Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9276 |
| ensemblid | ENSG00000184432.11 |
| hgncid | 2232 |
| symbol | COPB2 |
| name | COPI coat complex subunit beta 2 |
| refseq_nuc | NM_004766.3 |
| refseq_prot | NP_004757.1 |
| ensembl_nuc | ENST00000333188.10 |
| ensembl_prot | ENSP00000329419.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 139357406 |
| end | 139389647 |
| strand | - |
| ver | v1.2 |
| region | chr3:139357406-139389647 |
| region5000 | chr3:139352406-139394647 |
| regionname0 | COPB2_chr3_139357406_139389647 |
| regionname5000 | COPB2_chr3_139352406_139394647 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 906 | 259 | 92 | 60 | 59 | 12 | 34 | 46 | COPB2_chr3_139352406_139394647 | COPB2 | MPLRL others(901): Show |
chr3 | 139352406 | 139394647 |
| a0002 | 0/0 | 906 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | COPB2_chr3_139352406_139394647 | COPB2 | MPLRL others(901): Show |
chr3 | 139352406 | 139394647 |
| a0003 | 0/0 | 906 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COPB2_chr3_139352406_139394647 | COPB2 | MPLRL others(901): Show |
chr3 | 139352406 | 139394647 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2718 | 254 | 92 | 59 | 55 | 12 | 34 | COPB2_chr3_139352406_139394647 | COPB2 | ATGCC others(2713): Show |
chr3 | 139352406 | 139394647 | ||
| a0001c0002 | 0/0 | 2718 | 4 | 0 | 0 | 4 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | ATGCC others(2713): Show |
chr3 | 139352406 | 139394647 | ||
| a0001c0005 | 0/0 | 2718 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | ATGCC others(2713): Show |
chr3 | 139352406 | 139394647 | ||
| a0002c0003 | 0/0 | 2718 | 3 | 0 | 0 | 3 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | ATGCC others(2713): Show |
chr3 | 139352406 | 139394647 | ||
| a0003c0004 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | ATGCC others(2713): Show |
chr3 | 139352406 | 139394647 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3275 | 250 | 92 | 59 | 54 | 11 | 32 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| a0001c0001t0002 | 0/0 | 3275 | 2 | 0 | 0 | 0 | 1 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| a0001c0001t0003 | 0/0 | 3275 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| a0001c0001t0004 | 0/0 | 3275 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| a0001c0002t0001 | 0/0 | 3275 | 4 | 0 | 0 | 4 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| a0001c0005t0001 | 0/0 | 3275 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| a0002c0003t0001 | 0/0 | 3275 | 3 | 0 | 0 | 3 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| a0003c0004t0001 | 0/0 | 3275 | 2 | 0 | 0 | 2 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | CGTCA others(3270): Show |
chr3 | 139352406 | 139394647 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 1 | 5 | 2 | 3 | 6 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 5 | 9 | 1 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0003 | 0/0 | 10 | 8 | 0 | 2 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0005 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0006 | 0/0 | 6 | 4 | 1 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0008 | 0/0 | 5 | 3 | 0 | 1 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0009 | 0/0 | 5 | 2 | 1 | 0 | 0 | 2 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0018 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0001c0005t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0003c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| a0003c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0092 | EAS | CHS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01109 | hp2 | a0001 | c0005 | t0001 | g0152 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | CDX | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0154 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18953 | hp2 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18971 | hp2 | a0003 | c0004 | t0001 | g0058 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18981 | hp1 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19088 | hp1 | a0003 | c0004 | t0001 | g0059 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | USA | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0135 | REF | REF | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | COPB2_chr3_139352406_139394647 | COPB2 | chr3 | 139352406 | 139394647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139373274 | C | T | 1 | a0002 | 3 | HG00558.hp1 NA18953.hp2 NA18981.hp1 |
missense_variant | MODERATE | c.1033G>A | p.Val345Ile | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/22 | 1130/3275 | 1033/2721 | 345/906 | chr3 | 139373274 | |||
| chr3:139379155 | C | T | 1 | a0003 | 2 | NA18971.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.247G>A | p.Val83Met | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 4/22 | 344/3275 | 247/2721 | 83/906 | chr3 | 139379155 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139366607 | T | C | 1 | a0001c0005 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1845A>G | p.Lys615Lys | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/22 | 1942/3275 | 1845/2721 | 615/906 | chr3 | 139366607 | |||
| chr3:139379060 | A | G | 1 | a0001c0002 | 4 | HG00609.hp2 NA18970.hp1 NA18977.hp2 others(1): Show |
synonymous_variant | LOW | c.342T>C | p.Ile114Ile | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 4/22 | 439/3275 | 342/2721 | 114/906 | chr3 | 139379060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139357459 | A | G | 1 | a0001c0001t0003 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 22/22 | 404 | chr3 | 139357459 | ||||||
| chr3:139389587 | T | C | 1 | a0001c0001t0004 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/22 | 37 | chr3 | 139389587 | ||||||
| chr3:139389638 | C | T | 1 | a0001c0001t0002 | 2 | HG00140.hp1 HG03654.hp2 |
5_prime_UTR_variant | MODIFIER | c.-88G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/22 | 88 | chr3 | 139389638 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139357978 | G | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2626-20C>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 21/21 | chr3 | 139357978 | |||||||
| chr3:139358057 | A | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2626-99T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 21/21 | chr3 | 139358057 | |||||||
| chr3:139358120 | A | G | 1 | a0003c0004t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2625+80T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 21/21 | chr3 | 139358120 | |||||||
| chr3:139358132 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG00323.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2625+68C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 21/21 | chr3 | 139358132 | |||||||
| chr3:139358287 | A | AAGAT | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2554-20_2554-17dup others(4): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 20/21 | chr3 | 139358287 | |||||||
| chr3:139358335 | C | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2554-64G>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 20/21 | chr3 | 139358335 | |||||||
| chr3:139358359 | T | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0032 others(16): Show |
31 | HG00735.hp1 HG01099.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.2554-88A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 20/21 | chr3 | 139358359 | |||||||
| chr3:139358417 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2554-146C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 20/21 | chr3 | 139358417 | |||||||
| chr3:139358551 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG00609.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2553+193C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 20/21 | chr3 | 139358551 | |||||||
| chr3:139358573 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2553+171G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 20/21 | chr3 | 139358573 | |||||||
| chr3:139358685 | GA | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
21 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.2553+58delT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 20/21 | chr3 | 139358685 | |||||||
| chr3:139358857 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2485-45T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 19/21 | chr3 | 139358857 | |||||||
| chr3:139359462 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2211-100G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139359462 | |||||||
| chr3:139359768 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(22): Show |
44 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2211-406C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139359768 | |||||||
| chr3:139359771 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2211-409C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139359771 | |||||||
| chr3:139359786 | CTATTT | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0133 |
5 | HG01256.hp2 HG01515.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211-429_2211-425d others(7): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139359786 | |||||||
| chr3:139360132 | T | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
6 | HG01123.hp1 HG01496.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211-770A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360132 | |||||||
| chr3:139360172 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2211-810A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360172 | |||||||
| chr3:139360178 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2211-816C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360178 | |||||||
| chr3:139360192 | T | TAA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(17): Show |
38 | HG00323.hp2 HG00558.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2211-832_2211-831d others(4): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360192 | |||||||
| chr3:139360192 | T | TAAA | 4 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0079 others(1): Show |
5 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2211-833_2211-831d others(5): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360192 | |||||||
| chr3:139360192 | TA | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
168 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.2211-831delT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360192 | |||||||
| chr3:139360262 | A | G | 1 | a0001c0005t0001g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2210+819T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360262 | |||||||
| chr3:139360440 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2210+641G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360440 | |||||||
| chr3:139360517 | C | CA | 33 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0025 others(30): Show |
56 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.2210+563dupT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360517 | |||||||
| chr3:139360517 | C | CAA | 7 | a0001c0001t0001g0028 a0001c0001t0001g0081 a0001c0001t0001g0084 others(4): Show |
8 | HG01109.hp2 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2210+562_2210+563d others(4): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360517 | |||||||
| chr3:139360582 | G | A | 1 | a0001c0005t0001g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2210+499C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 17/21 | chr3 | 139360582 | |||||||
| chr3:139361536 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1996-241T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 16/21 | chr3 | 139361536 | |||||||
| chr3:139361661 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1996-366G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 16/21 | chr3 | 139361661 | |||||||
| chr3:139361847 | A | T | 1 | a0001c0001t0001g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1996-552T>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 16/21 | chr3 | 139361847 | |||||||
| chr3:139362181 | TAAAAC | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0048 |
4 | HG00733.hp1 HG01099.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1995+221_1995+225d others(7): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 16/21 | chr3 | 139362181 | |||||||
| chr3:139362385 | A | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1995+22T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 16/21 | chr3 | 139362385 | |||||||
| chr3:139362574 | TTA | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(33): Show |
63 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1885-59_1885-58del others(2): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139362574 | |||||||
| chr3:139362727 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1885-210T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139362727 | |||||||
| chr3:139363008 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1885-491T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363008 | |||||||
| chr3:139363325 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0076 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1885-808G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363325 | |||||||
| chr3:139363390 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1885-873A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363390 | |||||||
| chr3:139363399 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
152 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1885-882A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363399 | |||||||
| chr3:139363487 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1885-970A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363487 | |||||||
| chr3:139363501 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1885-984G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363501 | |||||||
| chr3:139363525 | A | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0100 others(9): Show |
22 | HG02155.hp2 HG02257.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1885-1008T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363525 | |||||||
| chr3:139363744 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1885-1227T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363744 | |||||||
| chr3:139363815 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0128 others(2): Show |
7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1885-1298C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363815 | |||||||
| chr3:139363901 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1885-1384G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363901 | |||||||
| chr3:139363938 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1885-1421T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139363938 | |||||||
| chr3:139364044 | A | AT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
46 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1885-1528dupA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139364044 | |||||||
| chr3:139364078 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
6 | HG01123.hp1 HG01496.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885-1561T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139364078 | |||||||
| chr3:139364271 | T | C | 1 | a0001c0001t0001g0016 | 3 | NA18988.hp2 NA19087.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1885-1754A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139364271 | |||||||
| chr3:139364422 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1885-1905C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139364422 | |||||||
| chr3:139364448 | G | T | 7 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG02559.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1885-1931C>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139364448 | |||||||
| chr3:139364716 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
7 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884+1852A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139364716 | |||||||
| chr3:139364928 | A | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1884+1640T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139364928 | |||||||
| chr3:139365113 | T | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0005t0001g0152 |
3 | HG01109.hp2 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1884+1455A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365113 | |||||||
| chr3:139365113 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1884+1455A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365113 | |||||||
| chr3:139365207 | TCCTACCA others(3): Show |
T | 1 | a0001c0001t0004g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1884+1351_1884+136 others(14): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365207 | |||||||
| chr3:139365412 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1884+1156A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365412 | |||||||
| chr3:139365446 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1884+1122G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365446 | |||||||
| chr3:139365640 | A | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
7 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1884+928T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365640 | |||||||
| chr3:139365780 | A | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1884+788T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365780 | |||||||
| chr3:139365875 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1884+693T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365875 | |||||||
| chr3:139365889 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1884+679G>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365889 | |||||||
| chr3:139365893 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1884+675G>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139365893 | |||||||
| chr3:139366114 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
214 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.1884+454T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139366114 | |||||||
| chr3:139366249 | A | AT | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1884+318dupA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139366249 | |||||||
| chr3:139366249 | AT | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0052 |
9 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1884+318delA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139366249 | |||||||
| chr3:139366258 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1884+310A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139366258 | |||||||
| chr3:139366424 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1884+144T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 15/21 | chr3 | 139366424 | |||||||
| chr3:139366838 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1677-63C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 14/21 | chr3 | 139366838 | |||||||
| chr3:139366863 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0113 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1677-88A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 14/21 | chr3 | 139366863 | |||||||
| chr3:139366896 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1676+119A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 14/21 | chr3 | 139366896 | |||||||
| chr3:139367293 | A | AT | 6 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0076 others(3): Show |
7 | HG02083.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-149dupA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 13/21 | chr3 | 139367293 | |||||||
| chr3:139367328 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1546-183G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 13/21 | chr3 | 139367328 | |||||||
| chr3:139367348 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546-203C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 13/21 | chr3 | 139367348 | |||||||
| chr3:139367845 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1545+300A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 13/21 | chr3 | 139367845 | |||||||
| chr3:139368393 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1402-105C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139368393 | |||||||
| chr3:139368394 | A | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(34): Show |
62 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.1402-106T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139368394 | |||||||
| chr3:139368451 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
7 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1402-163A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139368451 | |||||||
| chr3:139368609 | C | T | 1 | a0001c0001t0001g0007 | 5 | HG00438.hp1 NA18950.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.1402-321G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139368609 | |||||||
| chr3:139368679 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1402-391A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139368679 | |||||||
| chr3:139368789 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1401+472G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139368789 | |||||||
| chr3:139368847 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1401+414G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139368847 | |||||||
| chr3:139369153 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1401+108T>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 12/21 | chr3 | 139369153 | |||||||
| chr3:139369426 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1294+30T>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 11/21 | chr3 | 139369426 | |||||||
| chr3:139369639 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1206-95A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139369639 | |||||||
| chr3:139369729 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1206-185C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139369729 | |||||||
| chr3:139369824 | T | A | 1 | a0001c0001t0001g0031 | 2 | HG00738.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1206-280A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139369824 | |||||||
| chr3:139370125 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1206-581T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370125 | |||||||
| chr3:139370189 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1206-645A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370189 | |||||||
| chr3:139370311 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206-767G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370311 | |||||||
| chr3:139370333 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1206-789C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370333 | |||||||
| chr3:139370334 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
7 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1206-790G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370334 | |||||||
| chr3:139370371 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1206-827G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370371 | |||||||
| chr3:139370409 | T | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1206-865A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370409 | |||||||
| chr3:139370461 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1206-917G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370461 | |||||||
| chr3:139370760 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(41): Show |
80 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1205+963G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370760 | |||||||
| chr3:139370860 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1205+863A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370860 | |||||||
| chr3:139370942 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
39 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1205+781A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139370942 | |||||||
| chr3:139371106 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1205+617G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139371106 | |||||||
| chr3:139371323 | C | T | 1 | a0001c0001t0002g0020 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1205+400G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139371323 | |||||||
| chr3:139371487 | T | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1205+236A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139371487 | |||||||
| chr3:139371547 | T | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(33): Show |
63 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1205+176A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139371547 | |||||||
| chr3:139371639 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(5): Show |
14 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1205+84G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139371639 | |||||||
| chr3:139371652 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1205+71A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139371652 | |||||||
| chr3:139371674 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205+49T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 10/21 | chr3 | 139371674 | |||||||
| chr3:139371856 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(5): Show |
14 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1095-23T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139371856 | |||||||
| chr3:139371894 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1095-61C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139371894 | |||||||
| chr3:139372155 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1095-322A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139372155 | |||||||
| chr3:139372377 | G | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(33): Show |
63 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1095-544C>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139372377 | |||||||
| chr3:139372423 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1095-590T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139372423 | |||||||
| chr3:139372480 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1095-647T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139372480 | |||||||
| chr3:139372602 | G | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(41): Show |
80 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1094+611C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139372602 | |||||||
| chr3:139372674 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1094+539C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139372674 | |||||||
| chr3:139372823 | C | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1094+390G>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139372823 | |||||||
| chr3:139373175 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1094+38A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 9/21 | chr3 | 139373175 | |||||||
| chr3:139373633 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.894+33T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 8/21 | chr3 | 139373633 | |||||||
| chr3:139374000 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0097 |
2 | HG01257.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.752-192C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374000 | |||||||
| chr3:139374021 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.752-213C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374021 | |||||||
| chr3:139374282 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+207A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374282 | |||||||
| chr3:139374290 | AATGATGA others(8): Show |
A | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.751+184_751+198del others(15): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374290 | |||||||
| chr3:139374298 | C | CGAT | 38 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(35): Show |
56 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.751+188_751+190dup others(3): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374298 | |||||||
| chr3:139374298 | CGAT | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.751+188_751+190del others(3): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374298 | |||||||
| chr3:139374313 | T | TGAC | 4 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0099 others(1): Show |
13 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.751+175_751+176ins others(3): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374313 | |||||||
| chr3:139374367 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.751+122C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 7/21 | chr3 | 139374367 | |||||||
| chr3:139374644 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.652-56C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 6/21 | chr3 | 139374644 | |||||||
| chr3:139374740 | CTTG | C | 3 | a0002c0003t0001g0082 a0002c0003t0001g0091 a0002c0003t0001g0092 |
3 | HG00558.hp1 NA18953.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.652-155_652-153del others(3): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 6/21 | chr3 | 139374740 | |||||||
| chr3:139374803 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
214 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.652-215G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 6/21 | chr3 | 139374803 | |||||||
| chr3:139374838 | T | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
6 | HG01123.hp1 HG01496.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-250A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 6/21 | chr3 | 139374838 | |||||||
| chr3:139374954 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.652-366C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 6/21 | chr3 | 139374954 | |||||||
| chr3:139375235 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG02486.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.651+233G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 6/21 | chr3 | 139375235 | |||||||
| chr3:139375824 | T | G | 1 | a0002c0003t0001g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.505-210A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139375824 | |||||||
| chr3:139375850 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.505-236T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139375850 | |||||||
| chr3:139375970 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(5): Show |
14 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.505-356A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139375970 | |||||||
| chr3:139376743 | A | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0134 |
2 | HG03579.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.505-1129T>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376743 | |||||||
| chr3:139376745 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(36): Show |
75 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.505-1131A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376745 | |||||||
| chr3:139376747 | A | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(8): Show |
17 | HG00642.hp1 HG01261.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.505-1133T>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376747 | |||||||
| chr3:139376751 | A | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(27): Show |
55 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.505-1137T>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376751 | |||||||
| chr3:139376755 | T | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(8): Show |
17 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.505-1141A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376755 | |||||||
| chr3:139376780 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(41): Show |
80 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.505-1166G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376780 | |||||||
| chr3:139376802 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.505-1188G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376802 | |||||||
| chr3:139376810 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.505-1196G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376810 | |||||||
| chr3:139376823 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.505-1209G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376823 | |||||||
| chr3:139376875 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.504+1166C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376875 | |||||||
| chr3:139376912 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.504+1129C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139376912 | |||||||
| chr3:139377000 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
7 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+1041G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377000 | |||||||
| chr3:139377028 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0060 |
5 | HG02083.hp1 NA18986.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+1013G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377028 | |||||||
| chr3:139377039 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+1002C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377039 | |||||||
| chr3:139377071 | A | AT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.504+969dupA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377071 | |||||||
| chr3:139377211 | G | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
39 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.504+830C>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377211 | |||||||
| chr3:139377251 | A | AT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.504+789_504+790ins others(1): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377251 | |||||||
| chr3:139377252 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.504+789C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377252 | |||||||
| chr3:139377361 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0049 |
3 | NA18970.hp2 NA19006.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.504+680A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377361 | |||||||
| chr3:139377436 | A | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
214 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.504+605T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377436 | |||||||
| chr3:139377466 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.504+575A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377466 | |||||||
| chr3:139377693 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.504+348A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377693 | |||||||
| chr3:139377969 | T | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0125 others(5): Show |
13 | HG00642.hp1 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.504+72A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 5/21 | chr3 | 139377969 | |||||||
| chr3:139378320 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.356-131G>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 4/21 | chr3 | 139378320 | |||||||
| chr3:139378487 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.356-298A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 4/21 | chr3 | 139378487 | |||||||
| chr3:139378561 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.356-372A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 4/21 | chr3 | 139378561 | |||||||
| chr3:139378641 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.355+406G>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 4/21 | chr3 | 139378641 | |||||||
| chr3:139379353 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(34): Show |
62 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.228+27C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 3/21 | chr3 | 139379353 | |||||||
| chr3:139379515 | A | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(41): Show |
80 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.142-49T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139379515 | |||||||
| chr3:139379709 | T | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-243A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139379709 | |||||||
| chr3:139379999 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.142-533A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139379999 | |||||||
| chr3:139380003 | C | CT | 36 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(33): Show |
61 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.142-538dupA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380003 | |||||||
| chr3:139380003 | C | CTT | 4 | a0001c0001t0001g0036 a0001c0001t0001g0099 a0001c0001t0001g0122 others(1): Show |
5 | HG01891.hp1 HG02145.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-539_142-538dup others(2): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380003 | |||||||
| chr3:139380003 | CT | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(10): Show |
19 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-538delA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380003 | |||||||
| chr3:139380003 | CTTTTTT | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-543_142-538del others(6): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380003 | |||||||
| chr3:139380003 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-548_142-538del others(11): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380003 | |||||||
| chr3:139380008 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.142-542A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380008 | |||||||
| chr3:139380299 | C | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(34): Show |
62 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.142-833G>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380299 | |||||||
| chr3:139380522 | GGT | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0099 others(1): Show |
13 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-1058_142-1057d others(4): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380522 | |||||||
| chr3:139380648 | CTGAT | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0150 |
4 | HG01175.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-1186_142-1183d others(6): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380648 | |||||||
| chr3:139380757 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-1291T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380757 | |||||||
| chr3:139380777 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-1311A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380777 | |||||||
| chr3:139380803 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.142-1337G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380803 | |||||||
| chr3:139380830 | C | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-1364G>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380830 | |||||||
| chr3:139380926 | CAGAAGAA others(37): Show |
C | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.142-1504_142-1461d others(46): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380926 | |||||||
| chr3:139380961 | G | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0122 others(9): Show |
15 | HG01256.hp2 HG01515.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-1495C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139380961 | |||||||
| chr3:139381025 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-1559C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381025 | |||||||
| chr3:139381287 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-1821G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381287 | |||||||
| chr3:139381388 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.141+1910C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381388 | |||||||
| chr3:139381555 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.141+1743G>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381555 | |||||||
| chr3:139381692 | T | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0076 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+1606A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381692 | |||||||
| chr3:139381700 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.141+1598T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381700 | |||||||
| chr3:139381894 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.141+1404A>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381894 | |||||||
| chr3:139381915 | A | AAAAAC | 5 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0074 others(2): Show |
14 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1382_141+1383i others(7): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381915 | |||||||
| chr3:139381915 | A | AAAAC | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
137 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.141+1382_141+1383i others(6): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381915 | |||||||
| chr3:139381915 | A | AAAC | 13 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
21 | HG00323.hp2 HG00733.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.141+1382_141+1383i others(5): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381915 | |||||||
| chr3:139381915 | A | AAC | 22 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
41 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.141+1382_141+1383i others(4): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381915 | |||||||
| chr3:139381915 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.141+1383T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381915 | |||||||
| chr3:139381990 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.141+1308C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139381990 | |||||||
| chr3:139382294 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+1004C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382294 | |||||||
| chr3:139382338 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.141+960G>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382338 | |||||||
| chr3:139382470 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.141+828C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382470 | |||||||
| chr3:139382619 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(34): Show |
62 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.141+679C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382619 | |||||||
| chr3:139382627 | C | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0145 |
2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141+671G>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382627 | |||||||
| chr3:139382642 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.141+656G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382642 | |||||||
| chr3:139382918 | A | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG02486.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+380T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382918 | |||||||
| chr3:139382935 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(41): Show |
80 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.141+363C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382935 | |||||||
| chr3:139382995 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0099 others(1): Show |
13 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+303C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139382995 | |||||||
| chr3:139383188 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141+110T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139383188 | |||||||
| chr3:139383277 | A | G | 1 | a0002c0003t0001g0082 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.141+21T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139383277 | |||||||
| chr3:139383278 | C | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
152 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.141+20G>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 2/21 | chr3 | 139383278 | |||||||
| chr3:139383516 | A | AGGGGGGG others(37): Show |
1 | a0001c0001t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4-82_4-81insCCCCCC others(38): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139383516 | |||||||
| chr3:139383599 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.4-164A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139383599 | |||||||
| chr3:139383789 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4-354A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139383789 | |||||||
| chr3:139383810 | AAAAT | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.4-379_4-376delATTT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139383810 | |||||||
| chr3:139383825 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4-390G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139383825 | |||||||
| chr3:139383825 | CAT | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(36): Show |
75 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.4-392_4-391delAT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139383825 | |||||||
| chr3:139384020 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(5): Show |
14 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.4-585A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139384020 | |||||||
| chr3:139384339 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4-904A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139384339 | |||||||
| chr3:139384491 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4-1056T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139384491 | |||||||
| chr3:139384581 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4-1146C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139384581 | |||||||
| chr3:139384857 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4-1422T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139384857 | |||||||
| chr3:139385020 | ACGAAGTC others(31): Show |
A | 1 | a0001c0001t0001g0050 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4-1623_4-1586delCC others(36): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139385020 | |||||||
| chr3:139385097 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4-1662G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139385097 | |||||||
| chr3:139385293 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4-1858A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139385293 | |||||||
| chr3:139385307 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
7 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-1872C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139385307 | |||||||
| chr3:139385445 | CA | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0054 |
4 | HG00609.hp1 NA18956.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2011delT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139385445 | |||||||
| chr3:139386033 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0005t0001g0152 |
3 | HG01109.hp2 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4-2598G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386033 | |||||||
| chr3:139386047 | C | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.4-2612G>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386047 | |||||||
| chr3:139386139 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.4-2704A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386139 | |||||||
| chr3:139386164 | A | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4-2729T>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386164 | |||||||
| chr3:139386260 | CTTG | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
6 | HG01123.hp1 HG01496.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-2828_4-2826delCA others(1): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386260 | |||||||
| chr3:139386279 | CAG | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(33): Show |
66 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.4-2846_4-2845delCT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386279 | |||||||
| chr3:139386483 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4-3048G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386483 | |||||||
| chr3:139386553 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3+2995A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386553 | |||||||
| chr3:139386941 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3+2607C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139386941 | |||||||
| chr3:139387044 | C | CAA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(19): Show |
40 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.3+2502_3+2503dupTT | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139387044 | |||||||
| chr3:139387208 | CAAGA | C | 1 | a0001c0001t0001g0028 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3+2336_3+2339delTC others(2): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139387208 | |||||||
| chr3:139387208 | CAAGAAAG others(1): Show |
C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0100 a0001c0001t0001g0126 others(1): Show |
5 | HG04199.hp2 NA18971.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+2332_3+2339delTC others(6): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139387208 | |||||||
| chr3:139387264 | GAAAAAGA others(2): Show |
G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0005t0001g0152 |
3 | HG01109.hp2 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3+2275_3+2283delTT others(7): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139387264 | |||||||
| chr3:139387526 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3+2022G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139387526 | |||||||
| chr3:139387715 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3+1833G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139387715 | |||||||
| chr3:139387856 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3+1692A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139387856 | |||||||
| chr3:139388077 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3+1471C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388077 | |||||||
| chr3:139388288 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3+1260C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388288 | |||||||
| chr3:139388297 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3+1251A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388297 | |||||||
| chr3:139388391 | A | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.3+1157T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388391 | |||||||
| chr3:139388405 | T | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3+1143A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388405 | |||||||
| chr3:139388405 | T | TG | 53 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(50): Show |
91 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.3+1142dupC | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388405 | |||||||
| chr3:139388407 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3+1141C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388407 | |||||||
| chr3:139388415 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3+1133A>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388415 | |||||||
| chr3:139388497 | C | CCTCTGTT others(1): Show |
86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
151 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.3+1050_3+1051insAA others(6): Show |
COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388497 | |||||||
| chr3:139388501 | G | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3+1047C>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388501 | |||||||
| chr3:139388611 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG02486.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+937A>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388611 | |||||||
| chr3:139388626 | G | GT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0021 others(9): Show |
17 | HG00741.hp2 HG01175.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+921dupA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388626 | |||||||
| chr3:139388626 | GT | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
43 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3+921delA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388626 | |||||||
| chr3:139388753 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3+795C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388753 | |||||||
| chr3:139388796 | CT | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
206 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.3+751delA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388796 | |||||||
| chr3:139388828 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3+720C>T | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388828 | |||||||
| chr3:139388889 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3+659C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139388889 | |||||||
| chr3:139389360 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3+188G>A | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139389360 | |||||||
| chr3:139389408 | C | CTG | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
152 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.3+139_3+140insCA | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139389408 | |||||||
| chr3:139389460 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
6 | HG01123.hp1 HG01496.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+88T>C | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139389460 | |||||||
| chr3:139389533 | G | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
7 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+15C>G | COPB2 | ENSG00000184432.11 | transcript | ENST00000333188.10 | protein_coding | 1/21 | chr3 | 139389533 |