Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10642 |
|---|---|
| ensemblid | ENSG00000159217.10 |
| hgncid | 28866 |
| symbol | IGF2BP1 |
| name | insulin like growth factor 2 mRNA binding protein 1 |
| refseq_nuc | NM_006546.4 |
| refseq_prot | NP_006537.3 |
| ensembl_nuc | ENST00000290341.8 |
| ensembl_prot | ENSP00000290341.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 48997385 |
| end | 49056145 |
| strand | + |
| ver | v1.2 |
| region | chr17:48997385-49056145 |
| region5000 | chr17:48992385-49061145 |
| regionname0 | IGF2BP1_chr17_48997385_49056145 |
| regionname5000 | IGF2BP1_chr17_48992385_49061145 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 577 | 316 | 92 | 69 | 110 | 10 | 33 | 78 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0002 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0003 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1734 | 305 | 84 | 69 | 108 | 10 | 32 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| c0002 | 0/0 | 1734 | 7 | 7 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| c0003 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| c0004 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| c0005 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| c0006 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| c0007 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| c0008 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 7063 | 67 | 2 | 8 | 47 | 1 | 8 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0002 | 0/0 | 7065 | 48 | 25 | 14 | 2 | 1 | 6 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0003 | 0/0 | 7063 | 22 | 1 | 4 | 7 | 4 | 6 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0004 | 0/0 | 7065 | 21 | 1 | 5 | 15 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0005 | 0/0 | 7056 | 12 | 2 | 3 | 3 | 1 | 3 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0006 | 0/0 | 7065 | 11 | 2 | 1 | 6 | 0 | 2 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0007 | 0/0 | 7062 | 11 | 4 | 5 | 0 | 1 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0008 | 0/0 | 7065 | 10 | 10 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0009 | 0/0 | 7066 | 10 | 0 | 4 | 1 | 0 | 5 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0010 | 0/0 | 7066 | 9 | 4 | 2 | 3 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0011 | 0/0 | 7063 | 7 | 0 | 7 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0012 | 0/0 | 7064 | 5 | 0 | 0 | 5 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0013 | 0/0 | 7065 | 4 | 3 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0014 | 0/0 | 7064 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0015 | 0/0 | 7064 | 3 | 2 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0016 | 0/0 | 7066 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0017 | 0/0 | 7056 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0018 | 0/0 | 7065 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0019 | 0/0 | 7066 | 2 | 1 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0020 | 0/0 | 7065 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0021 | 0/0 | 7064 | 2 | 1 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0022 | 0/0 | 7064 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0023 | 0/0 | 7064 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0024 | 0/0 | 7066 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0025 | 0/0 | 7066 | 2 | 1 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0026 | 0/0 | 7063 | 2 | 1 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0027 | 0/0 | 7064 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0028 | 0/0 | 7055 | 2 | 1 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0029 | 0/0 | 7063 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0030 | 0/0 | 7062 | 2 | 0 | 1 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0031 | 0/0 | 7064 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0032 | 0/0 | 7065 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0033 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0034 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0035 | 0/0 | 7065 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0036 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0037 | 0/0 | 7065 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0038 | 0/0 | 7065 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0039 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0040 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0041 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0042 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0043 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0044 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0045 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0046 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0047 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0048 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0049 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0050 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0051 | 0/1 | 7063 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0052 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0053 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0054 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0055 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0056 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0057 | 0/0 | 7055 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0058 | 0/0 | 7065 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0059 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0060 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0061 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0062 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0063 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0064 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0065 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0066 | 0/0 | 7065 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0067 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0068 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0069 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0070 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0071 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| t0072 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1734 | 305 | 84 | 69 | 108 | 10 | 32 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0002 | 0/0 | 1734 | 7 | 7 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0003 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0005 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0006 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0008 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0002c0007 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0003c0004 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8796 | 65 | 2 | 7 | 46 | 1 | 8 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0002 | 0/0 | 8798 | 44 | 21 | 14 | 2 | 1 | 6 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0003 | 0/0 | 8796 | 21 | 1 | 4 | 7 | 4 | 5 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0004 | 0/0 | 8798 | 21 | 1 | 5 | 15 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0005 | 0/0 | 8789 | 12 | 2 | 3 | 3 | 1 | 3 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0006 | 0/0 | 8798 | 11 | 2 | 1 | 6 | 0 | 2 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0007 | 0/0 | 8795 | 11 | 4 | 5 | 0 | 1 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0008 | 0/0 | 8798 | 10 | 10 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0009 | 0/0 | 8799 | 9 | 0 | 4 | 1 | 0 | 4 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0010 | 0/0 | 8799 | 8 | 3 | 2 | 3 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0011 | 0/0 | 8796 | 7 | 0 | 7 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0012 | 0/0 | 8797 | 5 | 0 | 0 | 5 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0013 | 0/0 | 8798 | 4 | 3 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0014 | 0/0 | 8797 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0015 | 0/0 | 8797 | 3 | 2 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0016 | 0/0 | 8799 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0017 | 0/0 | 8789 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0018 | 0/0 | 8798 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0019 | 0/0 | 8799 | 2 | 1 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0020 | 0/0 | 8798 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0021 | 0/0 | 8797 | 2 | 1 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0022 | 0/0 | 8797 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0023 | 0/0 | 8797 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0024 | 0/0 | 8799 | 2 | 0 | 0 | 2 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0025 | 0/0 | 8799 | 2 | 1 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0026 | 0/0 | 8796 | 2 | 1 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0027 | 0/0 | 8797 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0028 | 0/0 | 8788 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0029 | 0/0 | 8796 | 2 | 0 | 2 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0030 | 0/0 | 8795 | 2 | 0 | 1 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0031 | 0/0 | 8797 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0032 | 0/0 | 8798 | 2 | 2 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0033 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0034 | 0/0 | 8795 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0035 | 0/0 | 8798 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0036 | 0/0 | 8797 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0037 | 0/0 | 8798 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0038 | 0/0 | 8798 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0039 | 0/0 | 8798 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0040 | 0/0 | 8797 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0041 | 0/0 | 8798 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0042 | 0/0 | 8798 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0044 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0045 | 0/0 | 8796 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0046 | 0/0 | 8797 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0047 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0048 | 0/0 | 8797 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0049 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0050 | 0/0 | 8798 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0051 | 0/1 | 8796 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0052 | 0/0 | 8798 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0053 | 0/0 | 8797 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0054 | 0/0 | 8797 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0055 | 0/0 | 8796 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0056 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0057 | 0/0 | 8788 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0058 | 0/0 | 8798 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0059 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0060 | 0/0 | 8789 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0061 | 0/0 | 8796 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0062 | 0/0 | 8796 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0064 | 0/0 | 8796 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0065 | 0/0 | 8797 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0066 | 0/0 | 8798 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0067 | 0/0 | 8796 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0068 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0069 | 0/0 | 8797 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0070 | 0/0 | 8798 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0001t0071 | 0/0 | 8798 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0002t0002 | 0/0 | 8798 | 3 | 3 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0002t0010 | 0/0 | 8799 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0002t0043 | 0/0 | 8798 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0002t0063 | 0/0 | 8798 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0002t0072 | 0/0 | 8798 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0003t0028 | 0/0 | 8788 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0005t0003 | 0/0 | 8796 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0006t0002 | 0/0 | 8798 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0001c0008t0001 | 0/0 | 8796 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0002c0007t0009 | 0/0 | 8799 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| a0003c0004t0001 | 0/0 | 8796 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | copy fasta | chr17 | 48992385 | 49061145 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0011g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0011g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0011g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0011g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0011g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0011g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0012g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0012g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0013g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0014g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0015g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0015g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0017g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0017g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0018g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0019g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0019g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0020g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0020g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0021g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0021g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0022g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0022g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0023g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0023g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0024g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0024g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0025g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0025g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0026g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0026g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0027g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0027g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0028g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0029g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0029g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0030g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0030g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0031g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0031g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0032g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0032g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0033g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0034g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0035g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0036g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0037g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0038g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0039g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0040g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0041g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0042g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0044g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0045g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0046g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0047g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0048g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0049g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0050g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0051g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0052g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0053g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0054g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0055g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0056g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0057g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0058g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0059g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0060g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0061g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0062g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0064g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0065g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0066g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0067g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0068g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0069g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0070g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0001t0071g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0002t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0002t0043g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0002t0063g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0002t0072g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0003t0028g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0005t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0006t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0001c0008t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0002c0007t0009g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| a0003c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0270 | EUR | GBR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0312 | EUR | GBR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0266 | EUR | GBR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0218 | EUR | FIN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00558 | hp1 | a0001 | c0001 | t0050 | g0030 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00558 | hp2 | a0001 | c0008 | t0001 | g0153 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00639 | hp1 | a0001 | c0001 | t0034 | g0264 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0232 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0259 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00642 | hp2 | a0001 | c0001 | t0009 | g0196 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0113 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00733 | hp2 | a0001 | c0001 | t0011 | g0258 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0203 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG00741 | hp2 | a0001 | c0001 | t0030 | g0201 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01069 | hp1 | a0001 | c0001 | t0022 | g0092 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0214 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0114 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01071 | hp1 | a0001 | c0001 | t0022 | g0091 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0115 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0257 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0166 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0231 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01167 | hp1 | a0001 | c0001 | t0020 | g0042 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01167 | hp2 | a0001 | c0001 | t0011 | g0256 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01168 | hp1 | a0001 | c0001 | t0011 | g0260 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01169 | hp1 | a0001 | c0001 | t0011 | g0255 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0038 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01175 | hp1 | a0001 | c0001 | t0038 | g0132 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01192 | hp1 | a0003 | c0004 | t0001 | g0170 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0055 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01255 | hp2 | a0001 | c0001 | t0023 | g0031 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0238 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01257 | hp1 | a0001 | c0001 | t0058 | g0112 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0309 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01258 | hp1 | a0001 | c0001 | t0010 | g0239 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0310 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0269 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01433 | hp2 | a0001 | c0001 | t0037 | g0069 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01496 | hp2 | a0001 | c0001 | t0029 | g0177 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01515 | hp1 | a0001 | c0001 | t0040 | g0169 | EUR | IBS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0202 | EUR | IBS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01516 | hp1 | a0001 | c0001 | t0030 | g0206 | EUR | IBS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0205 | EUR | IBS | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01884 | hp2 | a0001 | c0002 | t0043 | g0183 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0194 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01943 | hp1 | a0001 | c0001 | t0023 | g0013 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01975 | hp2 | a0001 | c0001 | t0021 | g0081 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02015 | hp1 | a0001 | c0001 | t0048 | g0020 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02055 | hp2 | a0001 | c0001 | t0019 | g0137 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02080 | hp2 | a0001 | c0001 | t0024 | g0287 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02083 | hp1 | a0001 | c0001 | t0012 | g0084 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02145 | hp1 | a0001 | c0002 | t0010 | g0184 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02145 | hp2 | a0001 | c0001 | t0013 | g0120 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02148 | hp2 | a0001 | c0001 | t0013 | g0224 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02155 | hp1 | a0001 | c0001 | t0039 | g0316 | EAS | CDX | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02258 | hp1 | a0001 | c0001 | t0014 | g0130 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0192 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02273 | hp1 | a0001 | c0001 | t0035 | g0228 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02273 | hp2 | a0001 | c0001 | t0029 | g0100 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02280 | hp1 | a0001 | c0001 | t0032 | g0008 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0217 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02572 | hp1 | a0001 | c0001 | t0031 | g0065 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02572 | hp2 | a0001 | c0001 | t0059 | g0089 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0211 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02615 | hp1 | a0001 | c0001 | t0071 | g0053 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02630 | hp2 | a0001 | c0002 | t0072 | g0007 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02647 | hp2 | a0001 | c0001 | t0047 | g0072 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0281 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02717 | hp1 | a0001 | c0001 | t0028 | g0149 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0215 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0087 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02809 | hp1 | a0001 | c0006 | t0002 | g0179 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0001 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0041 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0253 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0191 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0254 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0138 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0221 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02970 | hp1 | a0001 | c0001 | t0044 | g0039 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02970 | hp2 | a0001 | c0001 | t0070 | g0049 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02976 | hp1 | a0001 | c0001 | t0056 | g0186 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0154 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0193 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03130 | hp1 | a0001 | c0001 | t0042 | g0051 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03130 | hp2 | a0001 | c0001 | t0016 | g0045 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0142 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03139 | hp2 | a0001 | c0001 | t0069 | g0054 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0240 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0118 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0216 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03225 | hp2 | a0001 | c0001 | t0016 | g0117 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03486 | hp1 | a0001 | c0001 | t0033 | g0044 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03516 | hp1 | a0001 | c0001 | t0068 | g0061 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03516 | hp2 | a0001 | c0001 | t0016 | g0116 | AFR | ESN | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03540 | hp1 | a0001 | c0001 | t0049 | g0067 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03579 | hp1 | a0001 | c0002 | t0063 | g0188 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03579 | hp2 | a0001 | c0001 | t0064 | g0002 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03669 | hp1 | a0001 | c0005 | t0003 | g0246 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03704 | hp1 | a0001 | c0001 | t0025 | g0068 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03704 | hp2 | a0002 | c0007 | t0009 | g0198 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0168 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0071 | SAS | PJL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03831 | hp2 | a0001 | c0001 | t0066 | g0032 | SAS | BEB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | BEB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0158 | SAS | BEB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG04115 | hp1 | a0001 | c0001 | t0009 | g0088 | SAS | STU | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | STU | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG04184 | hp2 | a0001 | c0001 | t0054 | g0307 | SAS | BEB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0090 | SAS | STU | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0167 | SAS | STU | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | YRI | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0276 | AFR | YRI | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | CHB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18747 | hp1 | a0001 | c0001 | t0009 | g0230 | EAS | CHB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18747 | hp2 | a0001 | c0001 | t0061 | g0288 | EAS | CHB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18906 | hp1 | a0001 | c0001 | t0027 | g0314 | AFR | YRI | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0076 | AFR | YRI | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18946 | hp2 | a0001 | c0003 | t0028 | g0156 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18947 | hp1 | a0001 | c0001 | t0053 | g0103 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18947 | hp2 | a0001 | c0001 | t0018 | g0161 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18949 | hp1 | a0001 | c0001 | t0046 | g0005 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18949 | hp2 | a0001 | c0001 | t0052 | g0075 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18956 | hp1 | a0001 | c0001 | t0024 | g0029 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18978 | hp1 | a0001 | c0001 | t0067 | g0106 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18978 | hp2 | a0001 | c0001 | t0018 | g0159 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18979 | hp1 | a0001 | c0001 | t0012 | g0086 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18991 | hp2 | a0001 | c0001 | t0065 | g0250 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18995 | hp1 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19000 | hp2 | a0001 | c0001 | t0057 | g0150 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19001 | hp1 | a0001 | c0001 | t0060 | g0111 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19001 | hp2 | a0001 | c0001 | t0012 | g0293 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19007 | hp1 | a0001 | c0001 | t0036 | g0160 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19007 | hp2 | a0001 | c0001 | t0026 | g0247 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19030 | hp1 | a0001 | c0001 | t0045 | g0012 | AFR | LWK | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19030 | hp2 | a0001 | c0001 | t0032 | g0009 | AFR | LWK | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0190 | AFR | LWK | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0195 | AFR | LWK | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19057 | hp2 | a0001 | c0001 | t0055 | g0289 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19058 | hp2 | a0001 | c0001 | t0010 | g0048 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19067 | hp2 | a0001 | c0001 | t0010 | g0046 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19070 | hp2 | a0001 | c0001 | t0010 | g0047 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19084 | hp1 | a0001 | c0001 | t0019 | g0180 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19084 | hp2 | a0001 | c0001 | t0012 | g0300 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19085 | hp2 | a0001 | c0001 | t0041 | g0127 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0148 | AFR | YRI | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ASW | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ASW | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | GIH | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | GIH | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0311 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0204 | AMR | CLM | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02109 | hp1 | a0001 | c0001 | t0025 | g0066 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0315 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02486 | hp1 | a0001 | c0001 | t0026 | g0219 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0124 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | ACB | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0119 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG03471 | hp2 | a0001 | c0001 | t0062 | g0277 | AFR | MSL | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | USA | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | USA | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | USA | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | USA | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| NA21309 | hp2 | a0001 | c0001 | t0031 | g0064 | AFR | LWK | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0051 | g0182 | REF | REF | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0197 | REF | REF | IGF2BP1_chr17_48992385_49061145 | IGF2BP1 | chr17 | 48992385 | 49061145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49040068
|
T | A | 1 | a0003 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.795T>A | p.His265Gln | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/15 | 1156/8796 | 795/1734 | 265/577 | chr17 | 49040068 | ||
| chr17:49042297
|
A | G | 1 | a0002 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.997A>G | p.Ile333Val | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 9/15 | 1358/8796 | 997/1734 | 333/577 | chr17 | 49042297 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:49031929
|
G | A | 1 | a0001c0003 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.357G>A | p.Thr119Thr | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/15 | 718/8796 | 357/1734 | 119/577 | chr17 | 49031929 | ||
| chr17:49038231
|
C | T | 1 | a0001c0008 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.465C>T | p.Pro155Pro | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/15 | 826/8796 | 465/1734 | 155/577 | chr17 | 49038231 | ||
| chr17:49039981
|
C | T | 1 | a0001c0002 | 7 | HG01884.hp2 HG02145.hp1 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.708C>T | p.Asn236Asn | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/15 | 1069/8796 | 708/1734 | 236/577 | chr17 | 49039981 | ||
| chr17:49043493
|
C | T | 1 | a0001c0006 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.1143C>T | p.Ser381Ser | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 10/15 | 1504/8796 | 1143/1734 | 381/577 | chr17 | 49043493 | ||
| chr17:49049390
|
T | A | 1 | a0001c0005 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1680T>A | p.Val560Val | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2041/8796 | 1680/1734 | 560/577 | chr17 | 49049390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:48997611
|
A | G | 2 | a0001c0001t0032a0001c0002t0072 | 3 | HG02280.hp1 HG02630.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-135A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/15 | 135 | chr17 | 48997611 | |||||
| chr17:48997694
|
G | A | 1 | a0001c0001t0033 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/15 | 52 | chr17 | 48997694 | |||||
| chr17:48997703
|
T | G | 1 | a0001c0001t0034 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/15 | 43 | chr17 | 48997703 | |||||
| chr17:49049537
|
C | T | 1 | a0001c0001t0071 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*93C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 93 | chr17 | 49049537 | |||||
| chr17:49050005
|
G | T | 2 | a0001c0001t0069a0001c0001t0070 | 2 | HG02970.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*561G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 561 | chr17 | 49050005 | |||||
| chr17:49050170
|
A | G | 2 | a0001c0001t0011a0001c0001t0034 | 8 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*726A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 726 | chr17 | 49050170 | |||||
| chr17:49050177
|
C | T | 1 | a0001c0001t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*733C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 733 | chr17 | 49050177 | |||||
| chr17:49050233
|
C | T | 1 | a0001c0001t0031 | 2 | HG02572.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*789C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 789 | chr17 | 49050233 | |||||
| chr17:49050751
|
A | C | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1307 | chr17 | 49050751 | |||||
| chr17:49050752
|
G | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1308G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1308 | chr17 | 49050752 | |||||
| chr17:49050758
|
A | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1314 | chr17 | 49050758 | |||||
| chr17:49050766
|
T | G | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1322T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1322 | chr17 | 49050766 | |||||
| chr17:49050778
|
T | A | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1334 | chr17 | 49050778 | |||||
| chr17:49050779
|
T | G | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1335 | chr17 | 49050779 | |||||
| chr17:49050790
|
A | C | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1346 | chr17 | 49050790 | |||||
| chr17:49050793
|
A | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1349A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1349 | chr17 | 49050793 | |||||
| chr17:49050819
|
G | C | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1375G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1375 | chr17 | 49050819 | |||||
| chr17:49050820
|
T | A | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1376 | chr17 | 49050820 | |||||
| chr17:49050821
|
G | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1377G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1377 | chr17 | 49050821 | |||||
| chr17:49050843
|
A | G | 1 | a0001c0001t0066 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1399A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1399 | chr17 | 49050843 | |||||
| chr17:49050851
|
T | A | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1407 | chr17 | 49050851 | |||||
| chr17:49050853
|
G | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1409G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1409 | chr17 | 49050853 | |||||
| chr17:49050854
|
G | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1410G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1410 | chr17 | 49050854 | |||||
| chr17:49050861
|
C | A | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1417C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1417 | chr17 | 49050861 | |||||
| chr17:49050863
|
C | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1419C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1419 | chr17 | 49050863 | |||||
| chr17:49050865
|
T | A | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1421 | chr17 | 49050865 | |||||
| chr17:49050868
|
T | C | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1424 | chr17 | 49050868 | |||||
| chr17:49050874
|
G | A | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1430 | chr17 | 49050874 | |||||
| chr17:49050878
|
G | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1434G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1434 | chr17 | 49050878 | |||||
| chr17:49050885
|
C | T | 4 | a0001c0001t0003a0001c0001t0064a0001c0001t0065others(1): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1441C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1441 | chr17 | 49050885 | |||||
| chr17:49050900
|
A | T | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1456A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1456 | chr17 | 49050900 | |||||
| chr17:49050901
|
T | G | 1 | a0001c0001t0067 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1457T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1457 | chr17 | 49050901 | |||||
| chr17:49051417
|
A | T | 1 | a0001c0001t0030 | 2 | HG00741.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1973A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 1973 | chr17 | 49051417 | |||||
| chr17:49051488
|
G | A | 1 | a0001c0001t0017 | 2 | NA18522.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2044G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2044 | chr17 | 49051488 | |||||
| chr17:49051575
|
C | G | 2 | a0001c0002t0063a0001c0002t0072 | 2 | HG02630.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2131C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2131 | chr17 | 49051575 | |||||
| chr17:49051718
|
A | C | 1 | a0001c0001t0062 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2274A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2274 | chr17 | 49051718 | |||||
| chr17:49051759
|
G | A | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0010others(20): Show | 92 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2315G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2315 | chr17 | 49051759 | |||||
| chr17:49051775
|
C | T | 1 | a0001c0001t0061 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2331C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2331 | chr17 | 49051775 | |||||
| chr17:49051881
|
T | C | 2 | a0001c0001t0033a0001c0001t0044 | 2 | HG02970.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2437T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2437 | chr17 | 49051881 | |||||
| chr17:49052297
|
T | G | 1 | a0001c0001t0035 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2853T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2853 | chr17 | 49052297 | |||||
| chr17:49052300
|
A | T | 1 | a0001c0001t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2856A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2856 | chr17 | 49052300 | |||||
| chr17:49052370
|
A | G | 1 | a0001c0001t0060 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2926A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 2926 | chr17 | 49052370 | |||||
| chr17:49052613
|
G | T | 1 | a0001c0001t0017 | 2 | NA18522.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3169G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 3169 | chr17 | 49052613 | |||||
| chr17:49052704
|
T | G | 1 | a0001c0001t0045 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3260T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 3260 | chr17 | 49052704 | |||||
| chr17:49052852
|
T | C | 2 | a0001c0001t0018a0001c0001t0036 | 3 | NA18947.hp2 NA18978.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3408T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 3408 | chr17 | 49052852 | |||||
| chr17:49052868
|
G | C | 12 | a0001c0001t0004a0001c0001t0013a0001c0001t0022others(9): Show | 39 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3424G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 3424 | chr17 | 49052868 | |||||
| chr17:49053050
|
G | C | 2 | a0001c0001t0008a0001c0001t0015 | 13 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3606G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 3606 | chr17 | 49053050 | |||||
| chr17:49053237
|
G | C | 1 | a0001c0001t0037 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3793G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 3793 | chr17 | 49053237 | |||||
| chr17:49053482
|
C | T | 1 | a0001c0001t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4038C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 4038 | chr17 | 49053482 | |||||
| chr17:49053672
|
G | A | 1 | a0001c0001t0022 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4228G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 4228 | chr17 | 49053672 | |||||
| chr17:49054112
|
C | T | 1 | a0001c0001t0029 | 2 | HG01496.hp2 HG02273.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4668C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 4668 | chr17 | 49054112 | |||||
| chr17:49054311
|
G | A | 1 | a0001c0001t0064 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4867G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 4867 | chr17 | 49054311 | |||||
| chr17:49054539
|
A | G | 54 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(51): Show | 185 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*5095A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5095 | chr17 | 49054539 | |||||
| chr17:49054671
|
G | T | 1 | a0001c0002t0043 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5227G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5227 | chr17 | 49054671 | |||||
| chr17:49054810
|
G | A | 1 | a0001c0001t0051 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5366G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5366 | chr17 | 49054810 | |||||
| chr17:49054817
|
A | G | 1 | a0001c0001t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5373A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5373 | chr17 | 49054817 | |||||
| chr17:49054889
|
C | T | 2 | a0001c0001t0016a0001c0001t0059 | 4 | HG02572.hp2 HG03130.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5445C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5445 | chr17 | 49054889 | |||||
| chr17:49055052
|
G | A | 1 | a0001c0001t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5608G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5608 | chr17 | 49055052 | |||||
| chr17:49055062
|
C | G | 1 | a0001c0001t0042 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5618C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5618 | chr17 | 49055062 | |||||
| chr17:49055140
|
A | AT | 3 | a0001c0001t0008a0001c0001t0015a0001c0001t0027 | 15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5698dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5699 | INFO_REALIGN_3_PRIME | chr17 | 49055140 | ||||
| chr17:49055142
|
TA | T | 4 | a0001c0001t0007a0001c0001t0026a0001c0001t0030others(1): Show | 16 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5711delA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5711 | INFO_REALIGN_3_PRIME | chr17 | 49055142 | ||||
| chr17:49055143
|
A | T | 55 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(52): Show | 174 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*5699A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5699 | chr17 | 49055143 | |||||
| chr17:49055144
|
A | T | 1 | a0001c0001t0050 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5700A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5700 | chr17 | 49055144 | |||||
| chr17:49055155
|
A | C | 47 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(44): Show | 166 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*5711A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5711 | chr17 | 49055155 | |||||
| chr17:49055156
|
C | A | 2 | a0001c0001t0057a0001c0001t0068 | 2 | HG03516.hp1 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5712C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5712 | chr17 | 49055156 | |||||
| chr17:49055156
|
C | CA | 40 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(37): Show | 158 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*5712_*5713insA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5713 | chr17 | 49055156 | |||||
| chr17:49055157
|
C | A | 49 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(46): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*5713C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5713 | chr17 | 49055157 | |||||
| chr17:49055236
|
C | T | 1 | a0001c0001t0055 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5792C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5792 | chr17 | 49055236 | |||||
| chr17:49055289
|
C | T | 1 | a0001c0001t0054 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5845C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 5845 | chr17 | 49055289 | |||||
| chr17:49055457
|
T | C | 51 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(48): Show | 170 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*6013T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6013 | chr17 | 49055457 | |||||
| chr17:49055486
|
G | A | 7 | a0001c0001t0004a0001c0001t0023a0001c0001t0024others(4): Show | 29 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6042G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6042 | chr17 | 49055486 | |||||
| chr17:49055534
|
C | T | 1 | a0001c0001t0053 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6090C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6090 | chr17 | 49055534 | |||||
| chr17:49055821
|
C | A | 2 | a0001c0001t0016a0001c0001t0059 | 4 | HG02572.hp2 HG03130.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6377C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6377 | chr17 | 49055821 | |||||
| chr17:49055832
|
G | A | 1 | a0001c0001t0039 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6388G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6388 | chr17 | 49055832 | |||||
| chr17:49055836
|
G | GT | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(31): Show | 130 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*6414dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6415 | INFO_REALIGN_3_PRIME | chr17 | 49055836 | ||||
| chr17:49055836
|
G | GTT | 12 | a0001c0001t0009a0001c0001t0010a0001c0001t0016others(9): Show | 32 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*6413_*6414dupTT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6415 | INFO_REALIGN_3_PRIME | chr17 | 49055836 | ||||
| chr17:49055836
|
GTTTTTTT others(1): Show |
G | 6 | a0001c0001t0005a0001c0001t0017a0001c0001t0028others(3): Show | 18 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*6407_*6414delTTTT others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6407 | INFO_REALIGN_3_PRIME | chr17 | 49055836 | ||||
| chr17:49055859
|
A | T | 1 | a0001c0001t0020 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6415A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6415 | chr17 | 49055859 | |||||
| chr17:49055939
|
C | T | 6 | a0001c0001t0006a0001c0001t0018a0001c0001t0019others(3): Show | 18 | HG01081.hp1 HG01515.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*6495C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 15/15 | 6495 | chr17 | 49055939 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:48997933
|
C | T | 1 | a0001c0001t0001g0318 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.175+13C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48997933 | ||||||
| chr17:48998087
|
G | T | 1 | a0001c0001t0002g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.175+167G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998087 | ||||||
| chr17:48998088
|
C | T | 1 | a0001c0001t0002g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.175+168C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998088 | ||||||
| chr17:48998216
|
G | T | 1 | a0001c0001t0039g0316 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.175+296G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998216 | ||||||
| chr17:48998306
|
C | A | 2 | a0001c0001t0015g0001a0001c0001t0064g0002 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.175+386C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998306 | ||||||
| chr17:48998328
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.175+408G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998328 | ||||||
| chr17:48998331
|
C | T | 2 | a0001c0001t0027g0314a0001c0001t0027g0315 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.175+411C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998331 | ||||||
| chr17:48998455
|
G | A | 1 | a0001c0001t0046g0005 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.175+535G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998455 | ||||||
| chr17:48998553
|
G | A | 199 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0056others(196): Show | 199 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(196): Show |
intron_variant | MODIFIER | c.176-556G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998553 | ||||||
| chr17:48998559
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.176-550G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998559 | ||||||
| chr17:48998628
|
C | T | 13 | a0001c0001t0002g0185a0001c0001t0008g0190a0001c0001t0008g0191others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.176-481C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998628 | ||||||
| chr17:48998642
|
C | G | 1 | a0001c0001t0051g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.176-467C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48998642 | ||||||
| chr17:48999087
|
A | AT | 48 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0001t0001g0278others(45): Show | 48 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.176-10dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr17 | 48999087 | |||||
| chr17:48999101
|
A | C | 11 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0006g0163others(8): Show | 11 | HG01081.hp1 HG01515.hp1 HG02040.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.176-8A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48999101 | ||||||
| chr17:48999106
|
T | C | 5 | a0001c0001t0002g0011a0001c0001t0014g0010a0001c0001t0032g0008others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.176-3T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 1/14 | chr17 | 48999106 | ||||||
| chr17:48999188
|
C | CT | 5 | a0001c0001t0001g0174a0001c0001t0006g0171a0001c0001t0006g0172others(2): Show | 5 | NA18977.hp1 NA18984.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+19_236+20insT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999188 | ||||||
| chr17:48999189
|
G | T | 261 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0057others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.236+20G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999189 | ||||||
| chr17:48999190
|
G | C | 1 | a0003c0004t0001g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.236+21G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999190 | ||||||
| chr17:48999194
|
G | A | 3 | a0001c0001t0018g0159a0001c0001t0018g0161a0001c0001t0036g0160 | 3 | NA18947.hp2 NA18978.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.236+25G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999194 | ||||||
| chr17:48999195
|
G | C | 38 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0200others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.236+26G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999195 | ||||||
| chr17:48999356
|
T | TA | 270 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0056others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.236+197dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999356 | |||||
| chr17:48999362
|
A | G | 1 | a0001c0001t0001g0313 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.236+193A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999362 | ||||||
| chr17:48999370
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.236+201A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999370 | ||||||
| chr17:48999384
|
G | C | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236+215G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999384 | ||||||
| chr17:48999523
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.236+354A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999523 | ||||||
| chr17:48999611
|
C | T | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236+442C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 48999611 | ||||||
| chr17:48999923
|
G | GGT | 58 | a0001c0001t0001g0056a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 58 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.236+793_236+794dup others(2): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGT | 43 | a0001c0001t0001g0074a0001c0001t0001g0147a0001c0001t0001g0165others(40): Show | 43 | HG00609.hp1 HG00642.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.236+791_236+794dup others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGT | 7 | a0001c0001t0001g0070a0001c0001t0002g0225a0001c0001t0009g0071others(4): Show | 7 | HG01255.hp2 HG01934.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+789_236+794dup others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(1): Show |
7 | a0001c0001t0005g0146a0001c0001t0006g0163a0001c0001t0006g0164others(4): Show | 7 | HG00558.hp1 HG01433.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+787_236+794dup others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(3): Show |
7 | a0001c0001t0001g0162a0001c0001t0004g0291a0001c0001t0015g0001others(4): Show | 7 | HG01243.hp1 HG01975.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+785_236+794dup others(10): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(5): Show |
7 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0028others(4): Show | 7 | HG02109.hp1 HG02148.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+783_236+794dup others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(7): Show |
4 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(1): Show | 4 | NA18950.hp2 NA18962.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+781_236+794dup others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(9): Show |
3 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0048g0020 | 3 | HG00621.hp1 HG02015.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.236+779_236+794dup others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(11): Show |
4 | a0001c0001t0001g0062a0001c0001t0004g0063a0001c0001t0004g0282others(1): Show | 4 | HG00609.hp2 HG02074.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+777_236+794dup others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(13): Show |
1 | a0001c0001t0004g0019 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.236+775_236+794dup others(20): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(15): Show |
2 | a0001c0001t0004g0017a0001c0001t0004g0018 | 2 | HG01106.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.236+773_236+794dup others(22): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(17): Show |
2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.236+771_236+794dup others(24): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(19): Show |
1 | a0001c0001t0004g0014 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.236+769_236+794dup others(26): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(21): Show |
1 | a0001c0001t0004g0176 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.236+767_236+794dup others(28): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
G | GGTGTGTG others(27): Show |
1 | a0001c0001t0023g0013 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.236+761_236+794dup others(34): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
GGT | G | 32 | a0001c0001t0001g0006a0001c0001t0003g0218a0001c0001t0003g0220others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.236+793_236+794del others(2): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
GGTGT | G | 11 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 11 | HG02257.hp2 HG02280.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+791_236+794del others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
GGTGTGT | G | 3 | a0001c0001t0002g0143a0001c0001t0003g0275a0001c0001t0055g0289 | 3 | HG01192.hp2 HG02738.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.236+789_236+794del others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.236+785_236+794del others(10): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999923
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236+777_236+794del others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999923 | |||||
| chr17:48999949
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0002g0037a0001c0001t0020g0038 | 2 | HG01169.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.236+794_236+795ins others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999949 | |||||
| chr17:48999949
|
T | TGTGTGTG others(9): Show |
4 | a0001c0001t0002g0040a0001c0001t0002g0093a0001c0001t0020g0042others(1): Show | 4 | HG01167.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+789_236+804dup others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999949 | |||||
| chr17:48999961
|
T | TGTTC | 3 | a0001c0001t0006g0136a0001c0001t0006g0138a0001c0001t0019g0137 | 3 | HG02055.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.236+795_236+798dup others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 48999961 | |||||
| chr17:49000286
|
A | G | 236 | a0001c0001t0001g0134a0001c0001t0001g0162a0001c0001t0002g0003others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.236+1117A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000286 | ||||||
| chr17:49000320
|
G | C | 40 | a0001c0001t0002g0011a0001c0001t0002g0199a0001c0001t0005g0146others(37): Show | 40 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.236+1151G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000320 | ||||||
| chr17:49000321
|
G | T | 4 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0271others(1): Show | 4 | HG00544.hp2 HG00621.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+1152G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000321 | ||||||
| chr17:49000390
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.236+1221T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000390 | ||||||
| chr17:49000476
|
G | A | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.236+1307G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000476 | ||||||
| chr17:49000617
|
G | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.236+1448G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000617 | ||||||
| chr17:49000695
|
T | C | 2 | a0001c0001t0010g0238a0001c0001t0010g0239 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.236+1526T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000695 | ||||||
| chr17:49000870
|
C | G | 13 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.236+1701C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000870 | ||||||
| chr17:49000910
|
A | AGGCTCTT others(7): Show |
1 | a0001c0001t0006g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.236+1741_236+1742i others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49000910 | ||||||
| chr17:49000940
|
T | TA | 80 | a0001c0001t0002g0011a0001c0001t0002g0199a0001c0001t0003g0252others(77): Show | 80 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.236+1783dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49000940 | |||||
| chr17:49000993
|
T | TC | 181 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(178): Show | 181 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.236+1828dupC | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49000993 | |||||
| chr17:49001058
|
T | G | 38 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.236+1889T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49001058 | ||||||
| chr17:49001364
|
C | T | 1 | a0001c0006t0002g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.236+2195C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49001364 | ||||||
| chr17:49001561
|
T | C | 1 | a0001c0005t0003g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.236+2392T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49001561 | ||||||
| chr17:49001620
|
G | T | 1 | a0001c0001t0001g0308 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.236+2451G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49001620 | ||||||
| chr17:49001813
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.236+2644A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49001813 | ||||||
| chr17:49002054
|
C | A | 100 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0033others(97): Show | 100 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(97): Show |
intron_variant | MODIFIER | c.236+2885C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49002054 | ||||||
| chr17:49002699
|
A | AT | 23 | a0001c0001t0001g0110a0001c0001t0001g0162a0001c0001t0002g0003others(20): Show | 23 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.236+3546dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49002699 | |||||
| chr17:49002717
|
C | A | 1 | a0001c0001t0001g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.236+3548C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49002717 | ||||||
| chr17:49002901
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0095 | 2 | NA18944.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.236+3732G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49002901 | ||||||
| chr17:49003069
|
G | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.236+3900G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49003069 | ||||||
| chr17:49003311
|
C | T | 2 | a0001c0001t0033g0044a0001c0001t0044g0039 | 2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.236+4142C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49003311 | ||||||
| chr17:49003822
|
G | C | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236+4653G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49003822 | ||||||
| chr17:49004054
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0199a0001c0001t0014g0010 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.236+4885C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49004054 | ||||||
| chr17:49004094
|
C | G | 3 | a0001c0001t0001g0109a0001c0001t0051g0182a0003c0004t0001g0170 | 3 | HG01192.hp1 HG02148.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.236+4925C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49004094 | ||||||
| chr17:49004286
|
A | ACGAGAGG others(12): Show |
2 | a0001c0001t0003g0218a0001c0001t0003g0252 | 2 | HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.236+5120_236+5138d others(21): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49004286 | |||||
| chr17:49004306
|
CGGCTGCG | C | 177 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.236+5151_236+5157d others(9): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49004306 | |||||
| chr17:49004313
|
G | T | 1 | a0001c0001t0027g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.236+5144G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49004313 | ||||||
| chr17:49004518
|
G | A | 77 | a0001c0001t0002g0011a0001c0001t0002g0199a0001c0001t0004g0014others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.236+5349G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49004518 | ||||||
| chr17:49004529
|
C | A | 10 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.236+5360C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49004529 | ||||||
| chr17:49004882
|
T | C | 6 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0033others(3): Show | 6 | HG02559.hp1 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+5713T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49004882 | ||||||
| chr17:49005250
|
T | C | 1 | a0001c0001t0005g0146 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.236+6081T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49005250 | ||||||
| chr17:49005293
|
A | G | 1 | a0002c0007t0009g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.236+6124A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49005293 | ||||||
| chr17:49005413
|
G | A | 91 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(88): Show | 91 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.236+6244G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49005413 | ||||||
| chr17:49005524
|
G | A | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236+6355G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49005524 | ||||||
| chr17:49005929
|
G | T | 1 | a0001c0001t0066g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.236+6760G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49005929 | ||||||
| chr17:49006142
|
T | G | 1 | a0001c0001t0039g0316 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.236+6973T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49006142 | ||||||
| chr17:49006154
|
T | G | 1 | a0001c0001t0070g0049 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.236+6985T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49006154 | ||||||
| chr17:49006190
|
G | A | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236+7021G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49006190 | ||||||
| chr17:49006204
|
G | T | 10 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(7): Show | 10 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+7035G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49006204 | ||||||
| chr17:49006828
|
C | T | 1 | a0001c0001t0005g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.236+7659C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49006828 | ||||||
| chr17:49006898
|
G | A | 7 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+7729G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49006898 | ||||||
| chr17:49006912
|
A | T | 1 | a0001c0001t0003g0271 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.236+7743A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49006912 | ||||||
| chr17:49007171
|
C | T | 1 | a0001c0001t0039g0316 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.236+8002C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49007171 | ||||||
| chr17:49007237
|
T | C | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236+8068T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49007237 | ||||||
| chr17:49007300
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.236+8131A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49007300 | ||||||
| chr17:49007349
|
G | A | 177 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.236+8180G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49007349 | ||||||
| chr17:49007412
|
C | T | 3 | a0001c0001t0016g0045a0001c0001t0016g0117a0001c0001t0059g0089 | 3 | HG02572.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.236+8243C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49007412 | ||||||
| chr17:49007535
|
C | T | 1 | a0001c0001t0071g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236+8366C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49007535 | ||||||
| chr17:49007912
|
C | T | 1 | a0001c0001t0009g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.236+8743C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49007912 | ||||||
| chr17:49008172
|
C | CA | 34 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(31): Show | 34 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+9019dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49008172 | |||||
| chr17:49008172
|
C | CAA | 7 | a0001c0001t0004g0026a0001c0001t0013g0076a0001c0001t0013g0120others(4): Show | 7 | HG01071.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+9018_236+9019d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49008172 | |||||
| chr17:49008172
|
CA | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0107a0001c0001t0001g0108others(4): Show | 7 | HG03098.hp2 HG03654.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+9019delA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49008172 | |||||
| chr17:49008286
|
A | G | 38 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.236+9117A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49008286 | ||||||
| chr17:49008417
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.236+9248A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49008417 | ||||||
| chr17:49008532
|
C | A | 1 | a0001c0001t0012g0073 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.236+9363C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49008532 | ||||||
| chr17:49008947
|
T | C | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236+9778T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49008947 | ||||||
| chr17:49008988
|
C | G | 2 | a0001c0001t0020g0038a0001c0001t0020g0042 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.236+9819C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49008988 | ||||||
| chr17:49009131
|
G | A | 1 | a0001c0001t0007g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.236+9962G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49009131 | ||||||
| chr17:49009377
|
C | CTT | 181 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(178): Show | 181 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.236+10209_236+1021 others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49009377 | |||||
| chr17:49009411
|
T | A | 1 | a0001c0001t0005g0146 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.236+10242T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49009411 | ||||||
| chr17:49009412
|
A | T | 1 | a0001c0001t0002g0036 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.236+10243A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49009412 | ||||||
| chr17:49009459
|
C | T | 1 | a0001c0001t0009g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.236+10290C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49009459 | ||||||
| chr17:49009488
|
T | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.236+10319T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49009488 | ||||||
| chr17:49009709
|
TA | T | 16 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0166others(13): Show | 16 | HG01069.hp2 HG01081.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.236+10551delA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49009709 | |||||
| chr17:49009941
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.236+10772G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49009941 | ||||||
| chr17:49009972
|
C | T | 1 | a0001c0001t0071g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236+10803C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49009972 | ||||||
| chr17:49010076
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.236+10907G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49010076 | ||||||
| chr17:49010313
|
C | CT | 30 | a0001c0001t0001g0109a0001c0001t0001g0200a0001c0001t0001g0304others(27): Show | 30 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.236+11167dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49010313 | |||||
| chr17:49010313
|
CT | C | 12 | a0001c0001t0001g0082a0001c0001t0001g0096a0001c0001t0001g0107others(9): Show | 12 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+11167delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49010313 | |||||
| chr17:49010313
|
CTT | C | 21 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0033others(18): Show | 21 | HG01175.hp1 HG01243.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.236+11166_236+1116 others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49010313 | |||||
| chr17:49010313
|
CTTT | C | 78 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(75): Show | 78 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.236+11165_236+1116 others(7): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49010313 | |||||
| chr17:49010317
|
T | C | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+11148T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49010317 | ||||||
| chr17:49010318
|
T | C | 1 | a0001c0001t0008g0253 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+11149T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49010318 | ||||||
| chr17:49010319
|
T | C | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+11150T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49010319 | ||||||
| chr17:49010320
|
T | C | 1 | a0001c0001t0008g0253 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+11151T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49010320 | ||||||
| chr17:49010707
|
T | G | 1 | a0001c0001t0002g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.236+11538T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49010707 | ||||||
| chr17:49010794
|
A | C | 2 | a0001c0001t0030g0201a0001c0001t0030g0206 | 2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.236+11625A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49010794 | ||||||
| chr17:49011009
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.236+11840C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011009 | ||||||
| chr17:49011137
|
C | CA | 43 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0074others(40): Show | 43 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.236+11998dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
C | CAA | 18 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0098others(15): Show | 18 | HG00423.hp2 HG00741.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.236+11997_236+1199 others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
CAA | C | 11 | a0001c0001t0001g0085a0001c0001t0002g0033a0001c0001t0006g0163others(8): Show | 11 | HG01081.hp1 HG02055.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+11997_236+1199 others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
CAAA | C | 42 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0034others(39): Show | 42 | HG00735.hp2 HG01070.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.236+11996_236+1199 others(7): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
CAAAA | C | 39 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0058others(36): Show | 39 | HG00099.hp1 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.236+11995_236+1199 others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
CAAAAAAA | C | 8 | a0001c0001t0005g0281a0001c0001t0005g0310a0001c0001t0005g0311others(5): Show | 8 | HG00140.hp1 HG01123.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+11992_236+1199 others(11): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
CAAAAAAA others(1): Show |
C | 32 | a0001c0001t0002g0011a0001c0001t0002g0199a0001c0001t0005g0146others(29): Show | 32 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.236+11991_236+1199 others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
CAAAAAAA others(2): Show |
C | 11 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0017others(8): Show | 11 | HG01106.hp1 HG01952.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+11990_236+1199 others(13): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011137
|
CAAAAAAA others(3): Show |
C | 27 | a0001c0001t0004g0016a0001c0001t0004g0018a0001c0001t0004g0019others(24): Show | 27 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.236+11989_236+1199 others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011137 | |||||
| chr17:49011153
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.236+11988_236+1200 others(19): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011153 | |||||
| chr17:49011158
|
A | C | 45 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(42): Show | 45 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.236+11989A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011158 | ||||||
| chr17:49011163
|
A | C | 2 | a0001c0001t0033g0044a0001c0001t0044g0039 | 2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.236+11994A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011163 | ||||||
| chr17:49011165
|
A | C | 1 | a0001c0001t0001g0313 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.236+11996A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011165 | ||||||
| chr17:49011168
|
C | A | 15 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(12): Show | 15 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.236+11999C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011168 | ||||||
| chr17:49011415
|
C | T | 10 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(7): Show | 10 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+12246C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011415 | ||||||
| chr17:49011659
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.236+12490A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011659 | ||||||
| chr17:49011688
|
C | CA | 7 | a0001c0001t0001g0292a0001c0001t0001g0301a0001c0001t0004g0016others(4): Show | 7 | HG01433.hp1 HG01934.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+12532dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011688 | |||||
| chr17:49011779
|
G | A | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+12610G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011779 | ||||||
| chr17:49011849
|
A | AT | 28 | a0001c0001t0003g0205a0001c0001t0003g0218a0001c0001t0003g0220others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.236+12684dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011849 | |||||
| chr17:49011863
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.236+12694G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011863 | ||||||
| chr17:49011904
|
A | AT | 91 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0284others(88): Show | 91 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.236+12754dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011904 | |||||
| chr17:49011904
|
A | ATT | 86 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0002g0050others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.236+12753_236+1275 others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011904 | |||||
| chr17:49011904
|
A | ATTT | 12 | a0001c0001t0002g0040a0001c0001t0002g0052a0001c0001t0002g0060others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+12752_236+1275 others(7): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49011904 | |||||
| chr17:49011924
|
G | C | 7 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+12755G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49011924 | ||||||
| chr17:49012035
|
C | T | 9 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG02523.hp2 NA18946.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+12866C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012035 | ||||||
| chr17:49012201
|
G | A | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236+13032G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012201 | ||||||
| chr17:49012218
|
T | G | 7 | a0001c0001t0001g0097a0001c0001t0001g0147a0001c0001t0001g0162others(4): Show | 7 | NA18962.hp2 NA18973.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+13049T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012218 | ||||||
| chr17:49012225
|
G | T | 5 | a0001c0001t0013g0120a0001c0001t0022g0091a0001c0001t0022g0092others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+13056G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012225 | ||||||
| chr17:49012302
|
T | G | 2 | a0001c0001t0002g0011a0001c0001t0014g0010 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.236+13133T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012302 | ||||||
| chr17:49012355
|
C | A | 18 | a0001c0001t0002g0011a0001c0001t0002g0199a0001c0001t0009g0071others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.236+13186C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012355 | ||||||
| chr17:49012355
|
C | G | 169 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0033others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.236+13186C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012355 | ||||||
| chr17:49012523
|
G | A | 2 | a0001c0001t0027g0314a0001c0001t0027g0315 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.237-13095G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012523 | ||||||
| chr17:49012546
|
G | A | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0033others(87): Show | 90 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.237-13072G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012546 | ||||||
| chr17:49012662
|
C | T | 38 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.237-12956C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012662 | ||||||
| chr17:49012756
|
C | G | 2 | a0001c0001t0007g0202a0001c0001t0007g0211 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.237-12862C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012756 | ||||||
| chr17:49012936
|
G | C | 234 | a0001c0001t0001g0280a0001c0001t0002g0003a0001c0001t0002g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.237-12682G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49012936 | ||||||
| chr17:49013206
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.237-12412T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49013206 | ||||||
| chr17:49013225
|
CCAAA | C | 81 | a0001c0001t0001g0280a0001c0001t0002g0011a0001c0001t0002g0199others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.237-12388_237-1238 others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49013225 | |||||
| chr17:49013231
|
A | G | 2 | a0001c0001t0006g0163a0001c0001t0006g0164 | 2 | NA19074.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.237-12387A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49013231 | ||||||
| chr17:49013423
|
C | T | 54 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(51): Show | 54 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.237-12195C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49013423 | ||||||
| chr17:49013542
|
T | C | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.237-12076T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49013542 | ||||||
| chr17:49013543
|
A | G | 1 | a0001c0001t0004g0063 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.237-12075A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49013543 | ||||||
| chr17:49013921
|
C | A | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.237-11697C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49013921 | ||||||
| chr17:49014058
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(92): Show | 95 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.237-11560C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014058 | ||||||
| chr17:49014423
|
C | T | 1 | a0001c0001t0006g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.237-11195C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014423 | ||||||
| chr17:49014425
|
C | T | 5 | a0001c0001t0002g0011a0001c0001t0002g0035a0001c0001t0002g0036others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-11193C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014425 | ||||||
| chr17:49014511
|
G | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-11107G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014511 | ||||||
| chr17:49014524
|
G | A | 18 | a0001c0001t0006g0136a0001c0001t0006g0138a0001c0001t0006g0163others(15): Show | 18 | HG01081.hp1 HG01515.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-11094G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014524 | ||||||
| chr17:49014557
|
G | C | 10 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-11061G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014557 | ||||||
| chr17:49014714
|
C | T | 139 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(136): Show |
intron_variant | MODIFIER | c.237-10904C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014714 | ||||||
| chr17:49014786
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-10832A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014786 | ||||||
| chr17:49014890
|
G | T | 177 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.237-10728G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014890 | ||||||
| chr17:49014911
|
G | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-10707G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014911 | ||||||
| chr17:49014948
|
G | C | 179 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.237-10670G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49014948 | ||||||
| chr17:49016036
|
T | C | 94 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(91): Show | 94 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.237-9582T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016036 | ||||||
| chr17:49016202
|
A | G | 5 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-9416A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016202 | ||||||
| chr17:49016295
|
C | G | 1 | a0001c0001t0057g0150 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.237-9323C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016295 | ||||||
| chr17:49016336
|
C | T | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-9282C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016336 | ||||||
| chr17:49016370
|
C | T | 2 | a0001c0001t0003g0205a0001c0001t0003g0270 | 2 | HG00099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.237-9248C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016370 | ||||||
| chr17:49016412
|
T | C | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-9206T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016412 | ||||||
| chr17:49016418
|
C | CGT | 6 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-9184_237-9183d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49016418 | |||||
| chr17:49016426
|
T | C | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.237-9192T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016426 | ||||||
| chr17:49016467
|
C | T | 9 | a0001c0001t0002g0185a0001c0001t0056g0186a0001c0002t0002g0187others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-9151C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016467 | ||||||
| chr17:49016794
|
CCCGCCCG others(9): Show |
C | 3 | a0001c0001t0006g0136a0001c0001t0006g0138a0001c0001t0019g0137 | 3 | HG02055.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.237-8821_237-8806d others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49016794 | |||||
| chr17:49016912
|
C | G | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.237-8706C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49016912 | ||||||
| chr17:49017117
|
C | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-8501C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017117 | ||||||
| chr17:49017123
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.237-8495C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017123 | ||||||
| chr17:49017133
|
G | C | 1 | a0001c0001t0057g0150 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.237-8485G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017133 | ||||||
| chr17:49017149
|
G | A | 3 | a0001c0001t0005g0309a0001c0001t0005g0310a0001c0001t0005g0311 | 3 | HG01123.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.237-8469G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017149 | ||||||
| chr17:49017165
|
G | T | 1 | a0001c0001t0004g0022 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.237-8453G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017165 | ||||||
| chr17:49017237
|
T | C | 179 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.237-8381T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017237 | ||||||
| chr17:49017266
|
TCTTATCC others(6): Show |
T | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.237-8351_237-8339d others(15): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017266 | ||||||
| chr17:49017391
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-8227A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017391 | ||||||
| chr17:49017498
|
T | G | 1 | a0001c0001t0057g0150 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.237-8120T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017498 | ||||||
| chr17:49017571
|
T | A | 1 | a0001c0001t0009g0230 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.237-8047T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017571 | ||||||
| chr17:49017595
|
A | T | 1 | a0001c0001t0016g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.237-8023A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017595 | ||||||
| chr17:49017679
|
G | A | 102 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 102 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(99): Show |
intron_variant | MODIFIER | c.237-7939G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017679 | ||||||
| chr17:49017700
|
C | T | 4 | a0001c0001t0031g0064a0001c0001t0031g0065a0001c0001t0033g0044others(1): Show | 4 | HG02572.hp1 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-7918C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017700 | ||||||
| chr17:49017765
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.237-7853C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49017765 | ||||||
| chr17:49018062
|
C | T | 1 | a0001c0001t0028g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.237-7556C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49018062 | ||||||
| chr17:49018251
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.237-7367A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49018251 | ||||||
| chr17:49018397
|
G | C | 1 | a0001c0001t0002g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.237-7221G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49018397 | ||||||
| chr17:49018460
|
C | T | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.237-7158C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49018460 | ||||||
| chr17:49018518
|
G | A | 1 | a0001c0001t0011g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.237-7100G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49018518 | ||||||
| chr17:49018605
|
G | T | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.237-7013G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49018605 | ||||||
| chr17:49018657
|
C | CA | 11 | a0001c0001t0001g0299a0001c0001t0005g0146a0001c0001t0008g0190others(8): Show | 11 | HG01891.hp2 HG01952.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-6947dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49018657 | |||||
| chr17:49019300
|
G | A | 5 | a0001c0001t0003g0205a0001c0001t0003g0262a0001c0001t0003g0266others(2): Show | 5 | HG00099.hp2 HG00140.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-6318G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019300 | ||||||
| chr17:49019635
|
C | CATTTTAT others(20): Show |
6 | a0001c0001t0013g0076a0001c0001t0013g0120a0001c0001t0022g0091others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-5978_237-5952d others(29): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019635 | |||||
| chr17:49019702
|
T | C | 2 | a0001c0001t0027g0314a0001c0001t0027g0315 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.237-5916T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019702 | ||||||
| chr17:49019899
|
CTAATTTA others(12): Show |
C | 1 | a0001c0001t0003g0220 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.237-5716_237-5698d others(21): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019899 | |||||
| chr17:49019903
|
TTTATATA others(4): Show |
T | 1 | a0001c0001t0001g0098 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.237-5713_237-5703d others(13): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019903 | |||||
| chr17:49019904
|
T | TTA | 11 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0298others(8): Show | 11 | HG00140.hp2 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-5670_237-5669d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATA | 12 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0001g0140others(9): Show | 12 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-5672_237-5669d others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATATA | 7 | a0001c0001t0001g0082a0001c0001t0001g0109a0001c0001t0001g0139others(4): Show | 7 | HG00280.hp1 HG00741.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-5674_237-5669d others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATATAT others(1): Show |
12 | a0001c0001t0001g0085a0001c0001t0001g0200a0001c0001t0001g0283others(9): Show | 12 | HG01884.hp1 HG02486.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-5676_237-5669d others(10): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.237-5678_237-5669d others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0280a0001c0001t0007g0232 | 2 | HG00280.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.237-5680_237-5669d others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0234 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.237-5686_237-5669d others(20): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATATAT others(15): Show |
1 | a0001c0001t0001g0227 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.237-5690_237-5669d others(24): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0226 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.237-5692_237-5669d others(26): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTA | T | 10 | a0001c0001t0001g0279a0001c0001t0001g0295a0001c0001t0001g0306others(7): Show | 10 | HG01192.hp1 HG01358.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-5670_237-5669d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATA | T | 17 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0301others(14): Show | 17 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-5672_237-5669d others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATA | T | 3 | a0001c0001t0001g0056a0001c0001t0009g0230a0001c0001t0013g0076 | 3 | HG01099.hp1 NA18747.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.237-5674_237-5669d others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(1): Show |
T | 7 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0318others(4): Show | 7 | HG00609.hp1 HG01255.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-5676_237-5669d others(10): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(3): Show |
T | 26 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0097others(23): Show | 26 | HG00544.hp1 HG00733.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.237-5678_237-5669d others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(5): Show |
T | 3 | a0001c0001t0007g0203a0001c0001t0055g0289a0001c0001t0071g0053 | 3 | HG00741.hp1 HG02615.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.237-5680_237-5669d others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(7): Show |
T | 2 | a0001c0001t0001g0062a0001c0001t0001g0151 | 2 | HG03669.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.237-5682_237-5669d others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(9): Show |
T | 3 | a0001c0001t0001g0095a0001c0001t0003g0273a0001c0001t0070g0049 | 3 | HG02970.hp2 NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.237-5684_237-5669d others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0069g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.237-5686_237-5669d others(20): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0003g0272 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.237-5688_237-5669d others(22): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(15): Show |
T | 2 | a0001c0001t0003g0233a0001c0001t0003g0271 | 2 | HG00621.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.237-5690_237-5669d others(24): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(17): Show |
T | 1 | a0001c0001t0007g0204 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.237-5692_237-5669d others(26): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019904
|
TTATATAT others(21): Show |
T | 2 | a0001c0001t0003g0251a0001c0001t0025g0066 | 2 | HG02109.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.237-5696_237-5669d others(30): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019904 | |||||
| chr17:49019906
|
A | T | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.237-5712A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019906 | ||||||
| chr17:49019914
|
A | G | 7 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-5704A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019914 | ||||||
| chr17:49019928
|
A | T | 3 | a0001c0001t0006g0136a0001c0001t0006g0138a0001c0001t0019g0137 | 3 | HG02055.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.237-5690A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019928 | ||||||
| chr17:49019930
|
ATATATAT others(45): Show |
A | 1 | a0001c0001t0028g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.237-5687_237-5636d others(54): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019930 | ||||||
| chr17:49019931
|
TATATATA others(21): Show |
T | 3 | a0001c0001t0018g0159a0001c0001t0018g0161a0001c0001t0036g0160 | 3 | NA18947.hp2 NA18978.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.237-5685_237-5658d others(30): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019931 | |||||
| chr17:49019931
|
TATATATA others(45): Show |
T | 1 | a0001c0001t0017g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.237-5685_237-5634d others(54): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019931 | |||||
| chr17:49019932
|
A | T | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.237-5686A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019932 | ||||||
| chr17:49019932
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0003g0265 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.237-5684_237-5668d others(19): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019932 | |||||
| chr17:49019933
|
TATATATA others(19): Show |
T | 3 | a0001c0001t0006g0136a0001c0001t0006g0138a0001c0001t0019g0137 | 3 | HG02055.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.237-5683_237-5658d others(28): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019933 | |||||
| chr17:49019934
|
A | T | 3 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0175 | 3 | NA18977.hp1 NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.237-5684A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019934 | ||||||
| chr17:49019934
|
ATATATAT others(41): Show |
A | 1 | a0001c0001t0017g0276 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.237-5683_237-5636d others(50): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019934 | ||||||
| chr17:49019936
|
A | T | 7 | a0001c0001t0008g0217a0001c0001t0008g0253a0001c0001t0015g0254others(4): Show | 7 | HG02145.hp1 HG02155.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-5682A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019936 | ||||||
| chr17:49019936
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.237-5680_237-5668d others(15): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019936 | |||||
| chr17:49019936
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.237-5675_237-5662d others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019936 | |||||
| chr17:49019936
|
ATATATAT others(39): Show |
A | 2 | a0001c0001t0005g0155a0001c0001t0005g0312 | 2 | HG00140.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.237-5681_237-5636d others(48): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019936 | ||||||
| chr17:49019937
|
TATATATA others(39): Show |
T | 4 | a0001c0001t0005g0309a0001c0001t0005g0310a0001c0001t0060g0111others(1): Show | 4 | HG01257.hp2 HG01258.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5679_237-5634d others(48): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019937 | |||||
| chr17:49019937
|
TATATATA others(43): Show |
T | 1 | a0001c0001t0031g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.237-5671_237-5622d others(52): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019937 | |||||
| chr17:49019938
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0004g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.237-5669_237-5668i others(19): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(15): Show |
4 | a0001c0001t0004g0290a0001c0001t0046g0005a0001c0001t0048g0020others(1): Show | 4 | HG00558.hp1 HG02015.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5669_237-5668i others(24): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(13): Show |
4 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0063others(1): Show | 4 | HG01952.hp1 NA18956.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5669_237-5668i others(22): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(11): Show |
4 | a0001c0001t0004g0018a0001c0001t0004g0024a0001c0001t0004g0176others(1): Show | 4 | HG03831.hp2 NA18948.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5669_237-5668i others(20): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0004g0019a0001c0001t0004g0021a0001c0001t0004g0025others(1): Show | 4 | HG00609.hp2 HG00621.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5669_237-5668i others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(7): Show |
4 | a0001c0001t0004g0015a0001c0001t0004g0023a0001c0001t0004g0286others(1): Show | 4 | HG02080.hp2 HG02293.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-5669_237-5668i others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(59): Show |
1 | a0001c0001t0004g0285 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.237-5669_237-5668i others(68): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(5): Show |
4 | a0001c0001t0004g0022a0001c0001t0013g0224a0001c0001t0023g0013others(1): Show | 4 | HG01943.hp1 HG02148.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-5673_237-5662d others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0004g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.237-5671_237-5670i others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019938 | |||||
| chr17:49019938
|
A | T | 11 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0004g0291others(8): Show | 11 | HG01099.hp2 HG01255.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-5680A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019938 | ||||||
| chr17:49019938
|
ATATATAT others(37): Show |
A | 2 | a0001c0001t0005g0157a0001c0001t0057g0150 | 2 | HG02080.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.237-5679_237-5636d others(46): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019938 | ||||||
| chr17:49019939
|
TATATATA others(13): Show |
T | 3 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0175 | 3 | NA18977.hp1 NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.237-5677_237-5658d others(22): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019939 | |||||
| chr17:49019939
|
TATATATA others(37): Show |
T | 4 | a0001c0001t0005g0146a0001c0001t0005g0154a0001c0001t0005g0158others(1): Show | 4 | HG01123.hp1 HG02083.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5677_237-5634d others(46): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019939 | |||||
| chr17:49019939
|
TATATATA others(41): Show |
T | 4 | a0001c0001t0009g0114a0001c0001t0009g0115a0001c0001t0009g0196others(1): Show | 4 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5669_237-5622d others(50): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019939 | |||||
| chr17:49019940
|
A | G | 1 | a0001c0006t0002g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.237-5678A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019940 | ||||||
| chr17:49019940
|
A | T | 23 | a0001c0001t0002g0122a0001c0001t0002g0125a0001c0001t0002g0126others(20): Show | 23 | HG00099.hp1 HG00558.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.237-5678A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019940 | ||||||
| chr17:49019940
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0005g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237-5671_237-5662d others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019940 | |||||
| chr17:49019941
|
TATATATA others(11): Show |
T | 6 | a0001c0001t0002g0011a0001c0001t0002g0199a0001c0001t0014g0010others(3): Show | 6 | HG02145.hp1 HG02155.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-5675_237-5658d others(20): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019941 | |||||
| chr17:49019942
|
A | T | 23 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0059others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.237-5676A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019942 | ||||||
| chr17:49019942
|
ATATATAT others(33): Show |
A | 1 | a0001c0001t0005g0152 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.237-5675_237-5636d others(42): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019942 | ||||||
| chr17:49019943
|
TATATATT others(7): Show |
T | 1 | a0001c0001t0027g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.237-5673_237-5660d others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019943 | |||||
| chr17:49019943
|
TATATATT others(11): Show |
T | 5 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0010g0046others(2): Show | 5 | HG01099.hp2 HG01255.hp1 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-5673_237-5656d others(20): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019943 | |||||
| chr17:49019943
|
TATATATT others(13): Show |
T | 3 | a0001c0001t0008g0217a0001c0001t0008g0253a0001c0001t0015g0254 | 3 | HG02280.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.237-5673_237-5654d others(22): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019943 | |||||
| chr17:49019944
|
A | T | 7 | a0001c0001t0002g0052a0001c0001t0002g0058a0001c0001t0002g0131others(4): Show | 7 | HG01243.hp2 HG01433.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-5674A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019944 | ||||||
| chr17:49019945
|
TATATTTA others(5): Show |
T | 5 | a0001c0001t0008g0191a0001c0001t0008g0192a0001c0001t0008g0193others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-5671_237-5660d others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019945 | |||||
| chr17:49019945
|
TATATTTA others(7): Show |
T | 9 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0036others(6): Show | 9 | HG02280.hp1 HG02486.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-5671_237-5658d others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019945 | |||||
| chr17:49019945
|
TATATTTA others(9): Show |
T | 12 | a0001c0001t0002g0122a0001c0001t0002g0126a0001c0001t0002g0222others(9): Show | 12 | HG00099.hp1 HG00558.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-5671_237-5656d others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019945 | |||||
| chr17:49019945
|
TATATTTA others(11): Show |
T | 3 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216 | 3 | HG02630.hp1 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.237-5671_237-5654d others(20): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019945 | |||||
| chr17:49019946
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0302 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.237-5669_237-5668i others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019946 | |||||
| chr17:49019947
|
TATTTATA others(3): Show |
T | 1 | a0001c0001t0008g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.237-5669_237-5660d others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019947 | |||||
| chr17:49019947
|
TATTTATA others(5): Show |
T | 8 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0093others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-5669_237-5658d others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019947 | |||||
| chr17:49019947
|
TATTTATA others(7): Show |
T | 13 | a0001c0001t0002g0035a0001c0001t0002g0059a0001c0001t0002g0060others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.237-5669_237-5656d others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019947 | |||||
| chr17:49019949
|
TTTATATA others(3): Show |
T | 3 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0185 | 3 | HG01243.hp2 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.237-5668_237-5659d others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019949 | ||||||
| chr17:49019949
|
TTTATATA others(5): Show |
T | 5 | a0001c0001t0002g0058a0001c0001t0002g0131a0001c0001t0002g0133others(2): Show | 5 | HG01433.hp2 HG01934.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-5668_237-5657d others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019949 | ||||||
| chr17:49019950
|
T | A | 24 | a0001c0001t0001g0105a0001c0001t0001g0304a0001c0001t0002g0050others(21): Show | 24 | HG01081.hp1 HG01243.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.237-5668T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019950 | ||||||
| chr17:49019953
|
T | C | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.237-5665T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019953 | ||||||
| chr17:49019954
|
A | ATATT | 4 | a0001c0001t0002g0050a0001c0001t0006g0166a0001c0001t0014g0118others(1): Show | 4 | HG01081.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5662_237-5661i others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019954 | |||||
| chr17:49019954
|
A | T | 6 | a0001c0001t0002g0144a0001c0001t0006g0163a0001c0001t0006g0164others(3): Show | 6 | HG03130.hp1 HG04228.hp2 NA19074.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-5664A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019954 | ||||||
| chr17:49019955
|
T | C | 3 | a0001c0001t0009g0071a0001c0001t0045g0012a0001c0001t0064g0002 | 3 | HG03579.hp2 HG03710.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.237-5663T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019955 | ||||||
| chr17:49019955
|
T | TTTATATA others(13): Show |
1 | a0001c0001t0004g0028 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237-5663_237-5662i others(22): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019955 | ||||||
| chr17:49019955
|
TACAC | T | 10 | a0001c0001t0002g0178a0001c0001t0006g0168a0001c0001t0010g0240others(7): Show | 10 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-5645_237-5642d others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019955 | |||||
| chr17:49019955
|
TACACACA others(23): Show |
T | 2 | a0001c0001t0009g0088a0002c0007t0009g0198 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.237-5659_237-5630d others(32): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019955 | |||||
| chr17:49019955
|
TACACACA others(25): Show |
T | 1 | a0001c0001t0009g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.237-5661_237-5630d others(34): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019955 | |||||
| chr17:49019956
|
A | T | 5 | a0001c0001t0015g0001a0001c0001t0015g0055a0001c0001t0016g0045others(2): Show | 5 | HG01243.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-5662A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019956 | ||||||
| chr17:49019957
|
C | T | 20 | a0001c0001t0002g0050a0001c0001t0002g0144a0001c0001t0006g0163others(17): Show | 20 | HG01081.hp1 HG01243.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.237-5661C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019957 | ||||||
| chr17:49019958
|
A | T | 3 | a0001c0001t0016g0116a0001c0001t0031g0065a0001c0001t0033g0044 | 3 | HG02572.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237-5660A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019958 | ||||||
| chr17:49019959
|
C | T | 20 | a0001c0001t0002g0004a0001c0001t0002g0050a0001c0001t0002g0144others(17): Show | 20 | HG01081.hp1 HG01243.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.237-5659C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019959 | ||||||
| chr17:49019961
|
C | T | 8 | a0001c0001t0015g0001a0001c0001t0015g0055a0001c0001t0016g0045others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-5657C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019961 | ||||||
| chr17:49019963
|
C | T | 5 | a0001c0001t0015g0001a0001c0001t0015g0055a0001c0001t0016g0116others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-5655C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019963 | ||||||
| chr17:49019967
|
CACACACA others(21): Show |
C | 3 | a0001c0001t0016g0045a0001c0001t0016g0117a0001c0001t0044g0039 | 3 | HG02970.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.237-5641_237-5614d others(30): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019967 | |||||
| chr17:49019969
|
CACACACA others(19): Show |
C | 4 | a0001c0001t0005g0281a0001c0001t0016g0116a0001c0001t0031g0065others(1): Show | 4 | HG02572.hp1 HG02683.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-5641_237-5616d others(28): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019969 | |||||
| chr17:49019971
|
CACACATA others(17): Show |
C | 1 | a0001c0001t0005g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237-5641_237-5618d others(26): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019971 | |||||
| chr17:49019973
|
CACATACA others(31): Show |
C | 1 | a0001c0001t0009g0230 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.237-5643_237-5606d others(40): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019973 | |||||
| chr17:49019975
|
CATACACC others(29): Show |
C | 3 | a0001c0001t0009g0113a0001c0001t0059g0089a0001c0001t0071g0053 | 3 | HG00733.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.237-5639_237-5604d others(38): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019975 | |||||
| chr17:49019977
|
T | C | 20 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0107others(17): Show | 20 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.237-5641T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019977 | ||||||
| chr17:49019987
|
C | T | 2 | a0001c0001t0009g0088a0002c0007t0009g0198 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.237-5631C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019987 | ||||||
| chr17:49019987
|
CAT | C | 137 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(134): Show | 137 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.237-5623_237-5622d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019987 | |||||
| chr17:49019988
|
A | T | 7 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0114others(4): Show | 7 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-5630A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019988 | ||||||
| chr17:49019989
|
T | C | 14 | a0001c0001t0005g0146a0001c0001t0005g0154a0001c0001t0005g0155others(11): Show | 14 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.237-5629T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019989 | ||||||
| chr17:49019991
|
T | C | 14 | a0001c0001t0005g0146a0001c0001t0005g0154a0001c0001t0005g0155others(11): Show | 14 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.237-5627T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019991 | ||||||
| chr17:49019993
|
T | C | 15 | a0001c0001t0005g0146a0001c0001t0005g0154a0001c0001t0005g0155others(12): Show | 15 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-5625T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019993 | ||||||
| chr17:49019993
|
TATACAC | T | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-5623_237-5618d others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49019993 | |||||
| chr17:49019995
|
T | C | 25 | a0001c0001t0005g0146a0001c0001t0005g0152a0001c0001t0005g0154others(22): Show | 25 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.237-5623T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49019995 | ||||||
| chr17:49020009
|
C | T | 1 | a0001c0001t0006g0171 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.237-5609C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020009 | ||||||
| chr17:49020011
|
T | C | 10 | a0001c0001t0005g0152a0001c0001t0009g0087a0001c0001t0009g0088others(7): Show | 10 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-5607T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020011 | ||||||
| chr17:49020017
|
T | C | 1 | a0001c0001t0006g0171 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.237-5601T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020017 | ||||||
| chr17:49020017
|
TAC | T | 62 | a0001c0001t0003g0248a0001c0001t0004g0014a0001c0001t0004g0015others(59): Show | 62 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.237-5589_237-5588d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49020017 | |||||
| chr17:49020019
|
C | T | 79 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(76): Show | 79 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.237-5599C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020019 | ||||||
| chr17:49020029
|
C | T | 1 | a0001c0001t0006g0171 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.237-5589C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020029 | ||||||
| chr17:49020138
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.237-5480C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020138 | ||||||
| chr17:49020233
|
A | G | 6 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0110others(3): Show | 6 | HG02040.hp1 HG02257.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-5385A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020233 | ||||||
| chr17:49020556
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.237-5062A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49020556 | ||||||
| chr17:49020970
|
TA | T | 206 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0082others(203): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.237-4629delA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49020970 | |||||
| chr17:49020970
|
TAA | T | 15 | a0001c0001t0001g0298a0001c0001t0002g0003a0001c0001t0002g0004others(12): Show | 15 | HG01069.hp1 HG01257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-4630_237-4629d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49020970 | |||||
| chr17:49021030
|
C | A | 15 | a0001c0001t0007g0202a0001c0001t0007g0203a0001c0001t0007g0204others(12): Show | 15 | HG00639.hp2 HG00741.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-4588C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49021030 | ||||||
| chr17:49021056
|
C | T | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-4562C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49021056 | ||||||
| chr17:49021159
|
A | G | 14 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.237-4459A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49021159 | ||||||
| chr17:49021236
|
G | T | 1 | a0001c0001t0028g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.237-4382G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49021236 | ||||||
| chr17:49021315
|
C | G | 1 | a0001c0001t0071g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.237-4303C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49021315 | ||||||
| chr17:49021994
|
G | T | 1 | a0001c0001t0004g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.237-3624G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49021994 | ||||||
| chr17:49022025
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0033others(1): Show | 4 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-3593C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022025 | ||||||
| chr17:49022055
|
G | A | 3 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274 | 3 | NA18951.hp2 NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.237-3563G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022055 | ||||||
| chr17:49022213
|
G | T | 9 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(6): Show | 9 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-3405G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022213 | ||||||
| chr17:49022240
|
T | A | 5 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-3378T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022240 | ||||||
| chr17:49022412
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.237-3206C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022412 | ||||||
| chr17:49022424
|
C | T | 1 | a0001c0001t0016g0045 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.237-3194C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022424 | ||||||
| chr17:49022431
|
T | C | 1 | a0001c0001t0010g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.237-3187T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022431 | ||||||
| chr17:49022433
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.237-3185G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022433 | ||||||
| chr17:49022612
|
C | G | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.237-3006C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022612 | ||||||
| chr17:49022754
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.237-2864C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022754 | ||||||
| chr17:49022879
|
G | A | 2 | a0001c0001t0007g0221a0001c0001t0026g0219 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.237-2739G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022879 | ||||||
| chr17:49022920
|
T | C | 1 | a0001c0001t0067g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.237-2698T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022920 | ||||||
| chr17:49022987
|
T | C | 38 | a0001c0001t0005g0146a0001c0001t0005g0152a0001c0001t0005g0154others(35): Show | 38 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.237-2631T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49022987 | ||||||
| chr17:49023064
|
T | G | 1 | a0001c0001t0003g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.237-2554T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49023064 | ||||||
| chr17:49023134
|
C | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-2484C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49023134 | ||||||
| chr17:49023424
|
G | C | 1 | a0001c0001t0004g0023 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.237-2194G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49023424 | ||||||
| chr17:49023446
|
C | CT | 9 | a0001c0001t0007g0202a0001c0001t0007g0203a0001c0001t0007g0204others(6): Show | 9 | HG00639.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-2172_237-2171i others(3): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49023446 | ||||||
| chr17:49023466
|
C | G | 2 | a0001c0001t0015g0001a0001c0001t0015g0055 | 2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.237-2152C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49023466 | ||||||
| chr17:49023477
|
T | A | 4 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0171others(1): Show | 4 | HG02155.hp1 NA19074.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-2141T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49023477 | ||||||
| chr17:49023692
|
T | G | 1 | a0003c0004t0001g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.237-1926T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49023692 | ||||||
| chr17:49024069
|
A | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.237-1549A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49024069 | ||||||
| chr17:49024083
|
A | AT | 98 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.237-1507dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49024083 | |||||
| chr17:49024083
|
A | ATT | 17 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0005g0146others(14): Show | 17 | HG00140.hp1 HG01123.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-1508_237-1507d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49024083 | |||||
| chr17:49024083
|
AT | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0162others(16): Show | 19 | HG00099.hp1 HG01169.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-1507delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49024083 | |||||
| chr17:49024083
|
ATTTTTTT | A | 6 | a0001c0001t0011g0255a0001c0001t0011g0258a0001c0001t0011g0259others(3): Show | 6 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-1513_237-1507d others(9): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49024083 | |||||
| chr17:49024222
|
C | T | 1 | a0001c0001t0054g0307 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.237-1396C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49024222 | ||||||
| chr17:49024224
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.237-1394C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49024224 | ||||||
| chr17:49024338
|
C | T | 9 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1280C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49024338 | ||||||
| chr17:49024426
|
G | A | 1 | a0001c0001t0029g0100 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.237-1192G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49024426 | ||||||
| chr17:49024627
|
G | A | 175 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.237-991G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49024627 | ||||||
| chr17:49024676
|
A | G | 17 | a0001c0001t0005g0146a0001c0001t0005g0152a0001c0001t0005g0154others(14): Show | 17 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-942A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49024676 | ||||||
| chr17:49025254
|
A | G | 1 | a0001c0001t0005g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.237-364A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025254 | ||||||
| chr17:49025308
|
AAC | A | 3 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0171 | 3 | NA19074.hp1 NA19087.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.237-308_237-307del others(2): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025308 | |||||
| chr17:49025311
|
AAAGT | A | 10 | a0001c0001t0009g0090a0001c0001t0009g0113a0001c0001t0009g0114others(7): Show | 10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-306_237-303del others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025311 | ||||||
| chr17:49025311
|
AAAGTGTG others(7): Show |
A | 1 | a0001c0001t0016g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.237-306_237-293del others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025311 | ||||||
| chr17:49025311
|
AAAGTGTG others(11): Show |
A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-306_237-289del others(18): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025311 | ||||||
| chr17:49025312
|
A | G | 4 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0171others(1): Show | 4 | HG04115.hp1 NA19074.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-306A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025312 | ||||||
| chr17:49025313
|
A | AGT | 71 | a0001c0001t0001g0062a0001c0001t0001g0082a0001c0001t0001g0096others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.237-262_237-261dup others(2): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
A | AGTGT | 64 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0057others(61): Show | 64 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.237-264_237-261dup others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
A | AGTGTGT | 52 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0162others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.237-266_237-261dup others(6): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
A | AGTGTGTG others(1): Show |
12 | a0001c0001t0002g0317a0001c0001t0003g0251a0001c0001t0003g0268others(9): Show | 12 | HG00408.hp2 HG00609.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-268_237-261dup others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0002g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.237-270_237-261dup others(10): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0002g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.237-274_237-261dup others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
A | T | 5 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0171others(2): Show | 5 | HG00642.hp2 HG04115.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-305A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025313 | ||||||
| chr17:49025313
|
AGT | A | 43 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0318others(40): Show | 43 | HG01070.hp1 HG01123.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.237-262_237-261del others(2): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
AGTGT | A | 9 | a0001c0001t0001g0140a0001c0001t0002g0034a0001c0001t0002g0035others(6): Show | 9 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-264_237-261del others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
AGTGTGTG others(1): Show |
A | 3 | a0001c0001t0001g0147a0001c0001t0002g0011a0001c0001t0014g0010 | 3 | HG02896.hp1 HG02897.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.237-268_237-261del others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0071g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.237-270_237-261del others(10): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0006a0001c0001t0008g0193 | 2 | HG03017.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.237-272_237-261del others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025313
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.237-276_237-261del others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr17 | 49025313 | |||||
| chr17:49025357
|
T | TGTGTG | 3 | a0001c0001t0003g0265a0001c0001t0004g0026a0001c0001t0014g0118 | 3 | HG00423.hp1 HG03195.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.237-261_237-260ins others(5): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025357 | ||||||
| chr17:49025361
|
G | T | 1 | a0001c0001t0014g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.237-257G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025361 | ||||||
| chr17:49025441
|
C | T | 1 | a0001c0001t0065g0250 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.237-177C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 2/14 | chr17 | 49025441 | ||||||
| chr17:49025701
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.285+35A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | chr17 | 49025701 | ||||||
| chr17:49025760
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.285+94G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | chr17 | 49025760 | ||||||
| chr17:49025853
|
C | CT | 10 | a0001c0001t0004g0016a0001c0001t0006g0136a0001c0001t0006g0138others(7): Show | 10 | HG01934.hp1 HG02015.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+190dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr17 | 49025853 | |||||
| chr17:49025853
|
CTTTCTTT others(2): Show |
C | 55 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(52): Show | 55 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.285+191_285+199del others(9): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr17 | 49025853 | |||||
| chr17:49025856
|
TC | T | 5 | a0001c0001t0009g0071a0001c0001t0014g0130a0001c0001t0022g0092others(2): Show | 5 | HG01069.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+191delC | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | chr17 | 49025856 | ||||||
| chr17:49025857
|
C | T | 108 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(105): Show | 108 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.285+191C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | chr17 | 49025857 | ||||||
| chr17:49025857
|
CT | C | 19 | a0001c0001t0001g0098a0001c0001t0001g0226a0001c0001t0001g0236others(16): Show | 19 | HG00423.hp2 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.285+206delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr17 | 49025857 | |||||
| chr17:49025897
|
T | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.285+231T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | chr17 | 49025897 | ||||||
| chr17:49026078
|
C | T | 2 | a0001c0001t0008g0192a0001c0001t0008g0193 | 2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.286-388C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | chr17 | 49026078 | ||||||
| chr17:49026331
|
G | GACAGGTA others(3): Show |
1 | a0001c0001t0060g0111 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.286-133_286-124dup others(10): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr17 | 49026331 | |||||
| chr17:49026402
|
G | T | 13 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(10): Show | 13 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-64G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 3/14 | chr17 | 49026402 | ||||||
| chr17:49026619
|
TCCTTCCT others(9): Show |
T | 89 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(86): Show | 89 | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.337+114_337+129del others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026619 | |||||
| chr17:49026623
|
TCCTTCCT others(5): Show |
T | 1 | a0001c0001t0001g0237 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.337+122_337+133del others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026623 | |||||
| chr17:49026631
|
T | G | 3 | a0001c0001t0002g0121a0001c0001t0002g0178a0001c0006t0002g0179 | 3 | HG00735.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+114T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026631 | ||||||
| chr17:49026639
|
TCCTTCCT others(5): Show |
T | 1 | a0001c0001t0015g0001 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.337+134_337+145del others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026639 | |||||
| chr17:49026643
|
T | G | 79 | a0001c0001t0002g0121a0001c0001t0002g0178a0001c0001t0004g0014others(76): Show | 79 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.337+126T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026643 | ||||||
| chr17:49026647
|
G | T | 3 | a0001c0001t0002g0121a0001c0001t0002g0178a0001c0006t0002g0179 | 3 | HG00735.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+130G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026647 | ||||||
| chr17:49026651
|
G | T | 1 | a0001c0001t0010g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.337+134G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026651 | ||||||
| chr17:49026655
|
TCCTGCCT others(25): Show |
T | 1 | a0001c0001t0002g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.337+142_337+173del others(32): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026655 | |||||
| chr17:49026659
|
G | T | 2 | a0001c0001t0002g0178a0001c0006t0002g0179 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+142G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026659 | ||||||
| chr17:49026663
|
T | G | 2 | a0001c0001t0002g0178a0001c0006t0002g0179 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+146T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026663 | ||||||
| chr17:49026667
|
G | T | 2 | a0001c0001t0002g0178a0001c0006t0002g0179 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+150G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026667 | ||||||
| chr17:49026671
|
T | G | 2 | a0001c0001t0002g0178a0001c0006t0002g0179 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+154T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026671 | ||||||
| chr17:49026671
|
T | TCCTGCCT others(9): Show |
1 | a0001c0001t0027g0315 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.337+157_337+158ins others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026671 | |||||
| chr17:49026671
|
TCCTTCCT others(1): Show |
T | 93 | a0001c0001t0001g0151a0001c0001t0001g0298a0001c0001t0002g0003others(90): Show | 93 | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.337+198_337+205del others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026671 | |||||
| chr17:49026671
|
TCCTTCCT others(9): Show |
T | 31 | a0001c0001t0003g0205a0001c0001t0003g0218a0001c0001t0003g0233others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.337+190_337+205del others(16): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026671 | |||||
| chr17:49026707
|
TCCTGCCT others(5): Show |
T | 34 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(31): Show | 34 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.337+206_337+217del others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026707 | |||||
| chr17:49026727
|
TCCTGCCT others(5): Show |
T | 55 | a0001c0001t0001g0057a0001c0001t0001g0085a0001c0001t0001g0096others(52): Show | 55 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.337+226_337+237del others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026727 | |||||
| chr17:49026739
|
G | GCCTGCCT others(1): Show |
34 | a0001c0001t0001g0306a0001c0001t0004g0014a0001c0001t0004g0015others(31): Show | 34 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.337+243_337+250dup others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026739 | |||||
| chr17:49026739
|
GCCTGCCT others(1): Show |
G | 15 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0166others(12): Show | 15 | HG01081.hp1 HG01515.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.337+243_337+250del others(8): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49026739 | |||||
| chr17:49026944
|
C | T | 1 | a0001c0001t0071g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+427C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49026944 | ||||||
| chr17:49027070
|
A | T | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.337+553A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027070 | ||||||
| chr17:49027105
|
G | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.337+588G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027105 | ||||||
| chr17:49027245
|
G | A | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.337+728G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027245 | ||||||
| chr17:49027421
|
T | C | 1 | a0001c0001t0018g0161 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.337+904T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027421 | ||||||
| chr17:49027553
|
G | C | 1 | a0001c0001t0002g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.337+1036G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027553 | ||||||
| chr17:49027634
|
C | T | 1 | a0001c0001t0003g0275 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.337+1117C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027634 | ||||||
| chr17:49027668
|
C | T | 2 | a0001c0001t0033g0044a0001c0001t0044g0039 | 2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.337+1151C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027668 | ||||||
| chr17:49027708
|
C | T | 1 | a0001c0001t0007g0231 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.337+1191C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027708 | ||||||
| chr17:49027777
|
G | A | 2 | a0001c0001t0002g0178a0001c0006t0002g0179 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+1260G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027777 | ||||||
| chr17:49027831
|
G | C | 1 | a0003c0004t0001g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.337+1314G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027831 | ||||||
| chr17:49027853
|
G | GA | 57 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0062others(54): Show | 57 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.337+1364dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49027853 | |||||
| chr17:49027853
|
G | GAA | 12 | a0001c0001t0001g0074a0001c0001t0001g0139a0001c0001t0001g0237others(9): Show | 12 | HG00609.hp1 HG01496.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.337+1363_337+1364d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49027853 | |||||
| chr17:49027853
|
GA | G | 70 | a0001c0001t0002g0036a0001c0001t0002g0052a0001c0001t0002g0077others(67): Show | 70 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.337+1364delA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49027853 | |||||
| chr17:49027853
|
GAA | G | 105 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(102): Show | 105 | HG00099.hp1 HG00558.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.337+1363_337+1364d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49027853 | |||||
| chr17:49027853
|
GAAAAAAA others(4): Show |
G | 2 | a0001c0001t0069g0054a0001c0001t0070g0049 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.337+1354_337+1364d others(13): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49027853 | |||||
| chr17:49027889
|
G | A | 2 | a0001c0001t0021g0081a0001c0001t0035g0228 | 2 | HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.337+1372G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49027889 | ||||||
| chr17:49028069
|
A | G | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.337+1552A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49028069 | ||||||
| chr17:49028096
|
A | G | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.337+1579A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49028096 | ||||||
| chr17:49028174
|
C | A | 1 | a0001c0001t0001g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.337+1657C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49028174 | ||||||
| chr17:49028721
|
C | T | 10 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.337+2204C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49028721 | ||||||
| chr17:49029094
|
C | T | 1 | a0001c0001t0013g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.337+2577C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029094 | ||||||
| chr17:49029125
|
C | T | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.337+2608C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029125 | ||||||
| chr17:49029149
|
T | C | 2 | a0001c0001t0010g0238a0001c0001t0010g0239 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.337+2632T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029149 | ||||||
| chr17:49029163
|
CT | C | 92 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(89): Show | 92 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.337+2648delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49029163 | |||||
| chr17:49029179
|
A | G | 1 | a0001c0001t0019g0180 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.337+2662A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029179 | ||||||
| chr17:49029340
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.338-2570C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029340 | ||||||
| chr17:49029446
|
A | T | 16 | a0001c0001t0001g0057a0001c0001t0001g0096a0001c0001t0001g0181others(13): Show | 16 | HG00738.hp1 HG01978.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.338-2464A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029446 | ||||||
| chr17:49029516
|
T | G | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.338-2394T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029516 | ||||||
| chr17:49029794
|
A | AT | 6 | a0001c0001t0003g0268a0001c0001t0005g0157a0001c0001t0007g0232others(3): Show | 6 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-2098dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49029794 | |||||
| chr17:49029794
|
AT | A | 15 | a0001c0001t0001g0082a0001c0001t0001g0165a0001c0001t0001g0229others(12): Show | 15 | HG01074.hp1 HG01516.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.338-2098delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49029794 | |||||
| chr17:49029928
|
G | T | 92 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(89): Show | 92 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.338-1982G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49029928 | ||||||
| chr17:49030114
|
C | A | 1 | a0001c0001t0011g0258 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.338-1796C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030114 | ||||||
| chr17:49030141
|
C | CT | 16 | a0001c0001t0001g0062a0001c0001t0001g0279a0001c0001t0001g0280others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.338-1751dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49030141 | |||||
| chr17:49030141
|
CT | C | 162 | a0001c0001t0001g0141a0001c0001t0001g0229a0001c0001t0002g0003others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.338-1751delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49030141 | |||||
| chr17:49030141
|
CTT | C | 7 | a0001c0001t0002g0037a0001c0001t0002g0185a0001c0001t0004g0023others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.338-1752_338-1751d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49030141 | |||||
| chr17:49030323
|
G | A | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.338-1587G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030323 | ||||||
| chr17:49030341
|
C | T | 2 | a0001c0001t0007g0203a0001c0001t0007g0204 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.338-1569C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030341 | ||||||
| chr17:49030386
|
C | T | 2 | a0001c0001t0027g0314a0001c0001t0027g0315 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.338-1524C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030386 | ||||||
| chr17:49030421
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.338-1489C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030421 | ||||||
| chr17:49030444
|
T | A | 1 | a0001c0001t0060g0111 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.338-1466T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030444 | ||||||
| chr17:49030548
|
AG | A | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.338-1360delG | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49030548 | |||||
| chr17:49030575
|
A | G | 1 | a0001c0001t0025g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.338-1335A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030575 | ||||||
| chr17:49030714
|
C | T | 1 | a0001c0001t0003g0205 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.338-1196C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030714 | ||||||
| chr17:49030741
|
C | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.338-1169C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030741 | ||||||
| chr17:49030769
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.338-1141A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030769 | ||||||
| chr17:49030920
|
G | A | 92 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(89): Show | 92 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.338-990G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030920 | ||||||
| chr17:49030965
|
G | T | 1 | a0001c0001t0005g0152 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.338-945G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49030965 | ||||||
| chr17:49031011
|
A | T | 1 | a0001c0001t0060g0111 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.338-899A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031011 | ||||||
| chr17:49031122
|
T | C | 1 | a0001c0001t0060g0111 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.338-788T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031122 | ||||||
| chr17:49031174
|
G | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.338-736G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031174 | ||||||
| chr17:49031377
|
A | G | 1 | a0001c0001t0062g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338-533A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031377 | ||||||
| chr17:49031383
|
G | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.338-527G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031383 | ||||||
| chr17:49031446
|
G | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.338-464G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031446 | ||||||
| chr17:49031478
|
T | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.338-432T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031478 | ||||||
| chr17:49031501
|
C | CT | 7 | a0001c0001t0008g0209a0001c0001t0008g0215a0001c0001t0008g0216others(4): Show | 7 | HG02280.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.338-396dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr17 | 49031501 | |||||
| chr17:49031593
|
A | G | 168 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.338-317A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031593 | ||||||
| chr17:49031653
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.338-257C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031653 | ||||||
| chr17:49031667
|
C | T | 74 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.338-243C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031667 | ||||||
| chr17:49031802
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.338-108C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031802 | ||||||
| chr17:49031830
|
G | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.338-80G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 4/14 | chr17 | 49031830 | ||||||
| chr17:49032006
|
TG | T | 89 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.401+42delG | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49032006 | |||||
| chr17:49032065
|
C | G | 74 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.401+92C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032065 | ||||||
| chr17:49032100
|
T | C | 1 | a0001c0001t0009g0113 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.401+127T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032100 | ||||||
| chr17:49032204
|
A | G | 1 | a0001c0001t0005g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.401+231A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032204 | ||||||
| chr17:49032293
|
C | T | 10 | a0001c0001t0009g0071a0001c0001t0009g0090a0001c0001t0011g0255others(7): Show | 10 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.401+320C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032293 | ||||||
| chr17:49032297
|
G | C | 1 | a0001c0001t0064g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.401+324G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032297 | ||||||
| chr17:49032457
|
CT | C | 76 | a0001c0001t0001g0043a0001c0001t0004g0014a0001c0001t0004g0015others(73): Show | 76 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.401+488delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49032457 | |||||
| chr17:49032636
|
C | T | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(87): Show | 90 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.401+663C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032636 | ||||||
| chr17:49032810
|
A | G | 16 | a0001c0001t0001g0162a0001c0001t0006g0163a0001c0001t0006g0164others(13): Show | 16 | HG01081.hp1 HG01515.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.401+837A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032810 | ||||||
| chr17:49032883
|
T | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.401+910T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032883 | ||||||
| chr17:49032933
|
A | C | 1 | a0001c0001t0009g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.401+960A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49032933 | ||||||
| chr17:49033351
|
A | AT | 27 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(24): Show | 27 | HG01081.hp1 HG01515.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.401+1386dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49033351 | |||||
| chr17:49033422
|
A | G | 13 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(10): Show | 13 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.401+1449A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49033422 | ||||||
| chr17:49033641
|
C | T | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.401+1668C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49033641 | ||||||
| chr17:49033696
|
C | T | 1 | a0001c0001t0011g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.401+1723C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49033696 | ||||||
| chr17:49033993
|
A | C | 2 | a0001c0001t0007g0202a0001c0001t0007g0211 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.401+2020A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49033993 | ||||||
| chr17:49034037
|
C | T | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.401+2064C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034037 | ||||||
| chr17:49034077
|
GC | G | 316 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0056others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.401+2111delC | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49034077 | |||||
| chr17:49034115
|
C | CT | 35 | a0001c0001t0001g0200a0001c0001t0001g0279a0001c0001t0002g0035others(32): Show | 35 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.401+2162dupT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49034115 | |||||
| chr17:49034115
|
C | CTT | 7 | a0001c0001t0027g0314a0001c0002t0002g0187a0001c0002t0002g0195others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.401+2161_401+2162d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49034115 | |||||
| chr17:49034115
|
CT | C | 13 | a0001c0001t0001g0062a0001c0001t0006g0166a0001c0001t0007g0202others(10): Show | 13 | HG01081.hp1 HG01358.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.401+2162delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49034115 | |||||
| chr17:49034115
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0069g0054a0001c0001t0070g0049 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.401+2151_401+2162d others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49034115 | |||||
| chr17:49034116
|
T | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0292a0001c0001t0001g0294others(4): Show | 7 | HG00735.hp1 HG00738.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.401+2143T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034116 | ||||||
| chr17:49034172
|
C | T | 1 | a0001c0001t0025g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.401+2199C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034172 | ||||||
| chr17:49034349
|
C | T | 1 | a0001c0001t0051g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.401+2376C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034349 | ||||||
| chr17:49034356
|
C | T | 317 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0056others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.401+2383C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034356 | ||||||
| chr17:49034377
|
C | T | 33 | a0001c0001t0003g0205a0001c0001t0003g0218a0001c0001t0003g0220others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.401+2404C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034377 | ||||||
| chr17:49034384
|
G | A | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.401+2411G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034384 | ||||||
| chr17:49034385
|
T | C | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.401+2412T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034385 | ||||||
| chr17:49034505
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.401+2532A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034505 | ||||||
| chr17:49034745
|
C | A | 72 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(69): Show | 72 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.401+2772C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034745 | ||||||
| chr17:49034746
|
ACAAAAAA others(3): Show |
A | 17 | a0001c0001t0001g0162a0001c0001t0006g0136a0001c0001t0006g0163others(14): Show | 17 | HG01081.hp1 HG01515.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.401+2774_401+2783d others(12): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034746 | ||||||
| chr17:49034747
|
C | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(132): Show | 135 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.401+2774C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034747 | ||||||
| chr17:49034750
|
A | AC | 16 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(13): Show | 16 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.401+2777_401+2778i others(3): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034750 | ||||||
| chr17:49034754
|
A | AC | 40 | a0001c0001t0001g0108a0001c0001t0004g0014a0001c0001t0004g0015others(37): Show | 40 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.401+2781_401+2782i others(3): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034754 | ||||||
| chr17:49034755
|
A | AAC | 12 | a0001c0001t0005g0146a0001c0001t0005g0154a0001c0001t0005g0155others(9): Show | 12 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.401+2782_401+2783i others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034755 | ||||||
| chr17:49034755
|
A | AACAAAAA others(5): Show |
1 | a0001c0001t0005g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.401+2782_401+2783i others(14): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034755 | ||||||
| chr17:49034755
|
A | C | 64 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(61): Show | 64 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.401+2782A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034755 | ||||||
| chr17:49034756
|
C | A | 120 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.401+2783C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034756 | ||||||
| chr17:49034756
|
C | CAA | 7 | a0001c0001t0004g0063a0001c0001t0004g0290a0001c0001t0010g0240others(4): Show | 7 | HG02015.hp1 HG02074.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.401+2790_401+2791d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49034756 | |||||
| chr17:49034759
|
A | AC | 17 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(14): Show | 17 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.401+2786_401+2787i others(3): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034759 | ||||||
| chr17:49034759
|
A | C | 1 | a0001c0001t0071g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.401+2786A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034759 | ||||||
| chr17:49034762
|
A | C | 1 | a0001c0001t0071g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.401+2789A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034762 | ||||||
| chr17:49034763
|
A | C | 15 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(12): Show | 15 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.401+2790A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034763 | ||||||
| chr17:49034765
|
C | A | 18 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.401+2792C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034765 | ||||||
| chr17:49034774
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.401+2801C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034774 | ||||||
| chr17:49034775
|
G | A | 1 | a0001c0001t0029g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.401+2802G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49034775 | ||||||
| chr17:49035021
|
G | A | 2 | a0001c0001t0069g0054a0001c0001t0070g0049 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.401+3048G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035021 | ||||||
| chr17:49035046
|
C | T | 75 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.401+3073C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035046 | ||||||
| chr17:49035055
|
A | G | 1 | a0001c0001t0041g0127 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.401+3082A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035055 | ||||||
| chr17:49035212
|
A | G | 1 | a0001c0001t0058g0112 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.402-2956A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035212 | ||||||
| chr17:49035311
|
C | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402-2857C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035311 | ||||||
| chr17:49035329
|
C | T | 1 | a0001c0001t0065g0250 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.402-2839C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035329 | ||||||
| chr17:49035411
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.402-2757C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035411 | ||||||
| chr17:49035647
|
G | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402-2521G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035647 | ||||||
| chr17:49035650
|
G | A | 1 | a0001c0001t0064g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.402-2518G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035650 | ||||||
| chr17:49035952
|
C | A | 39 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(36): Show | 39 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.402-2216C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49035952 | ||||||
| chr17:49036050
|
A | G | 316 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0056others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.402-2118A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49036050 | ||||||
| chr17:49036078
|
GCGGGGTT others(13): Show |
G | 38 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.402-2066_402-2047d others(22): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49036078 | |||||
| chr17:49036121
|
G | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402-2047G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49036121 | ||||||
| chr17:49036476
|
T | TA | 14 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.402-1683dupA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49036476 | |||||
| chr17:49036671
|
T | C | 186 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(183): Show | 186 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.402-1497T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49036671 | ||||||
| chr17:49036715
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.402-1453C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49036715 | ||||||
| chr17:49036942
|
AAAAAC | A | 74 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.402-1211_402-1207d others(7): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr17 | 49036942 | |||||
| chr17:49036953
|
A | G | 1 | a0001c0001t0015g0001 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.402-1215A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49036953 | ||||||
| chr17:49037030
|
A | G | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.402-1138A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037030 | ||||||
| chr17:49037120
|
C | T | 38 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.402-1048C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037120 | ||||||
| chr17:49037125
|
C | T | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.402-1043C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037125 | ||||||
| chr17:49037153
|
T | C | 16 | a0001c0001t0001g0057a0001c0001t0001g0096a0001c0001t0001g0181others(13): Show | 16 | HG00738.hp1 HG01978.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.402-1015T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037153 | ||||||
| chr17:49037322
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402-846T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037322 | ||||||
| chr17:49037388
|
G | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402-780G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037388 | ||||||
| chr17:49037676
|
C | T | 74 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.402-492C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037676 | ||||||
| chr17:49037761
|
T | C | 1 | a0001c0001t0027g0315 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.402-407T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49037761 | ||||||
| chr17:49038038
|
T | G | 13 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(10): Show | 13 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.402-130T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 5/14 | chr17 | 49038038 | ||||||
| chr17:49038568
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.683+119T>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038568 | ||||||
| chr17:49038698
|
G | C | 1 | a0001c0001t0005g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.683+249G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038698 | ||||||
| chr17:49038845
|
C | T | 1 | a0001c0001t0004g0176 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.683+396C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038845 | ||||||
| chr17:49038873
|
AAT | A | 72 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(69): Show | 72 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.683+427_683+428del others(2): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr17 | 49038873 | |||||
| chr17:49038874
|
A | ATCTTT | 14 | a0001c0001t0008g0190a0001c0001t0008g0192a0001c0001t0008g0193others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.683+426_683+427ins others(5): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr17 | 49038874 | |||||
| chr17:49038874
|
A | ATCTTTTT others(18): Show |
1 | a0001c0001t0069g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.683+426_683+427ins others(25): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr17 | 49038874 | |||||
| chr17:49038874
|
A | ATCTTTTT others(19): Show |
1 | a0001c0001t0070g0049 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.683+426_683+427ins others(26): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr17 | 49038874 | |||||
| chr17:49038875
|
T | TC | 55 | a0001c0001t0001g0229a0001c0001t0002g0037a0001c0001t0002g0040others(52): Show | 55 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.683+426_683+427ins others(1): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038875 | ||||||
| chr17:49038875
|
TA | T | 3 | a0001c0001t0006g0172a0001c0001t0014g0010a0001c0001t0025g0068 | 3 | HG02897.hp2 HG03704.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.683+427delA | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038875 | ||||||
| chr17:49038876
|
A | C | 166 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0056others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.683+427A>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038876 | ||||||
| chr17:49038876
|
A | T | 75 | a0001c0001t0001g0229a0001c0001t0002g0037a0001c0001t0002g0040others(72): Show | 75 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.683+427A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038876 | ||||||
| chr17:49038877
|
T | C | 3 | a0001c0001t0006g0172a0001c0001t0014g0010a0001c0001t0025g0068 | 3 | HG02897.hp2 HG03704.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.683+428T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038877 | ||||||
| chr17:49038878
|
T | C | 72 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(69): Show | 72 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.683+429T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038878 | ||||||
| chr17:49038879
|
T | C | 1 | a0001c0003t0028g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.683+430T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038879 | ||||||
| chr17:49038883
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.683+434T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038883 | ||||||
| chr17:49038993
|
T | C | 1 | a0001c0001t0003g0272 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.683+544T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49038993 | ||||||
| chr17:49039002
|
C | T | 1 | a0001c0001t0025g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.683+553C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039002 | ||||||
| chr17:49039136
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.683+687A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039136 | ||||||
| chr17:49039140
|
T | C | 1 | a0001c0001t0013g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.683+691T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039140 | ||||||
| chr17:49039185
|
A | G | 1 | a0001c0001t0013g0120 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.683+736A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039185 | ||||||
| chr17:49039407
|
C | A | 1 | a0001c0001t0003g0263 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.684-550C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039407 | ||||||
| chr17:49039458
|
C | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.684-499C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039458 | ||||||
| chr17:49039533
|
T | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.684-424T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039533 | ||||||
| chr17:49039537
|
G | C | 1 | a0001c0001t0005g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.684-420G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039537 | ||||||
| chr17:49039568
|
G | A | 1 | a0001c0001t0004g0282 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.684-389G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039568 | ||||||
| chr17:49039598
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.684-359T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039598 | ||||||
| chr17:49039658
|
C | CTCAA | 3 | a0001c0001t0018g0159a0001c0001t0018g0161a0001c0001t0036g0160 | 3 | NA18947.hp2 NA18978.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.684-298_684-295dup others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr17 | 49039658 | |||||
| chr17:49039867
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.684-90C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 6/14 | chr17 | 49039867 | ||||||
| chr17:49040135
|
A | G | 2 | a0001c0001t0061g0288a0001c0008t0001g0153 | 2 | HG00558.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.818+44A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49040135 | ||||||
| chr17:49040327
|
C | T | 1 | a0001c0001t0057g0150 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.818+236C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49040327 | ||||||
| chr17:49040413
|
C | T | 92 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(89): Show | 92 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.818+322C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49040413 | ||||||
| chr17:49040601
|
G | A | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.818+510G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49040601 | ||||||
| chr17:49040726
|
A | G | 75 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.818+635A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49040726 | ||||||
| chr17:49040754
|
C | T | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.819-624C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49040754 | ||||||
| chr17:49041030
|
T | C | 1 | a0001c0001t0057g0150 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.819-348T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49041030 | ||||||
| chr17:49041044
|
C | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.819-334C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49041044 | ||||||
| chr17:49041100
|
G | A | 3 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274 | 3 | NA18951.hp2 NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.819-278G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49041100 | ||||||
| chr17:49041161
|
A | G | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.819-217A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 7/14 | chr17 | 49041161 | ||||||
| chr17:49041633
|
G | C | 8 | a0001c0001t0004g0016a0001c0001t0004g0018a0001c0001t0004g0019others(5): Show | 8 | HG00621.hp1 HG01255.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.941+133G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 8/14 | chr17 | 49041633 | ||||||
| chr17:49041773
|
G | A | 18 | a0001c0001t0009g0087a0001c0001t0009g0088a0001c0001t0009g0113others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.941+273G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 8/14 | chr17 | 49041773 | ||||||
| chr17:49042063
|
C | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.942-179C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 8/14 | chr17 | 49042063 | ||||||
| chr17:49042098
|
C | G | 2 | a0001c0001t0060g0111a0001c0003t0028g0156 | 2 | NA18946.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.942-144C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 8/14 | chr17 | 49042098 | ||||||
| chr17:49042470
|
C | T | 77 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1077+93C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 9/14 | chr17 | 49042470 | ||||||
| chr17:49043041
|
C | T | 1 | a0001c0001t0070g0049 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1078-387C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 9/14 | chr17 | 49043041 | ||||||
| chr17:49043105
|
A | G | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.1078-323A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 9/14 | chr17 | 49043105 | ||||||
| chr17:49043124
|
G | A | 1 | a0001c0001t0013g0224 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1078-304G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 9/14 | chr17 | 49043124 | ||||||
| chr17:49043414
|
T | C | 187 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(184): Show | 187 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1078-14T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 9/14 | chr17 | 49043414 | ||||||
| chr17:49043424
|
C | T | 1 | a0001c0001t0003g0275 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.1078-4C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 9/14 | chr17 | 49043424 | ||||||
| chr17:49043707
|
C | T | 1 | a0001c0001t0002g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1200+157C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 10/14 | chr17 | 49043707 | ||||||
| chr17:49043920
|
G | T | 2 | a0001c0001t0017g0148a0001c0001t0017g0276 | 2 | NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1201-47G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 10/14 | chr17 | 49043920 | ||||||
| chr17:49043928
|
A | G | 2 | a0001c0001t0012g0086a0001c0001t0052g0075 | 2 | NA18949.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1201-39A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 10/14 | chr17 | 49043928 | ||||||
| chr17:49043934
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1201-33G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 10/14 | chr17 | 49043934 | ||||||
| chr17:49043937
|
C | A | 2 | a0001c0001t0033g0044a0001c0001t0044g0039 | 2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1201-30C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 10/14 | chr17 | 49043937 | ||||||
| chr17:49044189
|
G | C | 31 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(28): Show | 31 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1320+103G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044189 | ||||||
| chr17:49044223
|
C | T | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1320+137C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044223 | ||||||
| chr17:49044230
|
C | T | 1 | a0001c0005t0003g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1320+144C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044230 | ||||||
| chr17:49044503
|
C | T | 4 | a0001c0001t0010g0046a0001c0001t0010g0047a0001c0001t0010g0048others(1): Show | 4 | NA19058.hp2 NA19067.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1320+417C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044503 | ||||||
| chr17:49044566
|
G | A | 1 | a0001c0001t0042g0051 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1321-425G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044566 | ||||||
| chr17:49044591
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1321-400G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044591 | ||||||
| chr17:49044652
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1321-339C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044652 | ||||||
| chr17:49044664
|
T | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 6 | HG01099.hp1 HG02040.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1321-327T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044664 | ||||||
| chr17:49044770
|
G | C | 1 | a0001c0001t0013g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1321-221G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044770 | ||||||
| chr17:49044785
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1321-206A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044785 | ||||||
| chr17:49044827
|
G | A | 4 | a0001c0001t0016g0045a0001c0001t0016g0116a0001c0001t0016g0117others(1): Show | 4 | HG02572.hp2 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321-164G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044827 | ||||||
| chr17:49044827
|
G | T | 2 | a0001c0001t0008g0209a0001c0001t0008g0217 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1321-164G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 11/14 | chr17 | 49044827 | ||||||
| chr17:49045125
|
C | T | 6 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0107others(3): Show | 6 | NA18947.hp1 NA18956.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395+60C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 12/14 | chr17 | 49045125 | ||||||
| chr17:49045130
|
G | A | 5 | a0001c0001t0005g0281a0001c0001t0005g0309a0001c0001t0005g0310others(2): Show | 5 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+65G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 12/14 | chr17 | 49045130 | ||||||
| chr17:49045156
|
C | T | 2 | a0001c0001t0069g0054a0001c0001t0070g0049 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1395+91C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 12/14 | chr17 | 49045156 | ||||||
| chr17:49045163
|
T | C | 93 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(90): Show | 93 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.1395+98T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 12/14 | chr17 | 49045163 | ||||||
| chr17:49045580
|
T | C | 170 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(167): Show | 170 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1396-310T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 12/14 | chr17 | 49045580 | ||||||
| chr17:49046061
|
T | C | 62 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(59): Show | 62 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.1527+40T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 13/14 | chr17 | 49046061 | ||||||
| chr17:49046390
|
C | T | 3 | a0001c0001t0002g0185a0001c0001t0020g0038a0001c0001t0020g0042 | 3 | HG01167.hp1 HG01169.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1641+17C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046390 | ||||||
| chr17:49046420
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1641+47G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046420 | ||||||
| chr17:49046421
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1641+48A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046421 | ||||||
| chr17:49046462
|
G | A | 12 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0079others(9): Show | 12 | HG00738.hp2 HG01070.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1641+89G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046462 | ||||||
| chr17:49046523
|
T | A | 1 | a0001c0001t0004g0021 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1641+150T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046523 | ||||||
| chr17:49046525
|
C | G | 38 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1641+152C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046525 | ||||||
| chr17:49046606
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1641+233A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046606 | ||||||
| chr17:49046635
|
A | G | 18 | a0001c0001t0005g0146a0001c0001t0005g0152a0001c0001t0005g0154others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1641+262A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046635 | ||||||
| chr17:49046663
|
G | A | 34 | a0001c0001t0005g0146a0001c0001t0005g0152a0001c0001t0005g0154others(31): Show | 34 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1641+290G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046663 | ||||||
| chr17:49046666
|
A | AAT | 14 | a0001c0001t0002g0037a0001c0001t0002g0040a0001c0001t0002g0050others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1641+306_1641+307d others(4): Show |
IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr17 | 49046666 | |||||
| chr17:49046752
|
A | G | 1 | a0001c0001t0070g0049 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1641+379A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046752 | ||||||
| chr17:49046772
|
C | T | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1641+399C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046772 | ||||||
| chr17:49046957
|
C | G | 3 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0171 | 3 | NA19074.hp1 NA19087.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1641+584C>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49046957 | ||||||
| chr17:49047074
|
C | A | 1 | a0001c0001t0003g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1641+701C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047074 | ||||||
| chr17:49047130
|
T | C | 13 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(10): Show | 13 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1641+757T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047130 | ||||||
| chr17:49047266
|
G | A | 17 | a0001c0001t0005g0146a0001c0001t0005g0152a0001c0001t0005g0154others(14): Show | 17 | HG00140.hp1 HG01123.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1641+893G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047266 | ||||||
| chr17:49047290
|
A | G | 5 | a0001c0001t0003g0205a0001c0001t0003g0262a0001c0001t0003g0266others(2): Show | 5 | HG00099.hp2 HG00140.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1641+917A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047290 | ||||||
| chr17:49047337
|
A | G | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1641+964A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047337 | ||||||
| chr17:49047398
|
T | C | 11 | a0001c0001t0009g0071a0001c0001t0009g0087a0001c0001t0009g0088others(8): Show | 11 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1641+1025T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047398 | ||||||
| chr17:49047418
|
T | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1641+1045T>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047418 | ||||||
| chr17:49047419
|
G | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1641+1046G>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047419 | ||||||
| chr17:49047517
|
G | A | 1 | a0001c0001t0038g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1641+1144G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047517 | ||||||
| chr17:49047529
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1641+1156A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047529 | ||||||
| chr17:49047540
|
G | T | 169 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1641+1167G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047540 | ||||||
| chr17:49047555
|
T | C | 1 | a0001c0001t0045g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1641+1182T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047555 | ||||||
| chr17:49047595
|
A | G | 31 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(28): Show | 31 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1641+1222A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047595 | ||||||
| chr17:49047714
|
CT | C | 78 | a0001c0001t0001g0162a0001c0001t0001g0306a0001c0001t0004g0014others(75): Show | 78 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1641+1358delT | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr17 | 49047714 | |||||
| chr17:49047857
|
G | A | 1 | a0001c0002t0043g0183 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1641+1484G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047857 | ||||||
| chr17:49047959
|
C | T | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0192others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1642-1393C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49047959 | ||||||
| chr17:49048010
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1642-1342C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048010 | ||||||
| chr17:49048017
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0208a0001c0001t0010g0124 | 3 | HG02486.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1642-1335C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048017 | ||||||
| chr17:49048226
|
C | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1642-1126C>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048226 | ||||||
| chr17:49048313
|
C | T | 2 | a0001c0001t0022g0091a0001c0001t0022g0092 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1642-1039C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048313 | ||||||
| chr17:49048399
|
C | T | 2 | a0001c0001t0031g0064a0001c0001t0031g0065 | 2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1642-953C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048399 | ||||||
| chr17:49048475
|
A | T | 2 | a0001c0001t0060g0111a0001c0003t0028g0156 | 2 | NA18946.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1642-877A>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048475 | ||||||
| chr17:49048620
|
T | C | 171 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0004others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1642-732T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048620 | ||||||
| chr17:49048622
|
T | C | 38 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1642-730T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048622 | ||||||
| chr17:49048630
|
G | A | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1642-722G>A | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048630 | ||||||
| chr17:49048716
|
A | G | 1 | a0001c0001t0013g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1642-636A>G | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048716 | ||||||
| chr17:49048775
|
G | T | 2 | a0001c0001t0033g0044a0001c0001t0044g0039 | 2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1642-577G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048775 | ||||||
| chr17:49048939
|
C | T | 3 | a0001c0001t0005g0309a0001c0001t0005g0310a0001c0001t0005g0311 | 3 | HG01123.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1642-413C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49048939 | ||||||
| chr17:49049139
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0033others(1): Show | 4 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1642-213C>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49049139 | ||||||
| chr17:49049315
|
G | T | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1642-37G>T | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49049315 | ||||||
| chr17:49049329
|
T | C | 1 | a0001c0001t0068g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1642-23T>C | IGF2BP1 | ENSG00000159217.10 | transcript | ENST00000290341.8 | protein_coding | 14/14 | chr17 | 49049329 |