Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 60677 |
|---|---|
| ensemblid | ENSG00000140488.16 |
| hgncid | 14059 |
| symbol | CELF6 |
| name | CUGBP Elav-like family member 6 |
| refseq_nuc | NM_052840.5 |
| refseq_prot | NP_443072.3 |
| ensembl_nuc | ENST00000287202.10 |
| ensembl_prot | ENSP00000287202.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 72284727 |
| end | 72320157 |
| strand | - |
| ver | v1.2 |
| region | chr15:72284727-72320157 |
| region5000 | chr15:72279727-72325157 |
| regionname0 | CELF6_chr15_72284727_72320157 |
| regionname5000 | CELF6_chr15_72279727_72325157 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 481 | 297 | 85 | 48 | 136 | 8 | 18 | 100 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0002 | 0/0 | 481 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0003 | 0/0 | 481 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0004 | 0/0 | 481 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1446 | 294 | 83 | 48 | 136 | 7 | 18 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| c0002 | 0/0 | 1446 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| c0003 | 0/0 | 1446 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| c0004 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| c0005 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| c0006 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1928 | 139 | 17 | 32 | 66 | 6 | 17 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0002 | 1/0 | 1928 | 121 | 54 | 8 | 57 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0003 | 0/0 | 1928 | 14 | 6 | 8 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0004 | 0/0 | 1928 | 10 | 0 | 0 | 10 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0005 | 0/0 | 1928 | 9 | 9 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0006 | 0/0 | 1928 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0007 | 0/0 | 1928 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0008 | 0/0 | 1928 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0009 | 0/0 | 1928 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0010 | 0/0 | 1928 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0011 | 0/0 | 1928 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| t0012 | 0/0 | 1928 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 20 | 2 | 2 | 13 | 0 | 3 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0002 | 0/1 | 13 | 2 | 1 | 8 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1446 | 294 | 83 | 48 | 136 | 7 | 18 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0002 | 0/0 | 1446 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0003 | 0/0 | 1446 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0002c0006 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0003c0005 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0004c0004 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3373 | 139 | 17 | 32 | 66 | 6 | 17 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0002 | 1/0 | 3373 | 116 | 50 | 8 | 57 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0003 | 0/0 | 3373 | 14 | 6 | 8 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0004 | 0/0 | 3373 | 10 | 0 | 0 | 10 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0005 | 0/0 | 3373 | 8 | 8 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0006 | 0/0 | 3373 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0007 | 0/0 | 3373 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0008 | 0/0 | 3373 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0009 | 0/0 | 3373 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0010 | 0/0 | 3373 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0011 | 0/0 | 3373 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0001t0012 | 0/0 | 3373 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0002t0002 | 0/0 | 3373 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0001c0003t0002 | 0/0 | 3373 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0002c0006t0005 | 0/0 | 3373 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0003c0005t0002 | 0/0 | 3373 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| a0004c0004t0002 | 0/0 | 3373 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | copy fasta | chr15 | 72279727 | 72325157 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 2 | 2 | 13 | 0 | 3 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0002 | 0/1 | 13 | 2 | 1 | 8 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0004g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0011g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0002c0006t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0003c0005t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| a0004c0004t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0012 | g0207 | EUR | GBR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00609 | hp2 | a0001 | c0001 | t0011 | g0206 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CDX | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CDX | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0086 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0131 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02976 | hp2 | a0002 | c0006 | t0005 | g0162 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03130 | hp2 | a0004 | c0004 | t0002 | g0033 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0163 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03486 | hp1 | a0003 | c0005 | t0002 | g0183 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | GWD | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | YRI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | YRI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | YRI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | LWK | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19063 | hp2 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19067 | hp2 | a0001 | c0001 | t0010 | g0067 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | YRI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ASW | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ASW | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0032 | EUR | TSI | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | USA | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | USA | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | LWK | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0192 | REF | REF | CELF6_chr15_72279727_72325157 | CELF6 | chr15 | 72279727 | 72325157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:72289180
|
C | T | 1 | a0002 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.988G>A | p.Gly330Ser | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 8/13 | 1271/3373 | 988/1446 | 330/481 | chr15 | 72289180 | ||
| chr15:72290139
|
C | G | 1 | a0003 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.511G>C | p.Gly171Arg | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 4/13 | 794/3373 | 511/1446 | 171/481 | chr15 | 72290139 | ||
| chr15:72319756
|
A | G | 1 | a0004 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.119T>C | p.Met40Thr | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/13 | 402/3373 | 119/1446 | 40/481 | chr15 | 72319756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:72288890
|
G | A | 1 | a0001c0002 | 2 | HG02886.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.1071C>T | p.Tyr357Tyr | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 9/13 | 1354/3373 | 1071/1446 | 357/481 | chr15 | 72288890 | ||
| chr15:72319854
|
C | T | 1 | a0001c0003 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.21G>A | p.Gly7Gly | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/13 | 304/3373 | 21/1446 | 7/481 | chr15 | 72319854 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:72284895
|
C | T | 1 | a0001c0001t0009 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1476G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 2370 | chr15 | 72284895 | |||||
| chr15:72284937
|
T | C | 1 | a0001c0001t0006 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1434A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 2328 | chr15 | 72284937 | |||||
| chr15:72285213
|
G | T | 2 | a0001c0001t0004a0001c0001t0010 | 11 | NA18948.hp2 NA18953.hp2 NA18964.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1158C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 2052 | chr15 | 72285213 | |||||
| chr15:72285541
|
G | C | 2 | a0001c0001t0004a0001c0001t0010 | 11 | NA18948.hp2 NA18953.hp2 NA18964.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*830C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 1724 | chr15 | 72285541 | |||||
| chr15:72285581
|
A | G | 1 | a0001c0001t0008 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*790T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 1684 | chr15 | 72285581 | |||||
| chr15:72285593
|
A | G | 1 | a0001c0001t0003 | 14 | HG01123.hp1 HG01361.hp1 HG01928.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*778T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 1672 | chr15 | 72285593 | |||||
| chr15:72285717
|
T | C | 1 | a0001c0001t0007 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*654A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 1548 | chr15 | 72285717 | |||||
| chr15:72285731
|
C | A | 5 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(2): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*640G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 1534 | chr15 | 72285731 | |||||
| chr15:72285742
|
T | C | 2 | a0001c0001t0005a0002c0006t0005 | 9 | HG01884.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*629A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 1523 | chr15 | 72285742 | |||||
| chr15:72286170
|
G | A | 1 | a0001c0001t0010 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*201C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 13/13 | 1095 | chr15 | 72286170 | |||||
| chr15:72319902
|
G | C | 1 | a0001c0001t0011 | 1 | HG00609.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/13 | 28 | chr15 | 72319902 | |||||
| chr15:72320075
|
G | A | 1 | a0001c0001t0012 | 1 | HG00099.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-201C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/13 | chr15 | 72320075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:72286409
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*29-67T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 12/12 | chr15 | 72286409 | ||||||
| chr15:72286413
|
C | G | 1 | a0001c0001t0002g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*29-71G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 12/12 | chr15 | 72286413 | ||||||
| chr15:72286450
|
T | A | 1 | a0001c0001t0002g0186 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*29-108A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 12/12 | chr15 | 72286450 | ||||||
| chr15:72286737
|
C | T | 5 | a0001c0001t0002g0064a0001c0001t0002g0108a0001c0001t0002g0110others(2): Show | 5 | HG00544.hp1 HG02040.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.*29-395G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 12/12 | chr15 | 72286737 | ||||||
| chr15:72286761
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0090 | 2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.*29-419G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 12/12 | chr15 | 72286761 | ||||||
| chr15:72286843
|
C | T | 10 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0136others(7): Show | 14 | HG01123.hp1 HG01361.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.*28+394G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 12/12 | chr15 | 72286843 | ||||||
| chr15:72287029
|
G | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(93): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.*28+208C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 12/12 | chr15 | 72287029 | ||||||
| chr15:72287555
|
A | C | 1 | a0001c0001t0002g0115 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1319-163T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 11/12 | chr15 | 72287555 | ||||||
| chr15:72287838
|
C | CT | 74 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0081others(71): Show | 107 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1319-447dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 11/12 | chr15 | 72287838 | ||||||
| chr15:72287838
|
CT | C | 7 | a0001c0001t0001g0072a0001c0001t0003g0018a0001c0001t0003g0193others(4): Show | 9 | HG01123.hp1 HG01168.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1319-447delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 11/12 | chr15 | 72287838 | ||||||
| chr15:72288118
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1318+190C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 11/12 | chr15 | 72288118 | ||||||
| chr15:72288691
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1094-73C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 9/12 | chr15 | 72288691 | ||||||
| chr15:72288768
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1093+100C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 9/12 | chr15 | 72288768 | ||||||
| chr15:72289320
|
C | G | 10 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0136others(7): Show | 14 | HG01123.hp1 HG01361.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.881-33G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 7/12 | chr15 | 72289320 | ||||||
| chr15:72289322
|
A | AC | 4 | a0001c0001t0001g0056a0001c0001t0001g0135a0001c0001t0002g0166others(1): Show | 4 | HG01109.hp1 HG02145.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-36dupG | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 7/12 | chr15 | 72289322 | ||||||
| chr15:72290056
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.524-38T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 4/12 | chr15 | 72290056 | ||||||
| chr15:72290341
|
A | C | 7 | a0001c0001t0002g0014a0001c0001t0002g0066a0001c0001t0004g0005others(4): Show | 15 | HG02083.hp2 NA18941.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.395-86T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290341 | ||||||
| chr15:72290349
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.395-94G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290349 | ||||||
| chr15:72290368
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.395-113T>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290368 | ||||||
| chr15:72290404
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.395-149A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290404 | ||||||
| chr15:72290441
|
G | T | 4 | a0001c0001t0002g0048a0001c0001t0002g0156a0001c0001t0002g0157others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-186C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290441 | ||||||
| chr15:72290459
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.395-204G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290459 | ||||||
| chr15:72290643
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.395-388C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290643 | ||||||
| chr15:72290687
|
G | C | 4 | a0001c0001t0002g0048a0001c0001t0002g0156a0001c0001t0002g0157others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-432C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290687 | ||||||
| chr15:72290846
|
C | T | 2 | a0001c0001t0002g0190a0001c0001t0002g0197 | 2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.395-591G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290846 | ||||||
| chr15:72290891
|
C | T | 2 | a0001c0001t0002g0065a0001c0001t0002g0169 | 2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.395-636G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72290891 | ||||||
| chr15:72291380
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.395-1125C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72291380 | ||||||
| chr15:72291496
|
T | C | 1 | a0001c0001t0001g0011 | 3 | HG01070.hp1 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.395-1241A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72291496 | ||||||
| chr15:72291744
|
G | A | 9 | a0001c0001t0002g0017a0001c0001t0002g0152a0001c0001t0002g0153others(6): Show | 11 | HG02486.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.395-1489C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72291744 | ||||||
| chr15:72291855
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(192): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.395-1600T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72291855 | ||||||
| chr15:72291877
|
G | A | 6 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 10 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.395-1622C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72291877 | ||||||
| chr15:72292016
|
C | A | 8 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0193others(5): Show | 12 | HG01123.hp1 HG01361.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.395-1761G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72292016 | ||||||
| chr15:72292575
|
T | C | 2 | a0001c0001t0002g0166a0001c0001t0007g0165 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.395-2320A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72292575 | ||||||
| chr15:72292888
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.395-2633C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72292888 | ||||||
| chr15:72293029
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.395-2774T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72293029 | ||||||
| chr15:72293256
|
A | G | 9 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 13 | HG00621.hp1 HG02083.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.395-3001T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72293256 | ||||||
| chr15:72293323
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(198): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.395-3068G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72293323 | ||||||
| chr15:72293368
|
CATTG | C | 9 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 13 | HG00621.hp1 HG02083.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.395-3117_395-3114d others(6): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72293368 | ||||||
| chr15:72293695
|
CT | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.395-3441delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72293695 | ||||||
| chr15:72293842
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0007g0165 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.395-3587C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72293842 | ||||||
| chr15:72293960
|
CT | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(203): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.395-3706delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72293960 | ||||||
| chr15:72294075
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.395-3820T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294075 | ||||||
| chr15:72294238
|
T | C | 7 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(4): Show | 9 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.395-3983A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294238 | ||||||
| chr15:72294307
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.395-4052C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294307 | ||||||
| chr15:72294377
|
G | A | 6 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 10 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.395-4122C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294377 | ||||||
| chr15:72294405
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-4150C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294405 | ||||||
| chr15:72294539
|
G | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0140 | 2 | HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.395-4284C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294539 | ||||||
| chr15:72294602
|
A | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0188 | 2 | NA19000.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.395-4347T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294602 | ||||||
| chr15:72294716
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.395-4461C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294716 | ||||||
| chr15:72294745
|
A | G | 1 | a0001c0001t0005g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395-4490T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294745 | ||||||
| chr15:72294792
|
A | T | 65 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(62): Show | 97 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.395-4537T>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294792 | ||||||
| chr15:72294805
|
C | G | 1 | a0001c0001t0003g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.395-4550G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294805 | ||||||
| chr15:72294937
|
C | T | 1 | a0001c0001t0012g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.395-4682G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294937 | ||||||
| chr15:72294977
|
C | CA | 20 | a0001c0001t0001g0096a0001c0001t0002g0006a0001c0001t0002g0028others(17): Show | 27 | HG00621.hp1 HG01496.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.395-4723dupT | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294977 | ||||||
| chr15:72294977
|
C | CAA | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(158): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.395-4724_395-4723d others(4): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294977 | ||||||
| chr15:72294977
|
C | CAAA | 10 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0100others(7): Show | 10 | HG01255.hp2 HG01361.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.395-4725_395-4723d others(5): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72294977 | ||||||
| chr15:72295069
|
C | A | 7 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(4): Show | 9 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.395-4814G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295069 | ||||||
| chr15:72295123
|
C | T | 24 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(21): Show | 33 | HG00621.hp1 HG01123.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.395-4868G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295123 | ||||||
| chr15:72295277
|
A | G | 6 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 10 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.395-5022T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295277 | ||||||
| chr15:72295284
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.395-5029G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295284 | ||||||
| chr15:72295593
|
G | C | 1 | a0001c0001t0002g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.395-5338C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295593 | ||||||
| chr15:72295636
|
G | C | 6 | a0001c0001t0002g0021a0001c0001t0002g0047a0001c0001t0002g0112others(3): Show | 7 | HG02615.hp1 HG02717.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.395-5381C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295636 | ||||||
| chr15:72295675
|
G | T | 28 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(25): Show | 47 | HG00544.hp2 HG00597.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.395-5420C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295675 | ||||||
| chr15:72295682
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.395-5427G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295682 | ||||||
| chr15:72295700
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(192): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.395-5445A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295700 | ||||||
| chr15:72295725
|
CA | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(153): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.395-5471delT | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295725 | ||||||
| chr15:72295728
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.395-5473T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295728 | ||||||
| chr15:72295778
|
G | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.395-5523C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72295778 | ||||||
| chr15:72296040
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.395-5785G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296040 | ||||||
| chr15:72296115
|
G | A | 72 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(69): Show | 106 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.395-5860C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296115 | ||||||
| chr15:72296132
|
G | C | 1 | a0001c0001t0002g0069 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.395-5877C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296132 | ||||||
| chr15:72296247
|
T | A | 72 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(69): Show | 106 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.395-5992A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296247 | ||||||
| chr15:72296299
|
C | A | 72 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(69): Show | 106 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.395-6044G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296299 | ||||||
| chr15:72296392
|
T | G | 80 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(77): Show | 115 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.395-6137A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296392 | ||||||
| chr15:72296574
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(192): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.395-6319C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296574 | ||||||
| chr15:72296585
|
C | A | 96 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(93): Show | 139 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.395-6330G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296585 | ||||||
| chr15:72296590
|
C | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(198): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.395-6335G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296590 | ||||||
| chr15:72296612
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.395-6357G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296612 | ||||||
| chr15:72296883
|
A | C | 2 | a0001c0001t0002g0152a0001c0001t0002g0155 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.395-6628T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296883 | ||||||
| chr15:72296921
|
C | T | 18 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0136others(15): Show | 23 | HG01123.hp1 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.395-6666G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72296921 | ||||||
| chr15:72297039
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.395-6784C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297039 | ||||||
| chr15:72297221
|
T | A | 1 | a0001c0001t0005g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.395-6966A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297221 | ||||||
| chr15:72297308
|
G | A | 8 | a0001c0001t0005g0030a0001c0001t0005g0159a0001c0001t0005g0160others(5): Show | 9 | HG01884.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.395-7053C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297308 | ||||||
| chr15:72297358
|
AC | A | 17 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(14): Show | 25 | HG00621.hp1 HG01123.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.395-7104delG | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297358 | ||||||
| chr15:72297467
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.395-7212A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297467 | ||||||
| chr15:72297488
|
T | C | 1 | a0001c0001t0005g0205 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.395-7233A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297488 | ||||||
| chr15:72297599
|
C | T | 6 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 10 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.394+7147G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297599 | ||||||
| chr15:72297712
|
T | G | 1 | a0001c0001t0001g0102 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.394+7034A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297712 | ||||||
| chr15:72297841
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394+6905C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297841 | ||||||
| chr15:72297868
|
C | T | 1 | a0001c0001t0012g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.394+6878G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297868 | ||||||
| chr15:72297998
|
T | G | 24 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(21): Show | 31 | HG01106.hp1 HG01123.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.394+6748A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72297998 | ||||||
| chr15:72298247
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.394+6499G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72298247 | ||||||
| chr15:72298484
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.394+6262C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72298484 | ||||||
| chr15:72299037
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0125 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.394+5709T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299037 | ||||||
| chr15:72299140
|
GGAGTTGT others(15): Show |
G | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.394+5584_394+5605d others(24): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299140 | ||||||
| chr15:72299185
|
G | A | 61 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(58): Show | 93 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.394+5561C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299185 | ||||||
| chr15:72299271
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.394+5475A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299271 | ||||||
| chr15:72299355
|
G | T | 1 | a0001c0001t0002g0017 | 3 | HG02622.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.394+5391C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299355 | ||||||
| chr15:72299362
|
C | CT | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.394+5383dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299362 | ||||||
| chr15:72299362
|
CT | C | 7 | a0001c0001t0001g0088a0001c0001t0002g0040a0001c0001t0002g0120others(4): Show | 7 | HG02895.hp2 HG03195.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+5383delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299362 | ||||||
| chr15:72299390
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.394+5356G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299390 | ||||||
| chr15:72299513
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.394+5233G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299513 | ||||||
| chr15:72299521
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.394+5225C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299521 | ||||||
| chr15:72299596
|
G | T | 22 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(19): Show | 29 | HG01106.hp1 HG01123.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.394+5150C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299596 | ||||||
| chr15:72299608
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.394+5138C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299608 | ||||||
| chr15:72299652
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.394+5094G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299652 | ||||||
| chr15:72299763
|
T | C | 1 | a0001c0001t0003g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394+4983A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299763 | ||||||
| chr15:72299820
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.394+4926C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299820 | ||||||
| chr15:72299845
|
C | A | 28 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(25): Show | 47 | HG00544.hp2 HG00597.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.394+4901G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299845 | ||||||
| chr15:72299870
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0081 | 2 | HG02027.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.394+4876C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72299870 | ||||||
| chr15:72300361
|
T | TA | 6 | a0001c0001t0001g0084a0001c0001t0001g0202a0001c0001t0002g0070others(3): Show | 6 | HG02148.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.394+4384dupT | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300361 | ||||||
| chr15:72300505
|
A | G | 6 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 10 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.394+4241T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300505 | ||||||
| chr15:72300611
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.394+4135T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300611 | ||||||
| chr15:72300655
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.394+4091C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300655 | ||||||
| chr15:72300685
|
T | G | 20 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(17): Show | 25 | HG01123.hp1 HG01361.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.394+4061A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300685 | ||||||
| chr15:72300780
|
G | A | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02895.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.394+3966C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300780 | ||||||
| chr15:72300790
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.394+3956G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300790 | ||||||
| chr15:72300852
|
A | AG | 3 | a0001c0001t0002g0123a0001c0001t0002g0186a0001c0001t0003g0193 | 3 | HG00621.hp2 HG01123.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.394+3893_394+3894i others(3): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300852 | ||||||
| chr15:72300852
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(189): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.394+3894T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300852 | ||||||
| chr15:72300989
|
A | AT | 19 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(16): Show | 24 | HG00621.hp1 HG01884.hp1 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.394+3756dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300989 | ||||||
| chr15:72300989
|
A | ATT | 9 | a0001c0001t0002g0197a0001c0001t0003g0018a0001c0001t0003g0019others(6): Show | 13 | HG01123.hp1 HG01361.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.394+3755_394+3756d others(4): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300989 | ||||||
| chr15:72300989
|
AT | A | 6 | a0001c0001t0002g0015a0001c0001t0002g0040a0001c0001t0002g0120others(3): Show | 8 | HG02886.hp1 HG03540.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.394+3756delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72300989 | ||||||
| chr15:72301091
|
C | T | 2 | a0001c0002t0002g0038a0001c0002t0002g0039 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.394+3655G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301091 | ||||||
| chr15:72301240
|
C | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.394+3506G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301240 | ||||||
| chr15:72301321
|
T | C | 17 | a0001c0001t0002g0197a0001c0001t0003g0018a0001c0001t0003g0019others(14): Show | 22 | HG01123.hp1 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.394+3425A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301321 | ||||||
| chr15:72301326
|
T | C | 61 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(58): Show | 93 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.394+3420A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301326 | ||||||
| chr15:72301596
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.394+3150C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301596 | ||||||
| chr15:72301734
|
A | AT | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(108): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.394+3011dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301734 | ||||||
| chr15:72301734
|
A | ATT | 18 | a0001c0001t0001g0046a0001c0001t0001g0059a0001c0001t0001g0060others(15): Show | 18 | HG00642.hp2 HG00741.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.394+3010_394+3011d others(4): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301734 | ||||||
| chr15:72301734
|
AT | A | 7 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0145others(4): Show | 11 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.394+3011delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301734 | ||||||
| chr15:72301756
|
A | C | 1 | a0001c0001t0007g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+2990T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301756 | ||||||
| chr15:72301800
|
G | A | 20 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(17): Show | 25 | HG01123.hp1 HG01361.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.394+2946C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301800 | ||||||
| chr15:72301987
|
G | A | 2 | a0001c0001t0003g0136a0001c0001t0003g0148 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394+2759C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72301987 | ||||||
| chr15:72302196
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.394+2550C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302196 | ||||||
| chr15:72302371
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.394+2375G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302371 | ||||||
| chr15:72302485
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(192): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.394+2261A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302485 | ||||||
| chr15:72302634
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.394+2112G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302634 | ||||||
| chr15:72302652
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.394+2094G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302652 | ||||||
| chr15:72302656
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.394+2090T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302656 | ||||||
| chr15:72302658
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02080.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.394+2088C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302658 | ||||||
| chr15:72302756
|
C | T | 5 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(2): Show | 7 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+1990G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302756 | ||||||
| chr15:72302757
|
G | A | 9 | a0001c0001t0002g0017a0001c0001t0002g0152a0001c0001t0002g0153others(6): Show | 11 | HG02486.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.394+1989C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302757 | ||||||
| chr15:72302974
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.394+1772G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72302974 | ||||||
| chr15:72303084
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.394+1662C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303084 | ||||||
| chr15:72303096
|
C | G | 5 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(2): Show | 7 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+1650G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303096 | ||||||
| chr15:72303230
|
A | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.394+1516T>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303230 | ||||||
| chr15:72303547
|
T | C | 61 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(58): Show | 93 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.394+1199A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303547 | ||||||
| chr15:72303663
|
C | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0029 | 4 | HG01891.hp2 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+1083G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303663 | ||||||
| chr15:72303762
|
G | A | 6 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 10 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.394+984C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303762 | ||||||
| chr15:72303766
|
C | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0092 | 2 | HG02080.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.394+980G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303766 | ||||||
| chr15:72303848
|
GTTTTGT | G | 5 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(2): Show | 7 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+892_394+897del others(6): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72303848 | ||||||
| chr15:72304140
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.394+606C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72304140 | ||||||
| chr15:72304162
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(191): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.394+584A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 3/12 | chr15 | 72304162 | ||||||
| chr15:72305248
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.346-454T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72305248 | ||||||
| chr15:72305364
|
G | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-570C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72305364 | ||||||
| chr15:72305726
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0089 | 2 | HG01255.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.346-932C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72305726 | ||||||
| chr15:72305814
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.346-1020G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72305814 | ||||||
| chr15:72305854
|
G | GT | 69 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0068others(66): Show | 100 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.346-1061dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72305854 | ||||||
| chr15:72305854
|
G | GTT | 7 | a0001c0001t0002g0027a0001c0001t0002g0115a0001c0001t0002g0156others(4): Show | 8 | HG02071.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.346-1062_346-1061d others(4): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72305854 | ||||||
| chr15:72305859
|
T | TG | 22 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(19): Show | 29 | HG01106.hp1 HG01123.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.346-1066_346-1065i others(3): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72305859 | ||||||
| chr15:72306175
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.346-1381C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306175 | ||||||
| chr15:72306255
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346-1461G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306255 | ||||||
| chr15:72306273
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(146): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.346-1479C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306273 | ||||||
| chr15:72306441
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.346-1647G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306441 | ||||||
| chr15:72306554
|
T | TA | 27 | a0001c0001t0001g0024a0001c0001t0002g0114a0001c0001t0002g0150others(24): Show | 34 | HG01106.hp1 HG01123.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.346-1761dupT | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306554 | ||||||
| chr15:72306554
|
T | TAA | 52 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0119others(49): Show | 84 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.346-1762_346-1761d others(4): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306554 | ||||||
| chr15:72306554
|
T | TAAA | 11 | a0001c0001t0002g0031a0001c0001t0002g0048a0001c0001t0002g0122others(8): Show | 12 | HG01346.hp1 HG02135.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-1763_346-1761d others(5): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306554 | ||||||
| chr15:72306554
|
TA | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0107a0001c0001t0001g0126others(3): Show | 6 | HG01169.hp1 HG02040.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-1761delT | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306554 | ||||||
| chr15:72306928
|
G | A | 1 | a0001c0001t0005g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.346-2134C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72306928 | ||||||
| chr15:72307002
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-2208G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307002 | ||||||
| chr15:72307070
|
G | A | 2 | a0001c0001t0003g0136a0001c0001t0003g0148 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.346-2276C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307070 | ||||||
| chr15:72307216
|
T | C | 61 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0017others(58): Show | 81 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.346-2422A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307216 | ||||||
| chr15:72307238
|
T | C | 25 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(22): Show | 32 | HG01106.hp1 HG01123.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.346-2444A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307238 | ||||||
| chr15:72307422
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.346-2628G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307422 | ||||||
| chr15:72307535
|
C | T | 2 | a0001c0001t0002g0166a0001c0001t0007g0165 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.346-2741G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307535 | ||||||
| chr15:72307671
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-2877C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307671 | ||||||
| chr15:72307722
|
T | C | 69 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(66): Show | 93 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.346-2928A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72307722 | ||||||
| chr15:72308086
|
C | T | 69 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(66): Show | 93 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.346-3292G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308086 | ||||||
| chr15:72308152
|
A | C | 69 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(66): Show | 93 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.346-3358T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308152 | ||||||
| chr15:72308176
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346-3382T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308176 | ||||||
| chr15:72308221
|
G | GT | 30 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0017others(27): Show | 43 | HG00621.hp2 HG01109.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.346-3428dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308221 | ||||||
| chr15:72308227
|
T | G | 20 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(17): Show | 25 | HG01123.hp1 HG01361.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.346-3433A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308227 | ||||||
| chr15:72308227
|
TTTTG | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-3437_346-3434d others(6): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308227 | ||||||
| chr15:72308290
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-3496C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308290 | ||||||
| chr15:72308306
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.346-3512C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308306 | ||||||
| chr15:72308376
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | NA19064.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.346-3582G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308376 | ||||||
| chr15:72308388
|
C | T | 8 | a0001c0001t0002g0017a0001c0001t0002g0166a0001c0001t0002g0168others(5): Show | 10 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.346-3594G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308388 | ||||||
| chr15:72308506
|
T | C | 69 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(66): Show | 93 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.346-3712A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308506 | ||||||
| chr15:72308607
|
C | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0107 | 3 | HG00140.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346-3813G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308607 | ||||||
| chr15:72308637
|
T | C | 61 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0017others(58): Show | 81 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.346-3843A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308637 | ||||||
| chr15:72308719
|
T | A | 5 | a0001c0001t0002g0064a0001c0001t0002g0108a0001c0001t0002g0110others(2): Show | 5 | HG00544.hp1 HG02040.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.346-3925A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308719 | ||||||
| chr15:72308741
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.346-3947A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308741 | ||||||
| chr15:72308745
|
AC | A | 5 | a0001c0001t0002g0017a0001c0001t0002g0168a0001c0001t0002g0169others(2): Show | 7 | HG02486.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.346-3952delG | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72308745 | ||||||
| chr15:72309015
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.346-4221G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309015 | ||||||
| chr15:72309122
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.346-4328T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309122 | ||||||
| chr15:72309200
|
G | A | 2 | a0001c0002t0002g0038a0001c0002t0002g0039 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.346-4406C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309200 | ||||||
| chr15:72309313
|
T | C | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346-4519A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309313 | ||||||
| chr15:72309323
|
A | G | 1 | a0001c0001t0002g0113 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.346-4529T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309323 | ||||||
| chr15:72309435
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346-4641G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309435 | ||||||
| chr15:72309437
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-4643G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309437 | ||||||
| chr15:72309497
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.346-4703C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309497 | ||||||
| chr15:72309514
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.346-4720C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309514 | ||||||
| chr15:72309704
|
T | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(2): Show | 9 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.346-4910A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72309704 | ||||||
| chr15:72310106
|
C | A | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02895.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.346-5312G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310106 | ||||||
| chr15:72310207
|
T | C | 1 | a0001c0001t0001g0012 | 3 | HG03834.hp1 NA18612.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.346-5413A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310207 | ||||||
| chr15:72310287
|
C | G | 68 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 92 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.346-5493G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310287 | ||||||
| chr15:72310368
|
A | G | 68 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 92 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.345+5477T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310368 | ||||||
| chr15:72310372
|
A | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02895.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.345+5473T>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310372 | ||||||
| chr15:72310497
|
T | C | 17 | a0001c0001t0002g0197a0001c0001t0003g0018a0001c0001t0003g0019others(14): Show | 22 | HG01123.hp1 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.345+5348A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310497 | ||||||
| chr15:72310546
|
C | CT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.345+5298dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310546 | ||||||
| chr15:72310656
|
T | A | 60 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0017others(57): Show | 80 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(77): Show |
intron_variant | MODIFIER | c.345+5189A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310656 | ||||||
| chr15:72310725
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 8 | HG00438.hp2 HG02015.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.345+5120T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310725 | ||||||
| chr15:72310738
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(192): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.345+5107A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310738 | ||||||
| chr15:72310783
|
T | C | 68 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 92 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.345+5062A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310783 | ||||||
| chr15:72310807
|
C | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(192): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.345+5038G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72310807 | ||||||
| chr15:72311021
|
T | C | 1 | a0001c0001t0007g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.345+4824A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311021 | ||||||
| chr15:72311126
|
TTTTC | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0125 | 3 | HG00738.hp1 HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345+4715_345+4718d others(6): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311126 | ||||||
| chr15:72311405
|
C | CT | 58 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0074others(55): Show | 78 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.345+4439dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311405 | ||||||
| chr15:72311405
|
C | CTT | 7 | a0001c0001t0002g0166a0001c0001t0002g0174a0001c0001t0002g0175others(4): Show | 7 | HG01346.hp1 HG01928.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.345+4438_345+4439d others(4): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311405 | ||||||
| chr15:72311694
|
A | C | 1 | a0001c0001t0002g0070 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.345+4151T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311694 | ||||||
| chr15:72311694
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(199): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.345+4151T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311694 | ||||||
| chr15:72311694
|
A | T | 2 | a0001c0001t0002g0166a0001c0001t0007g0165 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.345+4151T>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311694 | ||||||
| chr15:72311708
|
A | G | 62 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(59): Show | 82 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.345+4137T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311708 | ||||||
| chr15:72311723
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.345+4122C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311723 | ||||||
| chr15:72311821
|
A | G | 62 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(59): Show | 82 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.345+4024T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311821 | ||||||
| chr15:72311931
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.345+3914T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311931 | ||||||
| chr15:72311933
|
C | A | 2 | a0001c0001t0002g0112a0001c0001t0006g0131 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345+3912G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72311933 | ||||||
| chr15:72312241
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.345+3604C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72312241 | ||||||
| chr15:72312308
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(200): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.345+3537T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72312308 | ||||||
| chr15:72312444
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.345+3401A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72312444 | ||||||
| chr15:72312572
|
T | G | 27 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0003others(24): Show | 46 | HG00544.hp2 HG00597.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.345+3273A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72312572 | ||||||
| chr15:72313149
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0125 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.345+2696C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313149 | ||||||
| chr15:72313300
|
A | C | 26 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(23): Show | 37 | HG00621.hp2 HG01109.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.345+2545T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313300 | ||||||
| chr15:72313518
|
T | G | 60 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(57): Show | 80 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(77): Show |
intron_variant | MODIFIER | c.345+2327A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313518 | ||||||
| chr15:72313519
|
G | C | 4 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+2326C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313519 | ||||||
| chr15:72313617
|
T | G | 1 | a0001c0001t0004g0041 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.345+2228A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313617 | ||||||
| chr15:72313624
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.345+2221C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313624 | ||||||
| chr15:72313812
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0126 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.345+2033C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313812 | ||||||
| chr15:72313819
|
C | CTATT | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.345+2022_345+2025d others(6): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72313819 | ||||||
| chr15:72314208
|
G | C | 6 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(3): Show | 10 | HG00621.hp1 HG02083.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.345+1637C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314208 | ||||||
| chr15:72314235
|
G | C | 2 | a0001c0001t0003g0136a0001c0001t0003g0148 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.345+1610C>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314235 | ||||||
| chr15:72314270
|
G | T | 8 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(5): Show | 10 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.345+1575C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314270 | ||||||
| chr15:72314316
|
T | C | 70 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0006others(67): Show | 94 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(91): Show |
intron_variant | MODIFIER | c.345+1529A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314316 | ||||||
| chr15:72314589
|
G | GT | 45 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0034others(42): Show | 50 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.345+1255dupA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0002g0171a0001c0001t0002g0191 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.345+1243_345+1255d others(15): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(7): Show |
2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.345+1242_345+1255d others(16): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0003g0198a0001c0001t0005g0030a0002c0006t0005g0162 | 4 | HG02615.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+1241_345+1255d others(17): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(9): Show |
8 | a0001c0001t0002g0168a0001c0001t0002g0197a0001c0001t0003g0019others(5): Show | 10 | HG01884.hp1 HG01928.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.345+1240_345+1255d others(18): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(10): Show |
3 | a0001c0001t0003g0018a0001c0001t0003g0194a0001c0001t0005g0159 | 5 | HG01934.hp2 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+1239_345+1255d others(19): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(11): Show |
2 | a0001c0001t0003g0193a0001c0001t0003g0199 | 2 | HG01123.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.345+1238_345+1255d others(20): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(12): Show |
1 | a0001c0001t0002g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.345+1237_345+1255d others(21): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(13): Show |
1 | a0001c0001t0007g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.345+1236_345+1255d others(22): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
G | GTTTTTTT others(20): Show |
2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.345+1255_345+1256i others(29): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314589
|
GT | G | 12 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0002g0007others(9): Show | 16 | HG02040.hp1 HG02040.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.345+1255delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314589 | ||||||
| chr15:72314602
|
T | TTTTTTTT others(4): Show |
7 | a0001c0001t0002g0029a0001c0001t0002g0150a0001c0001t0002g0151others(4): Show | 8 | HG01106.hp1 HG01496.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1242_345+1243i others(13): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314602 | ||||||
| chr15:72314602
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0002g0028 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.345+1242_345+1243i others(14): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314602 | ||||||
| chr15:72314766
|
T | A | 1 | a0001c0001t0001g0133 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.345+1079A>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314766 | ||||||
| chr15:72314841
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.345+1004G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314841 | ||||||
| chr15:72314842
|
G | A | 8 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(5): Show | 10 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.345+1003C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314842 | ||||||
| chr15:72314922
|
C | A | 62 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(59): Show | 82 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.345+923G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314922 | ||||||
| chr15:72314931
|
C | G | 8 | a0001c0001t0005g0030a0001c0001t0005g0159a0001c0001t0005g0160others(5): Show | 9 | HG01884.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.345+914G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314931 | ||||||
| chr15:72314964
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.345+881G>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72314964 | ||||||
| chr15:72315031
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.345+814G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315031 | ||||||
| chr15:72315034
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.345+811C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315034 | ||||||
| chr15:72315055
|
G | T | 9 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(6): Show | 11 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.345+790C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315055 | ||||||
| chr15:72315088
|
C | T | 2 | a0001c0001t0002g0166a0001c0001t0007g0165 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.345+757G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315088 | ||||||
| chr15:72315258
|
C | T | 17 | a0001c0001t0002g0197a0001c0001t0003g0018a0001c0001t0003g0019others(14): Show | 22 | HG01123.hp1 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.345+587G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315258 | ||||||
| chr15:72315302
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.345+543C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315302 | ||||||
| chr15:72315325
|
A | T | 62 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(59): Show | 82 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.345+520T>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315325 | ||||||
| chr15:72315470
|
G | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02895.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.345+375C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315470 | ||||||
| chr15:72315696
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.345+149A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315696 | ||||||
| chr15:72315716
|
C | T | 1 | a0001c0001t0004g0041 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.345+129G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315716 | ||||||
| chr15:72315816
|
AT | A | 1 | a0001c0001t0002g0017 | 3 | HG02622.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.345+28delA | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315816 | ||||||
| chr15:72315821
|
C | A | 1 | a0001c0001t0002g0040 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.345+24G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315821 | ||||||
| chr15:72315822
|
A | C | 1 | a0001c0001t0002g0040 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.345+23T>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 2/12 | chr15 | 72315822 | ||||||
| chr15:72315985
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-58C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72315985 | ||||||
| chr15:72316286
|
C | T | 61 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(58): Show | 81 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.263-359G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72316286 | ||||||
| chr15:72316300
|
T | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-373A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72316300 | ||||||
| chr15:72316353
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-426G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72316353 | ||||||
| chr15:72316711
|
T | C | 32 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(29): Show | 45 | HG00621.hp2 HG01109.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.263-784A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72316711 | ||||||
| chr15:72316853
|
C | CAG | 62 | a0001c0001t0001g0172a0001c0001t0002g0004a0001c0001t0002g0007others(59): Show | 82 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.263-927_263-926ins others(2): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72316853 | ||||||
| chr15:72317050
|
T | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 12 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-1123A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317050 | ||||||
| chr15:72317306
|
G | A | 1 | a0001c0001t0011g0206 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.263-1379C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317306 | ||||||
| chr15:72317357
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(141): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.263-1430C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317357 | ||||||
| chr15:72317473
|
T | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01070.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.263-1546A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317473 | ||||||
| chr15:72317506
|
A | G | 2 | a0001c0002t0002g0038a0001c0002t0002g0039 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.263-1579T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317506 | ||||||
| chr15:72317550
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.263-1623T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317550 | ||||||
| chr15:72317588
|
C | T | 8 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0150others(5): Show | 10 | HG01106.hp1 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.263-1661G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317588 | ||||||
| chr15:72317655
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0139a0001c0001t0001g0140 | 5 | HG02109.hp2 HG02280.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1728A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317655 | ||||||
| chr15:72317668
|
CAATCATC others(4): Show |
C | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02080.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.263-1752_263-1742d others(13): Show |
CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317668 | ||||||
| chr15:72317918
|
T | C | 9 | a0001c0001t0002g0197a0001c0001t0003g0018a0001c0001t0003g0019others(6): Show | 13 | HG01123.hp1 HG01361.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.262+1695A>G | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72317918 | ||||||
| chr15:72318135
|
G | A | 7 | a0001c0001t0002g0006a0001c0001t0002g0143a0001c0001t0002g0144others(4): Show | 11 | HG00621.hp1 HG02083.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.262+1478C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72318135 | ||||||
| chr15:72318177
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.262+1436C>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72318177 | ||||||
| chr15:72318298
|
T | G | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.262+1315A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72318298 | ||||||
| chr15:72318319
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262+1294C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72318319 | ||||||
| chr15:72318380
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.262+1233A>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72318380 | ||||||
| chr15:72318508
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(141): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.262+1105G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72318508 | ||||||
| chr15:72319244
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG01123.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.262+369C>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72319244 | ||||||
| chr15:72319294
|
C | A | 1 | a0001c0001t0005g0205 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.262+319G>T | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72319294 | ||||||
| chr15:72319342
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.262+271T>C | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72319342 | ||||||
| chr15:72319524
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.262+89G>A | CELF6 | ENSG00000140488.16 | transcript | ENST00000287202.10 | protein_coding | 1/12 | chr15 | 72319524 |