chr13:46101336 | T | A | 1 | a0003c0003t0003g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.74+3600A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101336 | |||||||
| chr13:46101579 | C | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.74+3357G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101579 | |||||||
| chr13:46101598 | G | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 others(4): Show |
9 | HG01070.hp1 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+3338C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101598 | |||||||
| chr13:46101715 | CA | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(198): Show |
244 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.74+3220delT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101715 | |||||||
| chr13:46101832 | C | T | 1 | a0003c0003t0003g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.74+3104G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101832 | |||||||
| chr13:46101856 | C | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(209): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.74+3080G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46101856 | |||||||
| chr13:46102060 | A | G | 98 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(95): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.74+2876T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102060 | |||||||
| chr13:46102140 | T | C | 1 | a0001c0004t0001g0243 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.74+2796A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102140 | |||||||
| chr13:46102251 | G | T | 1 | a0003c0003t0003g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.74+2685C>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102251 | |||||||
| chr13:46102540 | C | CA | 23 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(20): Show |
28 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.74+2395dupT | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102540 | |||||||
| chr13:46102540 | C | CAA | 137 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0032 others(134): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.74+2394_74+2395dup others(2): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102540 | |||||||
| chr13:46102540 | C | CAAA | 29 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0001c0001t0001g0158 others(26): Show |
29 | HG00544.hp1 HG00621.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.74+2393_74+2395dup others(3): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102540 | |||||||
| chr13:46102540 | CAAAA | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(16): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.74+2392_74+2395del others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102540 | |||||||
| chr13:46102540 | CAAAAA | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+2391_74+2395del others(5): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102540 | |||||||
| chr13:46102592 | G | GCTTT | 26 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.74+2343_74+2344ins others(4): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102592 | |||||||
| chr13:46102592 | GT | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(110): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.74+2343delA | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102592 | |||||||
| chr13:46102593 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0165 |
2 | HG02895.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.74+2343A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102593 | |||||||
| chr13:46102594 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(110): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.74+2342A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102594 | |||||||
| chr13:46102597 | T | TTG | 68 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0125 others(65): Show |
85 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.74+2338_74+2339ins others(2): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102597 | |||||||
| chr13:46102598 | T | TG | 3 | a0002c0002t0002g0143 a0002c0002t0002g0144 a0002c0002t0002g0145 |
3 | HG02976.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.74+2337_74+2338ins others(1): Show |
CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102598 | |||||||
| chr13:46102786 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(137): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.74+2150G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102786 | |||||||
| chr13:46102821 | T | C | 2 | a0002c0002t0002g0023 a0002c0002t0002g0146 |
3 | HG01257.hp1 HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.74+2115A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102821 | |||||||
| chr13:46102866 | G | A | 4 | a0002c0002t0001g0257 a0002c0002t0001g0259 a0002c0002t0002g0258 others(1): Show |
4 | HG00639.hp1 HG02280.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.74+2070C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102866 | |||||||
| chr13:46102882 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(137): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.74+2054C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46102882 | |||||||
| chr13:46103193 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.74+1743T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103193 | |||||||
| chr13:46103237 | T | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(5): Show |
8 | HG01891.hp2 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+1699A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103237 | |||||||
| chr13:46103295 | G | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(5): Show |
8 | HG01891.hp2 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+1641C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103295 | |||||||
| chr13:46103297 | T | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18948.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.74+1639A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103297 | |||||||
| chr13:46103506 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+1430G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103506 | |||||||
| chr13:46103738 | G | A | 1 | a0003c0003t0003g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.74+1198C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103738 | |||||||
| chr13:46103942 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.74+994T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103942 | |||||||
| chr13:46103960 | C | T | 1 | a0001c0004t0001g0164 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.74+976G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46103960 | |||||||
| chr13:46104000 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.74+936T>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104000 | |||||||
| chr13:46104077 | C | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(5): Show |
8 | HG01891.hp2 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+859G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104077 | |||||||
| chr13:46104116 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.74+820C>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104116 | |||||||
| chr13:46104119 | TG | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+816delC | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104119 | |||||||
| chr13:46104121 | T | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+815A>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104121 | |||||||
| chr13:46104147 | C | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(5): Show |
8 | HG01891.hp2 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+789G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104147 | |||||||
| chr13:46104225 | A | T | 2 | a0002c0002t0001g0048 a0002c0002t0001g0049 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.74+711T>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104225 | |||||||
| chr13:46104241 | A | G | 1 | a0002c0002t0002g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.74+695T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104241 | |||||||
| chr13:46104456 | A | G | 2 | a0003c0003t0003g0011 a0003c0003t0003g0046 |
3 | HG01261.hp1 HG01981.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.74+480T>C | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104456 | |||||||
| chr13:46104500 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.74+436C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104500 | |||||||
| chr13:46104517 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.74+419A>G | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104517 | |||||||
| chr13:46104527 | C | A | 1 | a0001c0004t0002g0161 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.74+409G>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104527 | |||||||
| chr13:46104647 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.74+289C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104647 | |||||||
| chr13:46104730 | G | A | 1 | a0002c0002t0002g0163 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.74+206C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104730 | |||||||
| chr13:46104825 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+111C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104825 | |||||||
| chr13:46104826 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+110G>A | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104826 | |||||||
| chr13:46104904 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(110): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.74+32C>T | CPB2 | ENSG00000080618.17 | transcript | ENST00000181383.10 | protein_coding | 1/10 | chr13 | 46104904 |