Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80315 |
| ensemblid | ENSG00000113742.14 |
| hgncid | 21747 |
| symbol | CPEB4 |
| name | cytoplasmic polyadenylation element binding protein 4 |
| refseq_nuc | NM_030627.4 |
| refseq_prot | NP_085130.2 |
| ensembl_nuc | ENST00000265085.10 |
| ensembl_prot | ENSP00000265085.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 173888349 |
| end | 173961980 |
| strand | + |
| ver | v1.2 |
| region | chr5:173888349-173961980 |
| region5000 | chr5:173883349-173966980 |
| regionname0 | CPEB4_chr5_173888349_173961980 |
| regionname5000 | CPEB4_chr5_173883349_173966980 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 729 | 370 | 86 | 72 | 160 | 10 | 40 | 120 | CPEB4_chr5_173883349_173966980 | CPEB4 | MGDYG others(724): Show |
chr5 | 173883349 | 173966980 |
| a0002 | 0/0 | 729 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | MGDYG others(724): Show |
chr5 | 173883349 | 173966980 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2187 | 364 | 86 | 69 | 159 | 9 | 39 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 | ||
| a0001c0002 | 0/0 | 2187 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 | ||
| a0001c0003 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 | ||
| a0001c0004 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 | ||
| a0001c0005 | 0/0 | 2187 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 | ||
| a0001c0008 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 | ||
| a0002c0006 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 | ||
| a0002c0007 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ATGGG others(2182): Show |
chr5 | 173883349 | 173966980 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9418 | 70 | 0 | 17 | 50 | 0 | 3 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0002 | 0/0 | 9416 | 63 | 9 | 8 | 35 | 1 | 10 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0003 | 0/0 | 9417 | 42 | 11 | 8 | 19 | 1 | 3 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0004 | 0/0 | 9424 | 39 | 4 | 11 | 15 | 4 | 5 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9419): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0005 | 0/0 | 9417 | 39 | 13 | 9 | 10 | 1 | 6 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0006 | 1/0 | 9418 | 23 | 14 | 5 | 0 | 1 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0007 | 0/1 | 9417 | 17 | 1 | 4 | 9 | 1 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0008 | 0/0 | 9418 | 7 | 7 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0009 | 0/0 | 9412 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9407): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0010 | 0/0 | 9417 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0011 | 0/0 | 9417 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0012 | 0/0 | 9419 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9414): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0013 | 0/0 | 9418 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0014 | 0/0 | 9416 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0015 | 0/0 | 9417 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0016 | 0/0 | 9418 | 2 | 0 | 1 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0017 | 0/0 | 9418 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0019 | 0/0 | 9417 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0020 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0021 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0022 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0023 | 0/0 | 9417 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0024 | 0/0 | 9417 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0025 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0026 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0027 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0028 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0029 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0030 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0031 | 0/0 | 9418 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0032 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0033 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0034 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0035 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0036 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0037 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0038 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0039 | 0/0 | 9366 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9361): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0040 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0041 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0042 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0043 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0044 | 0/0 | 9418 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0045 | 0/0 | 9418 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0046 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0047 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0048 | 0/0 | 9417 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0049 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0050 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0051 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0052 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0053 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0054 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9418): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0055 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9419): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0056 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9419): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0057 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9419): Show |
chr5 | 173883349 | 173966980 |
| a0001c0001t0058 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9419): Show |
chr5 | 173883349 | 173966980 |
| a0001c0002t0018 | 0/0 | 9416 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0003t0002 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9411): Show |
chr5 | 173883349 | 173966980 |
| a0001c0004t0003 | 0/0 | 9417 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| a0001c0005t0004 | 0/0 | 9424 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9419): Show |
chr5 | 173883349 | 173966980 |
| a0001c0008t0004 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9419): Show |
chr5 | 173883349 | 173966980 |
| a0002c0006t0006 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9413): Show |
chr5 | 173883349 | 173966980 |
| a0002c0007t0005 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | ACTCG others(9412): Show |
chr5 | 173883349 | 173966980 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0008g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0008g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0010g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0012g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0014g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0015g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0015g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0016g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0016g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0017g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0017g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0019g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0020g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0021g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0022g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0023g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0024g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0025g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0026g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0027g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0028g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0029g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0030g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0031g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0032g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0033g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0034g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0035g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0036g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0037g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0038g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0039g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0040g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0041g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0042g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0043g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0044g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0045g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0046g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0047g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0048g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0049g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0050g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0051g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0052g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0053g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0054g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0055g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0056g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0057g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0001t0058g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0002t0018g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0004t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0005t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0001c0008t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0002c0006t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| a0002c0007t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0282 | EUR | GBR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | GBR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0273 | EUR | FIN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0099 | EUR | FIN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00408 | hp1 | a0001 | c0001 | t0020 | g0018 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00544 | hp2 | a0001 | c0001 | t0030 | g0306 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0131 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00735 | hp2 | a0001 | c0001 | t0031 | g0128 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0287 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0295 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0194 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0187 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01099 | hp1 | a0001 | c0001 | t0023 | g0176 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0133 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01109 | hp2 | a0001 | c0001 | t0048 | g0010 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01167 | hp1 | a0001 | c0002 | t0018 | g0013 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01167 | hp2 | a0001 | c0001 | t0025 | g0300 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0264 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01169 | hp2 | a0001 | c0002 | t0018 | g0013 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0288 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01255 | hp1 | a0001 | c0005 | t0004 | g0289 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0213 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0091 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0120 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01346 | hp1 | a0001 | c0001 | t0054 | g0297 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01433 | hp1 | a0001 | c0001 | t0024 | g0185 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0215 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0191 | EUR | IBS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01517 | hp2 | a0001 | c0004 | t0003 | g0048 | EUR | IBS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0211 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0047 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0090 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0188 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0294 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01952 | hp2 | a0001 | c0001 | t0016 | g0096 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0045 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02071 | hp1 | a0001 | c0001 | t0056 | g0265 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02080 | hp2 | a0001 | c0001 | t0040 | g0058 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02135 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02135 | hp2 | a0001 | c0001 | t0027 | g0256 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02145 | hp2 | a0001 | c0001 | t0022 | g0302 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02165 | hp2 | a0001 | c0001 | t0055 | g0267 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02257 | hp2 | a0002 | c0007 | t0005 | g0199 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0299 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0274 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0085 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0223 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02602 | hp1 | a0001 | c0001 | t0044 | g0139 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0171 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02622 | hp1 | a0001 | c0001 | t0021 | g0200 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02647 | hp1 | a0001 | c0001 | t0032 | g0102 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0312 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02735 | hp1 | a0001 | c0001 | t0016 | g0068 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0280 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02809 | hp2 | a0001 | c0001 | t0035 | g0158 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0043 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0243 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0182 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02970 | hp2 | a0001 | c0001 | t0019 | g0042 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0069 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0094 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0046 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0284 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0183 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0301 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03195 | hp2 | a0001 | c0001 | t0049 | g0259 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0308 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0186 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03453 | hp1 | a0002 | c0006 | t0006 | g0086 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0084 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0097 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03491 | hp2 | a0001 | c0001 | t0014 | g0039 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03492 | hp1 | a0001 | c0001 | t0014 | g0039 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0180 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03669 | hp1 | a0001 | c0001 | t0028 | g0012 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0006 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03704 | hp1 | a0001 | c0001 | t0046 | g0012 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0204 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03927 | hp2 | a0001 | c0001 | t0017 | g0100 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0298 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0078 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0285 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0245 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0281 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0003 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04228 | hp1 | a0001 | c0001 | t0045 | g0151 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0277 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0181 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18946 | hp1 | a0001 | c0001 | t0038 | g0051 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18951 | hp1 | a0001 | c0001 | t0029 | g0219 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18952 | hp2 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18959 | hp2 | a0001 | c0001 | t0057 | g0270 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18970 | hp1 | a0001 | c0001 | t0012 | g0093 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18981 | hp2 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18982 | hp1 | a0001 | c0001 | t0052 | g0054 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18986 | hp1 | a0001 | c0001 | t0051 | g0217 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18987 | hp2 | a0001 | c0001 | t0042 | g0007 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18991 | hp2 | a0001 | c0001 | t0058 | g0293 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18997 | hp2 | a0001 | c0001 | t0041 | g0114 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19007 | hp1 | a0001 | c0001 | t0039 | g0066 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19030 | hp2 | a0001 | c0001 | t0033 | g0044 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19079 | hp1 | a0001 | c0008 | t0004 | g0279 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19080 | hp1 | a0001 | c0001 | t0047 | g0189 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19082 | hp1 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19084 | hp2 | a0001 | c0001 | t0036 | g0055 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19087 | hp2 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19089 | hp1 | a0001 | c0001 | t0043 | g0147 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19089 | hp2 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19240 | hp1 | a0001 | c0001 | t0053 | g0148 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | ASW | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ASW | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0276 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0261 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20905 | hp1 | a0001 | c0001 | t0017 | g0101 | SAS | GIH | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | GIH | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02486 | hp1 | a0001 | c0001 | t0034 | g0071 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG02559 | hp2 | a0001 | c0001 | t0050 | g0010 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG06807 | hp1 | a0001 | c0001 | t0013 | g0040 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| HG06807 | hp2 | a0001 | c0001 | t0037 | g0126 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0210 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0170 | REF | REF | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0125 | REF | REF | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:173889866 | A | G | 1 | a0002 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.133A>G | p.Ile45Val | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1518/9418 | 133/2190 | 45/729 | chr5 | 173889866 | |||
| chr5:173889868 | A | G | 1 | a0002 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.135A>G | p.Ile45Met | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1520/9418 | 135/2190 | 45/729 | chr5 | 173889868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:173889853 | C | T | 1 | a0001c0008 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.120C>T | p.Ser40Ser | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1505/9418 | 120/2190 | 40/729 | chr5 | 173889853 | |||
| chr5:173890015 | G | A | 1 | a0001c0003 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.282G>A | p.Gln94Gln | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1667/9418 | 282/2190 | 94/729 | chr5 | 173890015 | |||
| chr5:173890363 | C | T | 1 | a0001c0005 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.630C>T | p.Phe210Phe | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 2015/9418 | 630/2190 | 210/729 | chr5 | 173890363 | |||
| chr5:173944977 | A | C | 1 | a0001c0002 | 2 | HG01167.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1293A>C | p.Ser431Ser | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/10 | 2678/9418 | 1293/2190 | 431/729 | chr5 | 173944977 | |||
| chr5:173953194 | G | A | 1 | a0001c0004 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.1884G>A | p.Ala628Ala | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/10 | 3269/9418 | 1884/2190 | 628/729 | chr5 | 173953194 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:173888413 | T | TGGC | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-1305_-1303dupGGC | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1302 | INFO_REALIGN_3_PRIME | chr5 | 173888413 | |||||
| chr5:173888657 | T | C | 1 | a0001c0001t0020 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1077T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1077 | chr5 | 173888657 | ||||||
| chr5:173888771 | C | T | 1 | a0001c0001t0053 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-963C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 963 | chr5 | 173888771 | ||||||
| chr5:173888858 | A | T | 1 | a0001c0001t0052 | 1 | NA18982.hp1 | 5_prime_UTR_variant | MODIFIER | c.-876A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 876 | chr5 | 173888858 | ||||||
| chr5:173888863 | C | G | 7 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0047 others(4): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-871C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | chr5 | 173888863 | |||||||
| chr5:173888880 | C | T | 1 | a0001c0001t0046 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-854C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 854 | chr5 | 173888880 | ||||||
| chr5:173889229 | A | G | 1 | a0001c0002t0018 | 2 | HG01167.hp1 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-505A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 505 | chr5 | 173889229 | ||||||
| chr5:173889471 | A | C | 1 | a0001c0001t0045 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-263A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 263 | chr5 | 173889471 | ||||||
| chr5:173889501 | T | C | 1 | a0001c0001t0021 | 1 | HG02622.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-233T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | chr5 | 173889501 | |||||||
| chr5:173889726 | G | A | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(33): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
5_prime_UTR_variant | MODIFIER | c.-8G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 8 | chr5 | 173889726 | ||||||
| chr5:173956153 | C | T | 1 | a0001c0001t0058 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 16 | chr5 | 173956153 | ||||||
| chr5:173956191 | C | A | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*54C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 54 | chr5 | 173956191 | ||||||
| chr5:173956498 | A | G | 1 | a0001c0001t0030 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*361A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 361 | chr5 | 173956498 | ||||||
| chr5:173956553 | G | A | 2 | a0001c0001t0022 a0001c0001t0031 |
2 | HG00735.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*416G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 416 | chr5 | 173956553 | ||||||
| chr5:173956603 | C | CTT | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*481_*482dupTT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 483 | INFO_REALIGN_3_PRIME | chr5 | 173956603 | |||||
| chr5:173956605 | T | A | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(7): Show |
59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*468T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 468 | chr5 | 173956605 | ||||||
| chr5:173956793 | C | T | 1 | a0001c0001t0024 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 656 | chr5 | 173956793 | ||||||
| chr5:173957129 | C | T | 1 | a0001c0001t0057 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 992 | chr5 | 173957129 | ||||||
| chr5:173957460 | A | C | 1 | a0001c0001t0013 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1323A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1323 | chr5 | 173957460 | ||||||
| chr5:173957539 | A | G | 1 | a0001c0001t0051 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1402 | chr5 | 173957539 | ||||||
| chr5:173957559 | C | T | 1 | a0001c0001t0029 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1422C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1422 | chr5 | 173957559 | ||||||
| chr5:173957660 | T | A | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1523T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1523 | chr5 | 173957660 | ||||||
| chr5:173958501 | A | G | 1 | a0001c0001t0050 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2364 | chr5 | 173958501 | ||||||
| chr5:173958676 | A | G | 1 | a0001c0001t0028 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2539A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2539 | chr5 | 173958676 | ||||||
| chr5:173958690 | T | TA | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2563dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2564 | INFO_REALIGN_3_PRIME | chr5 | 173958690 | |||||
| chr5:173958905 | G | C | 6 | a0001c0001t0007 a0001c0001t0047 a0001c0001t0048 others(3): Show |
21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2768G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2768 | chr5 | 173958905 | ||||||
| chr5:173959150 | AG | A | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3016delG | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3016 | INFO_REALIGN_3_PRIME | chr5 | 173959150 | |||||
| chr5:173959200 | C | T | 8 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0020 others(5): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3063C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3063 | chr5 | 173959200 | ||||||
| chr5:173959499 | G | C | 1 | a0001c0001t0047 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3362G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3362 | chr5 | 173959499 | ||||||
| chr5:173959506 | A | G | 1 | a0001c0001t0017 | 2 | HG03927.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3369A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3369 | chr5 | 173959506 | ||||||
| chr5:173959539 | A | T | 1 | a0001c0001t0056 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3402A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3402 | chr5 | 173959539 | ||||||
| chr5:173959623 | T | A | 1 | a0001c0001t0041 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3486T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3486 | chr5 | 173959623 | ||||||
| chr5:173959625 | A | T | 1 | a0001c0001t0041 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3488A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3488 | chr5 | 173959625 | ||||||
| chr5:173959676 | A | G | 1 | a0001c0001t0044 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3539A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3539 | chr5 | 173959676 | ||||||
| chr5:173959677 | T | C | 1 | a0001c0001t0016 | 2 | HG01952.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3540T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3540 | chr5 | 173959677 | ||||||
| chr5:173959874 | T | A | 1 | a0001c0001t0041 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3737T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3737 | chr5 | 173959874 | ||||||
| chr5:173960332 | C | A | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4195C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4195 | chr5 | 173960332 | ||||||
| chr5:173960467 | G | A | 1 | a0001c0001t0032 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4330G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4330 | chr5 | 173960467 | ||||||
| chr5:173960493 | C | T | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | HG02071.hp1 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4356C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4356 | chr5 | 173960493 | ||||||
| chr5:173960506 | T | C | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4369T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4369 | chr5 | 173960506 | ||||||
| chr5:173960528 | T | G | 2 | a0001c0001t0011 a0001c0001t0033 |
4 | HG01891.hp2 HG02055.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4391T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4391 | chr5 | 173960528 | ||||||
| chr5:173960699 | T | A | 1 | a0001c0001t0022 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4562 | chr5 | 173960699 | ||||||
| chr5:173960791 | C | T | 1 | a0001c0001t0040 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4654C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4654 | chr5 | 173960791 | ||||||
| chr5:173960823 | T | G | 1 | a0001c0001t0034 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4686T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4686 | chr5 | 173960823 | ||||||
| chr5:173960844 | G | T | 1 | a0001c0001t0010 | 3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4707G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4707 | chr5 | 173960844 | ||||||
| chr5:173960852 | A | G | 1 | a0001c0001t0023 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4715A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4715 | chr5 | 173960852 | ||||||
| chr5:173960866 | CTTTGA | C | 1 | a0001c0001t0009 | 3 | HG02965.hp2 HG03540.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4736_*4740delTTGA others(1): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4736 | INFO_REALIGN_3_PRIME | chr5 | 173960866 | |||||
| chr5:173960924 | T | C | 1 | a0001c0001t0035 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4787T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4787 | chr5 | 173960924 | ||||||
| chr5:173960932 | A | T | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(13): Show |
127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4795A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4795 | chr5 | 173960932 | ||||||
| chr5:173960957 | AGGATTTA others(44): Show |
A | 1 | a0001c0001t0039 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4821_*4871delGGAT others(47): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4821 | chr5 | 173960957 | ||||||
| chr5:173961047 | T | C | 1 | a0001c0001t0036 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4910T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4910 | chr5 | 173961047 | ||||||
| chr5:173961094 | G | A | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(13): Show |
127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4957G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4957 | chr5 | 173961094 | ||||||
| chr5:173961101 | T | C | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4964T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4964 | chr5 | 173961101 | ||||||
| chr5:173961308 | G | T | 8 | a0001c0001t0004 a0001c0001t0054 a0001c0001t0055 others(5): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*5171G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5171 | chr5 | 173961308 | ||||||
| chr5:173961340 | A | G | 1 | a0001c0001t0026 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5203A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5203 | chr5 | 173961340 | ||||||
| chr5:173961441 | G | A | 1 | a0001c0001t0037 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5304G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5304 | chr5 | 173961441 | ||||||
| chr5:173961516 | T | A | 1 | a0001c0001t0026 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5379T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5379 | chr5 | 173961516 | ||||||
| chr5:173961717 | AT | A | 28 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(25): Show |
130 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*5595delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5595 | INFO_REALIGN_3_PRIME | chr5 | 173961717 | |||||
| chr5:173961717 | ATT | A | 9 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0025 others(6): Show |
73 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*5594_*5595delTT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5594 | INFO_REALIGN_3_PRIME | chr5 | 173961717 | |||||
| chr5:173961752 | A | T | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(7): Show |
59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5615A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5615 | chr5 | 173961752 | ||||||
| chr5:173961864 | G | A | 1 | a0001c0001t0048 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5727G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5727 | chr5 | 173961864 | ||||||
| chr5:173961945 | C | CA | 9 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0042 others(6): Show |
49 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*5817dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5818 | INFO_REALIGN_3_PRIME | chr5 | 173961945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:173890981 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1125+123C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173890981 | |||||||
| chr5:173891146 | T | A | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+288T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891146 | |||||||
| chr5:173891147 | G | GAGAATCA others(81): Show |
13 | a0001c0001t0005g0038 a0001c0001t0005g0303 a0001c0001t0005g0304 others(10): Show |
15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+370_1125+371i others(90): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173891147 | ||||||
| chr5:173891249 | A | T | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+391A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891249 | |||||||
| chr5:173891251 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+393A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891251 | |||||||
| chr5:173891554 | G | A | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+696G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891554 | |||||||
| chr5:173891916 | AAAT | A | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+1060_1125+106 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173891916 | ||||||
| chr5:173891939 | G | C | 1 | a0001c0001t0013g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1125+1081G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891939 | |||||||
| chr5:173891984 | C | A | 1 | a0001c0001t0005g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1125+1126C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891984 | |||||||
| chr5:173892055 | T | C | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1125+1197T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892055 | |||||||
| chr5:173892102 | A | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+1244A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892102 | |||||||
| chr5:173892260 | G | A | 4 | a0001c0001t0011g0045 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1402G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892260 | |||||||
| chr5:173892274 | A | AT | 15 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
15 | HG01891.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+1431dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | ||||||
| chr5:173892274 | A | ATTTTTTT | 28 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(25): Show |
34 | HG00099.hp1 HG00280.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1125+1425_1125+143 others(11): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | ||||||
| chr5:173892274 | A | ATTTTTTT others(1): Show |
73 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 others(70): Show |
85 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1125+1424_1125+143 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | ||||||
| chr5:173892274 | A | ATTTTTTT others(2): Show |
49 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(46): Show |
57 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1125+1423_1125+143 others(13): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | ||||||
| chr5:173892274 | A | ATTTTTTT others(3): Show |
18 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0244 others(15): Show |
20 | HG00639.hp1 HG00673.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1125+1422_1125+143 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | ||||||
| chr5:173892274 | A | ATTTTTTT others(4): Show |
4 | a0001c0001t0002g0260 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG02071.hp2 HG02145.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1421_1125+143 others(15): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | ||||||
| chr5:173892674 | T | A | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+1816T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892674 | |||||||
| chr5:173892848 | A | G | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+1990A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892848 | |||||||
| chr5:173892997 | C | CTG | 44 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0024 others(41): Show |
54 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1125+2178_1125+217 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | C | CTGTG | 36 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0153 others(33): Show |
40 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1125+2176_1125+217 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | C | CTGTGTG | 11 | a0001c0001t0002g0036 a0001c0001t0002g0239 a0001c0001t0002g0240 others(8): Show |
13 | HG00544.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1125+2174_1125+217 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0005g0309 a0001c0001t0005g0310 a0001c0001t0005g0311 others(2): Show |
6 | HG00423.hp1 HG02683.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+2172_1125+217 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | C | CTGTGTGT others(3): Show |
3 | a0001c0001t0005g0203 a0001c0001t0005g0243 a0001c0001t0006g0155 |
3 | HG02257.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1125+2170_1125+217 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0005g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1125+2168_1125+217 others(16): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0003g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1125+2166_1125+217 others(18): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0006g0157 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1125+2164_1125+217 others(20): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | CTG | C | 57 | a0001c0001t0001g0018 a0001c0001t0001g0079 a0001c0001t0001g0081 others(54): Show |
66 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1125+2178_1125+217 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | CTGTG | C | 32 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0002g0206 others(29): Show |
38 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1125+2176_1125+217 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | CTGTGTG | C | 3 | a0001c0001t0004g0287 a0001c0001t0004g0288 a0001c0001t0005g0205 |
3 | HG00741.hp1 HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1125+2174_1125+217 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173892997 | CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0004g0286 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1125+2164_1125+217 others(20): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | ||||||
| chr5:173893030 | TGTGTGTG others(1): Show |
T | 3 | a0001c0001t0019g0042 a0001c0001t0019g0043 a0001c0001t0049g0259 |
3 | HG02886.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1125+2174_1125+218 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893030 | ||||||
| chr5:173893032 | TGTGTGA | T | 15 | a0001c0001t0004g0283 a0001c0001t0004g0284 a0001c0001t0007g0010 others(12): Show |
16 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1125+2176_1125+218 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893032 | ||||||
| chr5:173893034 | TGTGA | T | 5 | a0001c0001t0007g0030 a0001c0001t0007g0169 a0001c0001t0007g0186 others(2): Show |
6 | HG02015.hp1 HG02109.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+2178_1125+218 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893034 | ||||||
| chr5:173893036 | T | A | 6 | a0001c0001t0001g0111 a0001c0001t0004g0272 a0001c0001t0005g0201 others(3): Show |
6 | HG01952.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+2178T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893036 | |||||||
| chr5:173893036 | T | TGA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0109 others(7): Show |
14 | HG00438.hp1 HG00544.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.1125+2196_1125+219 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | ||||||
| chr5:173893036 | T | TGTGTGA | 6 | a0001c0001t0001g0121 a0001c0001t0005g0003 a0001c0001t0005g0009 others(3): Show |
7 | HG00558.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | ||||||
| chr5:173893036 | T | TGTGTGTG others(1): Show |
4 | a0001c0001t0005g0003 a0001c0001t0005g0028 a0001c0001t0005g0194 others(1): Show |
7 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | ||||||
| chr5:173893036 | T | TGTGTGTG others(3): Show |
13 | a0001c0001t0005g0029 a0001c0001t0005g0172 a0001c0001t0005g0174 others(10): Show |
15 | HG00558.hp2 HG01099.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | ||||||
| chr5:173893036 | T | TGTGTGTG others(5): Show |
9 | a0001c0001t0005g0026 a0001c0001t0005g0029 a0001c0001t0005g0041 others(6): Show |
10 | HG01243.hp1 HG01255.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(16): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | ||||||
| chr5:173893036 | TGA | T | 7 | a0001c0001t0002g0218 a0001c0001t0006g0094 a0001c0001t0006g0097 others(4): Show |
7 | HG01167.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+2196_1125+219 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | ||||||
| chr5:173893038 | A | T | 2 | a0001c0001t0002g0244 a0001c0001t0003g0168 |
2 | HG02723.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1125+2180A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893038 | |||||||
| chr5:173893152 | C | A | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1125+2294C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893152 | |||||||
| chr5:173893203 | T | C | 1 | a0001c0001t0004g0282 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1125+2345T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893203 | |||||||
| chr5:173893223 | A | G | 2 | a0001c0001t0006g0127 a0001c0001t0031g0128 |
2 | HG00735.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1125+2365A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893223 | |||||||
| chr5:173893424 | T | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(316): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1125+2566T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893424 | |||||||
| chr5:173893442 | C | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1125+2584C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893442 | |||||||
| chr5:173893456 | A | G | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1125+2598A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893456 | |||||||
| chr5:173893573 | GA | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(64): Show |
80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1125+2724delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893573 | ||||||
| chr5:173893696 | C | T | 3 | a0001c0001t0005g0201 a0001c0001t0021g0200 a0002c0007t0005g0199 |
3 | HG02257.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1125+2838C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893696 | |||||||
| chr5:173893812 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+2954G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893812 | |||||||
| chr5:173894193 | C | T | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+3335C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894193 | |||||||
| chr5:173894259 | G | A | 1 | a0001c0001t0035g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1125+3401G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894259 | |||||||
| chr5:173894295 | T | G | 1 | a0001c0001t0006g0131 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1125+3437T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894295 | |||||||
| chr5:173894336 | T | A | 1 | a0001c0001t0038g0051 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1125+3478T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894336 | |||||||
| chr5:173894342 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1125+3484G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894342 | |||||||
| chr5:173894395 | C | T | 1 | a0001c0001t0019g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1125+3537C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894395 | |||||||
| chr5:173894412 | A | G | 1 | a0001c0008t0004g0279 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1125+3554A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894412 | |||||||
| chr5:173894491 | G | A | 1 | a0001c0001t0030g0306 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1125+3633G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894491 | |||||||
| chr5:173894620 | C | CA | 52 | a0001c0001t0004g0280 a0001c0001t0005g0003 a0001c0001t0005g0009 others(49): Show |
64 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1125+3781dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173894620 | ||||||
| chr5:173894620 | CA | C | 58 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(55): Show |
67 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1125+3781delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173894620 | ||||||
| chr5:173894841 | C | A | 1 | a0001c0001t0004g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1125+3983C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894841 | |||||||
| chr5:173894925 | G | A | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+4067G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894925 | |||||||
| chr5:173895209 | T | C | 59 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(56): Show |
68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1125+4351T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895209 | |||||||
| chr5:173895239 | A | T | 1 | a0001c0001t0004g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1125+4381A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895239 | |||||||
| chr5:173895402 | A | G | 1 | a0001c0001t0006g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1125+4544A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895402 | |||||||
| chr5:173895531 | G | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(316): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1125+4673G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895531 | |||||||
| chr5:173895616 | T | C | 1 | a0001c0001t0006g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1125+4758T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895616 | |||||||
| chr5:173895816 | G | A | 1 | a0001c0001t0015g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1125+4958G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895816 | |||||||
| chr5:173895835 | C | G | 1 | a0001c0001t0003g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1125+4977C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895835 | |||||||
| chr5:173895836 | T | G | 1 | a0001c0001t0005g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1125+4978T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895836 | |||||||
| chr5:173896166 | C | T | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+5308C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896166 | |||||||
| chr5:173896199 | C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1125+5341C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896199 | |||||||
| chr5:173896653 | T | C | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1125+5795T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896653 | |||||||
| chr5:173896834 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1125+5976C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896834 | |||||||
| chr5:173897113 | T | C | 13 | a0001c0001t0005g0038 a0001c0001t0005g0303 a0001c0001t0005g0304 others(10): Show |
15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+6255T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897113 | |||||||
| chr5:173897426 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1125+6568T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897426 | |||||||
| chr5:173897574 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG00673.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1125+6716G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897574 | |||||||
| chr5:173897620 | A | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+6762A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897620 | |||||||
| chr5:173897711 | C | T | 1 | a0001c0001t0006g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1125+6853C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897711 | |||||||
| chr5:173897804 | G | T | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1125+6946G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897804 | |||||||
| chr5:173897869 | A | G | 1 | a0001c0001t0003g0077 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1125+7011A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897869 | |||||||
| chr5:173897877 | CAT | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+7020_1125+702 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897877 | |||||||
| chr5:173897905 | A | G | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+7047A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897905 | |||||||
| chr5:173897968 | G | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+7110G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897968 | |||||||
| chr5:173898591 | G | A | 1 | a0002c0006t0006g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1125+7733G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898591 | |||||||
| chr5:173898651 | G | A | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1125+7793G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898651 | |||||||
| chr5:173898715 | T | C | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+7857T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898715 | |||||||
| chr5:173898740 | G | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1125+7882G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898740 | |||||||
| chr5:173898834 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1125+7976G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898834 | |||||||
| chr5:173899123 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1125+8265C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899123 | |||||||
| chr5:173899196 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1125+8338C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899196 | |||||||
| chr5:173899577 | C | T | 109 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(106): Show |
130 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1125+8719C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899577 | |||||||
| chr5:173899711 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+8853A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899711 | |||||||
| chr5:173899738 | T | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+8880T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899738 | |||||||
| chr5:173899863 | A | G | 1 | a0001c0001t0004g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1125+9005A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899863 | |||||||
| chr5:173899888 | C | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+9030C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899888 | |||||||
| chr5:173900023 | C | G | 59 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(56): Show |
68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1125+9165C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900023 | |||||||
| chr5:173900143 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1125+9285C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900143 | |||||||
| chr5:173900195 | C | A | 17 | a0001c0001t0005g0009 a0001c0001t0005g0026 a0001c0001t0005g0041 others(14): Show |
20 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1125+9337C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900195 | |||||||
| chr5:173900386 | C | T | 1 | a0001c0001t0003g0017 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1125+9528C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900386 | |||||||
| chr5:173900405 | C | CA | 19 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(16): Show |
21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1125+9560dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173900405 | ||||||
| chr5:173900490 | A | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+9632A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900490 | |||||||
| chr5:173900538 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1125+9680C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900538 | |||||||
| chr5:173900637 | T | C | 1 | a0001c0005t0004g0289 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1125+9779T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900637 | |||||||
| chr5:173900686 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1125+9828T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900686 | |||||||
| chr5:173900790 | T | C | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1126-9733T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900790 | |||||||
| chr5:173900889 | C | G | 2 | a0001c0001t0002g0238 a0001c0001t0002g0258 |
2 | HG00639.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1126-9634C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900889 | |||||||
| chr5:173900933 | C | T | 6 | a0001c0001t0003g0016 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
7 | HG00438.hp2 HG00621.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126-9590C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900933 | |||||||
| chr5:173901017 | G | T | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-9506G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901017 | |||||||
| chr5:173901021 | G | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-9502G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901021 | |||||||
| chr5:173901202 | T | C | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-9321T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901202 | |||||||
| chr5:173901240 | T | C | 1 | a0001c0001t0003g0072 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1126-9283T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901240 | |||||||
| chr5:173901279 | A | G | 3 | a0001c0001t0005g0003 a0001c0001t0005g0194 a0001c0001t0005g0213 |
6 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-9244A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901279 | |||||||
| chr5:173901298 | A | G | 3 | a0001c0001t0004g0037 a0001c0001t0004g0277 a0001c0001t0004g0281 |
4 | HG01256.hp1 HG01258.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-9225A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901298 | |||||||
| chr5:173901329 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1126-9194A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901329 | |||||||
| chr5:173901518 | C | T | 2 | a0001c0001t0005g0312 a0001c0001t0014g0039 |
3 | HG02683.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1126-9005C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901518 | |||||||
| chr5:173901615 | C | A | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-8908C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901615 | |||||||
| chr5:173901617 | G | T | 20 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(17): Show |
22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-8906G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901617 | |||||||
| chr5:173901814 | C | G | 31 | a0001c0001t0005g0003 a0001c0001t0005g0009 a0001c0001t0005g0026 others(28): Show |
40 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1126-8709C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901814 | |||||||
| chr5:173901834 | A | G | 1 | a0001c0001t0003g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1126-8689A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901834 | |||||||
| chr5:173901958 | A | G | 1 | a0001c0001t0004g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1126-8565A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901958 | |||||||
| chr5:173902282 | T | C | 33 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0016 others(30): Show |
38 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1126-8241T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902282 | |||||||
| chr5:173902633 | T | C | 6 | a0001c0001t0003g0168 a0001c0001t0011g0045 a0001c0001t0011g0046 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-7890T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902633 | |||||||
| chr5:173902668 | C | T | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1126-7855C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902668 | |||||||
| chr5:173902749 | G | C | 1 | a0001c0001t0003g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1126-7774G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902749 | |||||||
| chr5:173902850 | C | T | 2 | a0001c0001t0004g0281 a0001c0001t0032g0102 |
2 | HG02647.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1126-7673C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902850 | |||||||
| chr5:173902886 | T | C | 1 | a0001c0001t0006g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1126-7637T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902886 | |||||||
| chr5:173902952 | T | G | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1126-7571T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902952 | |||||||
| chr5:173903060 | G | GA | 5 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0045g0151 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-7447dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173903060 | ||||||
| chr5:173903060 | GA | G | 49 | a0001c0001t0001g0146 a0001c0001t0001g0165 a0001c0001t0002g0236 others(46): Show |
55 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1126-7447delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173903060 | ||||||
| chr5:173903082 | A | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-7441A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903082 | |||||||
| chr5:173903461 | C | T | 1 | a0001c0001t0021g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1126-7062C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903461 | |||||||
| chr5:173903517 | A | C | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1126-7006A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903517 | |||||||
| chr5:173903540 | T | G | 2 | a0001c0001t0006g0090 a0001c0001t0006g0091 |
2 | HG01256.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1126-6983T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903540 | |||||||
| chr5:173903862 | GA | G | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1126-6658delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173903862 | ||||||
| chr5:173904271 | G | A | 33 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0016 others(30): Show |
38 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1126-6252G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904271 | |||||||
| chr5:173904590 | A | G | 44 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0016 others(41): Show |
51 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1126-5933A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904590 | |||||||
| chr5:173904655 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1126-5868T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904655 | |||||||
| chr5:173904678 | A | C | 1 | a0001c0001t0003g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1126-5845A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904678 | |||||||
| chr5:173904690 | A | T | 109 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(106): Show |
129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1126-5833A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904690 | |||||||
| chr5:173904727 | T | TC | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(255): Show |
300 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.1126-5795dupC | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904727 | ||||||
| chr5:173904848 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-5675A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904848 | |||||||
| chr5:173904962 | C | A | 1 | a0001c0001t0005g0309 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1126-5561C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904962 | |||||||
| chr5:173904972 | G | GATA | 27 | a0001c0001t0002g0214 a0001c0001t0002g0222 a0001c0001t0003g0014 others(24): Show |
30 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1126-5507_1126-550 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | ||||||
| chr5:173904972 | G | GATAATA | 4 | a0001c0001t0003g0076 a0001c0001t0006g0097 a0001c0001t0006g0098 others(1): Show |
4 | HG02647.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-5510_1126-550 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | ||||||
| chr5:173904972 | GATA | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
75 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1126-5507_1126-550 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | ||||||
| chr5:173904972 | GATAATA | G | 11 | a0001c0001t0001g0129 a0001c0001t0001g0152 a0001c0001t0001g0166 others(8): Show |
16 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1126-5510_1126-550 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | ||||||
| chr5:173905001 | TAATAATA others(11): Show |
T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-5519_1126-550 others(22): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905001 | ||||||
| chr5:173905004 | TAATAATA others(8): Show |
T | 2 | a0001c0001t0002g0248 a0001c0002t0018g0013 |
3 | HG01167.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1126-5516_1126-550 others(19): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905004 | ||||||
| chr5:173905007 | TAATAATA others(5): Show |
T | 9 | a0001c0001t0002g0032 a0001c0001t0002g0209 a0001c0001t0005g0243 others(6): Show |
11 | HG01167.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1126-5513_1126-550 others(16): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905007 | ||||||
| chr5:173905010 | TAATAATA others(2): Show |
T | 24 | a0001c0001t0002g0012 a0001c0001t0002g0034 a0001c0001t0002g0197 others(21): Show |
27 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1126-5510_1126-550 others(13): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905010 | ||||||
| chr5:173905013 | TAATAAA | T | 68 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0035 others(65): Show |
78 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1126-5507_1126-550 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905013 | ||||||
| chr5:173905014 | A | G | 4 | a0001c0001t0005g0205 a0001c0001t0009g0180 a0001c0001t0009g0181 others(1): Show |
4 | HG02965.hp2 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-5509A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905014 | |||||||
| chr5:173905016 | T | A | 2 | a0001c0001t0006g0131 a0002c0006t0006g0086 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1126-5507T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905016 | |||||||
| chr5:173905016 | TAAA | T | 59 | a0001c0001t0002g0004 a0001c0001t0002g0240 a0001c0001t0002g0242 others(56): Show |
66 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1126-5502_1126-550 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905016 | ||||||
| chr5:173905019 | A | T | 12 | a0001c0001t0001g0162 a0001c0001t0002g0214 a0001c0001t0002g0221 others(9): Show |
13 | HG00741.hp1 HG01175.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1126-5504A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905019 | |||||||
| chr5:173905374 | C | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-5149C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905374 | |||||||
| chr5:173905608 | T | C | 1 | a0001c0001t0005g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1126-4915T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905608 | |||||||
| chr5:173905639 | C | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-4884C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905639 | |||||||
| chr5:173905726 | G | A | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1126-4797G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905726 | |||||||
| chr5:173905763 | G | T | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-4760G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905763 | |||||||
| chr5:173906343 | T | C | 1 | a0001c0001t0005g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1126-4180T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906343 | |||||||
| chr5:173906583 | C | T | 108 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1126-3940C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906583 | |||||||
| chr5:173906719 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1126-3804T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906719 | |||||||
| chr5:173906847 | C | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-3676C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906847 | |||||||
| chr5:173906872 | A | T | 2 | a0001c0001t0016g0068 a0001c0001t0016g0096 |
2 | HG01952.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1126-3651A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906872 | |||||||
| chr5:173906906 | C | T | 17 | a0001c0001t0007g0010 a0001c0001t0007g0031 a0001c0001t0007g0169 others(14): Show |
18 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1126-3617C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906906 | |||||||
| chr5:173907025 | T | C | 25 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(22): Show |
27 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1126-3498T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907025 | |||||||
| chr5:173907127 | C | T | 6 | a0001c0001t0005g0026 a0001c0001t0005g0041 a0001c0001t0005g0172 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1126-3396C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907127 | |||||||
| chr5:173907181 | C | T | 20 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(17): Show |
22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-3342C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907181 | |||||||
| chr5:173907216 | T | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-3307T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907216 | |||||||
| chr5:173907267 | A | AAAC | 8 | a0001c0001t0004g0276 a0001c0001t0004g0280 a0001c0001t0005g0304 others(5): Show |
9 | HG00558.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1126-3229_1126-322 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173907267 | ||||||
| chr5:173907302 | G | A | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-3221G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907302 | |||||||
| chr5:173907380 | A | C | 1 | a0001c0001t0005g0029 | 2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1126-3143A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907380 | |||||||
| chr5:173907393 | C | T | 5 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0309 others(2): Show |
5 | HG00423.hp1 HG00558.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-3130C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907393 | |||||||
| chr5:173907398 | C | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(64): Show |
80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1126-3125C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907398 | |||||||
| chr5:173907473 | A | C | 1 | a0001c0001t0002g0198 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1126-3050A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907473 | |||||||
| chr5:173907498 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1126-3025C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907498 | |||||||
| chr5:173907514 | A | G | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1126-3009A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907514 | |||||||
| chr5:173907535 | C | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-2988C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907535 | |||||||
| chr5:173907576 | T | C | 109 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(106): Show |
129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1126-2947T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907576 | |||||||
| chr5:173907789 | G | A | 134 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(131): Show |
157 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.1126-2734G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907789 | |||||||
| chr5:173908283 | T | A | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-2240T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908283 | |||||||
| chr5:173908299 | A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-2224A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908299 | |||||||
| chr5:173908379 | G | A | 1 | a0001c0001t0004g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1126-2144G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908379 | |||||||
| chr5:173908601 | T | C | 1 | a0001c0001t0002g0206 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1126-1922T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908601 | |||||||
| chr5:173908654 | A | G | 3 | a0001c0001t0003g0016 a0001c0001t0003g0073 a0001c0001t0003g0075 |
4 | HG00621.hp2 HG02155.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-1869A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908654 | |||||||
| chr5:173908728 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1126-1795G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908728 | |||||||
| chr5:173908737 | G | C | 1 | a0001c0001t0004g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1126-1786G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908737 | |||||||
| chr5:173908823 | TTGTAA | T | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1126-1694_1126-169 others(9): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173908823 | ||||||
| chr5:173908920 | CTT | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1126-1601_1126-160 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173908920 | ||||||
| chr5:173909157 | A | G | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1126-1366A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909157 | |||||||
| chr5:173909243 | T | G | 1 | a0001c0001t0006g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1126-1280T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909243 | |||||||
| chr5:173909341 | G | C | 2 | a0001c0001t0015g0299 a0001c0001t0025g0300 |
2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1126-1182G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909341 | |||||||
| chr5:173909528 | G | A | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-995G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909528 | |||||||
| chr5:173909531 | AT | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(297): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1126-980delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173909531 | ||||||
| chr5:173909682 | T | C | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1126-841T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909682 | |||||||
| chr5:173909788 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1126-735C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909788 | |||||||
| chr5:173909789 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-734G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909789 | |||||||
| chr5:173909846 | G | A | 170 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1126-677G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909846 | |||||||
| chr5:173909856 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1126-667C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909856 | |||||||
| chr5:173909925 | G | A | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1126-598G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909925 | |||||||
| chr5:173909943 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1126-580T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909943 | |||||||
| chr5:173910130 | T | C | 1 | a0001c0001t0002g0202 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1126-393T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910130 | |||||||
| chr5:173910132 | C | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0052 |
3 | HG01099.hp2 HG01106.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1126-391C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910132 | |||||||
| chr5:173910168 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1126-355A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910168 | |||||||
| chr5:173910177 | A | G | 108 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1126-346A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910177 | |||||||
| chr5:173910178 | C | T | 108 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1126-345C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910178 | |||||||
| chr5:173910208 | A | AT | 8 | a0001c0001t0003g0168 a0001c0001t0011g0045 a0001c0001t0011g0046 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-303dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173910208 | ||||||
| chr5:173910228 | T | C | 1 | a0001c0001t0007g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1126-295T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910228 | |||||||
| chr5:173910292 | G | T | 1 | a0001c0001t0005g0243 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1126-231G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910292 | |||||||
| chr5:173910373 | G | A | 1 | a0001c0001t0023g0176 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1126-150G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910373 | |||||||
| chr5:173910621 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1207+17A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910621 | |||||||
| chr5:173910720 | T | G | 2 | a0001c0001t0003g0053 a0001c0001t0003g0062 |
2 | NA18959.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1207+116T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910720 | |||||||
| chr5:173910850 | T | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+246T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910850 | |||||||
| chr5:173910855 | A | G | 1 | a0001c0001t0004g0298 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1207+251A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910855 | |||||||
| chr5:173910882 | A | AT | 6 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0134 others(3): Show |
8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+286dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173910882 | ||||||
| chr5:173911024 | G | A | 3 | a0001c0001t0006g0094 a0001c0001t0006g0097 a0001c0001t0032g0102 |
3 | HG02647.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1207+420G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911024 | |||||||
| chr5:173911081 | T | TA | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1207+486dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911081 | ||||||
| chr5:173911141 | C | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0209 |
3 | NA18943.hp1 NA19058.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1207+537C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911141 | |||||||
| chr5:173911184 | C | T | 2 | a0001c0001t0006g0127 a0001c0001t0031g0128 |
2 | HG00735.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1207+580C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911184 | |||||||
| chr5:173911196 | G | T | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+592G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911196 | |||||||
| chr5:173911207 | C | A | 1 | a0001c0001t0044g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1207+603C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911207 | |||||||
| chr5:173911263 | G | A | 1 | a0001c0001t0006g0120 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1207+659G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911263 | |||||||
| chr5:173911273 | G | GT | 24 | a0001c0001t0002g0235 a0001c0001t0007g0010 a0001c0001t0007g0030 others(21): Show |
26 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1207+674dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911273 | ||||||
| chr5:173911279 | A | T | 170 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1207+675A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911279 | |||||||
| chr5:173911309 | C | T | 1 | a0001c0001t0051g0217 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1207+705C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911309 | |||||||
| chr5:173911386 | C | T | 1 | a0001c0001t0021g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1207+782C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911386 | |||||||
| chr5:173911397 | G | A | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+793G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911397 | |||||||
| chr5:173911523 | A | G | 1 | a0001c0001t0006g0090 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1207+919A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911523 | |||||||
| chr5:173911609 | C | T | 2 | a0001c0001t0004g0287 a0001c0001t0004g0288 |
2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1207+1005C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911609 | |||||||
| chr5:173911681 | G | GT | 11 | a0001c0001t0003g0065 a0001c0001t0003g0135 a0001c0001t0004g0264 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207+1100dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | ||||||
| chr5:173911681 | G | GTT | 35 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0266 others(32): Show |
41 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1207+1099_1207+110 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | ||||||
| chr5:173911681 | GT | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(172): Show |
207 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.1207+1100delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | ||||||
| chr5:173911681 | GTT | G | 28 | a0001c0001t0001g0092 a0001c0001t0001g0117 a0001c0001t0002g0011 others(25): Show |
32 | HG01943.hp1 HG02071.hp2 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.1207+1099_1207+110 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | ||||||
| chr5:173911758 | CTTCA | C | 5 | a0001c0001t0003g0156 a0001c0001t0005g0029 a0001c0001t0006g0155 others(2): Show |
6 | HG02145.hp1 HG02257.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207+1183_1207+118 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911758 | ||||||
| chr5:173911870 | G | C | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1207+1266G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911870 | |||||||
| chr5:173911912 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0134 others(3): Show |
8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+1308T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911912 | |||||||
| chr5:173912022 | G | A | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1207+1418G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912022 | |||||||
| chr5:173912041 | AT | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1207+1438delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912041 | |||||||
| chr5:173912058 | G | A | 2 | a0001c0001t0010g0027 a0001c0001t0010g0183 |
3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1207+1454G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912058 | |||||||
| chr5:173912132 | T | C | 1 | a0001c0001t0004g0281 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1207+1528T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912132 | |||||||
| chr5:173912219 | G | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+1615G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912219 | |||||||
| chr5:173912367 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1207+1763A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912367 | |||||||
| chr5:173912528 | T | C | 44 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(41): Show |
50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1207+1924T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912528 | |||||||
| chr5:173912626 | A | AT | 15 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0003g0059 others(12): Show |
20 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1207+2038dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173912626 | ||||||
| chr5:173912626 | AT | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0122 a0001c0001t0001g0140 others(18): Show |
22 | HG00280.hp2 HG00609.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1207+2038delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173912626 | ||||||
| chr5:173912642 | T | A | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2038T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912642 | |||||||
| chr5:173912643 | A | T | 1 | a0001c0001t0002g0234 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1207+2039A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912643 | |||||||
| chr5:173912647 | A | T | 1 | a0001c0001t0006g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1207+2043A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912647 | |||||||
| chr5:173912779 | A | T | 1 | a0002c0006t0006g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1207+2175A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912779 | |||||||
| chr5:173912839 | C | A | 59 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(56): Show |
68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1207+2235C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912839 | |||||||
| chr5:173912852 | A | G | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1207+2248A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912852 | |||||||
| chr5:173912882 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1207+2278C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912882 | |||||||
| chr5:173912883 | A | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(64): Show |
80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1207+2279A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912883 | |||||||
| chr5:173912910 | C | T | 1 | a0002c0006t0006g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1207+2306C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912910 | |||||||
| chr5:173912918 | C | CA | 111 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0123 others(108): Show |
131 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1207+2334dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173912918 | ||||||
| chr5:173913355 | G | A | 41 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0016 others(38): Show |
48 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1207+2751G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913355 | |||||||
| chr5:173913493 | T | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+2889T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913493 | |||||||
| chr5:173913914 | G | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+3310G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913914 | |||||||
| chr5:173913949 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1207+3345A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913949 | |||||||
| chr5:173914421 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1207+3817A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173914421 | |||||||
| chr5:173914613 | G | A | 1 | a0001c0001t0056g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1207+4009G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173914613 | |||||||
| chr5:173914656 | T | C | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1207+4052T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173914656 | |||||||
| chr5:173915146 | C | T | 1 | a0001c0001t0004g0275 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1207+4542C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915146 | |||||||
| chr5:173915174 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1207+4570G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915174 | |||||||
| chr5:173915463 | A | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+4859A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915463 | |||||||
| chr5:173915487 | C | T | 1 | a0001c0001t0005g0312 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1207+4883C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915487 | |||||||
| chr5:173915542 | C | A | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1207+4938C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915542 | |||||||
| chr5:173915747 | A | T | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1207+5143A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915747 | |||||||
| chr5:173915749 | G | A | 1 | a0001c0001t0009g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1207+5145G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915749 | |||||||
| chr5:173915755 | T | G | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1207+5151T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915755 | |||||||
| chr5:173915994 | C | T | 1 | a0001c0001t0004g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1207+5390C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915994 | |||||||
| chr5:173916099 | A | C | 1 | a0001c0001t0004g0274 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1207+5495A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916099 | |||||||
| chr5:173916230 | G | C | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+5626G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916230 | |||||||
| chr5:173916274 | A | G | 3 | a0001c0001t0004g0272 a0001c0001t0004g0273 a0001c0005t0004g0289 |
3 | HG00280.hp1 HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1207+5670A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916274 | |||||||
| chr5:173916296 | A | G | 1 | a0001c0001t0006g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1207+5692A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916296 | |||||||
| chr5:173916513 | G | A | 1 | a0001c0001t0005g0304 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1207+5909G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916513 | |||||||
| chr5:173916617 | C | T | 1 | a0001c0001t0006g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207+6013C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916617 | |||||||
| chr5:173916632 | G | C | 1 | a0001c0001t0003g0075 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1207+6028G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916632 | |||||||
| chr5:173916852 | A | G | 2 | a0001c0001t0006g0132 a0001c0001t0006g0136 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1207+6248A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916852 | |||||||
| chr5:173916897 | G | C | 108 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1207+6293G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916897 | |||||||
| chr5:173917101 | G | A | 170 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1207+6497G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917101 | |||||||
| chr5:173917150 | T | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+6546T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917150 | |||||||
| chr5:173917158 | A | G | 1 | a0001c0001t0031g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1207+6554A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917158 | |||||||
| chr5:173917175 | A | G | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1207+6571A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917175 | |||||||
| chr5:173917658 | G | A | 1 | a0001c0001t0005g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1207+7054G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917658 | |||||||
| chr5:173917874 | C | G | 1 | a0002c0006t0006g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1207+7270C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917874 | |||||||
| chr5:173917891 | G | C | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1207+7287G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917891 | |||||||
| chr5:173918020 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+7416A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918020 | |||||||
| chr5:173918083 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1207+7479A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918083 | |||||||
| chr5:173918223 | C | CTGTA | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1207+7620_1207+762 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173918223 | ||||||
| chr5:173918349 | C | T | 3 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0025g0300 |
3 | HG01167.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1207+7745C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918349 | |||||||
| chr5:173918406 | G | T | 33 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0016 others(30): Show |
38 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1207+7802G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918406 | |||||||
| chr5:173918484 | T | C | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1207+7880T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918484 | |||||||
| chr5:173918909 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1207+8305A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918909 | |||||||
| chr5:173918963 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1207+8359G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918963 | |||||||
| chr5:173919082 | C | T | 170 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1207+8478C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919082 | |||||||
| chr5:173919552 | C | G | 1 | a0001c0001t0035g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1207+8948C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919552 | |||||||
| chr5:173919575 | A | G | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1207+8971A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919575 | |||||||
| chr5:173919582 | G | C | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1207+8978G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919582 | |||||||
| chr5:173919617 | G | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+9013G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919617 | |||||||
| chr5:173919623 | G | A | 1 | a0001c0001t0005g0304 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1207+9019G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919623 | |||||||
| chr5:173919648 | T | C | 303 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(300): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1207+9044T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919648 | |||||||
| chr5:173919805 | C | G | 20 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(17): Show |
22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1207+9201C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919805 | |||||||
| chr5:173919830 | T | C | 3 | a0001c0001t0003g0077 a0001c0001t0003g0087 a0001c0001t0036g0055 |
3 | HG02602.hp2 NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1207+9226T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919830 | |||||||
| chr5:173919949 | G | C | 1 | a0001c0001t0003g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1207+9345G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919949 | |||||||
| chr5:173920072 | G | A | 3 | a0001c0001t0005g0038 a0001c0001t0005g0305 a0001c0001t0005g0313 |
4 | NA18947.hp2 NA18956.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+9468G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920072 | |||||||
| chr5:173920303 | T | G | 3 | a0001c0001t0003g0021 a0001c0001t0003g0149 a0001c0001t0006g0150 |
4 | HG02109.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+9699T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920303 | |||||||
| chr5:173920350 | G | C | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+9746G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920350 | |||||||
| chr5:173920385 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1207+9781A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920385 | |||||||
| chr5:173920565 | G | T | 1 | a0001c0001t0003g0080 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1207+9961G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920565 | |||||||
| chr5:173920817 | T | C | 1 | a0001c0001t0006g0120 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1207+10213T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920817 | |||||||
| chr5:173920868 | C | T | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1207+10264C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920868 | |||||||
| chr5:173920890 | C | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+10286C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920890 | |||||||
| chr5:173921153 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+10549G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921153 | |||||||
| chr5:173921328 | G | A | 1 | a0001c0001t0006g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1207+10724G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921328 | |||||||
| chr5:173921454 | G | A | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1207+10850G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921454 | |||||||
| chr5:173921476 | C | G | 2 | a0001c0001t0004g0283 a0001c0001t0004g0284 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1207+10872C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921476 | |||||||
| chr5:173921599 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1208-10851G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921599 | |||||||
| chr5:173921969 | T | C | 3 | a0001c0001t0004g0262 a0001c0001t0004g0266 a0001c0001t0004g0275 |
3 | NA18973.hp2 NA19075.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1208-10481T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921969 | |||||||
| chr5:173922042 | A | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-10408A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922042 | |||||||
| chr5:173922113 | A | G | 108 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1208-10337A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922113 | |||||||
| chr5:173922181 | C | T | 3 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0025g0300 |
3 | HG01167.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1208-10269C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922181 | |||||||
| chr5:173922286 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1208-10164A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922286 | |||||||
| chr5:173922333 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1208-10117C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922333 | |||||||
| chr5:173922401 | C | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-10049C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922401 | |||||||
| chr5:173922649 | T | A | 2 | a0001c0001t0006g0090 a0001c0001t0006g0091 |
2 | HG01256.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1208-9801T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922649 | |||||||
| chr5:173922754 | A | G | 50 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(47): Show |
59 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1208-9696A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922754 | |||||||
| chr5:173922788 | G | A | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1208-9662G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922788 | |||||||
| chr5:173922826 | C | T | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-9624C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922826 | |||||||
| chr5:173922837 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-9613A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922837 | |||||||
| chr5:173923402 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-9048A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923402 | |||||||
| chr5:173923556 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1208-8894T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923556 | |||||||
| chr5:173923562 | C | A | 1 | a0001c0001t0002g0234 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1208-8888C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923562 | |||||||
| chr5:173923813 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1208-8637C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923813 | |||||||
| chr5:173923814 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1208-8636T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923814 | |||||||
| chr5:173923987 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-8463G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923987 | |||||||
| chr5:173924078 | C | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-8372C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924078 | |||||||
| chr5:173924357 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1208-8093C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924357 | |||||||
| chr5:173924485 | C | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-7965C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924485 | |||||||
| chr5:173924756 | C | A | 1 | a0001c0001t0044g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1208-7694C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924756 | |||||||
| chr5:173924855 | G | A | 153 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(150): Show |
180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1208-7595G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924855 | |||||||
| chr5:173924858 | G | T | 153 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(150): Show |
180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1208-7592G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924858 | |||||||
| chr5:173924910 | A | G | 1 | a0001c0001t0006g0150 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1208-7540A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924910 | |||||||
| chr5:173925308 | T | C | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-7142T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925308 | |||||||
| chr5:173925350 | C | A | 48 | a0001c0001t0005g0003 a0001c0001t0005g0009 a0001c0001t0005g0026 others(45): Show |
59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1208-7100C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925350 | |||||||
| chr5:173925474 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0108 |
3 | HG00735.hp1 HG01261.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1208-6976G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925474 | |||||||
| chr5:173925712 | G | A | 1 | a0001c0001t0035g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1208-6738G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925712 | |||||||
| chr5:173925760 | G | A | 303 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(300): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1208-6690G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925760 | |||||||
| chr5:173925800 | T | C | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1208-6650T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925800 | |||||||
| chr5:173926429 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1208-6021T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926429 | |||||||
| chr5:173926511 | T | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-5939T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926511 | |||||||
| chr5:173926826 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1208-5624G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926826 | |||||||
| chr5:173926946 | C | T | 48 | a0001c0001t0005g0003 a0001c0001t0005g0009 a0001c0001t0005g0026 others(45): Show |
59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1208-5504C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926946 | |||||||
| chr5:173927007 | C | T | 3 | a0001c0001t0006g0094 a0001c0001t0006g0097 a0001c0001t0032g0102 |
3 | HG02647.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1208-5443C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927007 | |||||||
| chr5:173927010 | G | A | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1208-5440G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927010 | |||||||
| chr5:173927019 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1208-5431C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927019 | |||||||
| chr5:173927044 | G | A | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1208-5406G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927044 | |||||||
| chr5:173927157 | T | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-5293T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927157 | |||||||
| chr5:173927278 | G | C | 4 | a0001c0001t0006g0015 a0001c0001t0006g0069 a0001c0001t0006g0070 others(1): Show |
5 | HG02486.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-5172G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927278 | |||||||
| chr5:173927283 | T | C | 19 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(16): Show |
21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1208-5167T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927283 | |||||||
| chr5:173927339 | C | G | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1208-5111C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927339 | |||||||
| chr5:173927370 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1208-5080C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927370 | |||||||
| chr5:173927427 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-5023G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927427 | |||||||
| chr5:173927543 | C | T | 1 | a0001c0001t0034g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1208-4907C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927543 | |||||||
| chr5:173927620 | T | C | 1 | a0001c0001t0013g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1208-4830T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927620 | |||||||
| chr5:173927650 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1208-4800G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927650 | |||||||
| chr5:173927669 | C | T | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1208-4781C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927669 | |||||||
| chr5:173927731 | C | T | 19 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(16): Show |
21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1208-4719C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927731 | |||||||
| chr5:173927740 | GCACTC | G | 19 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(16): Show |
21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1208-4707_1208-470 others(9): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173927740 | ||||||
| chr5:173927839 | G | A | 170 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1208-4611G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927839 | |||||||
| chr5:173927907 | A | G | 1 | a0001c0001t0007g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1208-4543A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927907 | |||||||
| chr5:173927988 | A | T | 1 | a0001c0001t0002g0235 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-4462A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927988 | |||||||
| chr5:173928139 | C | T | 1 | a0001c0001t0007g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1208-4311C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928139 | |||||||
| chr5:173928387 | A | G | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1208-4063A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928387 | |||||||
| chr5:173928474 | C | T | 1 | a0001c0001t0006g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1208-3976C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928474 | |||||||
| chr5:173928585 | G | A | 3 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0025g0300 |
3 | HG01167.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1208-3865G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928585 | |||||||
| chr5:173928711 | C | T | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1208-3739C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928711 | |||||||
| chr5:173929285 | A | G | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1208-3165A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929285 | |||||||
| chr5:173929288 | T | A | 3 | a0001c0001t0012g0007 a0001c0001t0012g0093 a0001c0001t0042g0007 |
4 | NA18952.hp2 NA18970.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-3162T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929288 | |||||||
| chr5:173929434 | C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1208-3016C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929434 | |||||||
| chr5:173929538 | T | A | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1208-2912T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929538 | |||||||
| chr5:173929557 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-2893G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929557 | |||||||
| chr5:173929614 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1208-2836C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929614 | |||||||
| chr5:173929635 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-2815G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929635 | |||||||
| chr5:173929658 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1208-2792A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929658 | |||||||
| chr5:173929745 | A | G | 44 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(41): Show |
50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1208-2705A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929745 | |||||||
| chr5:173929749 | G | C | 44 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(41): Show |
50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1208-2701G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929749 | |||||||
| chr5:173929785 | G | A | 1 | a0001c0001t0044g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1208-2665G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929785 | |||||||
| chr5:173929801 | A | T | 1 | a0001c0001t0002g0235 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-2649A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929801 | |||||||
| chr5:173929826 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0138 a0001c0001t0001g0143 others(1): Show |
6 | HG01192.hp1 HG01243.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-2624A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929826 | |||||||
| chr5:173930039 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1208-2411C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930039 | |||||||
| chr5:173930056 | G | GT | 8 | a0001c0001t0002g0214 a0001c0001t0003g0159 a0001c0001t0004g0277 others(5): Show |
8 | HG02040.hp1 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208-2379dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173930056 | ||||||
| chr5:173930121 | C | A | 2 | a0001c0001t0004g0283 a0001c0001t0004g0284 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1208-2329C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930121 | |||||||
| chr5:173930200 | A | C | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1208-2250A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930200 | |||||||
| chr5:173930203 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-2247G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930203 | |||||||
| chr5:173930327 | G | A | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1208-2123G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930327 | |||||||
| chr5:173930392 | GCTCGTAG others(3): Show |
G | 8 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0266 others(5): Show |
8 | HG02071.hp1 HG02155.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208-2054_1208-204 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173930392 | ||||||
| chr5:173930403 | C | G | 50 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(47): Show |
59 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1208-2047C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930403 | |||||||
| chr5:173930533 | C | T | 108 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1208-1917C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930533 | |||||||
| chr5:173930671 | C | A | 1 | a0001c0001t0004g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1208-1779C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930671 | |||||||
| chr5:173930715 | G | A | 1 | a0001c0001t0003g0077 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1208-1735G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930715 | |||||||
| chr5:173930791 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1208-1659A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930791 | |||||||
| chr5:173930807 | T | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-1643T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930807 | |||||||
| chr5:173930829 | A | G | 1 | a0001c0001t0029g0219 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1208-1621A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930829 | |||||||
| chr5:173930990 | CA | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(280): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1208-1440delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173930990 | ||||||
| chr5:173931132 | A | T | 4 | a0001c0001t0005g0003 a0001c0001t0005g0194 a0001c0001t0005g0213 others(1): Show |
7 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-1318A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931132 | |||||||
| chr5:173931151 | G | A | 127 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(124): Show |
149 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1208-1299G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931151 | |||||||
| chr5:173931288 | G | A | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1208-1162G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931288 | |||||||
| chr5:173931334 | C | T | 42 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(39): Show |
48 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1208-1116C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931334 | |||||||
| chr5:173931954 | A | G | 28 | a0001c0001t0005g0003 a0001c0001t0005g0009 a0001c0001t0005g0026 others(25): Show |
37 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1208-496A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931954 | |||||||
| chr5:173931962 | T | C | 1 | a0001c0001t0002g0218 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1208-488T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931962 | |||||||
| chr5:173932048 | A | C | 48 | a0001c0001t0005g0003 a0001c0001t0005g0009 a0001c0001t0005g0026 others(45): Show |
59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1208-402A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932048 | |||||||
| chr5:173932081 | G | A | 2 | a0001c0001t0011g0047 a0001c0001t0033g0044 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1208-369G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932081 | |||||||
| chr5:173932149 | A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1208-301A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932149 | |||||||
| chr5:173932328 | A | G | 4 | a0001c0001t0002g0034 a0001c0001t0002g0232 a0001c0001t0002g0254 others(1): Show |
5 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-122A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932328 | |||||||
| chr5:173932373 | A | G | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG02040.hp2 NA18949.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-77A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932373 | |||||||
| chr5:173932678 | T | G | 1 | a0001c0001t0005g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1258+178T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173932678 | |||||||
| chr5:173932722 | A | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1258+222A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173932722 | |||||||
| chr5:173932998 | C | T | 94 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(91): Show |
112 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1258+498C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173932998 | |||||||
| chr5:173933282 | G | A | 1 | a0001c0001t0007g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1258+782G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933282 | |||||||
| chr5:173933519 | A | G | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1258+1019A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933519 | |||||||
| chr5:173933663 | G | C | 1 | a0001c0001t0005g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1258+1163G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933663 | |||||||
| chr5:173933898 | C | G | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1258+1398C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933898 | |||||||
| chr5:173933992 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1258+1492C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933992 | |||||||
| chr5:173933993 | G | A | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1258+1493G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933993 | |||||||
| chr5:173934537 | C | T | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1258+2037C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934537 | |||||||
| chr5:173934545 | G | A | 1 | a0001c0001t0006g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1258+2045G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934545 | |||||||
| chr5:173934699 | C | A | 1 | a0001c0001t0036g0055 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1258+2199C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934699 | |||||||
| chr5:173934707 | G | A | 1 | a0001c0001t0008g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1258+2207G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934707 | |||||||
| chr5:173934777 | G | A | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1258+2277G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934777 | |||||||
| chr5:173934826 | A | C | 1 | a0001c0001t0006g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1258+2326A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934826 | |||||||
| chr5:173934948 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1258+2448C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934948 | |||||||
| chr5:173935106 | C | T | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1258+2606C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935106 | |||||||
| chr5:173935274 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1258+2774C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935274 | |||||||
| chr5:173935309 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0134 others(3): Show |
8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258+2809T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935309 | |||||||
| chr5:173935454 | T | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(299): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1258+2954T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935454 | |||||||
| chr5:173935455 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1258+2955G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935455 | |||||||
| chr5:173935598 | A | G | 13 | a0001c0001t0005g0038 a0001c0001t0005g0303 a0001c0001t0005g0304 others(10): Show |
15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1258+3098A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935598 | |||||||
| chr5:173935723 | C | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1258+3223C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935723 | |||||||
| chr5:173935743 | C | T | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1258+3243C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935743 | |||||||
| chr5:173936463 | A | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0167 |
3 | HG01934.hp1 NA18943.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1258+3963A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936463 | |||||||
| chr5:173936664 | G | T | 134 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(131): Show |
157 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.1258+4164G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936664 | |||||||
| chr5:173936771 | A | G | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1258+4271A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936771 | |||||||
| chr5:173936814 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1258+4314C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936814 | |||||||
| chr5:173936814 | CT | C | 116 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(113): Show |
136 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1258+4329delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173936814 | ||||||
| chr5:173936848 | C | T | 5 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1258+4348C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936848 | |||||||
| chr5:173936886 | C | T | 134 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(131): Show |
157 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.1258+4386C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936886 | |||||||
| chr5:173936907 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1258+4407T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936907 | |||||||
| chr5:173936922 | G | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(299): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1258+4422G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936922 | |||||||
| chr5:173936953 | T | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0254 |
3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1258+4453T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936953 | |||||||
| chr5:173936974 | T | C | 1 | a0001c0001t0004g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1258+4474T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936974 | |||||||
| chr5:173937019 | C | CT | 9 | a0001c0001t0001g0050 a0001c0001t0001g0079 a0001c0001t0001g0119 others(6): Show |
9 | HG01192.hp1 HG02293.hp1 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258+4541dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173937019 | ||||||
| chr5:173937019 | CT | C | 45 | a0001c0001t0001g0109 a0001c0001t0002g0253 a0001c0001t0003g0057 others(42): Show |
51 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1258+4541delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173937019 | ||||||
| chr5:173937019 | CTT | C | 130 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(127): Show |
153 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.1258+4540_1258+454 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173937019 | ||||||
| chr5:173937021 | T | C | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1258+4521T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937021 | |||||||
| chr5:173937022 | T | C | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1258+4522T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937022 | |||||||
| chr5:173937090 | T | C | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1258+4590T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937090 | |||||||
| chr5:173937284 | C | T | 2 | a0001c0001t0010g0027 a0001c0001t0010g0183 |
3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1258+4784C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937284 | |||||||
| chr5:173937400 | G | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1258+4900G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937400 | |||||||
| chr5:173937874 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1259-5152T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937874 | |||||||
| chr5:173938076 | A | G | 1 | a0001c0001t0003g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1259-4950A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938076 | |||||||
| chr5:173938145 | A | G | 5 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1259-4881A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938145 | |||||||
| chr5:173938273 | T | C | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1259-4753T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938273 | |||||||
| chr5:173938290 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1259-4736A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938290 | |||||||
| chr5:173938307 | T | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1259-4719T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938307 | |||||||
| chr5:173938423 | A | G | 1 | a0001c0001t0045g0151 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1259-4603A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938423 | |||||||
| chr5:173938445 | C | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1259-4581C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938445 | |||||||
| chr5:173938484 | C | T | 1 | a0001c0001t0052g0054 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1259-4542C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938484 | |||||||
| chr5:173938500 | A | G | 1 | a0001c0001t0004g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1259-4526A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938500 | |||||||
| chr5:173938501 | T | TA | 17 | a0001c0001t0003g0005 a0001c0001t0003g0053 a0001c0001t0003g0056 others(14): Show |
19 | HG01069.hp1 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1259-4524dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173938501 | ||||||
| chr5:173938534 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1259-4492C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938534 | |||||||
| chr5:173938574 | C | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | NA18949.hp2 NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1259-4452C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938574 | |||||||
| chr5:173938712 | C | T | 1 | a0001c0001t0017g0101 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1259-4314C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938712 | |||||||
| chr5:173938757 | G | A | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1259-4269G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938757 | |||||||
| chr5:173938853 | C | T | 1 | a0001c0001t0006g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1259-4173C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938853 | |||||||
| chr5:173938858 | A | G | 1 | a0001c0001t0006g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1259-4168A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938858 | |||||||
| chr5:173938861 | A | ATATAATA others(9): Show |
1 | a0001c0001t0006g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1259-4165_1259-416 others(20): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938861 | |||||||
| chr5:173939103 | A | T | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1259-3923A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939103 | |||||||
| chr5:173939308 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1259-3718T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939308 | |||||||
| chr5:173939341 | GTACA | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(272): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1259-3656_1259-365 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173939341 | ||||||
| chr5:173939527 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1259-3499C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939527 | |||||||
| chr5:173939607 | A | G | 4 | a0001c0001t0005g0003 a0001c0001t0005g0194 a0001c0001t0005g0213 others(1): Show |
7 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1259-3419A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939607 | |||||||
| chr5:173939618 | C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1259-3408C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939618 | |||||||
| chr5:173939671 | C | T | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1259-3355C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939671 | |||||||
| chr5:173939742 | A | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0134 others(3): Show |
8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1259-3284A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939742 | |||||||
| chr5:173939753 | CT | C | 130 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0004 others(127): Show |
153 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.1259-3260delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173939753 | ||||||
| chr5:173939890 | T | C | 7 | a0001c0001t0003g0168 a0001c0001t0004g0268 a0001c0001t0011g0045 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1259-3136T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939890 | |||||||
| chr5:173939956 | C | CA | 57 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0011 others(54): Show |
66 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1259-3053dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173939956 | ||||||
| chr5:173939988 | T | C | 1 | a0001c0001t0003g0059 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1259-3038T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939988 | |||||||
| chr5:173940340 | T | C | 1 | a0001c0001t0004g0282 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1259-2686T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940340 | |||||||
| chr5:173940366 | T | C | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1259-2660T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940366 | |||||||
| chr5:173940391 | A | T | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1259-2635A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940391 | |||||||
| chr5:173940484 | T | C | 1 | a0001c0001t0004g0288 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1259-2542T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940484 | |||||||
| chr5:173940532 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1259-2494T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940532 | |||||||
| chr5:173940578 | G | C | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1259-2448G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940578 | |||||||
| chr5:173940583 | T | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1259-2443T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940583 | |||||||
| chr5:173940971 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1259-2055C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940971 | |||||||
| chr5:173941137 | A | G | 1 | a0001c0001t0006g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1259-1889A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941137 | |||||||
| chr5:173941177 | G | C | 3 | a0001c0001t0004g0037 a0001c0001t0004g0277 a0001c0001t0004g0281 |
4 | HG01256.hp1 HG01258.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259-1849G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941177 | |||||||
| chr5:173941548 | T | A | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1259-1478T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941548 | |||||||
| chr5:173941651 | T | TC | 19 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(16): Show |
21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1259-1374dupC | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173941651 | ||||||
| chr5:173941672 | A | C | 8 | a0001c0001t0005g0003 a0001c0001t0005g0028 a0001c0001t0005g0029 others(5): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1259-1354A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941672 | |||||||
| chr5:173941785 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1259-1241C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941785 | |||||||
| chr5:173941786 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0253 |
2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1259-1240G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941786 | |||||||
| chr5:173941810 | G | A | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259-1216G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941810 | |||||||
| chr5:173941817 | G | A | 42 | a0001c0001t0002g0202 a0001c0001t0003g0005 a0001c0001t0003g0014 others(39): Show |
49 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1259-1209G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941817 | |||||||
| chr5:173941827 | G | A | 1 | a0001c0001t0016g0096 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1259-1199G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941827 | |||||||
| chr5:173941916 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1259-1110C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941916 | |||||||
| chr5:173941989 | G | C | 1 | a0001c0001t0015g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1259-1037G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941989 | |||||||
| chr5:173941997 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1259-1029C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941997 | |||||||
| chr5:173942552 | T | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(67): Show |
83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1259-474T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942552 | |||||||
| chr5:173942558 | T | C | 1 | a0001c0001t0004g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1259-468T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942558 | |||||||
| chr5:173942642 | A | G | 1 | a0001c0001t0007g0193 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1259-384A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942642 | |||||||
| chr5:173942663 | A | G | 4 | a0001c0001t0011g0045 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259-363A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942663 | |||||||
| chr5:173942970 | T | C | 1 | a0001c0005t0004g0289 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1259-56T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942970 | |||||||
| chr5:173943312 | C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1282+263C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943312 | |||||||
| chr5:173943485 | A | G | 30 | a0001c0001t0005g0003 a0001c0001t0005g0009 a0001c0001t0005g0026 others(27): Show |
39 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1282+436A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943485 | |||||||
| chr5:173943489 | A | G | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1282+440A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943489 | |||||||
| chr5:173943660 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1282+611T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943660 | |||||||
| chr5:173943786 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(73): Show |
89 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282+737T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943786 | |||||||
| chr5:173944474 | C | CA | 7 | a0001c0001t0001g0106 a0001c0001t0003g0062 a0001c0001t0003g0156 others(4): Show |
7 | HG00735.hp2 HG01943.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1283-473dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 173944474 | ||||||
| chr5:173944474 | CA | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(129): Show |
155 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1283-473delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 173944474 | ||||||
| chr5:173944474 | CAA | C | 40 | a0001c0001t0002g0195 a0001c0001t0004g0001 a0001c0001t0004g0037 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1283-474_1283-473d others(4): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 173944474 | ||||||
| chr5:173944500 | T | A | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1283-467T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944500 | |||||||
| chr5:173944663 | C | A | 3 | a0001c0001t0005g0201 a0001c0001t0021g0200 a0002c0007t0005g0199 |
3 | HG02257.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1283-304C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944663 | |||||||
| chr5:173944914 | T | C | 1 | a0001c0001t0015g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1283-53T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944914 | |||||||
| chr5:173944938 | T | G | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1283-29T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944938 | |||||||
| chr5:173944941 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1283-26C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944941 | |||||||
| chr5:173945155 | G | T | 1 | a0001c0001t0002g0202 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1456+15G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945155 | |||||||
| chr5:173945181 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1456+41G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945181 | |||||||
| chr5:173945424 | C | G | 2 | a0001c0001t0004g0283 a0001c0001t0004g0284 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1456+284C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945424 | |||||||
| chr5:173945480 | C | CT | 41 | a0001c0001t0001g0081 a0001c0001t0004g0001 a0001c0001t0004g0037 others(38): Show |
47 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1456+345dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 173945480 | ||||||
| chr5:173945484 | T | A | 2 | a0001c0001t0003g0057 a0001c0001t0003g0061 |
2 | HG01123.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1456+344T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945484 | |||||||
| chr5:173945622 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+482G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945622 | |||||||
| chr5:173945647 | T | C | 1 | a0001c0001t0040g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1456+507T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945647 | |||||||
| chr5:173946100 | G | T | 4 | a0001c0001t0006g0015 a0001c0001t0006g0069 a0001c0001t0006g0070 others(1): Show |
5 | HG02486.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456+960G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946100 | |||||||
| chr5:173946140 | T | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+1000T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946140 | |||||||
| chr5:173946329 | A | G | 109 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(106): Show |
129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1456+1189A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946329 | |||||||
| chr5:173946485 | A | C | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+1345A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946485 | |||||||
| chr5:173946582 | G | A | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1456+1442G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946582 | |||||||
| chr5:173946887 | G | A | 4 | a0001c0001t0004g0269 a0001c0001t0004g0290 a0001c0001t0004g0291 others(1): Show |
4 | HG00423.hp2 NA18941.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456+1747G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946887 | |||||||
| chr5:173946945 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+1805A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946945 | |||||||
| chr5:173946965 | C | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1456+1825C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946965 | |||||||
| chr5:173947033 | A | G | 20 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(17): Show |
22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1456+1893A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947033 | |||||||
| chr5:173947155 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1456+2015T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947155 | |||||||
| chr5:173947164 | C | CT | 3 | a0001c0001t0005g0201 a0001c0001t0021g0200 a0002c0007t0005g0199 |
3 | HG02257.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1456+2027dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 173947164 | ||||||
| chr5:173947259 | G | A | 2 | a0001c0001t0004g0276 a0001c0001t0004g0280 |
2 | HG02738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1456+2119G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947259 | |||||||
| chr5:173947267 | G | A | 2 | a0001c0001t0004g0276 a0001c0001t0004g0280 |
2 | HG02738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1456+2127G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947267 | |||||||
| chr5:173947434 | C | T | 1 | a0001c0001t0004g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1457-2074C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947434 | |||||||
| chr5:173947435 | G | A | 1 | a0001c0001t0004g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1457-2073G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947435 | |||||||
| chr5:173947458 | C | T | 109 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(106): Show |
129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1457-2050C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947458 | |||||||
| chr5:173947494 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0112 a0001c0001t0001g0164 |
3 | NA18978.hp1 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1457-2014A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947494 | |||||||
| chr5:173947612 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1457-1896A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947612 | |||||||
| chr5:173947652 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1457-1856A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947652 | |||||||
| chr5:173947749 | T | C | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1457-1759T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947749 | |||||||
| chr5:173947751 | T | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(71): Show |
87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1457-1757T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947751 | |||||||
| chr5:173947757 | C | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1457-1751C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947757 | |||||||
| chr5:173947906 | G | A | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1457-1602G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947906 | |||||||
| chr5:173947952 | G | A | 108 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1457-1556G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947952 | |||||||
| chr5:173947983 | C | T | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1457-1525C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947983 | |||||||
| chr5:173948129 | A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1457-1379A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948129 | |||||||
| chr5:173948144 | A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1457-1364A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948144 | |||||||
| chr5:173948153 | A | C | 1 | a0001c0001t0003g0072 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1457-1355A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948153 | |||||||
| chr5:173948165 | T | A | 21 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1457-1343T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948165 | |||||||
| chr5:173948254 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1457-1254A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948254 | |||||||
| chr5:173948419 | C | T | 3 | a0001c0001t0005g0172 a0001c0001t0005g0178 a0001c0001t0005g0179 |
3 | HG01884.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1457-1089C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948419 | |||||||
| chr5:173948574 | G | A | 13 | a0001c0001t0005g0038 a0001c0001t0005g0303 a0001c0001t0005g0304 others(10): Show |
15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1457-934G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948574 | |||||||
| chr5:173948670 | G | C | 59 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(56): Show |
68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1457-838G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948670 | |||||||
| chr5:173948981 | G | A | 170 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1457-527G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948981 | |||||||
| chr5:173949084 | A | C | 1 | a0001c0001t0006g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1457-424A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173949084 | |||||||
| chr5:173949192 | C | T | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1457-316C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173949192 | |||||||
| chr5:173949503 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
splice_region_variant&intron_variant | LOW | c.1457-5A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173949503 | |||||||
| chr5:173949694 | A | G | 1 | a0001c0001t0002g0247 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1546+97A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 6/9 | chr5 | 173949694 | |||||||
| chr5:173949738 | A | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0134 others(3): Show |
8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+141A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 6/9 | chr5 | 173949738 | |||||||
| chr5:173950332 | T | C | 2 | a0001c0001t0010g0027 a0001c0001t0010g0183 |
3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1665+254T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950332 | |||||||
| chr5:173950432 | C | T | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1665+354C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950432 | |||||||
| chr5:173950466 | A | G | 171 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(168): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1665+388A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950466 | |||||||
| chr5:173950603 | C | CAAAAT | 13 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0092 others(10): Show |
17 | HG00544.hp1 HG00639.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.1665+555_1665+559d others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 173950603 | ||||||
| chr5:173950603 | CAAAAT | C | 135 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(132): Show |
158 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.1665+555_1665+559d others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 173950603 | ||||||
| chr5:173950614 | A | T | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1665+536A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950614 | |||||||
| chr5:173950633 | T | A | 39 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(36): Show |
45 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1665+555T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950633 | |||||||
| chr5:173950814 | G | A | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1665+736G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950814 | |||||||
| chr5:173950993 | G | A | 17 | a0001c0001t0005g0009 a0001c0001t0005g0026 a0001c0001t0005g0041 others(14): Show |
20 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1666-831G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950993 | |||||||
| chr5:173951177 | A | G | 44 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(41): Show |
50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1666-647A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951177 | |||||||
| chr5:173951281 | C | T | 1 | a0001c0001t0049g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1666-543C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951281 | |||||||
| chr5:173951283 | T | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1666-541T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951283 | |||||||
| chr5:173951313 | T | TA | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1666-502dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 173951313 | ||||||
| chr5:173951314 | A | T | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1666-510A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951314 | |||||||
| chr5:173951768 | T | C | 4 | a0001c0001t0004g0269 a0001c0001t0004g0290 a0001c0001t0004g0291 others(1): Show |
4 | HG00423.hp2 NA18941.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1666-56T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951768 | |||||||
| chr5:173951812 | T | C | 1 | a0001c0001t0022g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1666-12T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951812 | |||||||
| chr5:173952103 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1780+165G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952103 | |||||||
| chr5:173952344 | G | T | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1780+406G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952344 | |||||||
| chr5:173952538 | G | A | 2 | a0001c0001t0019g0042 a0001c0001t0019g0043 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1781-553G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952538 | |||||||
| chr5:173952643 | C | G | 1 | a0001c0001t0006g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1781-448C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952643 | |||||||
| chr5:173952692 | A | C | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1781-399A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952692 | |||||||
| chr5:173952713 | A | G | 1 | a0001c0001t0037g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1781-378A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952713 | |||||||
| chr5:173952794 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1781-297C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952794 | |||||||
| chr5:173953343 | C | T | 153 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(150): Show |
180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1962+71C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953343 | |||||||
| chr5:173953344 | G | A | 1 | a0001c0001t0003g0005 | 3 | HG01069.hp1 HG01074.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1962+72G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953344 | |||||||
| chr5:173953408 | T | C | 2 | a0001c0001t0015g0299 a0001c0001t0025g0300 |
2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1962+136T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953408 | |||||||
| chr5:173953592 | T | A | 174 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(171): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1962+320T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953592 | |||||||
| chr5:173953726 | CT | C | 170 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(167): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1962+468delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 173953726 | ||||||
| chr5:173953891 | C | T | 6 | a0001c0001t0007g0030 a0001c0001t0007g0031 a0001c0001t0007g0173 others(3): Show |
8 | HG02015.hp1 HG02135.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1962+619C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953891 | |||||||
| chr5:173953931 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0261 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1962+659A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953931 | |||||||
| chr5:173954172 | T | G | 3 | a0001c0001t0013g0040 a0001c0001t0013g0084 a0001c0001t0013g0085 |
3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1962+900T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954172 | |||||||
| chr5:173954270 | A | T | 2 | a0001c0001t0004g0272 a0001c0001t0004g0273 |
2 | HG00280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1962+998A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954270 | |||||||
| chr5:173954497 | C | T | 2 | a0001c0001t0010g0027 a0001c0001t0010g0183 |
3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1962+1225C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954497 | |||||||
| chr5:173954596 | C | G | 1 | a0001c0001t0002g0197 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1963-1314C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954596 | |||||||
| chr5:173954860 | G | T | 4 | a0001c0001t0015g0299 a0001c0001t0015g0301 a0001c0001t0022g0302 others(1): Show |
4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1963-1050G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954860 | |||||||
| chr5:173954945 | A | T | 1 | a0001c0001t0003g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1963-965A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954945 | |||||||
| chr5:173954946 | T | A | 16 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 others(13): Show |
21 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1963-964T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954946 | |||||||
| chr5:173954971 | C | T | 1 | a0001c0001t0004g0275 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1963-939C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954971 | |||||||
| chr5:173955265 | T | C | 1 | a0001c0002t0018g0013 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1963-645T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955265 | |||||||
| chr5:173955338 | CT | C | 9 | a0001c0001t0002g0207 a0001c0001t0002g0218 a0001c0001t0004g0271 others(6): Show |
9 | HG01167.hp2 HG01517.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1963-557delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 173955338 | ||||||
| chr5:173955445 | G | C | 1 | a0001c0001t0010g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1963-465G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955445 | |||||||
| chr5:173955474 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(316): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1963-436A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955474 | |||||||
| chr5:173955628 | T | C | 5 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0309 others(2): Show |
5 | HG00423.hp1 HG00558.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1963-282T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955628 | |||||||
| chr5:173955635 | C | T | 3 | a0001c0001t0003g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 |
3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1963-275C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955635 | |||||||
| chr5:173955758 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(70): Show |
86 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1963-152G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955758 | |||||||
| chr5:173955774 | A | G | 18 | a0001c0001t0007g0010 a0001c0001t0007g0030 a0001c0001t0007g0031 others(15): Show |
20 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1963-136A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955774 | |||||||
| chr5:173955838 | G | A | 1 | a0001c0001t0005g0177 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1963-72G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955838 |