Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10658 |
|---|---|
| ensemblid | ENSG00000149187.19 |
| hgncid | 2549 |
| symbol | CELF1 |
| name | CUGBP Elav-like family member 1 |
| refseq_nuc | NM_001376376.1 |
| refseq_prot | NP_001363305.1 |
| ensembl_nuc | ENST00000687097.1 |
| ensembl_prot | ENSP00000508525.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 47465937 |
| end | 47553132 |
| strand | - |
| ver | v1.2 |
| region | chr11:47465937-47553132 |
| region5000 | chr11:47460937-47558132 |
| regionname0 | CELF1_chr11_47465937_47553132 |
| regionname5000 | CELF1_chr11_47460937_47558132 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 514 | 340 | 84 | 56 | 148 | 10 | 40 | 118 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1545 | 335 | 81 | 55 | 148 | 10 | 39 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| c0002 | 0/0 | 1545 | 2 | 1 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| c0003 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| c0004 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 6587 | 111 | 37 | 12 | 53 | 2 | 6 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0002 | 0/0 | 6587 | 108 | 13 | 25 | 47 | 5 | 18 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0003 | 0/0 | 6588 | 71 | 3 | 13 | 42 | 2 | 11 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0004 | 0/0 | 6599 | 10 | 10 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0005 | 0/0 | 6588 | 6 | 6 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0006 | 0/0 | 6587 | 5 | 0 | 3 | 0 | 1 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0007 | 0/0 | 6589 | 3 | 3 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0008 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0009 | 0/0 | 6588 | 2 | 0 | 0 | 2 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0010 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0011 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0012 | 0/0 | 6587 | 2 | 0 | 0 | 0 | 0 | 2 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0013 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0014 | 0/0 | 6588 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0015 | 0/0 | 6588 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0016 | 1/0 | 6588 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0017 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0018 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0019 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0020 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0021 | 0/0 | 6588 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0022 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0023 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0024 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0025 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0026 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0027 | 0/0 | 6587 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| t0028 | 0/0 | 6588 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1545 | 335 | 81 | 55 | 148 | 10 | 39 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0002 | 0/0 | 1545 | 2 | 1 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0003 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0004 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8131 | 111 | 37 | 12 | 53 | 2 | 6 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0002 | 0/0 | 8131 | 105 | 12 | 24 | 47 | 5 | 17 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0003 | 0/0 | 8132 | 71 | 3 | 13 | 42 | 2 | 11 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0004 | 0/0 | 8143 | 10 | 10 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0005 | 0/0 | 8132 | 6 | 6 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0006 | 0/0 | 8131 | 5 | 0 | 3 | 0 | 1 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0007 | 0/0 | 8133 | 3 | 3 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0008 | 0/0 | 8131 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0009 | 0/0 | 8132 | 2 | 0 | 0 | 2 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0010 | 0/0 | 8131 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0012 | 0/0 | 8131 | 2 | 0 | 0 | 0 | 0 | 2 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0013 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0014 | 0/0 | 8132 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0015 | 0/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0016 | 1/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0017 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0018 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0019 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0020 | 0/0 | 8132 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0021 | 0/0 | 8132 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0022 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0023 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0024 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0025 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0026 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0027 | 0/0 | 8131 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0001t0028 | 0/0 | 8132 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0002t0002 | 0/0 | 8131 | 2 | 1 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0003t0011 | 0/0 | 8131 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| a0001c0004t0002 | 0/0 | 8131 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | copy fasta | chr11 | 47460937 | 47558132 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0009g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0012g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0012g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0013g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0015g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0016g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0017g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0018g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0020g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0022g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0023g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0024g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0025g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0026g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0027g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0028g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0003t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0003t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0004t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0316 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0078 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0111 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00558 | hp1 | a0001 | c0001 | t0009 | g0138 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0020 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00735 | hp2 | a0001 | c0001 | t0028 | g0035 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0104 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0300 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0079 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0117 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0052 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0310 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0314 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0275 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0299 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02165 | hp2 | a0001 | c0001 | t0026 | g0291 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02257 | hp1 | a0001 | c0001 | t0017 | g0251 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0189 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02293 | hp2 | a0001 | c0001 | t0021 | g0083 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0146 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02683 | hp1 | a0001 | c0001 | t0027 | g0227 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02896 | hp1 | a0001 | c0003 | t0011 | g0308 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0101 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02976 | hp2 | a0001 | c0001 | t0024 | g0320 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03098 | hp2 | a0001 | c0003 | t0011 | g0309 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0334 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03491 | hp1 | a0001 | c0001 | t0012 | g0249 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03492 | hp2 | a0001 | c0001 | t0012 | g0252 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03579 | hp1 | a0001 | c0001 | t0023 | g0221 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0113 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03942 | hp1 | a0001 | c0001 | t0015 | g0064 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04184 | hp2 | a0001 | c0004 | t0002 | g0303 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19060 | hp2 | a0001 | c0001 | t0022 | g0154 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19089 | hp2 | a0001 | c0001 | t0025 | g0287 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19090 | hp1 | a0001 | c0001 | t0020 | g0094 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ASW | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ASW | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | GIH | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | GIH | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02486 | hp1 | a0001 | c0001 | t0019 | g0185 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | USA | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | USA | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0133 | REF | REF | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0016 | g0335 | REF | REF | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47473134
|
A | C | 1 | a0001c0002 | 2 | HG01243.hp2 HG01884.hp2 |
synonymous_variant | LOW | c.1371T>G | p.Ser457Ser | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/15 | 1665/8132 | 1371/1545 | 457/514 | chr11 | 47473134 | ||
| chr11:47473218
|
G | A | 1 | a0001c0004 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1287C>T | p.Ala429Ala | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/15 | 1581/8132 | 1287/1545 | 429/514 | chr11 | 47473218 | ||
| chr11:47478887
|
G | A | 1 | a0001c0003 | 2 | HG02896.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.834C>T | p.His278His | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/15 | 1128/8132 | 834/1545 | 278/514 | chr11 | 47478887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47466046
|
C | A | 1 | a0001c0001t0021 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6184G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6184 | chr11 | 47466046 | |||||
| chr11:47466124
|
A | G | 1 | a0001c0001t0020 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6106T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6106 | chr11 | 47466124 | |||||
| chr11:47466130
|
A | AT | 1 | a0001c0001t0005 | 6 | HG02258.hp2 HG02486.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6099dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6099 | chr11 | 47466130 | |||||
| chr11:47466188
|
G | A | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 208 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*6042C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6042 | chr11 | 47466188 | |||||
| chr11:47466231
|
A | T | 1 | a0001c0001t0022 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5999T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5999 | chr11 | 47466231 | |||||
| chr11:47466562
|
C | CT | 7 | a0001c0001t0003a0001c0001t0009a0001c0001t0014others(4): Show | 78 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5667dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5667 | chr11 | 47466562 | |||||
| chr11:47466783
|
A | G | 1 | a0001c0001t0019 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5447T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5447 | chr11 | 47466783 | |||||
| chr11:47467038
|
G | A | 1 | a0001c0001t0023 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5192C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5192 | chr11 | 47467038 | |||||
| chr11:47467319
|
A | C | 1 | a0001c0001t0004 | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4911T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4911 | chr11 | 47467319 | |||||
| chr11:47467522
|
T | C | 1 | a0001c0001t0024 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4708A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4708 | chr11 | 47467522 | |||||
| chr11:47467595
|
G | A | 1 | a0001c0001t0025 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4635C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4635 | chr11 | 47467595 | |||||
| chr11:47467700
|
C | T | 1 | a0001c0001t0008 | 2 | HG02258.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4530G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4530 | chr11 | 47467700 | |||||
| chr11:47468148
|
G | C | 1 | a0001c0001t0006 | 5 | HG00323.hp2 HG01081.hp1 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4082C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4082 | chr11 | 47468148 | |||||
| chr11:47468227
|
A | AAG | 1 | a0001c0001t0007 | 3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4001_*4002dupCT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4002 | chr11 | 47468227 | |||||
| chr11:47468398
|
G | A | 1 | a0001c0001t0015 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3832C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 3832 | chr11 | 47468398 | |||||
| chr11:47468732
|
G | C | 1 | a0001c0001t0026 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 3498 | chr11 | 47468732 | |||||
| chr11:47469392
|
T | C | 1 | a0001c0001t0027 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2838A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2838 | chr11 | 47469392 | |||||
| chr11:47469653
|
G | A | 1 | a0001c0001t0010 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2577C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2577 | chr11 | 47469653 | |||||
| chr11:47469723
|
G | A | 1 | a0001c0003t0011 | 2 | HG02896.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2507C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2507 | chr11 | 47469723 | |||||
| chr11:47469856
|
A | G | 1 | a0001c0001t0018 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2374T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2374 | chr11 | 47469856 | |||||
| chr11:47470224
|
G | A | 1 | a0001c0001t0028 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2006C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2006 | chr11 | 47470224 | |||||
| chr11:47470286
|
CT | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 338 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1943delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 1943 | chr11 | 47470286 | |||||
| chr11:47470497
|
A | G | 1 | a0001c0001t0015 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1733T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 1733 | chr11 | 47470497 | |||||
| chr11:47470621
|
C | T | 1 | a0001c0001t0014 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1609G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 1609 | chr11 | 47470621 | |||||
| chr11:47471881
|
C | T | 1 | a0001c0001t0013 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*349G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 349 | chr11 | 47471881 | |||||
| chr11:47471897
|
T | C | 1 | a0001c0001t0012 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*333A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 333 | chr11 | 47471897 | |||||
| chr11:47553014
|
C | CGCTGCCT others(5): Show |
1 | a0001c0001t0004 | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-188_-177dupAACTGA others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/15 | 53492 | chr11 | 47553014 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47472432
|
A | G | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1418-75T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472432 | ||||||
| chr11:47472701
|
C | T | 1 | a0001c0001t0006g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1418-344G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472701 | ||||||
| chr11:47472843
|
A | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417+245T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472843 | ||||||
| chr11:47472989
|
A | C | 4 | a0001c0001t0001g0026a0001c0001t0002g0109a0001c0002t0002g0299others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417+99T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472989 | ||||||
| chr11:47473278
|
C | T | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0071others(3): Show | 6 | HG03942.hp1 NA18952.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-47G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473278 | ||||||
| chr11:47473352
|
C | A | 1 | a0001c0001t0002g0030 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1274-121G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473352 | ||||||
| chr11:47473367
|
G | C | 3 | a0001c0001t0002g0109a0001c0002t0002g0299a0001c0002t0002g0300 | 3 | HG01243.hp2 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1274-136C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473367 | ||||||
| chr11:47473389
|
G | A | 1 | a0001c0002t0002g0299 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1274-158C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473389 | ||||||
| chr11:47473650
|
G | A | 111 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(108): Show | 111 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1274-419C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473650 | ||||||
| chr11:47473662
|
G | A | 1 | a0001c0001t0014g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1274-431C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473662 | ||||||
| chr11:47473682
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1274-451C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473682 | ||||||
| chr11:47473897
|
TTTTCTTT others(7): Show |
T | 115 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1274-680_1274-667d others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473897 | ||||||
| chr11:47474194
|
G | T | 87 | a0001c0001t0001g0022a0001c0001t0002g0077a0001c0001t0003g0014others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1274-963C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474194 | ||||||
| chr11:47474468
|
A | G | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1273+868T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474468 | ||||||
| chr11:47474636
|
T | A | 1 | a0001c0001t0002g0262 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1273+700A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474636 | ||||||
| chr11:47474661
|
A | G | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1273+675T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474661 | ||||||
| chr11:47474754
|
C | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0001g0199others(1): Show | 4 | HG00558.hp2 NA18964.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+582G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474754 | ||||||
| chr11:47474843
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1273+493G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474843 | ||||||
| chr11:47474971
|
C | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+365G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474971 | ||||||
| chr11:47475093
|
C | T | 1 | a0001c0001t0008g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1273+243G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47475093 | ||||||
| chr11:47475275
|
C | T | 24 | a0001c0001t0002g0011a0001c0001t0002g0013a0001c0001t0002g0105others(21): Show | 24 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1273+61G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47475275 | ||||||
| chr11:47475591
|
G | A | 1 | a0001c0001t0026g0291 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1088-70C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475591 | ||||||
| chr11:47475606
|
G | C | 1 | a0001c0001t0002g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1088-85C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475606 | ||||||
| chr11:47475729
|
A | C | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1088-208T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475729 | ||||||
| chr11:47475735
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1088-214C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475735 | ||||||
| chr11:47475742
|
G | C | 1 | a0001c0001t0003g0076 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1088-221C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475742 | ||||||
| chr11:47475999
|
A | AT | 6 | a0001c0001t0001g0123a0001c0001t0002g0255a0001c0001t0002g0263others(3): Show | 6 | HG01169.hp2 HG01175.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088-479dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475999 | ||||||
| chr11:47476220
|
T | C | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1087+626A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476220 | ||||||
| chr11:47476383
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1087+463G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476383 | ||||||
| chr11:47476397
|
C | G | 6 | a0001c0001t0001g0319a0001c0001t0010g0101a0001c0001t0010g0102others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1087+449G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476397 | ||||||
| chr11:47476435
|
T | C | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087+411A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476435 | ||||||
| chr11:47476526
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1087+320A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476526 | ||||||
| chr11:47476736
|
T | C | 1 | a0001c0001t0003g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1087+110A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476736 | ||||||
| chr11:47477108
|
T | C | 6 | a0001c0001t0001g0319a0001c0001t0010g0101a0001c0001t0010g0102others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-149A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477108 | ||||||
| chr11:47477137
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.973+160A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477137 | ||||||
| chr11:47477210
|
A | C | 1 | a0001c0001t0003g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+87T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477210 | ||||||
| chr11:47477249
|
C | A | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.973+48G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477249 | ||||||
| chr11:47477260
|
G | C | 1 | a0001c0001t0003g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.973+37C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477260 | ||||||
| chr11:47477703
|
C | T | 1 | a0001c0001t0003g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.845-278G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477703 | ||||||
| chr11:47477860
|
A | G | 1 | a0001c0001t0027g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.845-435T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477860 | ||||||
| chr11:47477886
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.845-461G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477886 | ||||||
| chr11:47477968
|
G | C | 1 | a0001c0001t0003g0060 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.845-543C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477968 | ||||||
| chr11:47478664
|
A | AC | 3 | a0001c0001t0002g0280a0001c0001t0002g0282a0001c0001t0002g0288 | 3 | NA18956.hp1 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.844+212dupG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47478664 | ||||||
| chr11:47478715
|
T | C | 108 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.844+162A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47478715 | ||||||
| chr11:47478848
|
C | T | 59 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.844+29G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47478848 | ||||||
| chr11:47479086
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.769-134G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479086 | ||||||
| chr11:47479109
|
T | C | 4 | a0001c0001t0002g0278a0001c0001t0002g0289a0001c0001t0002g0292others(1): Show | 4 | HG00544.hp2 HG01978.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.769-157A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479109 | ||||||
| chr11:47479186
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0131 | 2 | NA18970.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.769-234G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479186 | ||||||
| chr11:47479269
|
C | T | 6 | a0001c0001t0001g0319a0001c0001t0010g0101a0001c0001t0010g0102others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.769-317G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479269 | ||||||
| chr11:47479438
|
T | A | 6 | a0001c0001t0001g0319a0001c0001t0010g0101a0001c0001t0010g0102others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.769-486A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479438 | ||||||
| chr11:47479656
|
C | G | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.769-704G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479656 | ||||||
| chr11:47479688
|
T | C | 1 | a0001c0001t0007g0124 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.769-736A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479688 | ||||||
| chr11:47480067
|
T | G | 104 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(101): Show | 104 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.769-1115A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480067 | ||||||
| chr11:47480089
|
C | CT | 10 | a0001c0001t0001g0319a0001c0001t0002g0255a0001c0001t0003g0039others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.769-1138dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480089 | ||||||
| chr11:47480089
|
CT | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0152a0001c0001t0002g0306others(4): Show | 7 | HG01081.hp2 HG01257.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.769-1138delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480089 | ||||||
| chr11:47480090
|
T | G | 12 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(9): Show | 12 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.769-1138A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480090 | ||||||
| chr11:47480336
|
C | T | 24 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(21): Show | 24 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.769-1384G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480336 | ||||||
| chr11:47480437
|
G | T | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.769-1485C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480437 | ||||||
| chr11:47480515
|
C | T | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.769-1563G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480515 | ||||||
| chr11:47480552
|
C | A | 1 | a0001c0001t0002g0302 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.769-1600G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480552 | ||||||
| chr11:47480738
|
T | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-1786A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480738 | ||||||
| chr11:47481081
|
GTTTTTTT others(16): Show |
G | 2 | a0001c0001t0007g0124a0001c0001t0007g0212 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.768+1591_768+1613d others(25): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481081 | ||||||
| chr11:47481081
|
GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0007g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.768+1590_768+1613d others(26): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481081 | ||||||
| chr11:47481081
|
GTTTTTTT others(21): Show |
G | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.768+1586_768+1613d others(30): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481081 | ||||||
| chr11:47481082
|
T | G | 5 | a0001c0001t0002g0272a0001c0001t0002g0274a0001c0001t0002g0275others(2): Show | 5 | HG01433.hp2 HG01517.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.768+1613A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481082 | ||||||
| chr11:47481093
|
T | C | 22 | a0001c0001t0002g0247a0001c0001t0002g0272a0001c0001t0002g0273others(19): Show | 22 | HG00544.hp2 HG00621.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.768+1602A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481093 | ||||||
| chr11:47481095
|
TC | T | 67 | a0001c0001t0002g0077a0001c0001t0003g0014a0001c0001t0003g0015others(64): Show | 67 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.768+1599delG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481095 | ||||||
| chr11:47481096
|
C | T | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0068others(3): Show | 6 | HG00597.hp1 HG01361.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+1599G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481096 | ||||||
| chr11:47481098
|
T | C | 5 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0068others(2): Show | 5 | HG01361.hp1 HG04115.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.768+1597A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481098 | ||||||
| chr11:47481099
|
C | T | 5 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0068others(2): Show | 5 | HG01361.hp1 HG04115.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.768+1596G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481099 | ||||||
| chr11:47481101
|
TC | T | 42 | a0001c0001t0002g0077a0001c0001t0003g0014a0001c0001t0003g0015others(39): Show | 42 | HG00323.hp1 HG00597.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.768+1593delG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481101 | ||||||
| chr11:47481102
|
C | CT | 32 | a0001c0001t0001g0096a0001c0001t0001g0119a0001c0001t0001g0123others(29): Show | 33 | HG00544.hp1 HG01884.hp1 HG02083.hp1 others(30): Show |
intron_variant | MODIFIER | c.768+1592dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | ||||||
| chr11:47481102
|
C | CTT | 11 | a0001c0001t0001g0026a0001c0001t0002g0028a0001c0001t0002g0029others(8): Show | 11 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.768+1591_768+1592d others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | ||||||
| chr11:47481102
|
C | CTTT | 82 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.768+1590_768+1592d others(5): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | ||||||
| chr11:47481102
|
C | CTTTT | 18 | a0001c0001t0002g0116a0001c0001t0002g0224a0001c0001t0002g0225others(15): Show | 18 | HG00621.hp2 HG01192.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.768+1589_768+1592d others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | ||||||
| chr11:47481102
|
C | T | 35 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0259others(32): Show | 35 | HG00438.hp2 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.768+1593G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | ||||||
| chr11:47481102
|
CT | C | 23 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0126others(20): Show | 23 | HG01243.hp1 HG01261.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.768+1592delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | ||||||
| chr11:47481102
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0008g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.768+1575_768+1592d others(20): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | ||||||
| chr11:47481106
|
T | C | 1 | a0001c0001t0003g0057 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.768+1589A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481106 | ||||||
| chr11:47481109
|
T | C | 1 | a0001c0001t0003g0044 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.768+1586A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481109 | ||||||
| chr11:47481198
|
G | A | 4 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+1497C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481198 | ||||||
| chr11:47481376
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.768+1319G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481376 | ||||||
| chr11:47481740
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.768+955G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481740 | ||||||
| chr11:47482030
|
C | T | 9 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0169others(6): Show | 9 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+665G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482030 | ||||||
| chr11:47482183
|
AGAGT | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.768+508_768+511del others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482183 | ||||||
| chr11:47482207
|
A | AAAAT | 105 | a0001c0001t0001g0319a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 105 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.768+484_768+487dup others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482207 | ||||||
| chr11:47482207
|
A | AAAATAAA others(1): Show |
4 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0230others(1): Show | 4 | HG02965.hp1 HG02976.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+480_768+487dup others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482207 | ||||||
| chr11:47482273
|
G | T | 1 | a0001c0001t0003g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.768+422C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482273 | ||||||
| chr11:47482523
|
G | T | 109 | a0001c0001t0001g0168a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 109 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.768+172C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482523 | ||||||
| chr11:47482890
|
C | T | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0071others(3): Show | 6 | HG03942.hp1 NA18952.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-34G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47482890 | ||||||
| chr11:47483097
|
TA | T | 80 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(77): Show | 80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.607-242delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483097 | ||||||
| chr11:47483125
|
G | A | 1 | a0001c0001t0014g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.607-269C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483125 | ||||||
| chr11:47483202
|
C | A | 1 | a0001c0001t0002g0237 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.606+251G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483202 | ||||||
| chr11:47483383
|
G | A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+70C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483383 | ||||||
| chr11:47483400
|
G | A | 1 | a0001c0001t0005g0332 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.606+53C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483400 | ||||||
| chr11:47483567
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0131 | 2 | NA18970.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.527-35A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47483567 | ||||||
| chr11:47483761
|
C | T | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-229G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47483761 | ||||||
| chr11:47483981
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.526+408A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47483981 | ||||||
| chr11:47484258
|
T | A | 1 | a0001c0001t0001g0131 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.526+131A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47484258 | ||||||
| chr11:47484317
|
C | CA | 14 | a0001c0001t0001g0096a0001c0001t0001g0123a0001c0001t0001g0150others(11): Show | 14 | HG01175.hp1 HG02738.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.526+71dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47484317 | ||||||
| chr11:47484331
|
C | A | 1 | a0001c0001t0002g0305 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526+58G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47484331 | ||||||
| chr11:47484588
|
G | C | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.392-65C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484588 | ||||||
| chr11:47484734
|
A | G | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.392-211T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484734 | ||||||
| chr11:47484747
|
C | T | 2 | a0001c0001t0002g0289a0001c0001t0025g0287 | 2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.392-224G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484747 | ||||||
| chr11:47484906
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0194others(6): Show | 9 | HG00408.hp1 HG00597.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.392-383C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484906 | ||||||
| chr11:47484924
|
CGCCTCG | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-407_392-402del others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484924 | ||||||
| chr11:47485186
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.392-663A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485186 | ||||||
| chr11:47485306
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.392-783C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485306 | ||||||
| chr11:47485500
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.392-977G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485500 | ||||||
| chr11:47485585
|
AT | A | 6 | a0001c0001t0001g0174a0001c0001t0001g0199a0001c0001t0001g0330others(3): Show | 6 | HG01257.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-1063delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485585 | ||||||
| chr11:47485717
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.391+1033C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485717 | ||||||
| chr11:47485744
|
G | A | 1 | a0001c0001t0027g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.391+1006C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485744 | ||||||
| chr11:47485810
|
C | G | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+940G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485810 | ||||||
| chr11:47485811
|
G | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+939C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485811 | ||||||
| chr11:47486085
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.391+665G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486085 | ||||||
| chr11:47486090
|
G | A | 2 | a0001c0001t0003g0297a0001c0001t0003g0298 | 2 | HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.391+660C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486090 | ||||||
| chr11:47486097
|
G | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+653C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486097 | ||||||
| chr11:47486103
|
A | G | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+647T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486103 | ||||||
| chr11:47486109
|
T | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+641A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486109 | ||||||
| chr11:47486110
|
A | G | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+640T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486110 | ||||||
| chr11:47486116
|
A | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+634T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486116 | ||||||
| chr11:47486122
|
G | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+628C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486122 | ||||||
| chr11:47486125
|
T | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+625A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486125 | ||||||
| chr11:47486131
|
C | A | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+619G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486131 | ||||||
| chr11:47486135
|
C | T | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+615G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486135 | ||||||
| chr11:47486136
|
A | G | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+614T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486136 | ||||||
| chr11:47486139
|
C | G | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+611G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486139 | ||||||
| chr11:47486140
|
A | T | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+610T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486140 | ||||||
| chr11:47486147
|
T | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+603A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486147 | ||||||
| chr11:47486148
|
G | A | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.391+602C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486148 | ||||||
| chr11:47486160
|
CA | C | 231 | a0001c0001t0001g0026a0001c0001t0001g0122a0001c0001t0001g0165others(228): Show | 232 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.391+589delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486160 | ||||||
| chr11:47486294
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.391+456G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486294 | ||||||
| chr11:47486339
|
C | A | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.391+411G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486339 | ||||||
| chr11:47486352
|
G | A | 1 | a0001c0001t0003g0321 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.391+398C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486352 | ||||||
| chr11:47486495
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.391+255G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486495 | ||||||
| chr11:47486821
|
T | C | 1 | a0001c0001t0002g0250 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.343-23A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47486821 | ||||||
| chr11:47486910
|
T | C | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-112A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47486910 | ||||||
| chr11:47486922
|
G | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0125a0001c0001t0001g0126others(11): Show | 14 | HG01496.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-124C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47486922 | ||||||
| chr11:47487043
|
T | C | 1 | a0001c0001t0002g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.342+116A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47487043 | ||||||
| chr11:47487312
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.260-71G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487312 | ||||||
| chr11:47487465
|
A | G | 21 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0274others(18): Show | 21 | HG00544.hp2 HG00621.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-224T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487465 | ||||||
| chr11:47487585
|
G | C | 80 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(77): Show | 80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.260-344C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487585 | ||||||
| chr11:47487813
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.260-572T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487813 | ||||||
| chr11:47487816
|
G | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0165a0001c0001t0001g0177others(4): Show | 7 | HG00558.hp2 HG00609.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-575C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487816 | ||||||
| chr11:47488148
|
C | A | 18 | a0001c0001t0002g0025a0001c0001t0002g0222a0001c0001t0002g0223others(15): Show | 18 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.259+689G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488148 | ||||||
| chr11:47488161
|
T | C | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.259+676A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488161 | ||||||
| chr11:47488175
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.259+662C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488175 | ||||||
| chr11:47488213
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259+624C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488213 | ||||||
| chr11:47488397
|
A | G | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.259+440T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488397 | ||||||
| chr11:47488428
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.259+409G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488428 | ||||||
| chr11:47488529
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.259+308C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488529 | ||||||
| chr11:47488777
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.259+60G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488777 | ||||||
| chr11:47488801
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259+36C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488801 | ||||||
| chr11:47489054
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0166 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.72-30A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489054 | ||||||
| chr11:47489195
|
C | T | 3 | a0001c0001t0003g0042a0001c0001t0003g0297a0001c0001t0003g0298 | 3 | HG00597.hp1 NA18962.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.72-171G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489195 | ||||||
| chr11:47489536
|
AATGC | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-516_72-513delGC others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489536 | ||||||
| chr11:47489863
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.72-839G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489863 | ||||||
| chr11:47489932
|
C | CTTGTTT | 3 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0309 | 3 | HG02451.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72-914_72-909dupAA others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489932 | ||||||
| chr11:47489932
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0057 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.72-909_72-908insAA others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489932 | ||||||
| chr11:47489935
|
G | GGTTTTTT others(12): Show |
1 | a0001c0001t0003g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTGTTTTT others(10): Show |
1 | a0001c0001t0002g0109 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTT | 8 | a0001c0001t0001g0151a0001c0001t0001g0170a0001c0001t0003g0060others(5): Show | 8 | HG00639.hp1 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-915_72-912dupAA others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTT | 7 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0003g0068others(4): Show | 7 | HG02965.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-916_72-912dupAA others(3): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT | 9 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(6): Show | 9 | HG02486.hp2 HG02622.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-918_72-912dupAA others(5): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(2): Show |
8 | a0001c0001t0001g0127a0001c0001t0002g0028a0001c0001t0002g0030others(5): Show | 8 | HG01071.hp2 HG01099.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-920_72-912dupAA others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(3): Show |
5 | a0001c0001t0001g0026a0001c0001t0003g0087a0001c0001t0004g0003others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-921_72-912dupAA others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(4): Show |
6 | a0001c0001t0002g0029a0001c0001t0003g0040a0001c0001t0004g0004others(3): Show | 6 | HG01192.hp2 HG02970.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-922_72-912dupAA others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(5): Show |
3 | a0001c0001t0004g0006a0001c0001t0004g0008a0001c0001t0019g0185 | 3 | HG02486.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.72-923_72-912dupAA others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0004g0001a0001c0001t0004g0002 | 3 | HG01884.hp1 HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.72-924_72-912dupAA others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(7): Show |
7 | a0001c0001t0002g0116a0001c0001t0002g0258a0001c0001t0002g0274others(4): Show | 7 | HG01517.hp2 HG03239.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-925_72-912dupAA others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(8): Show |
7 | a0001c0001t0002g0077a0001c0001t0002g0219a0001c0001t0002g0273others(4): Show | 7 | HG01433.hp2 HG01943.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-926_72-912dupAA others(13): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(9): Show |
22 | a0001c0001t0002g0220a0001c0001t0002g0224a0001c0001t0002g0236others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.72-927_72-912dupAA others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(10): Show |
38 | a0001c0001t0001g0096a0001c0001t0001g0145a0001c0001t0002g0025others(35): Show | 38 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.72-928_72-912dupAA others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(11): Show |
42 | a0001c0001t0001g0129a0001c0001t0002g0217a0001c0001t0002g0223others(39): Show | 42 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.72-929_72-912dupAA others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(12): Show |
15 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0002g0106others(12): Show | 15 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.72-930_72-912dupAA others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(13): Show |
13 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0152others(10): Show | 13 | HG00323.hp1 HG00642.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-931_72-912dupAA others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(14): Show |
9 | a0001c0001t0001g0178a0001c0001t0002g0244a0001c0001t0002g0267others(6): Show | 9 | HG01346.hp2 HG01943.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(19): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(15): Show |
7 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0128others(4): Show | 7 | HG01261.hp2 HG01358.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(20): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(16): Show |
8 | a0001c0001t0001g0169a0001c0001t0002g0012a0001c0001t0002g0228others(5): Show | 8 | HG00609.hp2 HG01255.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(21): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(17): Show |
3 | a0001c0001t0001g0192a0001c0001t0002g0314a0001c0001t0027g0227 | 3 | HG01517.hp1 HG02683.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.72-912_72-911insAA others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0003g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(23): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(19): Show |
4 | a0001c0001t0001g0150a0001c0001t0002g0311a0001c0001t0002g0312others(1): Show | 4 | HG00280.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(24): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(23): Show |
1 | a0001c0001t0001g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(28): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(24): Show |
1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(29): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(25): Show |
2 | a0001c0001t0001g0166a0001c0001t0007g0212 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.72-912_72-911insAA others(30): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(26): Show |
1 | a0001c0001t0006g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(31): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(28): Show |
1 | a0001c0001t0006g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(33): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(32): Show |
1 | a0001c0001t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(37): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(33): Show |
1 | a0001c0001t0002g0283 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(38): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | GTTTTTTT others(41): Show |
1 | a0001c0001t0007g0124 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(46): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
G | T | 1 | a0001c0001t0003g0057 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.72-911C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489935
|
GT | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0120a0001c0001t0001g0140others(14): Show | 17 | HG00558.hp1 HG02071.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.72-912delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | ||||||
| chr11:47489944
|
T | TTTTTTTT others(10): Show |
4 | a0001c0001t0002g0234a0001c0001t0002g0238a0001c0001t0002g0240others(1): Show | 4 | HG02083.hp2 NA18944.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-921_72-920insGA others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489944 | ||||||
| chr11:47490158
|
C | T | 1 | a0001c0001t0003g0075 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.72-1134G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490158 | ||||||
| chr11:47490183
|
G | A | 5 | a0001c0001t0001g0319a0001c0001t0003g0097a0001c0001t0024g0320others(2): Show | 5 | HG01175.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-1159C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490183 | ||||||
| chr11:47490425
|
G | GT | 20 | a0001c0001t0002g0029a0001c0001t0002g0238a0001c0001t0003g0031others(17): Show | 20 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.72-1402dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490425 | ||||||
| chr11:47490425
|
GT | G | 108 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.72-1402delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490425 | ||||||
| chr11:47490463
|
A | C | 2 | a0001c0001t0008g0098a0001c0001t0008g0099 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.72-1439T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490463 | ||||||
| chr11:47490586
|
G | A | 8 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(5): Show | 8 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-1562C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490586 | ||||||
| chr11:47490850
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1826G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490850 | ||||||
| chr11:47490995
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-1971C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490995 | ||||||
| chr11:47491103
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.72-2079G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491103 | ||||||
| chr11:47491250
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.72-2226G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491250 | ||||||
| chr11:47491255
|
CA | C | 152 | a0001c0001t0001g0096a0001c0001t0001g0141a0001c0001t0002g0011others(149): Show | 153 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.72-2232delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491255 | ||||||
| chr11:47491256
|
AG | A | 55 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.72-2233delC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491256 | ||||||
| chr11:47491573
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.72-2549T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491573 | ||||||
| chr11:47491578
|
A | G | 5 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-2554T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491578 | ||||||
| chr11:47492218
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0059 | 2 | HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.72-3194C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492218 | ||||||
| chr11:47492354
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3330G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492354 | ||||||
| chr11:47492586
|
G | A | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.72-3562C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492586 | ||||||
| chr11:47492646
|
C | G | 3 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.72-3622G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492646 | ||||||
| chr11:47492713
|
CAG | C | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-3691_72-3690del others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492713 | ||||||
| chr11:47492849
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-3825T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492849 | ||||||
| chr11:47492862
|
A | T | 1 | a0001c0001t0002g0315 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-3838T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492862 | ||||||
| chr11:47492863
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-3839C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492863 | ||||||
| chr11:47493004
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0003g0044 | 2 | HG04199.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.72-3980G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493004 | ||||||
| chr11:47493219
|
A | G | 1 | a0001c0001t0005g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.72-4195T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493219 | ||||||
| chr11:47493238
|
GCA | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4216_72-4215del others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493238 | ||||||
| chr11:47493270
|
G | A | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG01167.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.72-4246C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493270 | ||||||
| chr11:47493337
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-4313G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493337 | ||||||
| chr11:47493339
|
T | TA | 316 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(313): Show | 317 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.72-4316dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493339 | ||||||
| chr11:47493339
|
T | TAA | 6 | a0001c0001t0001g0121a0001c0001t0001g0143a0001c0001t0001g0177others(3): Show | 6 | HG02280.hp1 HG03831.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-4317_72-4316dup others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493339 | ||||||
| chr11:47493408
|
T | C | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.72-4384A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493408 | ||||||
| chr11:47493432
|
C | T | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.72-4408G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493432 | ||||||
| chr11:47493439
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.72-4415G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493439 | ||||||
| chr11:47493483
|
G | A | 10 | a0001c0001t0002g0116a0001c0001t0002g0310a0001c0001t0002g0311others(7): Show | 10 | HG00280.hp2 HG01255.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-4459C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493483 | ||||||
| chr11:47493507
|
CAAAAAGA others(4): Show |
C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4494_72-4484del others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493507 | ||||||
| chr11:47493513
|
G | GA | 36 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0142others(33): Show | 36 | HG00558.hp1 HG00621.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-4490dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493513 | ||||||
| chr11:47493513
|
GA | G | 85 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0141others(82): Show | 86 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.72-4490delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493513 | ||||||
| chr11:47493540
|
G | T | 1 | a0001c0001t0003g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.72-4516C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493540 | ||||||
| chr11:47493597
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.72-4573A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493597 | ||||||
| chr11:47493782
|
G | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4758C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493782 | ||||||
| chr11:47493875
|
C | G | 9 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(6): Show | 9 | NA18947.hp1 NA18963.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-4851G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493875 | ||||||
| chr11:47494009
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.72-4985A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494009 | ||||||
| chr11:47494189
|
G | C | 1 | a0001c0001t0002g0258 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.72-5165C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494189 | ||||||
| chr11:47494204
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72-5180T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494204 | ||||||
| chr11:47494306
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0149 | 2 | NA18985.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.71+5147C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494306 | ||||||
| chr11:47494345
|
A | G | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.71+5108T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494345 | ||||||
| chr11:47494417
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.71+5036C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494417 | ||||||
| chr11:47494502
|
A | G | 2 | a0001c0001t0001g0333a0001c0001t0013g0334 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.71+4951T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494502 | ||||||
| chr11:47494504
|
C | T | 3 | a0001c0001t0007g0016a0001c0001t0007g0124a0001c0001t0007g0212 | 3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.71+4949G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494504 | ||||||
| chr11:47494786
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0166 | 3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.71+4667G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494786 | ||||||
| chr11:47494888
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.71+4565A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494888 | ||||||
| chr11:47494909
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.71+4544T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494909 | ||||||
| chr11:47495053
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.71+4400C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495053 | ||||||
| chr11:47495399
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0180 | 2 | NA18982.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.71+4054A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495399 | ||||||
| chr11:47495452
|
G | A | 1 | a0001c0004t0002g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.71+4001C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495452 | ||||||
| chr11:47495482
|
A | C | 2 | a0001c0001t0002g0289a0001c0001t0025g0287 | 2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.71+3971T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495482 | ||||||
| chr11:47495482
|
A | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+3971T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495482 | ||||||
| chr11:47495757
|
T | A | 1 | a0001c0001t0002g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.71+3696A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495757 | ||||||
| chr11:47496045
|
T | A | 3 | a0001c0001t0002g0077a0001c0001t0003g0075a0001c0001t0003g0076 | 3 | HG01943.hp2 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.71+3408A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496045 | ||||||
| chr11:47496046
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.71+3407C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496046 | ||||||
| chr11:47496348
|
G | A | 24 | a0001c0001t0001g0018a0001c0001t0001g0123a0001c0001t0001g0143others(21): Show | 24 | HG00544.hp1 HG02083.hp1 HG02148.hp1 others(21): Show |
intron_variant | MODIFIER | c.71+3105C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496348 | ||||||
| chr11:47496649
|
C | T | 1 | a0001c0001t0023g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.71+2804G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496649 | ||||||
| chr11:47496769
|
A | T | 1 | a0001c0001t0002g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.71+2684T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496769 | ||||||
| chr11:47496800
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+2653G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496800 | ||||||
| chr11:47497004
|
T | C | 2 | a0001c0001t0002g0289a0001c0001t0025g0287 | 2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.71+2449A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497004 | ||||||
| chr11:47497123
|
G | C | 1 | a0001c0001t0001g0333 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.71+2330C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497123 | ||||||
| chr11:47497607
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.71+1846A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497607 | ||||||
| chr11:47497733
|
G | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+1720C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497733 | ||||||
| chr11:47498022
|
C | G | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.71+1431G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498022 | ||||||
| chr11:47498229
|
A | G | 1 | a0001c0001t0003g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71+1224T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498229 | ||||||
| chr11:47498242
|
ACAAAAAG others(2): Show |
A | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+1202_71+1210del others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498242 | ||||||
| chr11:47498768
|
G | C | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02257.hp2 HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71+685C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498768 | ||||||
| chr11:47498932
|
C | T | 2 | a0001c0001t0003g0048a0001c0001t0003g0081 | 2 | HG01361.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.71+521G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498932 | ||||||
| chr11:47499201
|
A | G | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.71+252T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47499201 | ||||||
| chr11:47499773
|
G | C | 2 | a0001c0001t0003g0066a0001c0001t0003g0103 | 2 | NA18990.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-81-169C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47499773 | ||||||
| chr11:47500005
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-81-401G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500005 | ||||||
| chr11:47500265
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-82+596A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500265 | ||||||
| chr11:47500393
|
C | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+468G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500393 | ||||||
| chr11:47500424
|
T | C | 1 | a0001c0001t0018g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-82+437A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500424 | ||||||
| chr11:47500512
|
T | C | 1 | a0001c0001t0018g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-82+349A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500512 | ||||||
| chr11:47500762
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0162a0001c0001t0001g0167others(1): Show | 4 | HG02083.hp1 HG03831.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+99C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500762 | ||||||
| chr11:47500936
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-153-4G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47500936 | ||||||
| chr11:47501117
|
T | A | 3 | a0001c0001t0007g0016a0001c0001t0007g0124a0001c0001t0007g0212 | 3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-153-185A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501117 | ||||||
| chr11:47501162
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-153-230A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501162 | ||||||
| chr11:47501257
|
G | C | 2 | a0001c0001t0003g0297a0001c0001t0003g0298 | 2 | HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-153-325C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501257 | ||||||
| chr11:47501322
|
CAGA | C | 75 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(72): Show | 75 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-153-393_-153-391d others(5): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501322 | ||||||
| chr11:47501586
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-654C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501586 | ||||||
| chr11:47501662
|
C | A | 78 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(75): Show | 78 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-153-730G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501662 | ||||||
| chr11:47501662
|
CA | C | 14 | a0001c0001t0001g0019a0001c0001t0001g0120a0001c0001t0001g0140others(11): Show | 14 | HG02071.hp2 HG02523.hp1 NA18982.hp2 others(11): Show |
intron_variant | MODIFIER | c.-153-731delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501662 | ||||||
| chr11:47501910
|
T | G | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-153-978A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501910 | ||||||
| chr11:47502026
|
G | A | 1 | a0001c0001t0003g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-153-1094C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502026 | ||||||
| chr11:47502037
|
C | T | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-153-1105G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502037 | ||||||
| chr11:47502075
|
T | C | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-153-1143A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502075 | ||||||
| chr11:47502289
|
G | T | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-153-1357C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502289 | ||||||
| chr11:47502301
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-1369G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502301 | ||||||
| chr11:47502444
|
A | T | 4 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0071others(1): Show | 4 | HG03942.hp1 NA18952.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-1512T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502444 | ||||||
| chr11:47502558
|
C | A | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-1626G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502558 | ||||||
| chr11:47502605
|
G | T | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-153-1673C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502605 | ||||||
| chr11:47502620
|
C | A | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-153-1688G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502620 | ||||||
| chr11:47502658
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-153-1726G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502658 | ||||||
| chr11:47502696
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-153-1764C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502696 | ||||||
| chr11:47502764
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-153-1832C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502764 | ||||||
| chr11:47502765
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-1833C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502765 | ||||||
| chr11:47502769
|
T | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-153-1837A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502769 | ||||||
| chr11:47502788
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-153-1856G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502788 | ||||||
| chr11:47502846
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-153-1914A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502846 | ||||||
| chr11:47502847
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-153-1915T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502847 | ||||||
| chr11:47502905
|
G | C | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-1973C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502905 | ||||||
| chr11:47502978
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-153-2046T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502978 | ||||||
| chr11:47503023
|
C | G | 2 | a0001c0001t0012g0249a0001c0001t0012g0252 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-153-2091G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503023 | ||||||
| chr11:47503118
|
G | C | 1 | a0001c0001t0002g0223 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-153-2186C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503118 | ||||||
| chr11:47503427
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-153-2495A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503427 | ||||||
| chr11:47503700
|
T | C | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-2768A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503700 | ||||||
| chr11:47503831
|
T | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-2899A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503831 | ||||||
| chr11:47504121
|
A | G | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-153-3189T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504121 | ||||||
| chr11:47504175
|
A | AAAAC | 4 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG03704.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-3247_-153-324 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504175 | ||||||
| chr11:47504452
|
C | A | 1 | a0001c0001t0003g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-153-3520G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504452 | ||||||
| chr11:47504500
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-153-3568G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504500 | ||||||
| chr11:47504552
|
ATGGGCAA others(1843): Show |
A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-5470_-153-362 others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504552 | ||||||
| chr11:47504601
|
T | TA | 5 | a0001c0001t0001g0151a0001c0001t0005g0021a0001c0001t0005g0186others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-3670dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504601 | ||||||
| chr11:47504626
|
C | A | 21 | a0001c0001t0002g0106a0001c0001t0002g0110a0001c0001t0002g0114others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.-153-3694G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504626 | ||||||
| chr11:47504718
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-153-3786T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504718 | ||||||
| chr11:47504728
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-153-3796G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504728 | ||||||
| chr11:47504902
|
C | CA | 113 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0001g0184others(110): Show | 113 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-153-3971dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504902 | ||||||
| chr11:47504902
|
C | CAA | 19 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(16): Show | 19 | HG02145.hp1 HG02486.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.-153-3972_-153-397 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504902 | ||||||
| chr11:47505304
|
T | C | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-4372A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505304 | ||||||
| chr11:47505440
|
T | A | 2 | a0001c0001t0002g0289a0001c0001t0025g0287 | 2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-153-4508A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505440 | ||||||
| chr11:47505500
|
G | T | 87 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-153-4568C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505500 | ||||||
| chr11:47505569
|
G | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-4637C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505569 | ||||||
| chr11:47505643
|
CA | C | 162 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(159): Show | 162 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-153-4712delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505643 | ||||||
| chr11:47505716
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG02809.hp2 HG02897.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153-4784G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505716 | ||||||
| chr11:47505840
|
C | T | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-153-4908G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505840 | ||||||
| chr11:47505936
|
C | CA | 106 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(103): Show | 106 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-153-5005dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505936 | ||||||
| chr11:47506074
|
A | T | 6 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-5142T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506074 | ||||||
| chr11:47506081
|
T | C | 1 | a0001c0001t0003g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-153-5149A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506081 | ||||||
| chr11:47506243
|
G | A | 25 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-153-5311C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506243 | ||||||
| chr11:47506286
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-5354G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506286 | ||||||
| chr11:47506437
|
GA | G | 8 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0169others(5): Show | 8 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153-5506delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506437 | ||||||
| chr11:47506563
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-5631C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506563 | ||||||
| chr11:47507016
|
C | A | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-6084G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507016 | ||||||
| chr11:47507413
|
A | G | 3 | a0001c0001t0003g0065a0001c0001t0003g0067a0001c0001t0003g0072 | 3 | NA18747.hp1 NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-153-6481T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507413 | ||||||
| chr11:47507462
|
A | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-6530T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507462 | ||||||
| chr11:47507485
|
G | A | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-153-6553C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507485 | ||||||
| chr11:47508072
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-7140T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508072 | ||||||
| chr11:47508203
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-153-7271A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508203 | ||||||
| chr11:47508297
|
T | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0120a0001c0001t0001g0140others(11): Show | 14 | HG02071.hp2 HG02523.hp1 NA18982.hp2 others(11): Show |
intron_variant | MODIFIER | c.-153-7365A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508297 | ||||||
| chr11:47508395
|
C | A | 98 | a0001c0001t0001g0096a0001c0001t0002g0028a0001c0001t0002g0029others(95): Show | 99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-153-7463G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508395 | ||||||
| chr11:47508472
|
G | A | 81 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(78): Show | 81 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-153-7540C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508472 | ||||||
| chr11:47508569
|
TAA | T | 144 | a0001c0001t0001g0018a0001c0001t0001g0198a0001c0001t0001g0319others(141): Show | 145 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-153-7639_-153-763 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508569 | ||||||
| chr11:47508569
|
TAAA | T | 182 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(179): Show | 182 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-153-7640_-153-763 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508569 | ||||||
| chr11:47508667
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-7735T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508667 | ||||||
| chr11:47508675
|
A | AAC | 119 | a0001c0001t0001g0148a0001c0001t0001g0202a0001c0001t0002g0011others(116): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-153-7745_-153-774 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508675 | ||||||
| chr11:47508697
|
C | T | 1 | a0001c0001t0019g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-153-7765G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508697 | ||||||
| chr11:47508703
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-7771A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508703 | ||||||
| chr11:47508977
|
C | T | 1 | a0001c0001t0002g0267 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-153-8045G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508977 | ||||||
| chr11:47509014
|
C | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-8082G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509014 | ||||||
| chr11:47509021
|
C | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-8089G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509021 | ||||||
| chr11:47509044
|
T | G | 1 | a0001c0001t0001g0338 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-153-8112A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509044 | ||||||
| chr11:47509084
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-153-8152A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509084 | ||||||
| chr11:47509257
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-153-8325C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509257 | ||||||
| chr11:47509283
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0282a0001c0001t0002g0288 | 3 | NA18956.hp1 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-153-8351C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509283 | ||||||
| chr11:47509445
|
T | C | 3 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | HG03041.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-153-8513A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509445 | ||||||
| chr11:47509509
|
G | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-8577C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509509 | ||||||
| chr11:47509801
|
C | T | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-8869G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509801 | ||||||
| chr11:47509897
|
C | CA | 161 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(158): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.-153-8966dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509897 | ||||||
| chr11:47509897
|
C | CAA | 151 | a0001c0001t0001g0096a0001c0001t0001g0121a0001c0001t0001g0132others(148): Show | 151 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-153-8967_-153-896 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509897 | ||||||
| chr11:47509897
|
C | CAAA | 7 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0246others(4): Show | 7 | HG02257.hp1 HG02683.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-8968_-153-896 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509897 | ||||||
| chr11:47509914
|
T | A | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-153-8982A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509914 | ||||||
| chr11:47510011
|
G | A | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-153-9079C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510011 | ||||||
| chr11:47510332
|
T | G | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-153-9400A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510332 | ||||||
| chr11:47510644
|
G | A | 2 | a0001c0001t0003g0036a0001c0001t0003g0045 | 2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-153-9712C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510644 | ||||||
| chr11:47510659
|
G | A | 1 | a0001c0001t0004g0001 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-153-9727C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510659 | ||||||
| chr11:47510843
|
T | G | 60 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(57): Show | 60 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-153-9911A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510843 | ||||||
| chr11:47510856
|
G | C | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-9924C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510856 | ||||||
| chr11:47510861
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-9929C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510861 | ||||||
| chr11:47510953
|
G | C | 1 | a0001c0001t0019g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-153-10021C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510953 | ||||||
| chr11:47511100
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-10168A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511100 | ||||||
| chr11:47511333
|
C | G | 2 | a0001c0001t0003g0048a0001c0001t0003g0081 | 2 | HG01361.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-153-10401G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511333 | ||||||
| chr11:47511354
|
C | CCTCTTGG others(15): Show |
338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-153-10423_-153-10 others(28): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511354 | ||||||
| chr11:47511743
|
C | G | 2 | a0001c0001t0008g0098a0001c0001t0008g0099 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-153-10811G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511743 | ||||||
| chr11:47511818
|
A | AG | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-10887dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511818 | ||||||
| chr11:47511883
|
C | G | 1 | a0001c0001t0002g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-153-10951G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511883 | ||||||
| chr11:47511886
|
T | C | 9 | a0001c0001t0002g0310a0001c0001t0002g0311a0001c0001t0002g0312others(6): Show | 9 | HG00280.hp2 HG01255.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-153-10954A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511886 | ||||||
| chr11:47511900
|
G | C | 1 | a0001c0001t0003g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-153-10968C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511900 | ||||||
| chr11:47511931
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-153-10999G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511931 | ||||||
| chr11:47512148
|
G | A | 2 | a0001c0001t0008g0098a0001c0001t0008g0099 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-153-11216C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512148 | ||||||
| chr11:47512166
|
G | T | 1 | a0001c0001t0002g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-11234C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512166 | ||||||
| chr11:47512167
|
T | G | 1 | a0001c0001t0002g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-11235A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512167 | ||||||
| chr11:47512173
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-153-11241C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512173 | ||||||
| chr11:47512204
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0181 | 2 | NA19004.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-153-11272C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512204 | ||||||
| chr11:47512207
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-153-11275G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512207 | ||||||
| chr11:47512372
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-153-11440G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512372 | ||||||
| chr11:47512399
|
T | C | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-153-11467A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512399 | ||||||
| chr11:47512452
|
AT | A | 286 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(283): Show | 287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-153-11521delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512452 | ||||||
| chr11:47512452
|
ATT | A | 14 | a0001c0001t0001g0026a0001c0001t0001g0134a0001c0001t0001g0167others(11): Show | 14 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-153-11522_-153-11 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512452 | ||||||
| chr11:47512584
|
C | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-11652G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512584 | ||||||
| chr11:47512951
|
T | G | 1 | a0001c0001t0002g0246 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-153-12019A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512951 | ||||||
| chr11:47513085
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-153-12153T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513085 | ||||||
| chr11:47513408
|
GT | G | 3 | a0001c0001t0002g0226a0001c0001t0010g0101a0001c0001t0010g0102 | 3 | HG02165.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-153-12477delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513408 | ||||||
| chr11:47513412
|
T | C | 108 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-153-12480A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513412 | ||||||
| chr11:47513412
|
T | TC | 8 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0169others(5): Show | 8 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153-12481dupG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513412 | ||||||
| chr11:47513413
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-153-12481G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513413 | ||||||
| chr11:47513461
|
CCT | C | 78 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(75): Show | 78 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-153-12531_-153-12 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513461 | ||||||
| chr11:47513580
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-153-12648G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513580 | ||||||
| chr11:47513584
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-153-12652G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513584 | ||||||
| chr11:47513665
|
C | T | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-153-12733G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513665 | ||||||
| chr11:47513792
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0167 | 2 | HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-153-12860C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513792 | ||||||
| chr11:47513930
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-12998G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513930 | ||||||
| chr11:47513931
|
C | CT | 19 | a0001c0001t0001g0319a0001c0001t0001g0322a0001c0001t0001g0323others(16): Show | 19 | HG00673.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.-153-13000dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | ||||||
| chr11:47513931
|
C | CTT | 201 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(198): Show | 202 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-153-13001_-153-13 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | ||||||
| chr11:47513931
|
C | CTTT | 78 | a0001c0001t0001g0177a0001c0001t0002g0024a0001c0001t0002g0025others(75): Show | 78 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-153-13002_-153-13 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | ||||||
| chr11:47513931
|
C | CTTTT | 28 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-153-13003_-153-13 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | ||||||
| chr11:47513931
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-12999G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | ||||||
| chr11:47513941
|
T | TTTC | 6 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0002g0261others(3): Show | 6 | HG01169.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-13010_-153-13 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513941 | ||||||
| chr11:47513992
|
G | C | 1 | a0001c0001t0002g0277 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-153-13060C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513992 | ||||||
| chr11:47514116
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-153-13184C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514116 | ||||||
| chr11:47514144
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0006others(3): Show | 7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-13212C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514144 | ||||||
| chr11:47514164
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-153-13232T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514164 | ||||||
| chr11:47514250
|
A | G | 1 | a0001c0001t0027g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-153-13318T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514250 | ||||||
| chr11:47514297
|
A | T | 7 | a0001c0001t0003g0023a0001c0001t0003g0055a0001c0001t0003g0056others(4): Show | 7 | NA18944.hp1 NA18945.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-13365T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514297 | ||||||
| chr11:47514304
|
T | C | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-13372A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514304 | ||||||
| chr11:47514685
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-153-13753T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514685 | ||||||
| chr11:47514692
|
C | CA | 123 | a0001c0001t0001g0019a0001c0001t0001g0122a0001c0001t0001g0156others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-153-13761dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514692 | ||||||
| chr11:47514692
|
C | CAA | 106 | a0001c0001t0001g0096a0001c0001t0001g0123a0001c0001t0001g0201others(103): Show | 107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.-153-13762_-153-13 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514692 | ||||||
| chr11:47514729
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-13797C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514729 | ||||||
| chr11:47514875
|
A | T | 1 | a0001c0001t0002g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-153-13943T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514875 | ||||||
| chr11:47514940
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-153-14008C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514940 | ||||||
| chr11:47514942
|
A | G | 2 | a0001c0001t0008g0098a0001c0001t0008g0099 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-153-14010T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514942 | ||||||
| chr11:47515068
|
T | C | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-153-14136A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515068 | ||||||
| chr11:47515099
|
G | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0267 | 2 | NA18971.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-153-14167C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515099 | ||||||
| chr11:47515301
|
G | A | 1 | a0001c0001t0003g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-153-14369C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515301 | ||||||
| chr11:47515426
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-14494T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515426 | ||||||
| chr11:47515578
|
A | C | 3 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | NA19065.hp2 NA19074.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-153-14646T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515578 | ||||||
| chr11:47515919
|
C | CTTAT | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-14991_-153-14 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515919 | ||||||
| chr11:47515981
|
A | G | 12 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(9): Show | 12 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-153-15049T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515981 | ||||||
| chr11:47515990
|
C | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0006others(3): Show | 7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-15058G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515990 | ||||||
| chr11:47516106
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0006others(3): Show | 7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-15174C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516106 | ||||||
| chr11:47516138
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-15206T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516138 | ||||||
| chr11:47516231
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-15299G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516231 | ||||||
| chr11:47516501
|
G | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-15569C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516501 | ||||||
| chr11:47516550
|
T | C | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-15618A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516550 | ||||||
| chr11:47516582
|
T | A | 1 | a0001c0001t0003g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-153-15650A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516582 | ||||||
| chr11:47516611
|
T | G | 5 | a0001c0001t0001g0319a0001c0001t0001g0330a0001c0001t0024g0320others(2): Show | 5 | HG02451.hp1 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-153-15679A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516611 | ||||||
| chr11:47516612
|
T | G | 1 | a0001c0001t0002g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-153-15680A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516612 | ||||||
| chr11:47516896
|
C | A | 1 | a0001c0001t0002g0317 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-153-15964G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516896 | ||||||
| chr11:47517037
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-153-16105T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517037 | ||||||
| chr11:47517124
|
G | A | 1 | a0001c0001t0003g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-153-16192C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517124 | ||||||
| chr11:47517153
|
G | A | 1 | a0001c0001t0001g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-153-16221C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517153 | ||||||
| chr11:47517159
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-153-16227T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517159 | ||||||
| chr11:47517260
|
G | GA | 43 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(40): Show | 43 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.-153-16329dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | ||||||
| chr11:47517260
|
GA | G | 100 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(97): Show | 100 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-153-16329delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | ||||||
| chr11:47517260
|
GAA | G | 7 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0162others(4): Show | 7 | HG02083.hp1 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-16330_-153-16 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | ||||||
| chr11:47517260
|
GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0002g0296 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-153-16338_-153-16 others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | ||||||
| chr11:47517261
|
A | G | 2 | a0001c0001t0003g0297a0001c0001t0003g0298 | 2 | HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-153-16329T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517261 | ||||||
| chr11:47517656
|
A | G | 100 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(97): Show | 100 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-153-16724T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517656 | ||||||
| chr11:47517656
|
A | T | 6 | a0001c0001t0001g0149a0001c0001t0002g0217a0001c0001t0002g0218others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-16724T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517656 | ||||||
| chr11:47517657
|
T | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0177 | 2 | NA19062.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-153-16725A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517657 | ||||||
| chr11:47517714
|
GC | G | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-153-16783delG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517714 | ||||||
| chr11:47517729
|
T | C | 3 | a0001c0001t0007g0016a0001c0001t0007g0124a0001c0001t0007g0212 | 3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-153-16797A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517729 | ||||||
| chr11:47517967
|
T | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-17035A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517967 | ||||||
| chr11:47518145
|
T | C | 77 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(74): Show | 77 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-153-17213A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518145 | ||||||
| chr11:47518440
|
C | G | 1 | a0001c0001t0005g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-153-17508G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518440 | ||||||
| chr11:47518455
|
C | T | 209 | a0001c0001t0001g0096a0001c0001t0002g0011a0001c0001t0002g0012others(206): Show | 210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-153-17523G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518455 | ||||||
| chr11:47518765
|
G | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG02809.hp2 HG02897.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153-17833C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518765 | ||||||
| chr11:47518800
|
C | T | 1 | a0001c0001t0006g0112 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-153-17868G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518800 | ||||||
| chr11:47518947
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | NA18988.hp2 NA18989.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-153-18015A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518947 | ||||||
| chr11:47519153
|
G | T | 1 | a0001c0001t0003g0014 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-153-18221C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519153 | ||||||
| chr11:47519285
|
C | G | 2 | a0001c0001t0002g0106a0001c0001t0002g0114 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-153-18353G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519285 | ||||||
| chr11:47519350
|
G | A | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-153-18418C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519350 | ||||||
| chr11:47519437
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-18505T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519437 | ||||||
| chr11:47519453
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-18521G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519453 | ||||||
| chr11:47519479
|
C | CTAAA | 27 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0145others(24): Show | 27 | HG00639.hp2 HG01258.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-153-18551_-153-18 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | ||||||
| chr11:47519479
|
C | CTAAATAA others(1): Show |
3 | a0001c0001t0001g0122a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02559.hp1 NA18953.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-153-18555_-153-18 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | ||||||
| chr11:47519479
|
CTAAA | C | 96 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(93): Show | 97 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-153-18551_-153-18 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | ||||||
| chr11:47519479
|
CTAAATAA others(1): Show |
C | 28 | a0001c0001t0001g0206a0001c0001t0002g0011a0001c0001t0002g0012others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-153-18555_-153-18 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | ||||||
| chr11:47519479
|
CTAAATAA others(5): Show |
C | 76 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0002g0259others(73): Show | 76 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-153-18559_-153-18 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | ||||||
| chr11:47519508
|
T | G | 2 | a0001c0002t0002g0299a0001c0002t0002g0300 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-153-18576A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519508 | ||||||
| chr11:47519512
|
T | G | 2 | a0001c0002t0002g0299a0001c0002t0002g0300 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-153-18580A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519512 | ||||||
| chr11:47519592
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-153-18660C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519592 | ||||||
| chr11:47519597
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-153-18665C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519597 | ||||||
| chr11:47519840
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0030 | 2 | HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-153-18908C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519840 | ||||||
| chr11:47519842
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-153-18910C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519842 | ||||||
| chr11:47519938
|
T | TA | 87 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-153-19007dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519938 | ||||||
| chr11:47520010
|
T | TA | 333 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(330): Show | 334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-153-19079dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520010 | ||||||
| chr11:47520027
|
A | AG | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0166 | 3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-153-19096dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520027 | ||||||
| chr11:47520109
|
G | C | 1 | a0001c0001t0003g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-153-19177C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520109 | ||||||
| chr11:47520229
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-153-19297A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520229 | ||||||
| chr11:47520306
|
GATACA | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0222a0001c0001t0003g0058 | 3 | HG03834.hp2 NA18942.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-153-19379_-153-19 others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520306 | ||||||
| chr11:47520765
|
T | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-19833A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520765 | ||||||
| chr11:47520821
|
C | T | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-19889G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520821 | ||||||
| chr11:47520836
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-19904C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520836 | ||||||
| chr11:47521079
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-20147T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521079 | ||||||
| chr11:47521204
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-20272C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521204 | ||||||
| chr11:47521207
|
G | A | 9 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(6): Show | 9 | NA18947.hp1 NA18963.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-153-20275C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521207 | ||||||
| chr11:47521576
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-153-20644G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521576 | ||||||
| chr11:47521597
|
A | G | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-20665T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521597 | ||||||
| chr11:47521769
|
A | C | 1 | a0001c0001t0003g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-153-20837T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521769 | ||||||
| chr11:47521913
|
A | AT | 108 | a0001c0001t0001g0156a0001c0001t0001g0180a0001c0001t0001g0190others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-153-20982dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521913 | ||||||
| chr11:47521915
|
T | G | 1 | a0001c0001t0003g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-153-20983A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521915 | ||||||
| chr11:47522213
|
G | A | 1 | a0001c0001t0002g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-153-21281C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522213 | ||||||
| chr11:47522310
|
G | A | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-21378C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522310 | ||||||
| chr11:47522322
|
T | TG | 3 | a0001c0001t0001g0141a0001c0001t0010g0101a0001c0001t0010g0102 | 3 | HG02896.hp2 HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-153-21391dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522322 | ||||||
| chr11:47522355
|
A | G | 3 | a0001c0001t0007g0016a0001c0001t0007g0124a0001c0001t0007g0212 | 3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-153-21423T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522355 | ||||||
| chr11:47522422
|
C | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0198 | 2 | NA18970.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-153-21490G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522422 | ||||||
| chr11:47522461
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-153-21529T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522461 | ||||||
| chr11:47522523
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-21591G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522523 | ||||||
| chr11:47522538
|
C | A | 1 | a0001c0001t0002g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-153-21606G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522538 | ||||||
| chr11:47522541
|
C | A | 329 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(326): Show | 330 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.-153-21609G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522541 | ||||||
| chr11:47522702
|
T | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-21770A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522702 | ||||||
| chr11:47522781
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-153-21849C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522781 | ||||||
| chr11:47522828
|
G | GA | 8 | a0001c0001t0001g0022a0001c0001t0001g0204a0001c0001t0002g0233others(5): Show | 8 | HG01192.hp2 HG02109.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153-21897dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522828 | ||||||
| chr11:47523069
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-153-22137T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523069 | ||||||
| chr11:47523105
|
A | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-22173T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523105 | ||||||
| chr11:47523235
|
G | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0006others(3): Show | 7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-22303C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523235 | ||||||
| chr11:47523299
|
A | T | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-153-22367T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523299 | ||||||
| chr11:47523415
|
C | T | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-22483G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523415 | ||||||
| chr11:47523522
|
A | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-22590T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523522 | ||||||
| chr11:47523616
|
A | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0001g0199others(1): Show | 4 | HG00558.hp2 NA18964.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-153-22684T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523616 | ||||||
| chr11:47523673
|
T | C | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-22741A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523673 | ||||||
| chr11:47523820
|
A | C | 1 | a0001c0001t0003g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-153-22888T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523820 | ||||||
| chr11:47523959
|
G | A | 3 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0307 | 3 | HG01071.hp2 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-153-23027C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523959 | ||||||
| chr11:47523970
|
T | C | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-153-23038A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523970 | ||||||
| chr11:47524145
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-153-23213T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524145 | ||||||
| chr11:47524317
|
C | A | 1 | a0001c0001t0003g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-153-23385G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524317 | ||||||
| chr11:47524488
|
C | CT | 4 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0286others(1): Show | 4 | HG03704.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-23557dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524488 | ||||||
| chr11:47524530
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-153-23598G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524530 | ||||||
| chr11:47524986
|
G | A | 1 | a0001c0001t0005g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-153-24054C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524986 | ||||||
| chr11:47525253
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-24321T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525253 | ||||||
| chr11:47525390
|
CCAA | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | NA18961.hp1 NA18972.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-24461_-153-24 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525390 | ||||||
| chr11:47525494
|
T | C | 78 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(75): Show | 78 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-153-24562A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525494 | ||||||
| chr11:47525628
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-153-24696G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525628 | ||||||
| chr11:47525726
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-153-24794G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525726 | ||||||
| chr11:47525861
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-153-24929G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525861 | ||||||
| chr11:47525928
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0053 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-153-25009_-153-24 others(19): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525928 | ||||||
| chr11:47525940
|
CA | C | 314 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(311): Show | 315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.-153-25009delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525940 | ||||||
| chr11:47526142
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-153-25210G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526142 | ||||||
| chr11:47526182
|
AGCCAGGT others(12): Show |
A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0166 | 3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-153-25269_-153-25 others(25): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526182 | ||||||
| chr11:47526262
|
G | A | 4 | a0001c0001t0002g0030a0001c0001t0002g0109a0001c0002t0002g0299others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-25330C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526262 | ||||||
| chr11:47526485
|
T | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-25553A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526485 | ||||||
| chr11:47526561
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-153-25629G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526561 | ||||||
| chr11:47526609
|
T | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-25677A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526609 | ||||||
| chr11:47526656
|
A | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0136 | 2 | HG01099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-153-25724T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526656 | ||||||
| chr11:47526766
|
C | T | 20 | a0001c0001t0003g0014a0001c0001t0003g0040a0001c0001t0003g0041others(17): Show | 20 | HG00673.hp2 HG00735.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-153-25834G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526766 | ||||||
| chr11:47526822
|
C | T | 2 | a0001c0001t0002g0316a0001c0001t0003g0055 | 2 | HG00280.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-153-25890G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526822 | ||||||
| chr11:47526907
|
T | C | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-25975A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526907 | ||||||
| chr11:47527050
|
T | TA | 13 | a0001c0001t0001g0143a0001c0001t0001g0165a0001c0001t0002g0105others(10): Show | 13 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.-154+25941dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527050 | ||||||
| chr11:47527068
|
T | C | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-154+25924A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527068 | ||||||
| chr11:47527113
|
C | T | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-154+25879G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527113 | ||||||
| chr11:47527216
|
T | C | 1 | a0001c0001t0002g0292 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-154+25776A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527216 | ||||||
| chr11:47527218
|
A | G | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+25774T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527218 | ||||||
| chr11:47527248
|
G | A | 9 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0169others(6): Show | 9 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+25744C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527248 | ||||||
| chr11:47527724
|
T | C | 6 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0006others(3): Show | 7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+25268A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527724 | ||||||
| chr11:47528101
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0028g0035 | 2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-154+24891G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528101 | ||||||
| chr11:47528208
|
A | G | 3 | a0001c0001t0002g0077a0001c0001t0003g0075a0001c0001t0003g0076 | 3 | HG01943.hp2 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-154+24784T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528208 | ||||||
| chr11:47528434
|
A | G | 1 | a0001c0001t0002g0318 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-154+24558T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528434 | ||||||
| chr11:47528446
|
A | AT | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+24545dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528446 | ||||||
| chr11:47528453
|
T | G | 1 | a0001c0001t0006g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-154+24539A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528453 | ||||||
| chr11:47528890
|
C | CA | 109 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(106): Show | 109 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-154+24101dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528890 | ||||||
| chr11:47529005
|
A | T | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-154+23987T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529005 | ||||||
| chr11:47529077
|
C | CT | 12 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0143others(9): Show | 12 | HG01346.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-154+23914dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529077 | ||||||
| chr11:47529139
|
G | A | 2 | a0001c0001t0002g0278a0001c0001t0002g0292 | 2 | HG00544.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-154+23853C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529139 | ||||||
| chr11:47529166
|
C | T | 3 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+23826G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529166 | ||||||
| chr11:47529188
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-154+23804G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529188 | ||||||
| chr11:47529254
|
T | C | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+23738A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529254 | ||||||
| chr11:47529283
|
GGGGACA | G | 77 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(74): Show | 77 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-154+23703_-154+23 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529283 | ||||||
| chr11:47529695
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+23297G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529695 | ||||||
| chr11:47529827
|
G | C | 1 | a0001c0001t0002g0109 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-154+23165C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529827 | ||||||
| chr11:47529914
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+23078G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529914 | ||||||
| chr11:47530087
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-154+22905C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530087 | ||||||
| chr11:47530502
|
T | C | 1 | a0001c0001t0003g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-154+22490A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530502 | ||||||
| chr11:47530623
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-154+22369C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530623 | ||||||
| chr11:47530749
|
G | GT | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+22242dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530749 | ||||||
| chr11:47530882
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+22110C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530882 | ||||||
| chr11:47530906
|
A | AC | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0271 | 3 | NA18985.hp2 NA19007.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-154+22085_-154+22 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530906 | ||||||
| chr11:47530934
|
C | A | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+22058G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530934 | ||||||
| chr11:47531027
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-154+21965G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531027 | ||||||
| chr11:47531180
|
G | A | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-154+21812C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531180 | ||||||
| chr11:47531265
|
C | A | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-154+21727G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531265 | ||||||
| chr11:47531272
|
C | CA | 22 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.-154+21719dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531272 | ||||||
| chr11:47531298
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0155a0001c0001t0001g0160 | 3 | NA18945.hp1 NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-154+21694C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531298 | ||||||
| chr11:47531474
|
TAGG | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0001g0199others(1): Show | 4 | HG00558.hp2 NA18964.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-154+21515_-154+21 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531474 | ||||||
| chr11:47531526
|
A | T | 1 | a0001c0001t0003g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-154+21466T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531526 | ||||||
| chr11:47531567
|
T | TCAAA | 321 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(318): Show | 322 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.-154+21421_-154+21 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531567 | ||||||
| chr11:47531567
|
T | TCAAACAA others(1): Show |
13 | a0001c0001t0001g0026a0001c0001t0002g0109a0001c0001t0002g0217others(10): Show | 13 | HG00280.hp2 HG01243.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+21417_-154+21 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531567 | ||||||
| chr11:47532035
|
A | AT | 13 | a0001c0001t0001g0017a0001c0001t0001g0132a0001c0001t0001g0133others(10): Show | 13 | HG01081.hp2 HG01099.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-154+20956dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532035 | ||||||
| chr11:47532040
|
T | A | 1 | a0001c0001t0003g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-154+20952A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532040 | ||||||
| chr11:47532041
|
T | A | 3 | a0001c0001t0001g0160a0001c0001t0003g0097a0001c0001t0028g0035 | 3 | HG00735.hp2 HG01175.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-154+20951A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532041 | ||||||
| chr11:47532053
|
CAG | C | 3 | a0001c0001t0003g0034a0001c0001t0003g0054a0001c0001t0003g0058 | 3 | HG03710.hp1 HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-154+20937_-154+20 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532053 | ||||||
| chr11:47532117
|
G | A | 10 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(7): Show | 10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+20875C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532117 | ||||||
| chr11:47532208
|
G | T | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-154+20784C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532208 | ||||||
| chr11:47532211
|
A | G | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+20781T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532211 | ||||||
| chr11:47532361
|
T | C | 1 | a0001c0001t0027g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-154+20631A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532361 | ||||||
| chr11:47532505
|
C | G | 331 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(328): Show | 332 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.-154+20487G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532505 | ||||||
| chr11:47532505
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0140a0001c0001t0001g0179 | 3 | NA18983.hp2 NA19083.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-154+20487G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532505 | ||||||
| chr11:47532785
|
G | A | 108 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-154+20207C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532785 | ||||||
| chr11:47533023
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-154+19969A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533023 | ||||||
| chr11:47533092
|
A | AT | 8 | a0001c0001t0001g0096a0001c0001t0001g0213a0001c0001t0001g0319others(5): Show | 8 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+19899dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533092 | ||||||
| chr11:47533225
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19767C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533225 | ||||||
| chr11:47533237
|
A | G | 3 | a0001c0001t0002g0232a0001c0001t0002g0245a0001c0001t0002g0265 | 3 | HG01071.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-154+19755T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533237 | ||||||
| chr11:47533346
|
G | A | 1 | a0001c0001t0006g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-154+19646C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533346 | ||||||
| chr11:47533451
|
C | A | 106 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(103): Show | 106 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-154+19541G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533451 | ||||||
| chr11:47533631
|
A | AATACATA others(5): Show |
1 | a0001c0001t0003g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-154+19360_-154+19 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533631 | ||||||
| chr11:47533631
|
A | ATAAATAC others(4): Show |
2 | a0001c0001t0003g0097a0001c0001t0028g0035 | 2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-154+19360_-154+19 others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533631 | ||||||
| chr11:47533635
|
A | AATAAATA others(5): Show |
4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0100others(1): Show | 4 | NA18939.hp2 NA18953.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19356_-154+19 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | ||||||
| chr11:47533635
|
A | AATAC | 4 | a0001c0001t0003g0075a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02148.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19353_-154+19 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | ||||||
| chr11:47533635
|
A | AATACATA others(1): Show |
245 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(242): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-154+19349_-154+19 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | ||||||
| chr11:47533635
|
A | AATACATA others(5): Show |
63 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0002g0283others(60): Show | 63 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-154+19345_-154+19 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | ||||||
| chr11:47533635
|
A | AATACATA others(9): Show |
3 | a0001c0001t0003g0051a0001c0001t0003g0078a0001c0001t0003g0084 | 3 | HG00323.hp1 HG01433.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-154+19341_-154+19 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | ||||||
| chr11:47533635
|
A | AATACATA others(13): Show |
7 | a0001c0001t0003g0023a0001c0001t0003g0055a0001c0001t0003g0056others(4): Show | 7 | NA18944.hp1 NA18945.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+19337_-154+19 others(26): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | ||||||
| chr11:47533635
|
A | C | 5 | a0001c0001t0001g0319a0001c0001t0003g0059a0001c0001t0003g0097others(2): Show | 5 | HG00558.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+19357T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | ||||||
| chr11:47533716
|
A | G | 3 | a0001c0001t0002g0232a0001c0001t0002g0245a0001c0001t0002g0265 | 3 | HG01071.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-154+19276T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533716 | ||||||
| chr11:47533779
|
C | T | 106 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(103): Show | 106 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-154+19213G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533779 | ||||||
| chr11:47533804
|
T | TA | 62 | a0001c0001t0001g0177a0001c0001t0001g0337a0001c0001t0001g0338others(59): Show | 62 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-154+19187_-154+19 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533804 | ||||||
| chr11:47533804
|
TCC | T | 15 | a0001c0001t0001g0135a0001c0001t0001g0153a0001c0001t0001g0322others(12): Show | 15 | HG02486.hp2 HG02615.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.-154+19186_-154+19 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533804 | ||||||
| chr11:47533805
|
C | A | 261 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(258): Show | 262 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.-154+19187G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533805 | ||||||
| chr11:47533807
|
C | A | 77 | a0001c0001t0001g0135a0001c0001t0001g0153a0001c0001t0001g0177others(74): Show | 77 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-154+19185G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533807 | ||||||
| chr11:47533808
|
C | A | 256 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(253): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.-154+19184G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533808 | ||||||
| chr11:47533809
|
C | A | 62 | a0001c0001t0001g0177a0001c0001t0001g0337a0001c0001t0001g0338others(59): Show | 62 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-154+19183G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533809 | ||||||
| chr11:47533809
|
C | CAA | 27 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(24): Show | 27 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-154+19181_-154+19 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533809 | ||||||
| chr11:47533809
|
CA | C | 114 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-154+19182delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533809 | ||||||
| chr11:47533811
|
A | C | 15 | a0001c0001t0001g0135a0001c0001t0001g0153a0001c0001t0001g0322others(12): Show | 15 | HG02486.hp2 HG02615.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.-154+19181T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533811 | ||||||
| chr11:47533812
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+19180T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533812 | ||||||
| chr11:47533814
|
A | C | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-154+19178T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533814 | ||||||
| chr11:47533815
|
A | C | 3 | a0001c0001t0024g0320a0001c0003t0011g0308a0001c0003t0011g0309 | 3 | HG02896.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+19177T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533815 | ||||||
| chr11:47533831
|
A | AAG | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+19160_-154+19 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533831 | ||||||
| chr11:47533842
|
T | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19150A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533842 | ||||||
| chr11:47534022
|
C | CT | 101 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(98): Show | 102 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-154+18969dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | ||||||
| chr11:47534022
|
C | CTT | 99 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(96): Show | 99 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-154+18968_-154+18 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | ||||||
| chr11:47534022
|
C | CTTT | 28 | a0001c0001t0002g0013a0001c0001t0002g0116a0001c0001t0002g0225others(25): Show | 28 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-154+18967_-154+18 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | ||||||
| chr11:47534022
|
C | T | 3 | a0001c0001t0024g0320a0001c0003t0011g0308a0001c0003t0011g0309 | 3 | HG02896.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+18970G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | ||||||
| chr11:47534045
|
G | T | 1 | a0001c0001t0002g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-154+18947C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534045 | ||||||
| chr11:47534127
|
C | G | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+18865G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534127 | ||||||
| chr11:47534198
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-154+18794A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534198 | ||||||
| chr11:47534232
|
A | G | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-154+18760T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534232 | ||||||
| chr11:47534531
|
C | A | 5 | a0001c0001t0006g0104a0001c0001t0006g0111a0001c0001t0006g0112others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+18461G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534531 | ||||||
| chr11:47534722
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-154+18270G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534722 | ||||||
| chr11:47534832
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+18160C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534832 | ||||||
| chr11:47534837
|
G | C | 1 | a0001c0001t0002g0224 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-154+18155C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534837 | ||||||
| chr11:47534996
|
A | T | 3 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+17996T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534996 | ||||||
| chr11:47535006
|
C | T | 3 | a0001c0001t0002g0106a0001c0001t0002g0114a0001c0001t0002g0115 | 3 | HG00642.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-154+17986G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535006 | ||||||
| chr11:47535031
|
G | C | 2 | a0001c0001t0002g0024a0001c0001t0002g0248 | 2 | HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-154+17961C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535031 | ||||||
| chr11:47535348
|
T | C | 9 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(6): Show | 9 | NA18947.hp1 NA18963.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+17644A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535348 | ||||||
| chr11:47535581
|
G | A | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+17411C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535581 | ||||||
| chr11:47535608
|
G | A | 8 | a0001c0001t0002g0106a0001c0001t0002g0114a0001c0001t0002g0115others(5): Show | 8 | HG00323.hp2 HG00642.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.-154+17384C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535608 | ||||||
| chr11:47535679
|
C | CA | 12 | a0001c0001t0001g0123a0001c0001t0001g0330a0001c0001t0001g0333others(9): Show | 12 | HG02257.hp2 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-154+17312dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535679 | ||||||
| chr11:47535679
|
C | CAA | 9 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(6): Show | 9 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+17311_-154+17 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535679 | ||||||
| chr11:47535688
|
A | T | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+17304T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535688 | ||||||
| chr11:47535692
|
A | AT | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+17299_-154+17 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535692 | ||||||
| chr11:47535692
|
A | T | 14 | a0001c0001t0001g0164a0001c0001t0001g0168a0001c0001t0001g0169others(11): Show | 14 | HG00438.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+17300T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535692 | ||||||
| chr11:47535693
|
A | T | 1 | a0001c0001t0003g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-154+17299T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535693 | ||||||
| chr11:47535696
|
T | A | 15 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(12): Show | 15 | HG02258.hp1 HG02486.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-154+17296A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535696 | ||||||
| chr11:47535804
|
C | T | 209 | a0001c0001t0001g0096a0001c0001t0002g0011a0001c0001t0002g0012others(206): Show | 210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-154+17188G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535804 | ||||||
| chr11:47535812
|
A | G | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-154+17180T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535812 | ||||||
| chr11:47535908
|
G | A | 1 | a0001c0004t0002g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-154+17084C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535908 | ||||||
| chr11:47535950
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-154+17042C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535950 | ||||||
| chr11:47536013
|
C | G | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-154+16979G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536013 | ||||||
| chr11:47536037
|
T | C | 9 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+16955A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536037 | ||||||
| chr11:47536240
|
C | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+16752G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536240 | ||||||
| chr11:47536309
|
T | C | 1 | a0001c0001t0002g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-154+16683A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536309 | ||||||
| chr11:47536319
|
T | C | 80 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(77): Show | 80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+16673A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536319 | ||||||
| chr11:47536557
|
T | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+16435A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536557 | ||||||
| chr11:47536668
|
G | A | 74 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.-154+16324C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536668 | ||||||
| chr11:47536757
|
C | G | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+16235G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536757 | ||||||
| chr11:47536964
|
C | T | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-154+16028G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536964 | ||||||
| chr11:47537245
|
A | AT | 19 | a0001c0001t0001g0096a0001c0001t0001g0325a0001c0001t0002g0247others(16): Show | 19 | HG00642.hp1 HG00741.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-154+15746dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537245 | ||||||
| chr11:47537245
|
AT | A | 106 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(103): Show | 106 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-154+15746delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537245 | ||||||
| chr11:47537265
|
T | G | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-154+15727A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537265 | ||||||
| chr11:47537306
|
G | A | 108 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-154+15686C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537306 | ||||||
| chr11:47537595
|
AT | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+15396delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537595 | ||||||
| chr11:47537836
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-154+15156A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537836 | ||||||
| chr11:47537874
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+15118G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537874 | ||||||
| chr11:47537918
|
CT | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0140a0001c0001t0001g0319others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+15073delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537918 | ||||||
| chr11:47538210
|
G | A | 1 | a0001c0001t0003g0015 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-154+14782C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538210 | ||||||
| chr11:47538250
|
A | T | 1 | a0001c0001t0002g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-154+14742T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538250 | ||||||
| chr11:47538420
|
G | A | 5 | a0001c0001t0002g0233a0001c0001t0002g0235a0001c0001t0002g0262others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+14572C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538420 | ||||||
| chr11:47538539
|
AGGCTGAG others(10): Show |
A | 1 | a0001c0001t0001g0137 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-154+14436_-154+14 others(23): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538539 | ||||||
| chr11:47538555
|
A | C | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+14437T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538555 | ||||||
| chr11:47538642
|
C | CA | 175 | a0001c0001t0001g0096a0001c0001t0002g0011a0001c0001t0002g0012others(172): Show | 175 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.-154+14349dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538642 | ||||||
| chr11:47538642
|
C | CAA | 8 | a0001c0001t0002g0245a0001c0001t0002g0259a0001c0001t0002g0289others(5): Show | 8 | HG00438.hp2 HG00597.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+14348_-154+14 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538642 | ||||||
| chr11:47538655
|
A | AT | 3 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0191 | 3 | HG02083.hp1 NA18747.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-154+14336_-154+14 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538655 | ||||||
| chr11:47538659
|
A | AT | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-154+14332_-154+14 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538659 | ||||||
| chr11:47538659
|
A | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0191 | 3 | HG02083.hp1 NA18747.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-154+14333T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538659 | ||||||
| chr11:47538881
|
T | C | 59 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-154+14111A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538881 | ||||||
| chr11:47538999
|
T | C | 2 | a0001c0002t0002g0299a0001c0002t0002g0300 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-154+13993A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538999 | ||||||
| chr11:47539229
|
T | TA | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+13762dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47539229 | ||||||
| chr11:47539275
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-154+13717G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47539275 | ||||||
| chr11:47539366
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-154+13626G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47539366 | ||||||
| chr11:47540132
|
T | C | 1 | a0001c0001t0003g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-154+12860A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540132 | ||||||
| chr11:47540285
|
T | G | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-154+12707A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540285 | ||||||
| chr11:47540313
|
C | T | 3 | a0001c0001t0002g0077a0001c0001t0003g0075a0001c0001t0003g0076 | 3 | HG01943.hp2 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-154+12679G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540313 | ||||||
| chr11:47540505
|
G | C | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+12487C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540505 | ||||||
| chr11:47540684
|
G | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0150a0001c0001t0001g0152others(3): Show | 6 | HG01496.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+12308C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540684 | ||||||
| chr11:47540689
|
C | T | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+12303G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540689 | ||||||
| chr11:47540885
|
A | AAAC | 105 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(102): Show | 105 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-154+12104_-154+12 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540885 | ||||||
| chr11:47540885
|
AAAC | A | 5 | a0001c0001t0001g0132a0001c0001t0001g0319a0001c0001t0024g0320others(2): Show | 5 | HG02293.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+12104_-154+12 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540885 | ||||||
| chr11:47540972
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+12020C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540972 | ||||||
| chr11:47541292
|
A | AC | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-154+11699dupG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541292 | ||||||
| chr11:47541496
|
G | GCCTGGCC others(25): Show |
1 | a0001c0001t0007g0124 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-154+11464_-154+11 others(38): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541496 | ||||||
| chr11:47541684
|
G | GTC | 51 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0027others(48): Show | 51 | HG00741.hp1 HG01071.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.-154+11306_-154+11 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541684 | ||||||
| chr11:47541686
|
C | CAAAGAAA others(5): Show |
2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-154+11294_-154+11 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541686
|
C | CG | 3 | a0001c0001t0004g0002a0001c0001t0004g0009a0001c0001t0007g0212 | 3 | HG02055.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11305_-154+11 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541686
|
C | CGAAAGAA others(87): Show |
1 | a0001c0001t0007g0124 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-154+11305_-154+11 others(100): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541686
|
C | CGAAAGAA others(220): Show |
1 | a0001c0001t0007g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-154+11305_-154+11 others(233): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541686
|
C | CT | 29 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(26): Show | 29 | HG00597.hp2 HG01099.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.-154+11305_-154+11 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541686
|
C | CTCA | 17 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0127others(14): Show | 17 | HG01192.hp1 HG01255.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-154+11305_-154+11 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541686
|
CAAAGAAA | C | 4 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0005others(1): Show | 5 | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11299_-154+11 others(13): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541686
|
CAAAGAAA others(8): Show |
C | 1 | a0001c0001t0004g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-154+11291_-154+11 others(21): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | ||||||
| chr11:47541687
|
A | C | 29 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0136others(26): Show | 29 | HG00597.hp2 HG01099.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.-154+11305T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541687 | ||||||
| chr11:47541687
|
A | T | 225 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(222): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-154+11305T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541687 | ||||||
| chr11:47541688
|
A | C | 225 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(222): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-154+11304T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541688 | ||||||
| chr11:47541689
|
AG | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0119a0001c0001t0001g0125others(18): Show | 21 | HG00280.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-154+11302delC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541689 | ||||||
| chr11:47541690
|
G | A | 301 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(298): Show | 301 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.-154+11302C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541690 | ||||||
| chr11:47541692
|
AAGAAAGA others(95): Show |
A | 8 | a0001c0001t0001g0319a0001c0001t0002g0274a0001c0001t0002g0275others(5): Show | 8 | HG01433.hp2 HG01517.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541692 | ||||||
| chr11:47541693
|
AGAAAGAA others(82): Show |
A | 2 | a0001c0001t0002g0109a0001c0001t0021g0083 | 2 | HG02293.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(95): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541693 | ||||||
| chr11:47541693
|
AGAAAGAA others(94): Show |
A | 16 | a0001c0001t0002g0273a0001c0001t0002g0276a0001c0001t0002g0277others(13): Show | 16 | HG00544.hp2 HG00621.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541693 | ||||||
| chr11:47541694
|
G | A | 296 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(293): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-154+11298C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541694 | ||||||
| chr11:47541696
|
AAGAAAGA others(91): Show |
A | 31 | a0001c0001t0002g0025a0001c0001t0002g0028a0001c0001t0002g0030others(28): Show | 31 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(104): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541696 | ||||||
| chr11:47541697
|
AGAAAGAA others(78): Show |
A | 2 | a0001c0001t0002g0259a0001c0001t0003g0048 | 2 | HG01975.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(91): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541697 | ||||||
| chr11:47541697
|
AGAAAGAA others(90): Show |
A | 30 | a0001c0001t0002g0024a0001c0001t0002g0228a0001c0001t0002g0229others(27): Show | 30 | HG00609.hp2 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(103): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541697 | ||||||
| chr11:47541698
|
G | A | 233 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(230): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-154+11294C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541698 | ||||||
| chr11:47541700
|
AAGAAAGA others(87): Show |
A | 5 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0230others(2): Show | 5 | HG02559.hp1 HG04228.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(100): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541700 | ||||||
| chr11:47541701
|
AGAAAGAA others(74): Show |
A | 4 | a0001c0001t0003g0034a0001c0001t0003g0044a0001c0001t0003g0050others(1): Show | 4 | HG02273.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(87): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541701 | ||||||
| chr11:47541701
|
AGAAAGAA others(86): Show |
A | 6 | a0001c0001t0002g0106a0001c0001t0002g0114a0001c0001t0002g0115others(3): Show | 6 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(99): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541701 | ||||||
| chr11:47541702
|
G | A | 163 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-154+11290C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541702 | ||||||
| chr11:47541705
|
AGAAAGAA others(70): Show |
A | 2 | a0001c0001t0001g0323a0001c0001t0013g0334 | 2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(83): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541705 | ||||||
| chr11:47541705
|
AGAAAGAA others(81): Show |
A | 3 | a0001c0001t0003g0039a0001c0001t0003g0095a0001c0001t0003g0216 | 3 | HG03239.hp2 NA18906.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(94): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541705 | ||||||
| chr11:47541706
|
G | A | 19 | a0001c0001t0001g0026a0001c0001t0001g0324a0001c0001t0001g0325others(16): Show | 19 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-154+11286C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541706 | ||||||
| chr11:47541707
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11285T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541707 | ||||||
| chr11:47541709
|
AGAAAGAA others(77): Show |
A | 6 | a0001c0001t0002g0217a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG00323.hp1 HG01257.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(90): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541709 | ||||||
| chr11:47541710
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11282C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541710 | ||||||
| chr11:47541712
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11280T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541712 | ||||||
| chr11:47541713
|
AGAAAGAA others(73): Show |
A | 14 | a0001c0001t0001g0330a0001c0001t0002g0077a0001c0001t0002g0307others(11): Show | 14 | HG00597.hp1 HG00642.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(86): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541713 | ||||||
| chr11:47541714
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11278C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541714 | ||||||
| chr11:47541717
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11275T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | ||||||
| chr11:47541717
|
AGAAAGAA others(45): Show |
A | 3 | a0001c0001t0001g0139a0001c0001t0001g0169a0001c0001t0001g0179 | 3 | HG01978.hp2 HG03486.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-154+11223_-154+11 others(58): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | ||||||
| chr11:47541717
|
AGAAAGAA others(57): Show |
A | 25 | a0001c0001t0001g0017a0001c0001t0001g0123a0001c0001t0001g0132others(22): Show | 25 | HG01081.hp2 HG01099.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(70): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | ||||||
| chr11:47541717
|
AGAAAGAA others(69): Show |
A | 20 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0184others(17): Show | 20 | HG00673.hp2 HG00735.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(82): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | ||||||
| chr11:47541718
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11274C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541718 | ||||||
| chr11:47541720
|
A | C | 2 | a0001c0001t0004g0002a0001c0001t0004g0009 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11272T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541720 | ||||||
| chr11:47541721
|
AGAAAGAA others(29): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-154+11235_-154+11 others(42): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541721 | ||||||
| chr11:47541721
|
AGAAAGAA others(53): Show |
A | 32 | a0001c0001t0001g0019a0001c0001t0001g0122a0001c0001t0001g0125others(29): Show | 32 | HG00280.hp2 HG01175.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(66): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541721 | ||||||
| chr11:47541721
|
AGAAAGAA others(65): Show |
A | 33 | a0001c0001t0001g0096a0001c0001t0001g0118a0001c0001t0001g0148others(30): Show | 33 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(78): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541721 | ||||||
| chr11:47541723
|
AAAGAACG others(32): Show |
A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11230_-154+11 others(45): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541723 | ||||||
| chr11:47541724
|
A | C | 1 | a0001c0001t0004g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-154+11268T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541724 | ||||||
| chr11:47541725
|
AGAACGAA others(9): Show |
A | 4 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0005others(1): Show | 5 | HG01884.hp1 HG02559.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11251_-154+11 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541725 | ||||||
| chr11:47541725
|
AGAACGAA others(49): Show |
A | 14 | a0001c0001t0001g0010a0001c0001t0001g0120a0001c0001t0001g0133others(11): Show | 14 | HG01081.hp1 HG01261.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(62): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541725 | ||||||
| chr11:47541725
|
AGAACGAA others(61): Show |
A | 61 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0027others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(74): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541725 | ||||||
| chr11:47541728
|
ACGAAAGA others(79): Show |
A | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-154+11178_-154+11 others(92): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541728 | ||||||
| chr11:47541729
|
C | A | 9 | a0001c0001t0002g0116a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+11263G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541729 | ||||||
| chr11:47541732
|
A | C | 3 | a0001c0001t0004g0002a0001c0001t0004g0003a0001c0001t0004g0009 | 3 | HG02055.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11260T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541732 | ||||||
| chr11:47541736
|
A | C | 1 | a0001c0001t0004g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-154+11256T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541736 | ||||||
| chr11:47541740
|
A | C | 1 | a0001c0001t0004g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-154+11252T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541740 | ||||||
| chr11:47541741
|
C | A | 9 | a0001c0001t0002g0116a0001c0001t0004g0002a0001c0001t0004g0003others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+11251G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541741 | ||||||
| chr11:47541744
|
A | C | 4 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0003others(1): Show | 5 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11248T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541744 | ||||||
| chr11:47541748
|
A | C | 3 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0008 | 3 | HG03225.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11244T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541748 | ||||||
| chr11:47541752
|
A | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0007 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-154+11240T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541752 | ||||||
| chr11:47541752
|
AAGAACGA others(51): Show |
A | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+11182_-154+11 others(64): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541752 | ||||||
| chr11:47541753
|
AGAACGAA others(21): Show |
A | 2 | a0001c0001t0004g0002a0001c0001t0004g0009 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(34): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541753 | ||||||
| chr11:47541756
|
A | C | 2 | a0001c0001t0004g0001a0001c0001t0004g0003 | 3 | HG01884.hp1 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-154+11236T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541756 | ||||||
| chr11:47541757
|
C | A | 10 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(7): Show | 11 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-154+11235G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541757 | ||||||
| chr11:47541760
|
A | C | 3 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0008 | 3 | HG03225.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11232T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541760 | ||||||
| chr11:47541764
|
A | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0007 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-154+11228T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541764 | ||||||
| chr11:47541767
|
A | G | 1 | a0001c0001t0007g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+11225T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541767 | ||||||
| chr11:47541768
|
A | C | 2 | a0001c0001t0004g0001a0001c0001t0004g0003 | 3 | HG01884.hp1 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-154+11224T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541768 | ||||||
| chr11:47541769
|
C | A | 11 | a0001c0001t0001g0199a0001c0001t0004g0001a0001c0001t0004g0003others(8): Show | 12 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-154+11223G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541769 | ||||||
| chr11:47541772
|
A | C | 3 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0008 | 3 | HG03225.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11220T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541772 | ||||||
| chr11:47541776
|
A | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0007 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-154+11216T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541776 | ||||||
| chr11:47541780
|
A | C | 1 | a0001c0001t0004g0001 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-154+11212T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541780 | ||||||
| chr11:47541781
|
C | A | 14 | a0001c0001t0001g0139a0001c0001t0001g0169a0001c0001t0001g0179others(11): Show | 15 | HG01884.hp1 HG01978.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-154+11211G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541781 | ||||||
| chr11:47541781
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11211G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541781 | ||||||
| chr11:47541782
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11210C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541782 | ||||||
| chr11:47541784
|
A | C | 3 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005 | 3 | HG02055.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11208T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541784 | ||||||
| chr11:47541786
|
G | A | 4 | a0001c0001t0002g0109a0001c0001t0002g0259a0001c0001t0003g0048others(1): Show | 4 | HG01975.hp2 HG02293.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11206C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541786 | ||||||
| chr11:47541788
|
A | C | 1 | a0001c0001t0004g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-154+11204T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541788 | ||||||
| chr11:47541790
|
G | A | 3 | a0001c0001t0002g0109a0001c0001t0002g0259a0001c0001t0021g0083 | 3 | HG02293.hp2 HG02451.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-154+11202C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541790 | ||||||
| chr11:47541791
|
A | AAAGAAAG others(531): Show |
1 | a0001c0001t0007g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+11200_-154+11 others(544): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541791 | ||||||
| chr11:47541793
|
C | A | 98 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(95): Show | 99 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(96): Show |
intron_variant | MODIFIER | c.-154+11199G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541793 | ||||||
| chr11:47541798
|
G | A | 93 | a0001c0001t0001g0319a0001c0001t0002g0024a0001c0001t0002g0025others(90): Show | 93 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-154+11194C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541798 | ||||||
| chr11:47541802
|
G | A | 80 | a0001c0001t0001g0319a0001c0001t0002g0024a0001c0001t0002g0025others(77): Show | 80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+11190C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541802 | ||||||
| chr11:47541806
|
G | A | 24 | a0001c0001t0001g0319a0001c0001t0002g0273a0001c0001t0002g0274others(21): Show | 24 | HG00544.hp2 HG00621.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-154+11186C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541806 | ||||||
| chr11:47541810
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11182C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541810 | ||||||
| chr11:47541811
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+11181T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541811 | ||||||
| chr11:47541821
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11171T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541821 | ||||||
| chr11:47541868
|
G | A | 1 | a0001c0004t0002g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-154+11124C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541868 | ||||||
| chr11:47542053
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+10939T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542053 | ||||||
| chr11:47542098
|
G | A | 2 | a0001c0001t0008g0098a0001c0001t0008g0099 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-154+10894C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542098 | ||||||
| chr11:47542172
|
C | G | 1 | a0001c0001t0002g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-154+10820G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542172 | ||||||
| chr11:47542188
|
G | C | 2 | a0001c0001t0001g0333a0001c0001t0013g0334 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-154+10804C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542188 | ||||||
| chr11:47542381
|
C | A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+10611G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542381 | ||||||
| chr11:47542383
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+10609C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542383 | ||||||
| chr11:47542433
|
G | T | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+10559C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542433 | ||||||
| chr11:47542496
|
A | AT | 21 | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0168others(18): Show | 21 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-154+10495dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542496 | ||||||
| chr11:47542496
|
AT | A | 24 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0165others(21): Show | 24 | HG00609.hp1 HG02109.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.-154+10495delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542496 | ||||||
| chr11:47542506
|
T | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+10486A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542506 | ||||||
| chr11:47542667
|
C | A | 1 | a0001c0001t0014g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-154+10325G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542667 | ||||||
| chr11:47542740
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-154+10252G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542740 | ||||||
| chr11:47542742
|
CGT | C | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+10248_-154+10 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542742 | ||||||
| chr11:47542787
|
C | G | 1 | a0001c0001t0003g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-154+10205G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542787 | ||||||
| chr11:47542889
|
T | C | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+10103A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542889 | ||||||
| chr11:47543035
|
G | A | 103 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-154+9957C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543035 | ||||||
| chr11:47543036
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-154+9956G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543036 | ||||||
| chr11:47543166
|
G | C | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+9826C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543166 | ||||||
| chr11:47543170
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0118a0001c0001t0001g0132others(11): Show | 14 | HG00280.hp1 HG00741.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+9822C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543170 | ||||||
| chr11:47543182
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-154+9810A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543182 | ||||||
| chr11:47543197
|
G | C | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0166 | 3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-154+9795C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543197 | ||||||
| chr11:47543233
|
A | G | 59 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-154+9759T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543233 | ||||||
| chr11:47543404
|
G | A | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-154+9588C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543404 | ||||||
| chr11:47543551
|
G | T | 28 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-154+9441C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543551 | ||||||
| chr11:47543586
|
T | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01175.hp1 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-154+9406A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543586 | ||||||
| chr11:47543639
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+9353C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543639 | ||||||
| chr11:47543663
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+9329T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543663 | ||||||
| chr11:47543726
|
A | G | 1 | a0001c0001t0003g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-154+9266T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543726 | ||||||
| chr11:47543761
|
TA | T | 107 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(104): Show | 107 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-154+9230delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543761 | ||||||
| chr11:47543784
|
C | T | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+9208G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543784 | ||||||
| chr11:47544358
|
G | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+8634C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544358 | ||||||
| chr11:47544613
|
A | C | 1 | a0001c0001t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-154+8379T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544613 | ||||||
| chr11:47544680
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-154+8312C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544680 | ||||||
| chr11:47544703
|
T | G | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-154+8289A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544703 | ||||||
| chr11:47544800
|
T | C | 102 | a0001c0001t0001g0096a0001c0001t0002g0028a0001c0001t0002g0029others(99): Show | 103 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-154+8192A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544800 | ||||||
| chr11:47544859
|
G | A | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+8133C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544859 | ||||||
| chr11:47544946
|
C | G | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-154+8046G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544946 | ||||||
| chr11:47545109
|
A | C | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+7883T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545109 | ||||||
| chr11:47545195
|
C | G | 1 | a0001c0001t0006g0112 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-154+7797G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545195 | ||||||
| chr11:47545196
|
G | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0125others(26): Show | 29 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-154+7796C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545196 | ||||||
| chr11:47545337
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-154+7655G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545337 | ||||||
| chr11:47545431
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-154+7561T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545431 | ||||||
| chr11:47545502
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7490T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545502 | ||||||
| chr11:47545604
|
C | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00408.hp1 HG00597.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+7388G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545604 | ||||||
| chr11:47545643
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-154+7349T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545643 | ||||||
| chr11:47545700
|
T | C | 20 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0061others(17): Show | 20 | HG00558.hp1 HG00673.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-154+7292A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545700 | ||||||
| chr11:47545799
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-154+7193C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545799 | ||||||
| chr11:47545850
|
C | CGT | 4 | a0001c0001t0002g0106a0001c0001t0002g0114a0001c0001t0002g0245others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7140_-154+714 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | ||||||
| chr11:47545850
|
C | T | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+7142G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | ||||||
| chr11:47545850
|
CGTGTGTG others(15): Show |
C | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+7120_-154+714 others(26): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | ||||||
| chr11:47545850
|
CGTGTGTG others(21): Show |
C | 19 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0065others(16): Show | 19 | HG00558.hp1 HG00673.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.-154+7114_-154+714 others(32): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | ||||||
| chr11:47545852
|
TGTGTGTG others(11): Show |
T | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-154+7122_-154+713 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545852 | ||||||
| chr11:47545858
|
TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-154+7122_-154+713 others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545858 | ||||||
| chr11:47545862
|
TGTGTCTG others(1): Show |
T | 4 | a0001c0001t0001g0122a0001c0001t0002g0109a0001c0002t0002g0299others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7122_-154+712 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545862 | ||||||
| chr11:47545865
|
GTC | G | 4 | a0001c0001t0002g0232a0001c0001t0002g0247a0001c0001t0002g0279others(1): Show | 4 | HG01346.hp1 HG01433.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7125_-154+712 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545865 | ||||||
| chr11:47545866
|
TCTGC | T | 3 | a0001c0001t0002g0272a0001c0001t0004g0004a0001c0001t0004g0005 | 3 | HG03017.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+7122_-154+712 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545866 | ||||||
| chr11:47545867
|
C | CTG | 22 | a0001c0001t0002g0024a0001c0001t0002g0107a0001c0001t0002g0110others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-154+7123_-154+712 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
C | CTGTG | 33 | a0001c0001t0002g0228a0001c0001t0002g0234a0001c0001t0002g0235others(30): Show | 33 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-154+7124_-154+712 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
C | CTGTGTG | 6 | a0001c0001t0002g0225a0001c0001t0002g0229a0001c0001t0002g0233others(3): Show | 6 | HG02071.hp1 HG02683.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+7124_-154+712 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
C | CTGTGTGT others(1): Show |
5 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0288others(2): Show | 5 | HG01517.hp2 HG03239.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+7124_-154+712 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
C | CTGTGTGT others(13): Show |
1 | a0001c0001t0002g0246 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-154+7124_-154+712 others(24): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
C | G | 7 | a0001c0001t0002g0245a0001c0001t0004g0001a0001c0001t0004g0002others(4): Show | 8 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+7125G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
CTGCG | C | 123 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-154+7121_-154+712 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
CTGCGTG | C | 14 | a0001c0001t0001g0026a0001c0001t0001g0121a0001c0001t0001g0137others(11): Show | 14 | HG01081.hp2 HG01346.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.-154+7119_-154+712 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
CTGCGTGT others(1): Show |
C | 3 | a0001c0001t0001g0027a0001c0001t0001g0193a0001c0001t0003g0039 | 3 | HG00609.hp1 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-154+7117_-154+712 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545867
|
CTGCGTGT others(7): Show |
C | 1 | a0001c0001t0002g0302 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-154+7111_-154+712 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | ||||||
| chr11:47545868
|
TGC | T | 11 | a0001c0001t0001g0192a0001c0001t0001g0331a0001c0001t0002g0244others(8): Show | 11 | HG01361.hp1 HG01975.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.-154+7122_-154+712 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545868 | ||||||
| chr11:47545870
|
C | T | 151 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0120others(148): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-154+7122G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545870 | ||||||
| chr11:47545871
|
G | C | 5 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(2): Show | 6 | HG01884.hp1 HG02559.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+7121C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545871 | ||||||
| chr11:47545873
|
G | C | 1 | a0001c0001t0004g0003 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-154+7119C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545873 | ||||||
| chr11:47545875
|
G | C | 2 | a0001c0001t0004g0004a0001c0001t0004g0005 | 2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+7117C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545875 | ||||||
| chr11:47545901
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-154+7091C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545901 | ||||||
| chr11:47545903
|
G | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0166others(5): Show | 8 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+7089C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545903 | ||||||
| chr11:47545905
|
G | A | 132 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0096others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-154+7087C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545905 | ||||||
| chr11:47545905
|
G | GTA | 4 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0305others(1): Show | 4 | HG01099.hp2 HG01257.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-154+7085_-154+708 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545905 | ||||||
| chr11:47545907
|
A | G | 26 | a0001c0001t0002g0013a0001c0001t0002g0106a0001c0001t0002g0107others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.-154+7085T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545907 | ||||||
| chr11:47545909
|
A | G | 2 | a0001c0001t0002g0116a0001c0001t0006g0104 | 2 | HG01081.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-154+7083T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545909 | ||||||
| chr11:47545915
|
A | T | 12 | a0001c0001t0001g0336a0001c0001t0002g0228a0001c0001t0002g0229others(9): Show | 12 | HG01358.hp2 HG03471.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.-154+7077T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | ||||||
| chr11:47545915
|
AT | A | 81 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(78): Show | 81 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.-154+7076delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | ||||||
| chr11:47545915
|
ATT | A | 6 | a0001c0001t0001g0026a0001c0001t0002g0011a0001c0001t0002g0012others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+7075_-154+707 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | ||||||
| chr11:47545915
|
ATTT | A | 24 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0130others(21): Show | 24 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-154+7074_-154+707 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | ||||||
| chr11:47545917
|
T | A | 112 | a0001c0001t0001g0096a0001c0001t0001g0322a0001c0001t0001g0324others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.-154+7075A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545917 | ||||||
| chr11:47545918
|
T | A | 80 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(77): Show | 80 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-154+7074A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545918 | ||||||
| chr11:47545919
|
T | A | 8 | a0001c0001t0001g0026a0001c0001t0002g0077a0001c0001t0003g0075others(5): Show | 8 | HG00323.hp1 HG00642.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+7073A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545919 | ||||||
| chr11:47545921
|
T | A | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-154+7071A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545921 | ||||||
| chr11:47546003
|
C | G | 3 | a0001c0001t0003g0042a0001c0001t0003g0297a0001c0001t0003g0298 | 3 | HG00597.hp1 NA18962.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-154+6989G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546003 | ||||||
| chr11:47546012
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0030 | 2 | HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-154+6980C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546012 | ||||||
| chr11:47546236
|
C | CTT | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+6754_-154+675 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546236 | ||||||
| chr11:47546236
|
CT | C | 301 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(298): Show | 302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.-154+6755delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546236 | ||||||
| chr11:47546253
|
T | G | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-154+6739A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546253 | ||||||
| chr11:47546256
|
G | C | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-154+6736C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546256 | ||||||
| chr11:47546257
|
C | G | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-154+6735G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546257 | ||||||
| chr11:47546270
|
C | CG | 29 | a0001c0001t0001g0018a0001c0001t0001g0139a0001c0001t0001g0143others(26): Show | 29 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-154+6721dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546270 | ||||||
| chr11:47546270
|
C | G | 1 | a0001c0001t0004g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-154+6722G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546270 | ||||||
| chr11:47546270
|
C | T | 1 | a0001c0001t0007g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+6722G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546270 | ||||||
| chr11:47546276
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-154+6716G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546276 | ||||||
| chr11:47546277
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-154+6715C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546277 | ||||||
| chr11:47546322
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-154+6670T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546322 | ||||||
| chr11:47546425
|
C | G | 1 | a0001c0001t0027g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-154+6567G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546425 | ||||||
| chr11:47546522
|
C | T | 77 | a0001c0001t0001g0096a0001c0001t0002g0077a0001c0001t0003g0014others(74): Show | 77 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-154+6470G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546522 | ||||||
| chr11:47546525
|
C | T | 1 | a0001c0001t0004g0003 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-154+6467G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546525 | ||||||
| chr11:47546699
|
T | C | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+6293A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546699 | ||||||
| chr11:47546750
|
T | C | 4 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0250others(1): Show | 4 | HG01167.hp2 HG01258.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+6242A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546750 | ||||||
| chr11:47546792
|
C | G | 80 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(77): Show | 80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+6200G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546792 | ||||||
| chr11:47546892
|
T | C | 334 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-154+6100A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546892 | ||||||
| chr11:47547049
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+5943T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547049 | ||||||
| chr11:47547057
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-154+5935G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547057 | ||||||
| chr11:47547065
|
C | A | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+5927G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CA | 6 | a0001c0001t0001g0339a0001c0001t0002g0109a0001c0001t0010g0101others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+5926dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAA | 7 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0002g0226others(4): Show | 7 | HG02165.hp1 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+5925_-154+592 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAA | 61 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0002g0011others(58): Show | 62 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-154+5924_-154+592 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAA | 38 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.-154+5923_-154+592 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAA | 27 | a0001c0001t0001g0010a0001c0001t0001g0141a0001c0001t0001g0142others(24): Show | 27 | HG00621.hp2 HG00642.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.-154+5922_-154+592 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAAA | 32 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(29): Show | 32 | HG00544.hp1 HG01175.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-154+5921_-154+592 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAAAA | 22 | a0001c0001t0001g0026a0001c0001t0001g0119a0001c0001t0001g0123others(19): Show | 22 | HG00558.hp2 HG00609.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-154+5920_-154+592 others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAAAA others(1): Show |
19 | a0001c0001t0001g0022a0001c0001t0001g0120a0001c0001t0001g0121others(16): Show | 19 | HG00280.hp1 HG00408.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-154+5919_-154+592 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0187a0001c0001t0001g0200a0001c0001t0001g0201others(6): Show | 9 | HG02109.hp1 HG02486.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+5918_-154+592 others(13): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0122a0001c0001t0001g0202a0001c0001t0001g0207others(2): Show | 5 | HG02258.hp2 HG02698.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+5917_-154+592 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-154+5916_-154+592 others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-154+5915_-154+592 others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
CAA | C | 13 | a0001c0001t0003g0023a0001c0001t0003g0034a0001c0001t0003g0080others(10): Show | 13 | HG01175.hp2 HG01361.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-154+5925_-154+592 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
CAAA | C | 63 | a0001c0001t0002g0077a0001c0001t0003g0014a0001c0001t0003g0015others(60): Show | 63 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-154+5924_-154+592 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(4): Show | 7 | HG01081.hp2 HG01099.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.-154+5919_-154+592 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547065
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0108 | 3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-154+5914_-154+592 others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | ||||||
| chr11:47547088
|
A | G | 1 | a0001c0001t0007g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+5904T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547088 | ||||||
| chr11:47547174
|
G | T | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+5818C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547174 | ||||||
| chr11:47547307
|
T | C | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0264 | 3 | NA18990.hp2 NA18995.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-154+5685A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547307 | ||||||
| chr11:47547394
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-154+5598T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547394 | ||||||
| chr11:47547508
|
T | A | 1 | a0001c0001t0002g0258 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-154+5484A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547508 | ||||||
| chr11:47547624
|
G | A | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+5368C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547624 | ||||||
| chr11:47547681
|
AAAG | A | 91 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(88): Show | 91 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-154+5308_-154+531 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547681 | ||||||
| chr11:47547682
|
AAG | A | 15 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(12): Show | 15 | HG00408.hp2 HG01261.hp1 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-154+5308_-154+530 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547682 | ||||||
| chr11:47547846
|
G | C | 1 | a0001c0001t0002g0265 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-154+5146C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547846 | ||||||
| chr11:47547849
|
T | C | 10 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(7): Show | 10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+5143A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547849 | ||||||
| chr11:47548054
|
A | G | 3 | a0001c0001t0007g0016a0001c0001t0007g0124a0001c0001t0007g0212 | 3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-154+4938T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548054 | ||||||
| chr11:47548192
|
G | A | 2 | a0001c0003t0011g0308a0001c0003t0011g0309 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+4800C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548192 | ||||||
| chr11:47548227
|
C | T | 13 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+4765G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548227 | ||||||
| chr11:47548403
|
C | G | 2 | a0001c0001t0003g0097a0001c0001t0028g0035 | 2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-154+4589G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548403 | ||||||
| chr11:47548518
|
T | G | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+4474A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548518 | ||||||
| chr11:47548865
|
C | CA | 124 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0096others(121): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-154+4126dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548865 | ||||||
| chr11:47548865
|
C | CAA | 13 | a0001c0001t0002g0012a0001c0001t0002g0116a0001c0001t0002g0266others(10): Show | 13 | HG00438.hp1 HG00735.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-154+4125_-154+412 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548865 | ||||||
| chr11:47548865
|
CA | C | 18 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(15): Show | 18 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-154+4126delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548865 | ||||||
| chr11:47549059
|
T | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp1 HG02698.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+3933A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549059 | ||||||
| chr11:47549171
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+3821C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549171 | ||||||
| chr11:47549479
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+3513T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549479 | ||||||
| chr11:47549809
|
G | T | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+3183C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549809 | ||||||
| chr11:47549812
|
T | G | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+3180A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549812 | ||||||
| chr11:47549816
|
T | G | 1 | a0001c0001t0003g0100 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-154+3176A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549816 | ||||||
| chr11:47549820
|
G | GT | 85 | a0001c0001t0001g0096a0001c0001t0001g0119a0001c0001t0001g0120others(82): Show | 85 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-154+3171dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549820 | ||||||
| chr11:47549820
|
G | T | 1 | a0001c0001t0003g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-154+3172C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549820 | ||||||
| chr11:47549848
|
G | A | 2 | a0001c0001t0010g0101a0001c0001t0010g0102 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+3144C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549848 | ||||||
| chr11:47549905
|
C | T | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033 | 3 | HG00741.hp1 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-154+3087G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549905 | ||||||
| chr11:47550013
|
G | C | 338 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(335): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-154+2979C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550013 | ||||||
| chr11:47550064
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-154+2928G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550064 | ||||||
| chr11:47550082
|
T | C | 1 | a0001c0001t0006g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-154+2910A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550082 | ||||||
| chr11:47550216
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-154+2776G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550216 | ||||||
| chr11:47550239
|
C | CA | 14 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0319others(11): Show | 14 | HG01071.hp2 HG01175.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+2752dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550239 | ||||||
| chr11:47550243
|
A | C | 1 | a0001c0001t0006g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-154+2749T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550243 | ||||||
| chr11:47550256
|
T | C | 108 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-154+2736A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550256 | ||||||
| chr11:47550291
|
G | C | 1 | a0001c0001t0026g0291 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-154+2701C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550291 | ||||||
| chr11:47550303
|
G | A | 108 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-154+2689C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550303 | ||||||
| chr11:47550340
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+2652C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550340 | ||||||
| chr11:47550369
|
A | G | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(3): Show | 6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+2623T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550369 | ||||||
| chr11:47550404
|
G | A | 108 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-154+2588C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550404 | ||||||
| chr11:47550415
|
C | T | 59 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-154+2577G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550415 | ||||||
| chr11:47550460
|
G | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+2532C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550460 | ||||||
| chr11:47550639
|
T | C | 1 | a0001c0001t0002g0292 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-154+2353A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550639 | ||||||
| chr11:47550727
|
G | A | 80 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(77): Show | 80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+2265C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550727 | ||||||
| chr11:47550742
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+2250C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550742 | ||||||
| chr11:47551039
|
TA | T | 319 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(316): Show | 320 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.-154+1952delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551039 | ||||||
| chr11:47551342
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-154+1650G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551342 | ||||||
| chr11:47551404
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+1588C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551404 | ||||||
| chr11:47551497
|
T | C | 1 | a0001c0001t0003g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-154+1495A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551497 | ||||||
| chr11:47551541
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-154+1451A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551541 | ||||||
| chr11:47551542
|
G | A | 5 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+1450C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551542 | ||||||
| chr11:47551574
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+1418G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551574 | ||||||
| chr11:47551790
|
G | A | 80 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0222others(77): Show | 80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+1202C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551790 | ||||||
| chr11:47552013
|
T | TA | 7 | a0001c0001t0001g0301a0001c0001t0002g0302a0001c0001t0003g0297others(4): Show | 7 | HG00597.hp1 HG00609.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+978dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552013 | ||||||
| chr11:47552013
|
TA | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG00558.hp2 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+978delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552013 | ||||||
| chr11:47552056
|
T | C | 1 | a0001c0001t0002g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-154+936A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552056 | ||||||
| chr11:47552378
|
G | C | 3 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0307 | 3 | HG01071.hp2 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-154+614C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552378 | ||||||
| chr11:47552380
|
G | C | 4 | a0001c0001t0001g0319a0001c0001t0024g0320a0001c0003t0011g0308others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+612C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552380 | ||||||
| chr11:47552529
|
C | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | HG01175.hp1 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-154+463G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552529 | ||||||
| chr11:47552658
|
G | C | 1 | a0001c0001t0002g0318 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-154+334C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552658 | ||||||
| chr11:47552726
|
G | A | 9 | a0001c0001t0002g0310a0001c0001t0002g0311a0001c0001t0002g0312others(6): Show | 9 | HG00280.hp2 HG01255.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+266C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552726 | ||||||
| chr11:47552777
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0024g0320 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+215C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552777 | ||||||
| chr11:47552823
|
G | A | 1 | a0001c0001t0003g0321 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-154+169C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552823 | ||||||
| chr11:47552864
|
A | G | 321 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(318): Show | 322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.-154+128T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552864 | ||||||
| chr11:47552908
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-154+84C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552908 |