Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3479 |
|---|---|
| ensemblid | ENSG00000017427.17 |
| hgncid | 5464 |
| symbol | IGF1 |
| name | insulin like growth factor 1 |
| refseq_nuc | NM_000618.5 |
| refseq_prot | NP_000609.1 |
| ensembl_nuc | ENST00000337514.11 |
| ensembl_prot | ENSP00000337612.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 102395874 |
| end | 102480563 |
| strand | - |
| ver | v1.2 |
| region | chr12:102395874-102480563 |
| region5000 | chr12:102390874-102485563 |
| regionname0 | IGF1_chr12_102395874_102480563 |
| regionname5000 | IGF1_chr12_102390874_102485563 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 153 | 359 | 83 | 68 | 158 | 14 | 34 | 118 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0002 | 0/0 | 153 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 462 | 358 | 82 | 68 | 158 | 14 | 34 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| c0002 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| c0003 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 6818 | 59 | 16 | 16 | 19 | 2 | 5 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0002 | 0/0 | 6819 | 43 | 12 | 5 | 18 | 4 | 4 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0003 | 0/0 | 6820 | 37 | 0 | 4 | 31 | 2 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0004 | 0/0 | 6818 | 37 | 0 | 9 | 27 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0005 | 1/0 | 6816 | 9 | 3 | 3 | 0 | 1 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0006 | 0/0 | 6820 | 8 | 1 | 0 | 6 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0007 | 0/0 | 6822 | 6 | 1 | 1 | 4 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0008 | 0/0 | 6820 | 6 | 0 | 0 | 2 | 0 | 4 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0009 | 0/0 | 6828 | 4 | 0 | 0 | 4 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0010 | 0/0 | 6820 | 4 | 4 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0011 | 0/0 | 6818 | 4 | 0 | 0 | 4 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0012 | 0/0 | 6821 | 4 | 3 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0013 | 0/0 | 6817 | 4 | 3 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0014 | 0/0 | 6817 | 4 | 0 | 1 | 2 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0015 | 0/0 | 6819 | 4 | 0 | 1 | 3 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0016 | 0/0 | 6815 | 4 | 4 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0017 | 0/0 | 6820 | 3 | 0 | 0 | 1 | 0 | 2 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0018 | 0/0 | 6818 | 3 | 0 | 0 | 2 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0019 | 0/0 | 6816 | 3 | 3 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0020 | 0/0 | 6815 | 3 | 2 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0021 | 0/0 | 6820 | 3 | 0 | 0 | 3 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0022 | 0/0 | 6815 | 3 | 1 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0023 | 0/0 | 6819 | 3 | 0 | 3 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0024 | 0/0 | 6821 | 3 | 0 | 1 | 0 | 0 | 2 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0025 | 0/0 | 6820 | 3 | 0 | 2 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0026 | 0/0 | 6824 | 3 | 1 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0027 | 0/0 | 6818 | 3 | 0 | 2 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0028 | 0/0 | 6817 | 3 | 0 | 2 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0029 | 0/0 | 6818 | 2 | 0 | 1 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0030 | 0/0 | 6819 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0031 | 0/0 | 6820 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0032 | 0/0 | 6818 | 2 | 0 | 0 | 1 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0033 | 0/0 | 6822 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0034 | 0/0 | 6816 | 2 | 2 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0035 | 0/0 | 6818 | 2 | 1 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0036 | 0/0 | 6814 | 2 | 2 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0037 | 0/0 | 6822 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0038 | 0/0 | 6822 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0039 | 0/0 | 6819 | 2 | 0 | 1 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0040 | 0/0 | 6822 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0041 | 0/0 | 6817 | 2 | 0 | 1 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0042 | 0/0 | 6818 | 2 | 2 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0043 | 0/0 | 6820 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0044 | 0/0 | 6818 | 2 | 0 | 0 | 0 | 2 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0045 | 0/0 | 6815 | 2 | 0 | 1 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0046 | 0/0 | 6819 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0047 | 0/0 | 6820 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0048 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0049 | 0/0 | 6818 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0050 | 0/0 | 6825 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0051 | 0/0 | 6818 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0052 | 0/0 | 6818 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0053 | 0/0 | 6825 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0054 | 0/0 | 6821 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0055 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0056 | 0/0 | 6824 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0057 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0058 | 0/0 | 6821 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0059 | 0/0 | 6818 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0060 | 0/0 | 6816 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0061 | 0/0 | 6815 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0062 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0063 | 0/0 | 6815 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0064 | 0/0 | 6818 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0065 | 0/0 | 6814 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0066 | 0/0 | 6823 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0067 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0068 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0069 | 0/0 | 6816 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0070 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0071 | 0/0 | 6819 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0072 | 0/0 | 6820 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0073 | 0/0 | 6818 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0074 | 0/0 | 6818 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0075 | 0/0 | 6818 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0076 | 0/0 | 6814 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0077 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0078 | 0/0 | 6831 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0079 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0080 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0081 | 0/0 | 6817 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0082 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0083 | 0/0 | 6818 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0084 | 0/0 | 6817 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0085 | 0/0 | 6818 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0086 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0087 | 0/0 | 6816 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0088 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0089 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0090 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0091 | 0/0 | 6818 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0092 | 0/0 | 6813 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0093 | 0/0 | 6828 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0094 | 0/0 | 6820 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0095 | 0/0 | 6818 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0096 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| t0097 | 0/0 | 6818 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 462 | 358 | 82 | 68 | 158 | 14 | 34 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0002 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0002c0003 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7279 | 59 | 16 | 16 | 19 | 2 | 5 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0002 | 0/0 | 7280 | 43 | 12 | 5 | 18 | 4 | 4 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0003 | 0/0 | 7281 | 37 | 0 | 4 | 31 | 2 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0004 | 0/0 | 7279 | 37 | 0 | 9 | 27 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0005 | 1/0 | 7277 | 9 | 3 | 3 | 0 | 1 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0006 | 0/0 | 7281 | 8 | 1 | 0 | 6 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0007 | 0/0 | 7283 | 6 | 1 | 1 | 4 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0008 | 0/0 | 7281 | 6 | 0 | 0 | 2 | 0 | 4 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0009 | 0/0 | 7289 | 4 | 0 | 0 | 4 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0010 | 0/0 | 7281 | 4 | 4 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0011 | 0/0 | 7279 | 4 | 0 | 0 | 4 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0012 | 0/0 | 7282 | 4 | 3 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0013 | 0/0 | 7278 | 4 | 3 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0014 | 0/0 | 7278 | 4 | 0 | 1 | 2 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0015 | 0/0 | 7280 | 4 | 0 | 1 | 3 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0016 | 0/0 | 7276 | 4 | 4 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0017 | 0/0 | 7281 | 3 | 0 | 0 | 1 | 0 | 2 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0018 | 0/0 | 7279 | 3 | 0 | 0 | 2 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0019 | 0/0 | 7277 | 3 | 3 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0020 | 0/0 | 7276 | 3 | 2 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0021 | 0/0 | 7281 | 3 | 0 | 0 | 3 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0022 | 0/0 | 7276 | 3 | 1 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0023 | 0/0 | 7280 | 3 | 0 | 3 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0024 | 0/0 | 7282 | 3 | 0 | 1 | 0 | 0 | 2 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0025 | 0/0 | 7281 | 3 | 0 | 2 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0026 | 0/0 | 7285 | 3 | 1 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0027 | 0/0 | 7279 | 3 | 0 | 2 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0028 | 0/0 | 7278 | 3 | 0 | 2 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0029 | 0/0 | 7279 | 2 | 0 | 1 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0030 | 0/0 | 7280 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0031 | 0/0 | 7281 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0032 | 0/0 | 7279 | 2 | 0 | 0 | 1 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0033 | 0/0 | 7283 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0034 | 0/0 | 7277 | 2 | 2 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0035 | 0/0 | 7279 | 2 | 1 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0036 | 0/0 | 7275 | 2 | 2 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0037 | 0/0 | 7283 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0038 | 0/0 | 7283 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0039 | 0/0 | 7280 | 2 | 0 | 1 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0040 | 0/0 | 7283 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0041 | 0/0 | 7278 | 2 | 0 | 1 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0042 | 0/0 | 7279 | 2 | 2 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0043 | 0/0 | 7281 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0044 | 0/0 | 7279 | 2 | 0 | 0 | 0 | 2 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0045 | 0/0 | 7276 | 2 | 0 | 1 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0046 | 0/0 | 7280 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0047 | 0/0 | 7281 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0048 | 0/0 | 7283 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0049 | 0/0 | 7279 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0050 | 0/0 | 7286 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0051 | 0/0 | 7279 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0052 | 0/0 | 7279 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0053 | 0/0 | 7286 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0054 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0055 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0056 | 0/0 | 7285 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0057 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0058 | 0/0 | 7282 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0059 | 0/0 | 7279 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0060 | 0/0 | 7277 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0061 | 0/0 | 7276 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0062 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0064 | 0/0 | 7279 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0065 | 0/0 | 7275 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0066 | 0/0 | 7284 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0067 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0068 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0069 | 0/0 | 7277 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0070 | 0/0 | 7287 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0071 | 0/0 | 7280 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0072 | 0/0 | 7281 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0073 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0074 | 0/0 | 7279 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0075 | 0/0 | 7279 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0076 | 0/0 | 7275 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0077 | 0/0 | 7295 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0078 | 0/0 | 7292 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0080 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0081 | 0/0 | 7278 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0082 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0083 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0084 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0085 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0086 | 0/0 | 7283 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0087 | 0/0 | 7277 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0088 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0089 | 0/0 | 7280 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0090 | 0/0 | 7274 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0091 | 0/0 | 7279 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0092 | 0/0 | 7274 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0093 | 0/0 | 7289 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0094 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0095 | 0/0 | 7279 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0096 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0001t0097 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0001c0002t0079 | 0/0 | 7293 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| a0002c0003t0063 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | copy fasta | chr12 | 102390874 | 102485563 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0008g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0008g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0009g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0009g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0009g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0009g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0011g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0011g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0011g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0012g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0013g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0014g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0014g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0015g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0015g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0015g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0015g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0016g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0016g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0017g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0017g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0017g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0018g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0018g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0018g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0019g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0019g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0020g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0020g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0020g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0021g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0021g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0021g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0022g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0022g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0022g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0023g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0023g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0023g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0024g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0024g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0024g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0025g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0025g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0025g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0026g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0026g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0026g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0027g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0027g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0027g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0028g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0028g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0028g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0029g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0029g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0030g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0031g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0031g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0032g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0032g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0033g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0033g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0034g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0034g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0035g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0035g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0036g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0036g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0037g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0037g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0038g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0038g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0039g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0039g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0040g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0040g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0041g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0041g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0042g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0042g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0043g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0043g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0044g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0045g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0045g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0046g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0046g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0047g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0048g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0049g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0050g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0051g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0052g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0053g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0054g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0055g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0056g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0057g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0058g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0059g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0060g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0061g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0062g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0064g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0065g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0066g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0067g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0068g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0069g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0070g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0071g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0072g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0073g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0074g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0075g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0076g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0077g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0078g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0080g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0081g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0082g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0083g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0084g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0085g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0086g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0087g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0088g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0089g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0090g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0091g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0092g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0093g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0094g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0095g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0096g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0001t0097g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0001c0002t0079g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| a0002c0003t0063g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0081 | g0105 | EUR | GBR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0249 | EUR | GBR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | FIN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0251 | EUR | FIN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0092 | EUR | FIN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00408 | hp2 | a0001 | c0001 | t0031 | g0265 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00423 | hp1 | a0001 | c0001 | t0084 | g0300 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00558 | hp1 | a0001 | c0001 | t0015 | g0090 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00597 | hp1 | a0001 | c0001 | t0043 | g0214 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00639 | hp1 | a0001 | c0001 | t0030 | g0001 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0098 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00642 | hp2 | a0001 | c0001 | t0061 | g0055 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00733 | hp1 | a0001 | c0001 | t0029 | g0112 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0057 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG00741 | hp2 | a0001 | c0001 | t0015 | g0174 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0331 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01071 | hp1 | a0001 | c0001 | t0030 | g0001 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0332 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01074 | hp1 | a0001 | c0001 | t0025 | g0114 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0315 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01109 | hp1 | a0001 | c0001 | t0045 | g0019 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01167 | hp1 | a0001 | c0001 | t0023 | g0023 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01167 | hp2 | a0001 | c0001 | t0056 | g0011 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01168 | hp1 | a0001 | c0001 | t0038 | g0137 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01168 | hp2 | a0001 | c0001 | t0076 | g0115 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01169 | hp1 | a0001 | c0001 | t0038 | g0138 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01169 | hp2 | a0001 | c0001 | t0023 | g0022 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01192 | hp1 | a0001 | c0001 | t0028 | g0107 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01192 | hp2 | a0001 | c0001 | t0075 | g0143 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01243 | hp2 | a0001 | c0001 | t0052 | g0132 | AMR | PUR | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01257 | hp1 | a0001 | c0001 | t0026 | g0341 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01258 | hp2 | a0001 | c0001 | t0026 | g0342 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01346 | hp1 | a0001 | c0001 | t0027 | g0097 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0338 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0326 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01361 | hp2 | a0001 | c0001 | t0023 | g0043 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0207 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01515 | hp1 | a0001 | c0001 | t0092 | g0156 | EUR | IBS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0180 | EUR | IBS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01516 | hp2 | a0001 | c0001 | t0044 | g0004 | EUR | IBS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01517 | hp2 | a0001 | c0001 | t0044 | g0004 | EUR | IBS | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01884 | hp2 | a0001 | c0001 | t0089 | g0255 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01891 | hp1 | a0001 | c0001 | t0094 | g0007 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01928 | hp2 | a0001 | c0001 | t0024 | g0064 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0318 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01943 | hp2 | a0001 | c0001 | t0049 | g0127 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0352 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01952 | hp2 | a0001 | c0001 | t0041 | g0336 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01975 | hp1 | a0001 | c0001 | t0039 | g0133 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0335 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01978 | hp2 | a0001 | c0001 | t0027 | g0125 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01981 | hp2 | a0001 | c0001 | t0025 | g0096 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01993 | hp1 | a0001 | c0001 | t0091 | g0124 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0311 | AMR | PEL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0266 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02040 | hp2 | a0001 | c0001 | t0083 | g0296 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02080 | hp1 | a0001 | c0001 | t0022 | g0025 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0059 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02129 | hp1 | a0001 | c0001 | t0032 | g0252 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0302 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02135 | hp2 | a0001 | c0001 | t0085 | g0312 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02145 | hp2 | a0001 | c0001 | t0054 | g0229 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CDX | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CDX | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | CDX | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0231 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02258 | hp2 | a0001 | c0001 | t0070 | g0078 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0039 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02280 | hp2 | a0001 | c0001 | t0034 | g0146 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0045 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0261 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0179 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02622 | hp1 | a0001 | c0001 | t0067 | g0042 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0274 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02630 | hp2 | a0001 | c0001 | t0034 | g0201 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02683 | hp1 | a0001 | c0001 | t0053 | g0082 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0169 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02698 | hp1 | a0001 | c0001 | t0048 | g0128 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0291 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02717 | hp1 | a0001 | c0001 | t0077 | g0151 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02723 | hp1 | a0001 | c0001 | t0062 | g0254 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02723 | hp2 | a0001 | c0001 | t0068 | g0038 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02738 | hp2 | a0001 | c0001 | t0050 | g0212 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02818 | hp1 | a0001 | c0001 | t0020 | g0079 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02818 | hp2 | a0001 | c0001 | t0090 | g0021 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02886 | hp1 | a0001 | c0001 | t0095 | g0240 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02886 | hp2 | a0001 | c0001 | t0036 | g0202 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02896 | hp1 | a0001 | c0001 | t0019 | g0015 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0183 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0031 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03017 | hp1 | a0001 | c0001 | t0017 | g0235 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03017 | hp2 | a0001 | c0001 | t0047 | g0344 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03041 | hp1 | a0001 | c0001 | t0082 | g0185 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03098 | hp2 | a0001 | c0001 | t0055 | g0244 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0178 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03139 | hp1 | a0001 | c0002 | t0079 | g0147 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0233 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03209 | hp1 | a0001 | c0001 | t0064 | g0155 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03209 | hp2 | a0001 | c0001 | t0096 | g0008 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03225 | hp1 | a0002 | c0003 | t0063 | g0081 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03239 | hp1 | a0001 | c0001 | t0013 | g0165 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03239 | hp2 | a0001 | c0001 | t0014 | g0058 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0012 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03486 | hp2 | a0001 | c0001 | t0086 | g0205 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03490 | hp1 | a0001 | c0001 | t0024 | g0103 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03490 | hp2 | a0001 | c0001 | t0071 | g0104 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0289 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03491 | hp2 | a0001 | c0001 | t0032 | g0135 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03492 | hp1 | a0001 | c0001 | t0024 | g0093 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0290 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03516 | hp1 | a0001 | c0001 | t0059 | g0028 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | ESN | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0016 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03579 | hp1 | a0001 | c0001 | t0088 | g0206 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03579 | hp2 | a0001 | c0001 | t0093 | g0243 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0150 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03710 | hp1 | a0001 | c0001 | t0035 | g0046 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03710 | hp2 | a0001 | c0001 | t0029 | g0113 | SAS | PJL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03831 | hp1 | a0001 | c0001 | t0017 | g0236 | SAS | BEB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03834 | hp1 | a0001 | c0001 | t0060 | g0056 | SAS | BEB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG04115 | hp1 | a0001 | c0001 | t0051 | g0210 | SAS | STU | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG04115 | hp2 | a0001 | c0001 | t0018 | g0298 | SAS | STU | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0287 | SAS | BEB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | CHB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0307 | EAS | CHB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | CHB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0232 | AFR | YRI | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18941 | hp2 | a0001 | c0001 | t0011 | g0348 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18942 | hp1 | a0001 | c0001 | t0037 | g0159 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18942 | hp2 | a0001 | c0001 | t0087 | g0192 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18947 | hp1 | a0001 | c0001 | t0033 | g0355 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18953 | hp2 | a0001 | c0001 | t0037 | g0186 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18957 | hp2 | a0001 | c0001 | t0012 | g0100 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18962 | hp2 | a0001 | c0001 | t0039 | g0070 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18964 | hp1 | a0001 | c0001 | t0045 | g0161 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18967 | hp1 | a0001 | c0001 | t0069 | g0259 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18967 | hp2 | a0001 | c0001 | t0021 | g0345 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18972 | hp2 | a0001 | c0001 | t0040 | g0354 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0264 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18978 | hp2 | a0001 | c0001 | t0014 | g0176 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18980 | hp2 | a0001 | c0001 | t0015 | g0148 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18982 | hp2 | a0001 | c0001 | t0040 | g0303 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18984 | hp1 | a0001 | c0001 | t0033 | g0329 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18986 | hp1 | a0001 | c0001 | t0073 | g0065 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18988 | hp2 | a0001 | c0001 | t0022 | g0020 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18989 | hp1 | a0001 | c0001 | t0097 | g0327 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18992 | hp2 | a0001 | c0001 | t0046 | g0204 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0309 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18998 | hp1 | a0001 | c0001 | t0041 | g0256 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18998 | hp2 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18999 | hp1 | a0001 | c0001 | t0043 | g0193 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19000 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19003 | hp1 | a0001 | c0001 | t0018 | g0339 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19004 | hp2 | a0001 | c0001 | t0007 | g0238 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19030 | hp2 | a0001 | c0001 | t0035 | g0073 | AFR | LWK | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | LWK | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19043 | hp2 | a0001 | c0001 | t0078 | g0157 | AFR | LWK | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19060 | hp1 | a0001 | c0001 | t0027 | g0170 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19060 | hp2 | a0001 | c0001 | t0066 | g0035 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19062 | hp2 | a0001 | c0001 | t0021 | g0347 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19065 | hp1 | a0001 | c0001 | t0009 | g0328 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19066 | hp2 | a0001 | c0001 | t0011 | g0351 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19068 | hp1 | a0001 | c0001 | t0025 | g0087 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19068 | hp2 | a0001 | c0001 | t0011 | g0346 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19074 | hp2 | a0001 | c0001 | t0031 | g0106 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19075 | hp1 | a0001 | c0001 | t0058 | g0181 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19075 | hp2 | a0001 | c0001 | t0046 | g0149 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19076 | hp2 | a0001 | c0001 | t0014 | g0085 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19077 | hp2 | a0001 | c0001 | t0021 | g0350 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19078 | hp1 | a0001 | c0001 | t0065 | g0349 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0194 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19081 | hp1 | a0001 | c0001 | t0017 | g0141 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19085 | hp1 | a0001 | c0001 | t0015 | g0153 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19090 | hp1 | a0001 | c0001 | t0072 | g0237 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19090 | hp2 | a0001 | c0001 | t0018 | g0334 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19240 | hp1 | a0001 | c0001 | t0057 | g0010 | AFR | YRI | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20129 | hp1 | a0001 | c0001 | t0022 | g0281 | AFR | ASW | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20129 | hp2 | a0001 | c0001 | t0080 | g0275 | AFR | ASW | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20752 | hp1 | a0001 | c0001 | t0020 | g0083 | EUR | TSI | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0246 | EUR | TSI | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | GIH | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0288 | SAS | GIH | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01123 | hp1 | a0001 | c0001 | t0028 | g0099 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG01123 | hp2 | a0001 | c0001 | t0074 | g0066 | AMR | CLM | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02109 | hp2 | a0001 | c0001 | t0020 | g0080 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02486 | hp2 | a0001 | c0001 | t0042 | g0241 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02559 | hp1 | a0001 | c0001 | t0036 | g0257 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0014 | AFR | ACB | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03471 | hp1 | a0001 | c0001 | t0042 | g0242 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG06807 | hp1 | a0001 | c0001 | t0026 | g0340 | AFR | USA | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0184 | AFR | USA | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA18955 | hp2 | a0001 | c0001 | t0009 | g0310 | EAS | JPT | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | USA | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0048 | REF | REF | IGF1_chr12_102390874_102485563 | IGF1 | chr12 | 102390874 | 102485563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102419568
|
C | T | 1 | a0002 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.343G>A | p.Ala115Thr | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/4 | 525/7277 | 343/462 | 115/153 | chr12 | 102419568 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102475707
|
C | T | 1 | a0001c0002 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.156G>A | p.Thr52Thr | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/4 | 338/7277 | 156/462 | 52/153 | chr12 | 102475707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102396074
|
C | G | 9 | a0001c0001t0003a0001c0001t0007a0001c0001t0017others(6): Show | 54 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*6433G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 6433 | chr12 | 102396074 | |||||
| chr12:102396123
|
G | A | 2 | a0001c0001t0019a0001c0001t0020 | 6 | HG02109.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6384C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 6384 | chr12 | 102396123 | |||||
| chr12:102396196
|
A | G | 1 | a0001c0001t0010 | 4 | HG02257.hp2 HG03139.hp2 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6311T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 6311 | chr12 | 102396196 | |||||
| chr12:102396414
|
C | T | 9 | a0001c0001t0003a0001c0001t0007a0001c0001t0017others(6): Show | 54 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*6093G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 6093 | chr12 | 102396414 | |||||
| chr12:102396712
|
C | T | 1 | a0001c0001t0091 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5795G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 5795 | chr12 | 102396712 | |||||
| chr12:102396788
|
C | CT | 12 | a0001c0001t0004a0001c0001t0008a0001c0001t0009others(9): Show | 63 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*5718dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 5718 | chr12 | 102396788 | |||||
| chr12:102396969
|
G | A | 1 | a0001c0001t0068 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5538C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 5538 | chr12 | 102396969 | |||||
| chr12:102397002
|
A | T | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(45): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*5505T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 5505 | chr12 | 102397002 | |||||
| chr12:102397237
|
A | C | 1 | a0001c0001t0034 | 2 | HG02280.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5270T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 5270 | chr12 | 102397237 | |||||
| chr12:102397305
|
A | C | 1 | a0001c0001t0067 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5202T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 5202 | chr12 | 102397305 | |||||
| chr12:102397768
|
G | A | 1 | a0001c0001t0072 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4739C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4739 | chr12 | 102397768 | |||||
| chr12:102397770
|
C | A | 1 | a0001c0001t0074 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4737G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4737 | chr12 | 102397770 | |||||
| chr12:102397971
|
A | G | 1 | a0001c0001t0094 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4536T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4536 | chr12 | 102397971 | |||||
| chr12:102398022
|
TA | T | 3 | a0001c0001t0020a0001c0001t0062a0002c0003t0063 | 5 | HG02109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4484delT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4484 | chr12 | 102398022 | |||||
| chr12:102398086
|
T | TA | 30 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(27): Show | 111 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*4420dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4420 | chr12 | 102398086 | |||||
| chr12:102398086
|
TA | T | 9 | a0001c0001t0042a0001c0001t0055a0001c0001t0057others(6): Show | 10 | HG01891.hp1 HG02486.hp2 HG02717.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4420delT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4420 | chr12 | 102398086 | |||||
| chr12:102398096
|
A | C | 1 | a0001c0001t0060 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4411T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4411 | chr12 | 102398096 | |||||
| chr12:102398498
|
C | T | 1 | a0001c0001t0059 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4009G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4009 | chr12 | 102398498 | |||||
| chr12:102398499
|
G | A | 1 | a0001c0001t0055 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4008C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 4008 | chr12 | 102398499 | |||||
| chr12:102398531
|
G | C | 1 | a0001c0001t0085 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3976C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3976 | chr12 | 102398531 | |||||
| chr12:102398536
|
T | C | 1 | a0001c0001t0075 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3971A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3971 | chr12 | 102398536 | |||||
| chr12:102398590
|
C | G | 1 | a0001c0001t0055 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3917G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3917 | chr12 | 102398590 | |||||
| chr12:102399107
|
A | ATG | 22 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(19): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3398_*3399dupCA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3399 | chr12 | 102399107 | |||||
| chr12:102399107
|
A | ATGTG | 15 | a0001c0001t0003a0001c0001t0010a0001c0001t0012others(12): Show | 66 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3396_*3399dupCACA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3399 | chr12 | 102399107 | |||||
| chr12:102399107
|
A | ATGTGTG | 6 | a0001c0001t0007a0001c0001t0040a0001c0001t0042others(3): Show | 13 | HG01496.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3394_*3399dupCACA others(2): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3399 | chr12 | 102399107 | |||||
| chr12:102399107
|
A | ATGTGTGT others(1): Show |
6 | a0001c0001t0026a0001c0001t0050a0001c0001t0053others(3): Show | 8 | HG01167.hp2 HG01257.hp1 HG01258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3392_*3399dupCACA others(4): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3399 | chr12 | 102399107 | |||||
| chr12:102399107
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0009 | 4 | HG02080.hp2 NA18955.hp2 NA18994.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3390_*3399dupCACA others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3399 | chr12 | 102399107 | |||||
| chr12:102399107
|
A | ATGTGTGT others(9): Show |
3 | a0001c0001t0078a0001c0001t0093a0001c0002t0079 | 3 | HG03139.hp1 HG03579.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3384_*3399dupCACA others(12): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3399 | chr12 | 102399107 | |||||
| chr12:102399107
|
A | ATGTGTGT others(13): Show |
1 | a0001c0001t0077 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3380_*3399dupCACA others(16): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3399 | chr12 | 102399107 | |||||
| chr12:102399107
|
ATG | A | 7 | a0001c0001t0022a0001c0001t0036a0001c0001t0045others(4): Show | 11 | HG01109.hp1 HG01515.hp1 HG02080.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3398_*3399delCA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3398 | chr12 | 102399107 | |||||
| chr12:102399107
|
ATGTG | A | 3 | a0001c0001t0065a0001c0001t0076a0001c0001t0090 | 3 | HG01168.hp2 HG02818.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3396_*3399delCACA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3396 | chr12 | 102399107 | |||||
| chr12:102399119
|
G | A | 3 | a0001c0001t0020a0001c0001t0062a0002c0003t0063 | 5 | HG02109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3388C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3388 | chr12 | 102399119 | |||||
| chr12:102399281
|
G | C | 1 | a0001c0001t0023 | 3 | HG01167.hp1 HG01169.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3226C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 3226 | chr12 | 102399281 | |||||
| chr12:102399791
|
C | T | 49 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(46): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*2716G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2716 | chr12 | 102399791 | |||||
| chr12:102399855
|
A | G | 9 | a0001c0001t0004a0001c0001t0008a0001c0001t0009others(6): Show | 56 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2652T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2652 | chr12 | 102399855 | |||||
| chr12:102400008
|
A | C | 9 | a0001c0001t0004a0001c0001t0008a0001c0001t0009others(6): Show | 56 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2499T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2499 | chr12 | 102400008 | |||||
| chr12:102400131
|
C | CT | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(55): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*2375dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2375 | chr12 | 102400131 | |||||
| chr12:102400131
|
CT | C | 10 | a0001c0001t0016a0001c0001t0028a0001c0001t0046others(7): Show | 16 | HG00099.hp1 HG00642.hp2 HG01123.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2375delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2375 | chr12 | 102400131 | |||||
| chr12:102400143
|
T | C | 3 | a0001c0001t0020a0001c0001t0062a0002c0003t0063 | 5 | HG02109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2364A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2364 | chr12 | 102400143 | |||||
| chr12:102400241
|
A | C | 3 | a0001c0001t0011a0001c0001t0021a0001c0001t0065 | 8 | HG02132.hp1 NA18941.hp2 NA18967.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2266T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2266 | chr12 | 102400241 | |||||
| chr12:102400241
|
A | G | 1 | a0001c0001t0064 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2266T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2266 | chr12 | 102400241 | |||||
| chr12:102400443
|
T | C | 1 | a0001c0001t0049 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2064A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 2064 | chr12 | 102400443 | |||||
| chr12:102400658
|
C | T | 1 | a0001c0001t0089 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1849G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 1849 | chr12 | 102400658 | |||||
| chr12:102400736
|
C | T | 1 | a0001c0001t0083 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1771G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 1771 | chr12 | 102400736 | |||||
| chr12:102400737
|
G | A | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(50): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*1770C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 1770 | chr12 | 102400737 | |||||
| chr12:102401150
|
A | C | 1 | a0001c0001t0052 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 1357 | chr12 | 102401150 | |||||
| chr12:102401286
|
C | G | 1 | a0001c0001t0051 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 1221 | chr12 | 102401286 | |||||
| chr12:102401736
|
A | G | 1 | a0001c0001t0050 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*771T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 771 | chr12 | 102401736 | |||||
| chr12:102401752
|
CTT | C | 5 | a0001c0001t0042a0001c0001t0093a0001c0001t0094others(2): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*753_*754delAA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 753 | chr12 | 102401752 | |||||
| chr12:102402244
|
A | T | 7 | a0001c0001t0017a0001c0001t0030a0001c0001t0031others(4): Show | 12 | HG00408.hp2 HG00639.hp1 HG01071.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*263T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 263 | chr12 | 102402244 | |||||
| chr12:102402244
|
AT | A | 9 | a0001c0001t0026a0001c0001t0040a0001c0001t0041others(6): Show | 14 | HG01257.hp1 HG01258.hp2 HG01891.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*262delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 262 | chr12 | 102402244 | |||||
| chr12:102402246
|
T | A | 21 | a0001c0001t0004a0001c0001t0008a0001c0001t0015others(18): Show | 76 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*261A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 261 | chr12 | 102402246 | |||||
| chr12:102402247
|
T | A | 4 | a0001c0001t0093a0001c0001t0094a0001c0001t0095others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*260A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 260 | chr12 | 102402247 | |||||
| chr12:102402248
|
T | A | 1 | a0001c0001t0097 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 259 | chr12 | 102402248 | |||||
| chr12:102402402
|
A | G | 1 | a0001c0001t0029 | 2 | HG00733.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 4/4 | 105 | chr12 | 102402402 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102402744
|
G | C | 208 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(205): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.403-178C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102402744 | ||||||
| chr12:102402872
|
C | A | 1 | a0001c0001t0011g0005 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.403-306G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102402872 | ||||||
| chr12:102402933
|
A | G | 4 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190others(1): Show | 4 | NA18945.hp2 NA18946.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-367T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102402933 | ||||||
| chr12:102403013
|
G | T | 20 | a0001c0001t0001g0063a0001c0001t0001g0120a0001c0001t0001g0121others(17): Show | 20 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.403-447C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403013 | ||||||
| chr12:102403314
|
C | G | 1 | a0001c0001t0051g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.403-748G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403314 | ||||||
| chr12:102403418
|
A | G | 200 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(197): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.403-852T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403418 | ||||||
| chr12:102403431
|
C | T | 1 | a0001c0001t0034g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403-865G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403431 | ||||||
| chr12:102403452
|
G | A | 1 | a0001c0001t0054g0229 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403-886C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403452 | ||||||
| chr12:102403463
|
G | GT | 7 | a0001c0001t0001g0140a0001c0001t0002g0074a0001c0001t0003g0224others(4): Show | 7 | HG00280.hp2 HG01943.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.403-898dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403463 | ||||||
| chr12:102403515
|
G | A | 205 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(202): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.403-949C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403515 | ||||||
| chr12:102403623
|
AT | A | 47 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(44): Show | 49 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.403-1058delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403623 | ||||||
| chr12:102403623
|
ATT | A | 13 | a0001c0001t0001g0094a0001c0001t0001g0109a0001c0001t0001g0273others(10): Show | 13 | HG01167.hp2 HG01192.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-1059_403-1058d others(4): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403623 | ||||||
| chr12:102403623
|
ATTT | A | 124 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(121): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.403-1060_403-1058d others(5): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403623 | ||||||
| chr12:102403623
|
ATTTT | A | 131 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0002g0002others(128): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.403-1061_403-1058d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403623 | ||||||
| chr12:102403623
|
ATTTTT | A | 8 | a0001c0001t0002g0171a0001c0001t0002g0203a0001c0001t0004g0304others(5): Show | 8 | HG01515.hp1 HG02976.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-1062_403-1058d others(7): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403623 | ||||||
| chr12:102403623
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(1): Show | 4 | HG02109.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-1068_403-1058d others(13): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403623 | ||||||
| chr12:102403632
|
T | G | 1 | a0001c0001t0053g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.403-1066A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403632 | ||||||
| chr12:102403684
|
T | C | 1 | a0001c0001t0004g0324 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.403-1118A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403684 | ||||||
| chr12:102403747
|
C | A | 1 | a0001c0001t0003g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.403-1181G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403747 | ||||||
| chr12:102403822
|
T | G | 1 | a0001c0001t0045g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.403-1256A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102403822 | ||||||
| chr12:102404399
|
G | A | 48 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(45): Show | 50 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.403-1833C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404399 | ||||||
| chr12:102404425
|
G | A | 1 | a0001c0001t0004g0326 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.403-1859C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404425 | ||||||
| chr12:102404601
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0015g0174 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.403-2035T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404601 | ||||||
| chr12:102404750
|
G | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0020g0079others(1): Show | 4 | HG01255.hp2 HG01261.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-2184C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404750 | ||||||
| chr12:102404757
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.403-2191A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404757 | ||||||
| chr12:102404760
|
G | T | 9 | a0001c0001t0001g0094a0001c0001t0002g0144a0001c0001t0002g0152others(6): Show | 9 | HG00597.hp2 HG01167.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.403-2194C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404760 | ||||||
| chr12:102404763
|
G | GT | 330 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.403-2198dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404763 | ||||||
| chr12:102404763
|
G | GTT | 9 | a0001c0001t0001g0108a0001c0001t0013g0014a0001c0001t0013g0037others(6): Show | 9 | HG00558.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-2199_403-2198d others(4): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404763 | ||||||
| chr12:102404819
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.403-2253C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102404819 | ||||||
| chr12:102405076
|
G | GCTTT | 123 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(120): Show | 123 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.403-2514_403-2511d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405076 | ||||||
| chr12:102405076
|
G | GCTTTCTT others(1): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0037g0159 | 3 | HG02027.hp2 NA18942.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.403-2518_403-2511d others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405076 | ||||||
| chr12:102405139
|
G | A | 4 | a0001c0001t0001g0268a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-2573C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405139 | ||||||
| chr12:102405208
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.403-2642A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405208 | ||||||
| chr12:102405251
|
T | TAATTTTT others(313): Show |
1 | a0001c0001t0006g0262 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.403-2686_403-2685i others(322): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405251 | ||||||
| chr12:102405251
|
T | TAATTTTT others(314): Show |
34 | a0001c0001t0002g0002a0001c0001t0002g0029a0001c0001t0002g0030others(31): Show | 36 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.403-2686_403-2685i others(323): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405251 | ||||||
| chr12:102405251
|
T | TAATTTTT others(315): Show |
17 | a0001c0001t0002g0006a0001c0001t0002g0060a0001c0001t0002g0074others(14): Show | 17 | HG00280.hp2 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.403-2686_403-2685i others(324): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405251 | ||||||
| chr12:102405251
|
T | TAATTTTT others(316): Show |
1 | a0001c0001t0013g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.403-2686_403-2685i others(325): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405251 | ||||||
| chr12:102405313
|
C | T | 50 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(47): Show | 50 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.403-2747G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405313 | ||||||
| chr12:102405458
|
C | A | 278 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(275): Show | 280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.403-2892G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405458 | ||||||
| chr12:102405820
|
A | G | 69 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(66): Show | 69 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.403-3254T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405820 | ||||||
| chr12:102405883
|
T | C | 1 | a0001c0001t0004g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.403-3317A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102405883 | ||||||
| chr12:102406089
|
G | A | 4 | a0001c0001t0010g0009a0001c0001t0010g0231a0001c0001t0010g0232others(1): Show | 4 | HG02257.hp2 HG03139.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-3523C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102406089 | ||||||
| chr12:102406296
|
G | A | 6 | a0001c0001t0010g0009a0001c0001t0010g0231a0001c0001t0010g0232others(3): Show | 6 | HG01167.hp2 HG02257.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-3730C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102406296 | ||||||
| chr12:102406406
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.403-3840A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102406406 | ||||||
| chr12:102406614
|
C | T | 1 | a0001c0001t0004g0295 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.403-4048G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102406614 | ||||||
| chr12:102406874
|
C | G | 1 | a0001c0001t0003g0228 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.403-4308G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102406874 | ||||||
| chr12:102407025
|
C | T | 91 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0017others(88): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.403-4459G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407025 | ||||||
| chr12:102407094
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0005g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.403-4541_403-4529d others(15): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CA | C | 7 | a0001c0001t0005g0047a0001c0001t0005g0076a0001c0001t0005g0251others(4): Show | 7 | HG00323.hp1 HG00423.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.403-4529delT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAA | C | 21 | a0001c0001t0003g0188a0001c0001t0003g0190a0001c0001t0003g0223others(18): Show | 21 | HG01071.hp2 HG01934.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.403-4530_403-4529d others(4): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAA | C | 47 | a0001c0001t0003g0018a0001c0001t0003g0072a0001c0001t0003g0189others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.403-4531_403-4529d others(5): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAA | C | 31 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0142others(28): Show | 33 | HG01099.hp1 HG01256.hp2 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.403-4532_403-4529d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0026g0340a0001c0001t0026g0342a0001c0001t0040g0354 | 3 | HG01258.hp2 HG06807.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.403-4538_403-4529d others(12): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0026g0341a0001c0001t0040g0303a0001c0001t0042g0241others(2): Show | 5 | HG01257.hp1 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-4539_403-4529d others(13): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0093g0243a0001c0001t0094g0007a0001c0001t0096g0008 | 3 | HG01891.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.403-4540_403-4529d others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0034g0146a0001c0001t0034g0201 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.403-4541_403-4529d others(15): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0070g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.403-4543_403-4529d others(17): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0007g0207a0001c0001t0007g0208 | 2 | HG01496.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.403-4545_403-4529d others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0045g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.403-4546_403-4529d others(20): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0002g0027a0001c0001t0002g0145a0001c0001t0006g0264 | 3 | HG02572.hp2 HG04184.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.403-4547_403-4529d others(21): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(13): Show |
C | 96 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0017others(93): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.403-4548_403-4529d others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(14): Show |
C | 2 | a0001c0001t0002g0075a0001c0001t0002g0180 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.403-4549_403-4529d others(23): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(17): Show |
C | 2 | a0001c0001t0038g0137a0001c0001t0076g0115 | 2 | HG01168.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.403-4552_403-4529d others(26): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(18): Show |
C | 102 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(99): Show | 102 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.403-4553_403-4529d others(27): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407094
|
CAAAAAAA others(21): Show |
C | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403-4556_403-4529d others(30): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407094 | ||||||
| chr12:102407150
|
A | G | 56 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(53): Show | 56 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.403-4584T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407150 | ||||||
| chr12:102407157
|
C | T | 275 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(272): Show | 277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.403-4591G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407157 | ||||||
| chr12:102407166
|
T | C | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403-4600A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407166 | ||||||
| chr12:102407252
|
G | A | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403-4686C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407252 | ||||||
| chr12:102407326
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.403-4760T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407326 | ||||||
| chr12:102407592
|
A | G | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-5026T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407592 | ||||||
| chr12:102407709
|
G | C | 2 | a0001c0001t0040g0303a0001c0001t0040g0354 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.403-5143C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407709 | ||||||
| chr12:102407741
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0278 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.403-5175G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102407741 | ||||||
| chr12:102408091
|
A | G | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-5525T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102408091 | ||||||
| chr12:102408199
|
G | A | 2 | a0001c0001t0034g0146a0001c0001t0034g0201 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.403-5633C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102408199 | ||||||
| chr12:102408461
|
T | C | 202 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(199): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.403-5895A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102408461 | ||||||
| chr12:102408487
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.403-5921T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102408487 | ||||||
| chr12:102408607
|
C | T | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-6041G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102408607 | ||||||
| chr12:102408767
|
G | A | 3 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281 | 3 | HG03516.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.403-6201C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102408767 | ||||||
| chr12:102408794
|
T | C | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-6228A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102408794 | ||||||
| chr12:102409118
|
T | C | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403-6552A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409118 | ||||||
| chr12:102409176
|
G | A | 1 | a0001c0001t0003g0024 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.403-6610C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409176 | ||||||
| chr12:102409215
|
C | T | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-6649G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409215 | ||||||
| chr12:102409265
|
A | AAGAGCCC others(13): Show |
1 | a0001c0001t0038g0138 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.403-6719_403-6700d others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409265 | ||||||
| chr12:102409565
|
C | A | 6 | a0001c0001t0004g0062a0001c0001t0004g0317a0001c0001t0004g0326others(3): Show | 6 | HG01346.hp2 HG01361.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-6999G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409565 | ||||||
| chr12:102409620
|
A | G | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-7054T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409620 | ||||||
| chr12:102409671
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.403-7105C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409671 | ||||||
| chr12:102409870
|
TCTTTTTA others(5): Show |
T | 1 | a0001c0001t0042g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.403-7316_403-7305d others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409870 | ||||||
| chr12:102409989
|
G | A | 11 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.403-7423C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102409989 | ||||||
| chr12:102410115
|
A | T | 185 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(182): Show | 187 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.403-7549T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102410115 | ||||||
| chr12:102410509
|
G | A | 11 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.403-7943C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102410509 | ||||||
| chr12:102410541
|
C | A | 11 | a0001c0001t0009g0059a0001c0001t0009g0309a0001c0001t0009g0310others(8): Show | 11 | HG01257.hp1 HG01258.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.403-7975G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102410541 | ||||||
| chr12:102410766
|
G | A | 1 | a0001c0001t0059g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.403-8200C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102410766 | ||||||
| chr12:102410942
|
G | T | 2 | a0001c0001t0024g0093a0001c0001t0024g0103 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.403-8376C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102410942 | ||||||
| chr12:102411070
|
C | G | 2 | a0001c0001t0024g0093a0001c0001t0024g0103 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.402+8439G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102411070 | ||||||
| chr12:102411244
|
C | T | 1 | a0001c0001t0006g0261 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.402+8265G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102411244 | ||||||
| chr12:102411470
|
G | A | 1 | a0001c0001t0004g0308 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.402+8039C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102411470 | ||||||
| chr12:102411475
|
C | A | 2 | a0001c0001t0020g0079a0001c0001t0020g0080 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.402+8034G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102411475 | ||||||
| chr12:102412164
|
C | A | 1 | a0001c0001t0002g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.402+7345G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412164 | ||||||
| chr12:102412405
|
C | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0074a0001c0001t0002g0075others(1): Show | 5 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+7104G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412405 | ||||||
| chr12:102412419
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.402+7090G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412419 | ||||||
| chr12:102412497
|
A | G | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+7012T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412497 | ||||||
| chr12:102412527
|
C | T | 178 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(175): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.402+6982G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412527 | ||||||
| chr12:102412635
|
T | C | 3 | a0001c0001t0013g0014a0001c0001t0013g0037a0001c0001t0013g0045 | 3 | HG01884.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.402+6874A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412635 | ||||||
| chr12:102412838
|
A | G | 1 | a0001c0001t0085g0312 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.402+6671T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412838 | ||||||
| chr12:102412840
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.402+6669T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412840 | ||||||
| chr12:102412841
|
C | T | 1 | a0001c0001t0014g0176 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.402+6668G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102412841 | ||||||
| chr12:102413355
|
G | T | 1 | a0001c0001t0019g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.402+6154C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102413355 | ||||||
| chr12:102413609
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.402+5900T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102413609 | ||||||
| chr12:102413707
|
C | T | 1 | a0001c0001t0012g0100 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.402+5802G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102413707 | ||||||
| chr12:102413773
|
G | T | 1 | a0001c0001t0056g0011 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.402+5736C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102413773 | ||||||
| chr12:102413851
|
C | CAAGCTAC others(26): Show |
1 | a0001c0001t0066g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.402+5625_402+5657d others(35): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102413851 | ||||||
| chr12:102413892
|
G | A | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.402+5617C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102413892 | ||||||
| chr12:102413993
|
G | C | 1 | a0001c0001t0018g0298 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.402+5516C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102413993 | ||||||
| chr12:102414389
|
G | T | 1 | a0001c0001t0040g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.402+5120C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102414389 | ||||||
| chr12:102414577
|
A | C | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.402+4932T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102414577 | ||||||
| chr12:102414686
|
A | G | 203 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(200): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.402+4823T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102414686 | ||||||
| chr12:102415074
|
A | G | 1 | a0001c0001t0097g0327 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.402+4435T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415074 | ||||||
| chr12:102415172
|
C | G | 2 | a0001c0001t0016g0178a0001c0001t0016g0274 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.402+4337G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415172 | ||||||
| chr12:102415256
|
T | TCATC | 5 | a0001c0001t0004g0313a0001c0001t0004g0330a0001c0001t0004g0333others(2): Show | 5 | HG00423.hp1 HG02630.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+4249_402+4252d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415256 | ||||||
| chr12:102415256
|
TCATC | T | 157 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.402+4249_402+4252d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415256 | ||||||
| chr12:102415256
|
TCATCCAT others(1): Show |
T | 161 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0067others(158): Show | 163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.402+4245_402+4252d others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415256 | ||||||
| chr12:102415256
|
TCATCCAT others(5): Show |
T | 1 | a0001c0001t0004g0062 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.402+4241_402+4252d others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415256 | ||||||
| chr12:102415256
|
TCATCCAT others(13): Show |
T | 2 | a0001c0001t0004g0297a0001c0001t0004g0353 | 2 | NA18975.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.402+4233_402+4252d others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415256 | ||||||
| chr12:102415376
|
T | TA | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.402+4132dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415376 | ||||||
| chr12:102415410
|
A | G | 1 | a0001c0001t0018g0334 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.402+4099T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415410 | ||||||
| chr12:102415543
|
T | TTTCC | 61 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(58): Show | 62 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.402+3962_402+3965d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(1): Show |
64 | a0001c0001t0001g0094a0001c0001t0001g0116a0001c0001t0001g0117others(61): Show | 64 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.402+3958_402+3965d others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(5): Show |
25 | a0001c0001t0001g0063a0001c0001t0001g0118a0001c0001t0001g0119others(22): Show | 25 | HG00741.hp1 HG01099.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.402+3954_402+3965d others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(9): Show |
7 | a0001c0001t0001g0134a0001c0001t0004g0287a0001c0001t0004g0294others(4): Show | 7 | HG01978.hp2 HG02074.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+3950_402+3965d others(18): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(13): Show |
1 | a0001c0001t0091g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.402+3946_402+3965d others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(25): Show |
2 | a0001c0001t0023g0022a0001c0001t0023g0023 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.402+3965_402+3966i others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(29): Show |
1 | a0001c0001t0012g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.402+3965_402+3966i others(38): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(37): Show |
1 | a0001c0001t0029g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.402+3965_402+3966i others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(29): Show |
35 | a0001c0001t0001g0109a0001c0001t0002g0002a0001c0001t0002g0017others(32): Show | 36 | HG00099.hp1 HG01192.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.402+3965_402+3966i others(38): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(33): Show |
32 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0088others(29): Show | 32 | HG00280.hp2 HG00741.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.402+3965_402+3966i others(42): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(37): Show |
21 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0091others(18): Show | 21 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+3965_402+3966i others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(41): Show |
22 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0086others(19): Show | 23 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.402+3965_402+3966i others(50): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(45): Show |
3 | a0001c0001t0001g0356a0001c0001t0029g0112a0001c0001t0072g0237 | 3 | HG00733.hp1 NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.402+3965_402+3966i others(54): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(49): Show |
2 | a0001c0001t0001g0292a0001c0001t0002g0006 | 2 | HG00408.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.402+3965_402+3966i others(58): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(33): Show |
3 | a0001c0001t0020g0083a0001c0001t0045g0019a0001c0001t0090g0021 | 3 | HG01109.hp1 HG02818.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.402+3965_402+3966i others(42): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(37): Show |
4 | a0001c0001t0011g0005a0001c0001t0011g0346a0001c0001t0021g0345others(1): Show | 4 | HG02132.hp1 NA18967.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+3965_402+3966i others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(41): Show |
2 | a0001c0001t0011g0348a0001c0001t0021g0347 | 2 | NA18941.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.402+3965_402+3966i others(50): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(45): Show |
2 | a0001c0001t0011g0351a0001c0001t0021g0350 | 2 | NA19066.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.402+3965_402+3966i others(54): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(45): Show |
1 | a0001c0001t0020g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.402+3965_402+3966i others(54): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(49): Show |
1 | a0001c0001t0020g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.402+3965_402+3966i others(58): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(49): Show |
1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+3965_402+3966i others(58): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(49): Show |
1 | a0001c0001t0062g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.402+3965_402+3966i others(58): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
T | TTTCCTTC others(53): Show |
1 | a0001c0001t0089g0255 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.402+3965_402+3966i others(62): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
TTTCC | T | 11 | a0001c0001t0003g0209a0001c0001t0003g0224a0001c0001t0003g0245others(8): Show | 12 | HG00733.hp2 HG01106.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.402+3962_402+3965d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415543
|
TTTCCTTC others(1): Show |
T | 5 | a0001c0001t0005g0076a0001c0001t0005g0077a0001c0001t0005g0282others(2): Show | 5 | HG00642.hp2 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+3958_402+3965d others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415543 | ||||||
| chr12:102415544
|
T | TTCCTTCC others(25): Show |
8 | a0001c0001t0001g0123a0001c0001t0002g0053a0001c0001t0002g0092others(5): Show | 8 | HG00323.hp2 HG01257.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.402+3964_402+3965i others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415544 | ||||||
| chr12:102415544
|
T | TTCCTTCC others(29): Show |
3 | a0001c0001t0019g0012a0001c0001t0019g0015a0001c0001t0019g0016 | 3 | HG02896.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.402+3964_402+3965i others(38): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415544 | ||||||
| chr12:102415548
|
T | TTCCTTCC others(21): Show |
5 | a0001c0001t0001g0120a0001c0001t0002g0036a0001c0001t0002g0044others(2): Show | 5 | HG01081.hp1 HG01081.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+3960_402+3961i others(30): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415548 | ||||||
| chr12:102415548
|
T | TTCCTTCC others(29): Show |
1 | a0002c0003t0063g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.402+3960_402+3961i others(38): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415548 | ||||||
| chr12:102415592
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG00408.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.402+3917A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415592 | ||||||
| chr12:102415596
|
T | C | 4 | a0001c0001t0002g0017a0001c0001t0002g0027a0001c0001t0042g0242others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+3913A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415596 | ||||||
| chr12:102415596
|
T | TTCCC | 3 | a0001c0001t0042g0241a0001c0001t0093g0243a0001c0001t0095g0240 | 3 | HG02486.hp2 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.402+3909_402+3912d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415596 | ||||||
| chr12:102415596
|
T | TTCCTTCC others(5): Show |
1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.402+3912_402+3913i others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415596 | ||||||
| chr12:102415852
|
G | C | 53 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(50): Show | 55 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.402+3657C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415852 | ||||||
| chr12:102415957
|
G | A | 1 | a0001c0001t0037g0186 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.402+3552C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102415957 | ||||||
| chr12:102416249
|
C | T | 1 | a0001c0001t0002g0102 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.402+3260G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102416249 | ||||||
| chr12:102416407
|
C | A | 4 | a0001c0001t0005g0076a0001c0001t0005g0077a0001c0001t0005g0282others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+3102G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102416407 | ||||||
| chr12:102416491
|
T | C | 194 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(191): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.402+3018A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102416491 | ||||||
| chr12:102416532
|
A | G | 1 | a0001c0001t0004g0343 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.402+2977T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102416532 | ||||||
| chr12:102416582
|
C | T | 1 | a0001c0001t0046g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.402+2927G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102416582 | ||||||
| chr12:102416620
|
T | C | 283 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(280): Show | 285 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.402+2889A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102416620 | ||||||
| chr12:102416818
|
C | T | 348 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(345): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.402+2691G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102416818 | ||||||
| chr12:102417219
|
T | TGAA | 283 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(280): Show | 285 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.402+2287_402+2289d others(5): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102417219 | ||||||
| chr12:102417328
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.402+2181G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102417328 | ||||||
| chr12:102417461
|
A | G | 54 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(51): Show | 56 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.402+2048T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102417461 | ||||||
| chr12:102417846
|
G | T | 2 | a0001c0001t0034g0146a0001c0001t0034g0201 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.402+1663C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102417846 | ||||||
| chr12:102418260
|
C | A | 1 | a0001c0001t0031g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.402+1249G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418260 | ||||||
| chr12:102418327
|
T | C | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+1182A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418327 | ||||||
| chr12:102418424
|
C | T | 2 | a0001c0001t0062g0254a0001c0001t0089g0255 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.402+1085G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418424 | ||||||
| chr12:102418581
|
A | G | 1 | a0001c0001t0082g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.402+928T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418581 | ||||||
| chr12:102418621
|
C | T | 2 | a0001c0001t0024g0093a0001c0001t0024g0103 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.402+888G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418621 | ||||||
| chr12:102418639
|
C | G | 1 | a0001c0001t0002g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.402+870G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418639 | ||||||
| chr12:102418740
|
G | A | 1 | a0001c0001t0012g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.402+769C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418740 | ||||||
| chr12:102418748
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.402+761C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418748 | ||||||
| chr12:102418914
|
G | A | 4 | a0001c0001t0016g0183a0001c0001t0016g0184a0001c0001t0080g0275others(1): Show | 4 | HG02976.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+595C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102418914 | ||||||
| chr12:102419050
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.402+459G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102419050 | ||||||
| chr12:102419478
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.402+31C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 3/3 | chr12 | 102419478 | ||||||
| chr12:102419846
|
G | T | 3 | a0001c0001t0013g0014a0001c0001t0013g0037a0001c0001t0013g0045 | 3 | HG01884.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.221-156C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102419846 | ||||||
| chr12:102419854
|
C | T | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.221-164G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102419854 | ||||||
| chr12:102419939
|
A | G | 11 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-249T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102419939 | ||||||
| chr12:102419970
|
T | C | 4 | a0001c0001t0010g0009a0001c0001t0010g0231a0001c0001t0010g0232others(1): Show | 4 | HG02257.hp2 HG03139.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-280A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102419970 | ||||||
| chr12:102420036
|
C | T | 2 | a0001c0001t0007g0207a0001c0001t0007g0208 | 2 | HG01496.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.221-346G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102420036 | ||||||
| chr12:102420190
|
A | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0285 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.221-500T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102420190 | ||||||
| chr12:102420468
|
A | G | 1 | a0001c0001t0005g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.221-778T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102420468 | ||||||
| chr12:102420554
|
C | G | 203 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(200): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.221-864G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102420554 | ||||||
| chr12:102421105
|
A | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-1415T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102421105 | ||||||
| chr12:102421248
|
T | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0285 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.221-1558A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102421248 | ||||||
| chr12:102421324
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.221-1634G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102421324 | ||||||
| chr12:102421476
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0172 | 2 | HG00673.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.221-1786C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102421476 | ||||||
| chr12:102421966
|
G | A | 1 | a0001c0001t0006g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.221-2276C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102421966 | ||||||
| chr12:102421980
|
G | A | 53 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(50): Show | 55 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.221-2290C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102421980 | ||||||
| chr12:102422022
|
C | CA | 73 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0004g0062others(70): Show | 73 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.221-2333dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422022 | ||||||
| chr12:102422079
|
C | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0026a0001c0001t0002g0027 | 3 | HG02572.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.221-2389G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422079 | ||||||
| chr12:102422351
|
G | A | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-2661C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422351 | ||||||
| chr12:102422573
|
G | T | 1 | a0001c0001t0094g0007 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.221-2883C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422573 | ||||||
| chr12:102422655
|
A | G | 1 | a0001c0001t0004g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.221-2965T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422655 | ||||||
| chr12:102422701
|
GAT | G | 204 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(201): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.221-3013_221-3012d others(4): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422701 | ||||||
| chr12:102422745
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.221-3055G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422745 | ||||||
| chr12:102422818
|
A | T | 1 | a0001c0001t0003g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.221-3128T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102422818 | ||||||
| chr12:102423252
|
A | G | 1 | a0001c0001t0064g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221-3562T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423252 | ||||||
| chr12:102423259
|
G | GA | 22 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0144others(19): Show | 23 | HG01256.hp1 HG01258.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.221-3570dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423259 | ||||||
| chr12:102423259
|
GA | G | 98 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0061others(95): Show | 99 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.221-3570delT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423259 | ||||||
| chr12:102423259
|
GAA | G | 111 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0034others(108): Show | 111 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.221-3571_221-3570d others(4): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423259 | ||||||
| chr12:102423259
|
GAAA | G | 9 | a0001c0001t0001g0091a0001c0001t0004g0306a0001c0001t0009g0328others(6): Show | 9 | HG01257.hp1 HG01258.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-3572_221-3570d others(5): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423259 | ||||||
| chr12:102423293
|
G | A | 5 | a0001c0001t0026g0340a0001c0001t0026g0341a0001c0001t0026g0342others(2): Show | 5 | HG01257.hp1 HG01258.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-3603C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423293 | ||||||
| chr12:102423343
|
T | C | 1 | a0001c0001t0020g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.221-3653A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423343 | ||||||
| chr12:102423366
|
A | G | 2 | a0001c0001t0004g0287a0001c0001t0047g0344 | 2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.221-3676T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423366 | ||||||
| chr12:102423585
|
A | G | 1 | a0001c0001t0003g0224 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.221-3895T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423585 | ||||||
| chr12:102423649
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-3959A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102423649 | ||||||
| chr12:102424225
|
T | C | 1 | a0001c0001t0002g0029 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.221-4535A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424225 | ||||||
| chr12:102424239
|
C | CT | 10 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0006g0262others(7): Show | 10 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-4550dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424239 | ||||||
| chr12:102424239
|
CT | C | 43 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0089others(40): Show | 43 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.221-4550delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424239 | ||||||
| chr12:102424303
|
A | G | 1 | a0001c0001t0027g0097 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.221-4613T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424303 | ||||||
| chr12:102424390
|
T | C | 1 | a0001c0001t0028g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.221-4700A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424390 | ||||||
| chr12:102424555
|
G | C | 1 | a0001c0001t0039g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.221-4865C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424555 | ||||||
| chr12:102424642
|
G | C | 1 | a0001c0001t0003g0219 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.221-4952C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424642 | ||||||
| chr12:102424804
|
C | A | 1 | a0001c0001t0014g0085 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221-5114G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424804 | ||||||
| chr12:102424845
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.221-5155C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424845 | ||||||
| chr12:102424886
|
T | C | 1 | a0001c0001t0042g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.221-5196A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102424886 | ||||||
| chr12:102425225
|
G | T | 2 | a0001c0001t0002g0102a0001c0001t0045g0161 | 2 | NA18964.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.221-5535C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102425225 | ||||||
| chr12:102425466
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | HG00642.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.221-5776G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102425466 | ||||||
| chr12:102425478
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.221-5788G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102425478 | ||||||
| chr12:102425547
|
A | T | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-5857T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102425547 | ||||||
| chr12:102425713
|
T | G | 1 | a0001c0001t0027g0097 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.221-6023A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102425713 | ||||||
| chr12:102425821
|
T | C | 277 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(274): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.221-6131A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102425821 | ||||||
| chr12:102425969
|
A | G | 2 | a0001c0001t0004g0287a0001c0001t0047g0344 | 2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.221-6279T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102425969 | ||||||
| chr12:102426032
|
G | A | 1 | a0001c0001t0056g0011 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.221-6342C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102426032 | ||||||
| chr12:102426192
|
T | C | 1 | a0001c0001t0046g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.221-6502A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102426192 | ||||||
| chr12:102426413
|
T | A | 7 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0004g0321others(4): Show | 7 | NA18944.hp1 NA18957.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-6723A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102426413 | ||||||
| chr12:102426545
|
A | C | 2 | a0001c0001t0003g0209a0001c0001t0003g0215 | 2 | NA18612.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.221-6855T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102426545 | ||||||
| chr12:102426606
|
T | C | 1 | a0001c0001t0056g0011 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.221-6916A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102426606 | ||||||
| chr12:102426609
|
G | A | 73 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0004g0062others(70): Show | 73 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.221-6919C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102426609 | ||||||
| chr12:102426663
|
G | A | 1 | a0001c0001t0003g0224 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.221-6973C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102426663 | ||||||
| chr12:102427092
|
C | T | 9 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0297others(6): Show | 9 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-7402G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102427092 | ||||||
| chr12:102427240
|
A | G | 4 | a0001c0001t0016g0183a0001c0001t0016g0184a0001c0001t0080g0275others(1): Show | 4 | HG02976.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-7550T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102427240 | ||||||
| chr12:102427377
|
C | A | 277 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(274): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.221-7687G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102427377 | ||||||
| chr12:102427386
|
C | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0012g0039 | 3 | HG02280.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.221-7696G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102427386 | ||||||
| chr12:102427688
|
C | T | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-7998G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102427688 | ||||||
| chr12:102427710
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.221-8020C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102427710 | ||||||
| chr12:102428072
|
A | G | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-8382T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428072 | ||||||
| chr12:102428230
|
T | G | 1 | a0001c0001t0042g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.221-8540A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428230 | ||||||
| chr12:102428236
|
G | GTATATAT others(5): Show |
6 | a0001c0001t0013g0014a0001c0001t0013g0037a0001c0001t0013g0045others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-8558_221-8547d others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0046g0149a0001c0001t0046g0204 | 2 | NA18992.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.221-8547_221-8546i others(18): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(13): Show |
16 | a0001c0001t0001g0052a0001c0001t0001g0196a0001c0001t0001g0268others(13): Show | 16 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(15): Show |
4 | a0001c0001t0001g0270a0001c0001t0001g0276a0001c0001t0002g0177others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(24): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(17): Show |
3 | a0001c0001t0001g0032a0001c0001t0014g0098a0001c0001t0029g0113 | 3 | HG00639.hp2 HG00673.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.221-8547_221-8546i others(26): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(21): Show |
6 | a0001c0001t0001g0069a0001c0001t0001g0293a0001c0001t0002g0203others(3): Show | 6 | HG01123.hp1 HG01928.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(30): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(23): Show |
20 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0164others(17): Show | 20 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(32): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(25): Show |
24 | a0001c0001t0001g0033a0001c0001t0001g0084a0001c0001t0001g0086others(21): Show | 24 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(27): Show |
22 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0116others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(36): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(29): Show |
25 | a0001c0001t0001g0013a0001c0001t0001g0063a0001c0001t0001g0068others(22): Show | 25 | HG01433.hp1 HG01433.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(38): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(31): Show |
22 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0002g0029others(19): Show | 22 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(40): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(33): Show |
9 | a0001c0001t0001g0091a0001c0001t0001g0126a0001c0001t0001g0182others(6): Show | 10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(42): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(35): Show |
15 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0001t0002g0041others(12): Show | 16 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(44): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(37): Show |
14 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0123others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(39): Show |
4 | a0001c0001t0001g0034a0001c0001t0002g0071a0001c0001t0006g0261others(1): Show | 4 | HG02056.hp1 HG02523.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-8547_221-8546i others(48): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(41): Show |
1 | a0001c0001t0021g0347 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.221-8547_221-8546i others(50): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATATAT others(43): Show |
1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.221-8547_221-8546i others(52): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATGTAT others(29): Show |
1 | a0001c0001t0089g0255 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.221-8547_221-8546i others(38): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428236
|
G | GTATGTAT others(35): Show |
1 | a0001c0001t0062g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.221-8547_221-8546i others(44): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428236 | ||||||
| chr12:102428248
|
A | ATACTATA others(10): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02027.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.221-8559_221-8558i others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428248 | ||||||
| chr12:102428249
|
T | TATATATA others(30): Show |
1 | a0001c0001t0019g0015 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.221-8560_221-8559i others(39): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428249 | ||||||
| chr12:102428250
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02027.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.221-8560C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428250 | ||||||
| chr12:102428750
|
A | G | 197 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(194): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.221-9060T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102428750 | ||||||
| chr12:102429084
|
C | T | 55 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(52): Show | 57 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.221-9394G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102429084 | ||||||
| chr12:102429341
|
G | A | 1 | a0001c0001t0014g0098 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.221-9651C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102429341 | ||||||
| chr12:102429700
|
A | G | 203 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(200): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.221-10010T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102429700 | ||||||
| chr12:102429741
|
C | T | 276 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(273): Show | 278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.221-10051G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102429741 | ||||||
| chr12:102429772
|
C | G | 11 | a0001c0001t0002g0092a0001c0001t0028g0099a0001c0001t0028g0107others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-10082G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102429772 | ||||||
| chr12:102429814
|
A | C | 1 | a0001c0001t0080g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.221-10124T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102429814 | ||||||
| chr12:102429934
|
T | C | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.221-10244A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102429934 | ||||||
| chr12:102430122
|
G | A | 57 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(54): Show | 57 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.221-10432C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102430122 | ||||||
| chr12:102430212
|
T | G | 11 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-10522A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102430212 | ||||||
| chr12:102430436
|
C | T | 1 | a0001c0001t0071g0104 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.221-10746G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102430436 | ||||||
| chr12:102430861
|
C | T | 1 | a0001c0001t0021g0345 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.221-11171G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102430861 | ||||||
| chr12:102430946
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.221-11256T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102430946 | ||||||
| chr12:102431143
|
T | C | 204 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(201): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.221-11453A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102431143 | ||||||
| chr12:102431773
|
G | A | 1 | a0001c0001t0083g0296 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.221-12083C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102431773 | ||||||
| chr12:102431874
|
C | T | 1 | a0001c0001t0036g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.221-12184G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102431874 | ||||||
| chr12:102431955
|
C | T | 1 | a0001c0001t0014g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.221-12265G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102431955 | ||||||
| chr12:102432194
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0027 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.221-12504G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432194 | ||||||
| chr12:102432195
|
G | A | 1 | a0001c0001t0042g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.221-12505C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432195 | ||||||
| chr12:102432303
|
G | A | 2 | a0001c0001t0034g0146a0001c0001t0034g0201 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.221-12613C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432303 | ||||||
| chr12:102432362
|
T | C | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.221-12672A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432362 | ||||||
| chr12:102432538
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.221-12848G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432538 | ||||||
| chr12:102432555
|
C | T | 1 | a0001c0001t0059g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.221-12865G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432555 | ||||||
| chr12:102432563
|
G | T | 1 | a0001c0001t0003g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.221-12873C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432563 | ||||||
| chr12:102432566
|
GAGCACAG others(8): Show |
G | 1 | a0001c0001t0005g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.221-12891_221-1287 others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432566 | ||||||
| chr12:102432632
|
T | C | 1 | a0001c0001t0062g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.221-12942A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432632 | ||||||
| chr12:102432668
|
G | A | 1 | a0001c0001t0006g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.221-12978C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432668 | ||||||
| chr12:102432745
|
G | A | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-13055C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432745 | ||||||
| chr12:102432750
|
C | G | 11 | a0001c0001t0009g0059a0001c0001t0009g0309a0001c0001t0009g0310others(8): Show | 11 | HG01257.hp1 HG01258.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-13060G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432750 | ||||||
| chr12:102432847
|
AATAC | A | 75 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0004g0062others(72): Show | 75 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.221-13161_221-1315 others(8): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102432847 | ||||||
| chr12:102433145
|
G | A | 1 | a0001c0001t0077g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.221-13455C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102433145 | ||||||
| chr12:102433267
|
G | C | 277 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(274): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.221-13577C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102433267 | ||||||
| chr12:102433357
|
C | T | 3 | a0001c0001t0010g0231a0001c0001t0010g0232a0001c0001t0010g0233 | 3 | HG02257.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.221-13667G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102433357 | ||||||
| chr12:102433421
|
C | G | 1 | a0001c0001t0001g0292 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.221-13731G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102433421 | ||||||
| chr12:102433663
|
G | C | 197 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(194): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.221-13973C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102433663 | ||||||
| chr12:102434100
|
G | T | 1 | a0001c0001t0033g0355 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.221-14410C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434100 | ||||||
| chr12:102434146
|
CT | C | 7 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0053others(4): Show | 7 | HG02647.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-14457delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434146 | ||||||
| chr12:102434147
|
T | TC | 15 | a0001c0001t0001g0126a0001c0001t0002g0092a0001c0001t0024g0064others(12): Show | 15 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.221-14458_221-1445 others(5): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434147 | ||||||
| chr12:102434148
|
T | C | 183 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(180): Show | 185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.221-14458A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434148 | ||||||
| chr12:102434149
|
T | C | 5 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0053others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-14459A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434149 | ||||||
| chr12:102434294
|
C | T | 1 | a0001c0002t0079g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.221-14604G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434294 | ||||||
| chr12:102434298
|
C | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0013g0014others(2): Show | 5 | HG00741.hp1 HG01099.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-14608G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434298 | ||||||
| chr12:102434301
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.221-14611G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434301 | ||||||
| chr12:102434353
|
T | C | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.221-14663A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434353 | ||||||
| chr12:102434490
|
T | C | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-14800A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434490 | ||||||
| chr12:102434526
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.221-14836G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434526 | ||||||
| chr12:102434761
|
C | A | 5 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-15071G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102434761 | ||||||
| chr12:102435275
|
G | A | 2 | a0001c0001t0004g0325a0001c0001t0008g0305 | 2 | NA18998.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.221-15585C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102435275 | ||||||
| chr12:102435401
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.221-15711G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102435401 | ||||||
| chr12:102435402
|
G | A | 18 | a0001c0001t0001g0052a0001c0001t0001g0196a0001c0001t0001g0268others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.221-15712C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102435402 | ||||||
| chr12:102435880
|
C | T | 1 | a0001c0001t0041g0336 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.221-16190G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102435880 | ||||||
| chr12:102435942
|
T | C | 1 | a0001c0001t0053g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.221-16252A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102435942 | ||||||
| chr12:102435975
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.221-16285G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102435975 | ||||||
| chr12:102436082
|
T | C | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-16392A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102436082 | ||||||
| chr12:102436230
|
T | C | 277 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(274): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.221-16540A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102436230 | ||||||
| chr12:102436302
|
C | T | 1 | a0001c0001t0051g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.221-16612G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102436302 | ||||||
| chr12:102436304
|
C | T | 1 | a0001c0001t0091g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.221-16614G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102436304 | ||||||
| chr12:102436754
|
G | A | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-17064C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102436754 | ||||||
| chr12:102436926
|
G | A | 2 | a0001c0001t0002g0171a0001c0001t0002g0203 | 2 | NA18970.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.221-17236C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102436926 | ||||||
| chr12:102437714
|
G | A | 1 | a0001c0001t0086g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.221-18024C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102437714 | ||||||
| chr12:102437883
|
A | G | 1 | a0002c0003t0063g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.221-18193T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102437883 | ||||||
| chr12:102437944
|
T | G | 203 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(200): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.221-18254A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102437944 | ||||||
| chr12:102438008
|
T | G | 5 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-18318A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102438008 | ||||||
| chr12:102438284
|
G | T | 1 | a0001c0001t0006g0260 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.221-18594C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102438284 | ||||||
| chr12:102438374
|
C | A | 1 | a0001c0001t0059g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.221-18684G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102438374 | ||||||
| chr12:102438425
|
T | C | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-18735A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102438425 | ||||||
| chr12:102438453
|
A | G | 1 | a0001c0001t0051g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.221-18763T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102438453 | ||||||
| chr12:102438734
|
A | G | 9 | a0001c0001t0011g0005a0001c0001t0011g0346a0001c0001t0011g0348others(6): Show | 9 | HG01981.hp2 HG02132.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-19044T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102438734 | ||||||
| chr12:102438807
|
T | C | 3 | a0001c0001t0010g0231a0001c0001t0010g0232a0001c0001t0010g0233 | 3 | HG02257.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.221-19117A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102438807 | ||||||
| chr12:102439188
|
G | A | 3 | a0001c0001t0016g0178a0001c0001t0016g0183a0001c0001t0016g0274 | 3 | HG02622.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.221-19498C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102439188 | ||||||
| chr12:102439531
|
G | A | 11 | a0001c0001t0002g0092a0001c0001t0024g0064a0001c0001t0024g0093others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-19841C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102439531 | ||||||
| chr12:102439542
|
C | T | 1 | a0001c0001t0016g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.221-19852G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102439542 | ||||||
| chr12:102439594
|
C | T | 1 | a0001c0001t0020g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.221-19904G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102439594 | ||||||
| chr12:102439718
|
G | GA | 265 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.221-20029dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102439718 | ||||||
| chr12:102439744
|
G | A | 3 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200 | 3 | NA18964.hp2 NA19003.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.221-20054C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102439744 | ||||||
| chr12:102440102
|
C | A | 2 | a0001c0001t0008g0289a0001c0001t0008g0290 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.221-20412G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440102 | ||||||
| chr12:102440107
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0074a0001c0001t0002g0075others(1): Show | 5 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-20417C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440107 | ||||||
| chr12:102440199
|
T | G | 2 | a0001c0001t0036g0202a0001c0001t0088g0206 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.221-20509A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440199 | ||||||
| chr12:102440232
|
G | A | 277 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(274): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.221-20542C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440232 | ||||||
| chr12:102440256
|
T | G | 1 | a0001c0001t0041g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.221-20566A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440256 | ||||||
| chr12:102440291
|
C | G | 1 | a0001c0001t0015g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.221-20601G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440291 | ||||||
| chr12:102440479
|
A | G | 11 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-20789T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440479 | ||||||
| chr12:102440495
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0015g0090 | 2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.221-20805G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440495 | ||||||
| chr12:102440709
|
G | A | 1 | a0001c0001t0037g0186 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.221-21019C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440709 | ||||||
| chr12:102440824
|
C | T | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-21134G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440824 | ||||||
| chr12:102440846
|
T | G | 4 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(1): Show | 4 | HG02109.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-21156A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440846 | ||||||
| chr12:102440939
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.221-21249C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440939 | ||||||
| chr12:102440941
|
T | C | 1 | a0001c0001t0043g0193 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.221-21251A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102440941 | ||||||
| chr12:102441090
|
A | G | 73 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0004g0062others(70): Show | 73 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.221-21400T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441090 | ||||||
| chr12:102441124
|
G | A | 1 | a0001c0001t0020g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.221-21434C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441124 | ||||||
| chr12:102441302
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.221-21612T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441302 | ||||||
| chr12:102441346
|
T | C | 1 | a0001c0001t0057g0010 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.221-21656A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441346 | ||||||
| chr12:102441492
|
T | C | 6 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0004g0321others(3): Show | 6 | NA18944.hp1 NA18957.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-21802A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441492 | ||||||
| chr12:102441788
|
T | C | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-22098A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441788 | ||||||
| chr12:102441903
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0025g0114 | 3 | HG01074.hp1 HG01099.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.221-22213T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441903 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(35): Show |
3 | a0001c0001t0038g0137a0001c0001t0038g0138a0001c0001t0076g0115 | 3 | HG01168.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(47): Show |
1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(58): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(38): Show |
2 | a0001c0001t0002g0017a0001c0001t0002g0027 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(49): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(41): Show |
1 | a0001c0001t0077g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(52): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(44): Show |
1 | a0001c0001t0051g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(55): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(56): Show |
1 | a0001c0001t0048g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(67): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(8): Show |
1 | a0001c0001t0016g0183 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(17): Show |
2 | a0001c0001t0001g0279a0001c0001t0045g0161 | 2 | HG01243.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(28): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(20): Show |
2 | a0001c0001t0001g0196a0001c0001t0001g0276 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(31): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(23): Show |
4 | a0001c0001t0001g0272a0001c0001t0028g0107a0001c0001t0028g0179others(1): Show | 4 | HG01192.hp1 HG02602.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(26): Show |
3 | a0001c0001t0012g0100a0001c0001t0028g0099a0001c0001t0092g0156 | 3 | HG01123.hp1 HG01515.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(37): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(29): Show |
2 | a0001c0001t0078g0157a0001c0001t0081g0105 | 2 | HG00099.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(40): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(32): Show |
5 | a0001c0001t0001g0129a0001c0001t0001g0140a0001c0001t0001g0253others(2): Show | 5 | HG01934.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(43): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(35): Show |
2 | a0001c0001t0001g0134a0001c0001t0068g0038 | 2 | HG02723.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(38): Show |
3 | a0001c0001t0012g0039a0001c0001t0073g0065a0001c0002t0079g0147 | 3 | HG02280.hp1 HG03139.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(49): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(41): Show |
3 | a0001c0001t0001g0116a0001c0001t0002g0040a0001c0001t0039g0070 | 3 | HG00280.hp1 HG03041.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(52): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(44): Show |
1 | a0001c0001t0002g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(55): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(50): Show |
1 | a0001c0001t0090g0021 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(61): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(56): Show |
1 | a0001c0001t0045g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(67): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(5): Show |
2 | a0001c0001t0002g0075a0001c0001t0002g0180 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(16): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(8): Show |
13 | a0001c0001t0001g0052a0001c0001t0001g0270a0001c0001t0001g0271others(10): Show | 14 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(11): Show |
6 | a0001c0001t0002g0029a0001c0001t0002g0074a0001c0001t0006g0264others(3): Show | 7 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(14): Show |
12 | a0001c0001t0001g0263a0001c0001t0002g0030a0001c0001t0002g0071others(9): Show | 12 | HG00597.hp2 HG00642.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(25): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(32): Show |
1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(43): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(17): Show |
9 | a0001c0001t0002g0060a0001c0001t0002g0171a0001c0001t0002g0203others(6): Show | 9 | HG00733.hp1 HG02523.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(28): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(20): Show |
14 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(31): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(23): Show |
12 | a0001c0001t0001g0268a0001c0001t0002g0006a0001c0001t0002g0102others(9): Show | 12 | HG01433.hp1 HG01952.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(26): Show |
13 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0122others(10): Show | 13 | HG00673.hp2 HG01928.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(37): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(29): Show |
9 | a0001c0001t0001g0117a0001c0001t0001g0126a0001c0001t0001g0139others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(40): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(32): Show |
5 | a0001c0001t0001g0063a0001c0001t0027g0125a0001c0001t0039g0133others(2): Show | 5 | HG01975.hp1 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(43): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(35): Show |
7 | a0001c0001t0001g0111a0001c0001t0001g0120a0001c0001t0001g0164others(4): Show | 7 | HG01081.hp1 HG01081.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(38): Show |
5 | a0001c0001t0001g0293a0001c0001t0002g0036a0001c0001t0022g0020others(2): Show | 5 | HG02486.hp2 HG03041.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(49): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(41): Show |
3 | a0001c0001t0002g0050a0001c0001t0002g0154a0001c0001t0067g0042 | 3 | HG02622.hp1 HG02897.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(52): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(44): Show |
2 | a0001c0001t0001g0121a0001c0001t0002g0026 | 2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(55): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(62): Show |
1 | a0001c0001t0041g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(73): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(8): Show |
1 | a0001c0001t0094g0007 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(11): Show |
1 | a0001c0001t0032g0135 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(14): Show |
1 | a0001c0001t0093g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(25): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(17): Show |
1 | a0001c0001t0042g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(28): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(20): Show |
6 | a0001c0001t0001g0095a0001c0001t0001g0109a0001c0001t0001g0230others(3): Show | 6 | HG00639.hp2 HG02015.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(31): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(23): Show |
8 | a0001c0001t0001g0136a0001c0001t0001g0356a0001c0001t0011g0346others(5): Show | 8 | NA18941.hp2 NA18942.hp1 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(26): Show |
7 | a0001c0001t0001g0110a0001c0001t0001g0292a0001c0001t0002g0145others(4): Show | 7 | HG00408.hp1 HG01346.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(37): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(206): Show |
1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(217): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(29): Show |
1 | a0001c0001t0001g0013 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(40): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(32): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0084a0001c0001t0001g0108others(1): Show | 4 | HG02135.hp1 HG02258.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(43): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(38): Show |
5 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0002g0053others(2): Show | 5 | HG01516.hp1 HG02647.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(49): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(41): Show |
1 | a0001c0001t0014g0085 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(52): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTGC others(47): Show |
1 | a0001c0001t0095g0240 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(58): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTTC others(20): Show |
1 | a0001c0001t0004g0307 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(31): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTGCTTC others(38): Show |
1 | a0001c0001t0032g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.221-22217_221-2221 others(49): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(8): Show |
2 | a0001c0001t0004g0297a0001c0001t0020g0080 | 2 | HG02109.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(11): Show |
2 | a0001c0001t0004g0353a0001c0001t0008g0291 | 2 | HG02698.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(14): Show |
8 | a0001c0001t0004g0308a0001c0001t0004g0311a0001c0001t0008g0288others(5): Show | 8 | HG01993.hp2 HG02135.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(25): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(17): Show |
7 | a0001c0001t0004g0294a0001c0001t0004g0320a0001c0001t0004g0321others(4): Show | 7 | HG01346.hp2 HG01361.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(28): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(20): Show |
5 | a0001c0001t0004g0287a0001c0001t0004g0304a0001c0001t0004g0306others(2): Show | 5 | HG04184.hp1 NA18945.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(31): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(23): Show |
5 | a0001c0001t0004g0316a0001c0001t0004g0318a0001c0001t0004g0319others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(26): Show |
10 | a0001c0001t0004g0299a0001c0001t0004g0315a0001c0001t0004g0325others(7): Show | 10 | HG01099.hp1 HG01884.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(37): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(29): Show |
8 | a0001c0001t0002g0280a0001c0001t0004g0301a0001c0001t0004g0333others(5): Show | 8 | HG01952.hp1 HG02040.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(40): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(32): Show |
7 | a0001c0001t0002g0269a0001c0001t0004g0062a0001c0001t0004g0295others(4): Show | 7 | HG02071.hp1 HG02155.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-22217_221-2221 others(43): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(35): Show |
2 | a0001c0001t0004g0330a0001c0001t0084g0300 | 2 | HG00423.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(46): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(38): Show |
3 | a0001c0001t0004g0302a0001c0001t0004g0313a0001c0001t0018g0298 | 3 | HG02129.hp2 HG04115.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(49): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(41): Show |
2 | a0001c0001t0022g0281a0001c0001t0034g0201 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.221-22217_221-2221 others(52): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
G | GCTTCTTC others(104): Show |
1 | a0001c0001t0034g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.221-22217_221-2221 others(115): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441906
|
GCTTCTTC others(5): Show |
G | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-22228_221-2221 others(16): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441906 | ||||||
| chr12:102441908
|
T | TGCTTCTT others(155): Show |
1 | a0001c0001t0025g0114 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.221-22219_221-2221 others(166): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441908 | ||||||
| chr12:102441909
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.221-22219A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441909 | ||||||
| chr12:102441909
|
T | G | 8 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0118others(5): Show | 8 | HG00741.hp1 HG01070.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-22219A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441909 | ||||||
| chr12:102441912
|
T | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0123others(2): Show | 5 | HG01070.hp2 HG01257.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-22222A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441912 | ||||||
| chr12:102441915
|
C | CCTTCTT | 4 | a0001c0001t0003g0215a0001c0001t0005g0282a0001c0001t0007g0187others(1): Show | 4 | HG03540.hp2 NA18953.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-22231_221-2222 others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | CCTTCTTC others(2): Show |
17 | a0001c0001t0003g0003a0001c0001t0003g0197a0001c0001t0003g0209others(14): Show | 18 | HG00099.hp2 HG00597.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.221-22234_221-2222 others(13): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | CCTTCTTC others(5): Show |
17 | a0001c0001t0003g0018a0001c0001t0003g0024a0001c0001t0003g0072others(14): Show | 17 | HG01256.hp2 HG02056.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.221-22237_221-2222 others(16): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | CCTTCTTC others(8): Show |
7 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190others(4): Show | 7 | HG00323.hp1 NA18940.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-22240_221-2222 others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | CCTTCTTC others(11): Show |
9 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0213others(6): Show | 9 | HG00423.hp2 HG01106.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-22243_221-2222 others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | CCTTCTTC others(14): Show |
3 | a0001c0001t0003g0248a0001c0001t0054g0229a0001c0001t0057g0010 | 3 | HG01074.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.221-22246_221-2222 others(25): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | CCTTCTTC others(17): Show |
3 | a0001c0001t0003g0200a0001c0001t0014g0058a0001c0001t0044g0004 | 4 | HG01516.hp2 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-22249_221-2222 others(28): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | CCTTCTTC others(23): Show |
1 | a0001c0001t0059g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.221-22255_221-2222 others(34): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441915
|
C | T | 275 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(272): Show | 277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.221-22225G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441915 | ||||||
| chr12:102441921
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.221-22231A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441921 | ||||||
| chr12:102441921
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-22231A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441921 | ||||||
| chr12:102441924
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-22234A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441924 | ||||||
| chr12:102441927
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-22237A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441927 | ||||||
| chr12:102441930
|
T | C | 1 | a0001c0001t0006g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.221-22240A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441930 | ||||||
| chr12:102441933
|
T | TCTTCTTC others(179): Show |
1 | a0001c0001t0001g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.221-22244_221-2224 others(190): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441933 | ||||||
| chr12:102441940
|
C | CTTCTTCT others(164): Show |
1 | a0001c0001t0026g0341 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.221-22251_221-2225 others(175): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441940 | ||||||
| chr12:102441940
|
C | CTTCTTCT others(161): Show |
1 | a0001c0001t0026g0342 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.221-22251_221-2225 others(172): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441940 | ||||||
| chr12:102441940
|
C | CTTCTTCT others(188): Show |
1 | a0001c0001t0040g0303 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.221-22251_221-2225 others(199): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441940 | ||||||
| chr12:102441940
|
C | CTTCTTCT others(185): Show |
1 | a0001c0001t0026g0340 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.221-22251_221-2225 others(196): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441940 | ||||||
| chr12:102441940
|
C | CTTCTTCT others(208): Show |
1 | a0001c0001t0040g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.221-22251_221-2225 others(219): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441940 | ||||||
| chr12:102441941
|
T | C | 1 | a0001c0001t0074g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.221-22251A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441941 | ||||||
| chr12:102441948
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0130 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.221-22258A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441948 | ||||||
| chr12:102441951
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.221-22261A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441951 | ||||||
| chr12:102441952
|
C | CTTCTTCT others(238): Show |
1 | a0001c0001t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.221-22263_221-2226 others(249): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441952 | ||||||
| chr12:102441953
|
T | TCCTTCTC others(183): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0130 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.221-22264_221-2226 others(194): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441953 | ||||||
| chr12:102441953
|
T | TTCTCCTT others(162): Show |
1 | a0001c0001t0001g0069 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.221-22264_221-2226 others(173): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441953 | ||||||
| chr12:102441953
|
T | TTCTTCTC others(165): Show |
1 | a0001c0001t0074g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.221-22264_221-2226 others(176): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441953 | ||||||
| chr12:102441953
|
T | TTCTTCTT others(189): Show |
1 | a0001c0001t0001g0123 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.221-22264_221-2226 others(200): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441953 | ||||||
| chr12:102441953
|
T | TTCTTCTT others(200): Show |
1 | a0001c0001t0001g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.221-22264_221-2226 others(211): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441953 | ||||||
| chr12:102441955
|
C | CTTCTTCT others(6): Show |
1 | a0001c0001t0070g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.221-22266_221-2226 others(17): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441955 | ||||||
| chr12:102441956
|
T | TTC | 8 | a0001c0001t0002g0006a0001c0001t0002g0175a0001c0001t0012g0054others(5): Show | 8 | HG01433.hp1 HG02486.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-22267_221-2226 others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441956 | ||||||
| chr12:102441956
|
T | TTCTTCTT others(22): Show |
1 | a0001c0001t0004g0322 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.221-22267_221-2226 others(33): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441956 | ||||||
| chr12:102441957
|
T | TCTTCTTC others(27): Show |
1 | a0001c0001t0050g0212 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.221-22268_221-2226 others(38): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441957 | ||||||
| chr12:102441957
|
T | TCTTCTTC others(45): Show |
1 | a0001c0001t0009g0059 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.221-22268_221-2226 others(56): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441957 | ||||||
| chr12:102441958
|
T | C | 66 | a0001c0001t0001g0111a0001c0001t0002g0269a0001c0001t0002g0280others(63): Show | 68 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.221-22268A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441958 | ||||||
| chr12:102441959
|
T | C | 6 | a0001c0001t0002g0175a0001c0001t0012g0054a0001c0001t0019g0015others(3): Show | 6 | HG01433.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-22269A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441959 | ||||||
| chr12:102441960
|
T | C | 1 | a0001c0001t0050g0212 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.221-22270A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441960 | ||||||
| chr12:102441962
|
T | C | 1 | a0001c0001t0066g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.221-22272A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441962 | ||||||
| chr12:102441963
|
T | C | 1 | a0001c0001t0005g0049 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.221-22273A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441963 | ||||||
| chr12:102441965
|
T | C | 1 | a0001c0001t0066g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.221-22275A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102441965 | ||||||
| chr12:102442081
|
C | T | 203 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(200): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.221-22391G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442081 | ||||||
| chr12:102442127
|
T | C | 1 | a0001c0001t0014g0098 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.221-22437A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442127 | ||||||
| chr12:102442135
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0037g0159 | 3 | HG02027.hp2 NA18942.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.221-22445C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442135 | ||||||
| chr12:102442288
|
C | T | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-22598G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442288 | ||||||
| chr12:102442496
|
A | G | 1 | a0001c0001t0004g0304 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.221-22806T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442496 | ||||||
| chr12:102442510
|
G | C | 3 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281 | 3 | HG03516.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.221-22820C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442510 | ||||||
| chr12:102442908
|
T | G | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-23218A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442908 | ||||||
| chr12:102442940
|
T | C | 2 | a0001c0001t0029g0112a0001c0001t0029g0113 | 2 | HG00733.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.221-23250A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102442940 | ||||||
| chr12:102443040
|
A | G | 1 | a0001c0001t0011g0005 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.221-23350T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102443040 | ||||||
| chr12:102443178
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.221-23488A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102443178 | ||||||
| chr12:102443402
|
G | A | 2 | a0001c0001t0014g0098a0001c0001t0032g0135 | 2 | HG00639.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.221-23712C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102443402 | ||||||
| chr12:102443428
|
G | A | 2 | a0001c0001t0002g0171a0001c0001t0002g0203 | 2 | NA18970.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.221-23738C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102443428 | ||||||
| chr12:102443851
|
G | A | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221-24161C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102443851 | ||||||
| chr12:102443951
|
C | G | 3 | a0001c0001t0042g0241a0001c0001t0093g0243a0001c0001t0095g0240 | 3 | HG02486.hp2 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.221-24261G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102443951 | ||||||
| chr12:102444027
|
A | T | 3 | a0001c0001t0009g0309a0001c0001t0009g0310a0001c0001t0009g0328 | 3 | NA18955.hp2 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.221-24337T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444027 | ||||||
| chr12:102444085
|
T | C | 277 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(274): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.221-24395A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444085 | ||||||
| chr12:102444191
|
G | A | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-24501C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444191 | ||||||
| chr12:102444260
|
T | C | 1 | a0001c0001t0004g0317 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.221-24570A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444260 | ||||||
| chr12:102444345
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0001g0253a0001c0001t0027g0125others(3): Show | 6 | HG01243.hp2 HG01934.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-24655G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444345 | ||||||
| chr12:102444350
|
G | A | 203 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(200): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.221-24660C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444350 | ||||||
| chr12:102444403
|
A | G | 1 | a0001c0001t0004g0317 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.221-24713T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444403 | ||||||
| chr12:102444446
|
C | A | 1 | a0001c0001t0075g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.221-24756G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444446 | ||||||
| chr12:102444509
|
C | T | 1 | a0001c0001t0067g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.221-24819G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444509 | ||||||
| chr12:102444655
|
T | C | 1 | a0001c0001t0089g0255 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.221-24965A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444655 | ||||||
| chr12:102444709
|
G | A | 1 | a0001c0001t0085g0312 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.221-25019C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444709 | ||||||
| chr12:102444714
|
A | G | 1 | a0001c0001t0004g0308 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.221-25024T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444714 | ||||||
| chr12:102444737
|
C | T | 263 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(260): Show | 265 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.221-25047G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444737 | ||||||
| chr12:102444794
|
G | C | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-25104C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444794 | ||||||
| chr12:102444812
|
G | A | 1 | a0001c0001t0036g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.221-25122C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102444812 | ||||||
| chr12:102445022
|
G | A | 1 | a0001c0001t0072g0237 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.221-25332C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445022 | ||||||
| chr12:102445121
|
G | A | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-25431C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445121 | ||||||
| chr12:102445218
|
A | C | 4 | a0001c0001t0008g0288a0001c0001t0008g0289a0001c0001t0008g0290others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-25528T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445218 | ||||||
| chr12:102445218
|
A | G | 273 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(270): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.221-25528T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445218 | ||||||
| chr12:102445235
|
C | T | 1 | a0001c0001t0091g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.221-25545G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445235 | ||||||
| chr12:102445336
|
A | C | 277 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(274): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.221-25646T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445336 | ||||||
| chr12:102445664
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0004g0338 | 2 | HG01346.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.221-25974G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445664 | ||||||
| chr12:102445669
|
A | G | 1 | a0001c0001t0067g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.221-25979T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445669 | ||||||
| chr12:102445756
|
C | T | 2 | a0001c0001t0024g0093a0001c0001t0024g0103 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.221-26066G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102445756 | ||||||
| chr12:102446226
|
G | A | 1 | a0001c0001t0011g0005 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.221-26536C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102446226 | ||||||
| chr12:102446397
|
C | G | 73 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0004g0062others(70): Show | 73 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.221-26707G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102446397 | ||||||
| chr12:102446522
|
T | C | 1 | a0001c0001t0003g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.221-26832A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102446522 | ||||||
| chr12:102446679
|
A | G | 345 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(342): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.221-26989T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102446679 | ||||||
| chr12:102446716
|
A | G | 1 | a0001c0001t0017g0141 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.221-27026T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102446716 | ||||||
| chr12:102446884
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0002g0172 | 2 | HG00673.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.221-27194T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102446884 | ||||||
| chr12:102447078
|
T | C | 2 | a0001c0001t0036g0202a0001c0001t0088g0206 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.221-27388A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102447078 | ||||||
| chr12:102447243
|
G | A | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-27553C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102447243 | ||||||
| chr12:102447612
|
G | A | 1 | a0001c0001t0004g0304 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.221-27922C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102447612 | ||||||
| chr12:102447669
|
T | G | 1 | a0001c0001t0013g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.220+27974A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102447669 | ||||||
| chr12:102447866
|
A | G | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+27777T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102447866 | ||||||
| chr12:102447995
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02027.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.220+27648T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102447995 | ||||||
| chr12:102448033
|
G | A | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.220+27610C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448033 | ||||||
| chr12:102448048
|
C | T | 73 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0004g0062others(70): Show | 73 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.220+27595G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448048 | ||||||
| chr12:102448105
|
G | GT | 345 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(342): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.220+27537dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448105 | ||||||
| chr12:102448132
|
G | A | 3 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0228 | 3 | HG00423.hp2 HG02523.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.220+27511C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448132 | ||||||
| chr12:102448440
|
C | T | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.220+27203G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448440 | ||||||
| chr12:102448456
|
G | A | 2 | a0001c0001t0029g0112a0001c0001t0029g0113 | 2 | HG00733.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.220+27187C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448456 | ||||||
| chr12:102448481
|
T | C | 2 | a0001c0001t0006g0264a0001c0001t0006g0267 | 2 | NA18977.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.220+27162A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448481 | ||||||
| chr12:102448537
|
G | T | 6 | a0001c0001t0026g0340a0001c0001t0026g0341a0001c0001t0026g0342others(3): Show | 7 | HG00639.hp1 HG01071.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+27106C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448537 | ||||||
| chr12:102448545
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.220+27098C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448545 | ||||||
| chr12:102448606
|
G | A | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+27037C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448606 | ||||||
| chr12:102448613
|
G | A | 5 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+27030C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448613 | ||||||
| chr12:102448639
|
T | C | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+27004A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448639 | ||||||
| chr12:102448689
|
T | TAA | 7 | a0001c0001t0004g0294a0001c0001t0004g0315a0001c0001t0004g0316others(4): Show | 7 | HG01099.hp1 HG02074.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+26952_220+2695 others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
T | TAAA | 43 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0295others(40): Show | 43 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.220+26951_220+2695 others(7): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
T | TAAAA | 9 | a0001c0001t0004g0297a0001c0001t0004g0299a0001c0001t0004g0301others(6): Show | 9 | HG02080.hp2 HG02132.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+26950_220+2695 others(8): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
TA | T | 15 | a0001c0001t0003g0225a0001c0001t0003g0250a0001c0001t0010g0231others(12): Show | 15 | HG00642.hp2 HG01106.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+26953delT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
TAA | T | 45 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(42): Show | 47 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.220+26952_220+2695 others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
TAAA | T | 9 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200others(6): Show | 9 | HG01074.hp2 HG01167.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+26951_220+2695 others(7): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
TAAAA | T | 10 | a0001c0001t0001g0033a0001c0001t0001g0095a0001c0001t0001g0136others(7): Show | 10 | HG00323.hp1 HG01168.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+26950_220+2695 others(8): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
TAAAAA | T | 170 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0034others(167): Show | 172 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.220+26949_220+2695 others(9): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448689
|
TAAAAAA | T | 19 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0131others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.220+26948_220+2695 others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448689 | ||||||
| chr12:102448695
|
A | AT | 3 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281 | 3 | HG03516.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.220+26947_220+2694 others(5): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448695 | ||||||
| chr12:102448697
|
A | T | 2 | a0001c0001t0034g0146a0001c0001t0034g0201 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.220+26946T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448697 | ||||||
| chr12:102448701
|
A | T | 98 | a0001c0001t0001g0052a0001c0001t0001g0089a0001c0001t0001g0196others(95): Show | 100 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.220+26942T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448701 | ||||||
| chr12:102448702
|
A | T | 11 | a0001c0001t0002g0092a0001c0001t0012g0100a0001c0001t0013g0165others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+26941T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448702 | ||||||
| chr12:102448933
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.220+26710G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102448933 | ||||||
| chr12:102449211
|
T | C | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+26432A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102449211 | ||||||
| chr12:102449380
|
C | G | 1 | a0001c0001t0062g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.220+26263G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102449380 | ||||||
| chr12:102449452
|
C | G | 1 | a0001c0001t0085g0312 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.220+26191G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102449452 | ||||||
| chr12:102449536
|
T | C | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+26107A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102449536 | ||||||
| chr12:102449681
|
G | T | 1 | a0001c0001t0009g0309 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.220+25962C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102449681 | ||||||
| chr12:102449976
|
C | T | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+25667G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102449976 | ||||||
| chr12:102449992
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0037g0159 | 3 | HG02027.hp2 NA18942.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.220+25651C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102449992 | ||||||
| chr12:102450029
|
C | T | 8 | a0001c0001t0011g0005a0001c0001t0011g0346a0001c0001t0011g0348others(5): Show | 8 | HG02132.hp1 NA18941.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+25614G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102450029 | ||||||
| chr12:102450101
|
G | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | HG00642.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.220+25542C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102450101 | ||||||
| chr12:102450284
|
A | G | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0012g0039 | 3 | HG02280.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.220+25359T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102450284 | ||||||
| chr12:102450458
|
G | A | 282 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(279): Show | 284 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.220+25185C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102450458 | ||||||
| chr12:102450809
|
C | A | 1 | a0001c0001t0002g0092 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.220+24834G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102450809 | ||||||
| chr12:102450832
|
G | A | 1 | a0001c0001t0086g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.220+24811C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102450832 | ||||||
| chr12:102450948
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0029g0112a0001c0001t0029g0113 | 3 | HG00733.hp1 HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.220+24695A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102450948 | ||||||
| chr12:102451083
|
C | G | 2 | a0001c0001t0001g0089a0001c0001t0015g0090 | 2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.220+24560G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102451083 | ||||||
| chr12:102451615
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0074a0001c0001t0002g0075others(1): Show | 5 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+24028C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102451615 | ||||||
| chr12:102451617
|
A | G | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+24026T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102451617 | ||||||
| chr12:102451766
|
G | T | 276 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(273): Show | 278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.220+23877C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102451766 | ||||||
| chr12:102452028
|
C | T | 2 | a0001c0001t0004g0331a0001c0001t0004g0332 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.220+23615G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452028 | ||||||
| chr12:102452034
|
G | A | 1 | a0001c0001t0015g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.220+23609C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452034 | ||||||
| chr12:102452037
|
C | T | 5 | a0001c0001t0028g0099a0001c0001t0028g0107a0001c0001t0028g0179others(2): Show | 5 | HG00099.hp1 HG01123.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+23606G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452037 | ||||||
| chr12:102452241
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220+23402C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452241 | ||||||
| chr12:102452242
|
A | G | 55 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0024others(52): Show | 57 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.220+23401T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452242 | ||||||
| chr12:102452261
|
C | CA | 72 | a0001c0001t0001g0052a0001c0001t0001g0089a0001c0001t0001g0271others(69): Show | 73 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.220+23381dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452261
|
C | CAA | 41 | a0001c0001t0001g0034a0001c0001t0001g0095a0001c0001t0001g0196others(38): Show | 42 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.220+23380_220+2338 others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452261
|
C | CAAA | 70 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0061others(67): Show | 70 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.220+23379_220+2338 others(7): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452261
|
C | CAAAA | 20 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0094others(17): Show | 20 | HG00741.hp1 HG01074.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.220+23378_220+2338 others(8): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452261
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0020g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.220+23371_220+2338 others(15): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452261
|
C | CAAAAAAA others(5): Show |
1 | a0002c0003t0063g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.220+23370_220+2338 others(16): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452261
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0062g0254a0001c0001t0089g0255 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.220+23368_220+2338 others(18): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452261
|
CA | C | 92 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0003g0003others(89): Show | 94 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.220+23381delT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452261 | ||||||
| chr12:102452726
|
A | G | 202 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(199): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.220+22917T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452726 | ||||||
| chr12:102452871
|
A | G | 1 | a0001c0001t0032g0135 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.220+22772T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452871 | ||||||
| chr12:102452963
|
A | G | 1 | a0001c0001t0068g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220+22680T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102452963 | ||||||
| chr12:102453025
|
G | A | 2 | a0001c0001t0004g0331a0001c0001t0004g0332 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.220+22618C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102453025 | ||||||
| chr12:102453159
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.220+22484T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102453159 | ||||||
| chr12:102453168
|
C | T | 2 | a0001c0001t0042g0241a0001c0001t0095g0240 | 2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.220+22475G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102453168 | ||||||
| chr12:102453298
|
A | G | 345 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(342): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.220+22345T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102453298 | ||||||
| chr12:102453310
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220+22333C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102453310 | ||||||
| chr12:102453741
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.220+21902G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102453741 | ||||||
| chr12:102454468
|
G | A | 62 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.220+21175C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102454468 | ||||||
| chr12:102454564
|
C | T | 57 | a0001c0001t0004g0062a0001c0001t0004g0287a0001c0001t0004g0294others(54): Show | 57 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.220+21079G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102454564 | ||||||
| chr12:102454823
|
T | C | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+20820A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102454823 | ||||||
| chr12:102455248
|
T | C | 1 | a0001c0001t0011g0348 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.220+20395A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102455248 | ||||||
| chr12:102455334
|
A | G | 2 | a0001c0001t0007g0207a0001c0001t0007g0208 | 2 | HG01496.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.220+20309T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102455334 | ||||||
| chr12:102455528
|
G | A | 1 | a0001c0001t0055g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+20115C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102455528 | ||||||
| chr12:102455553
|
G | C | 1 | a0001c0001t0004g0323 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.220+20090C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102455553 | ||||||
| chr12:102455964
|
T | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG00673.hp2 HG02135.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+19679A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102455964 | ||||||
| chr12:102456058
|
A | T | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0093g0243others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+19585T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456058 | ||||||
| chr12:102456061
|
A | G | 3 | a0001c0001t0001g0111a0001c0001t0029g0112a0001c0001t0029g0113 | 3 | HG00733.hp1 HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.220+19582T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456061 | ||||||
| chr12:102456166
|
C | G | 1 | a0001c0001t0071g0104 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.220+19477G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456166 | ||||||
| chr12:102456208
|
T | C | 5 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+19435A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456208 | ||||||
| chr12:102456221
|
G | GGT | 35 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0134others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.220+19420_220+1942 others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
G | GGTGT | 19 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0197others(16): Show | 20 | HG01496.hp1 HG02015.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.220+19418_220+1942 others(8): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
G | GGTGTGT | 5 | a0001c0001t0003g0198a0001c0001t0003g0217a0001c0001t0003g0227others(2): Show | 5 | HG01074.hp2 HG02976.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+19416_220+1942 others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
G | GGTGTGTG others(1): Show |
3 | a0001c0001t0003g0191a0001c0001t0056g0011a0001c0001t0057g0010 | 3 | HG01167.hp2 NA18949.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.220+19414_220+1942 others(12): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0003g0216 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.220+19412_220+1942 others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGT | G | 99 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0052others(96): Show | 99 | HG00423.hp1 HG00642.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.220+19420_220+1942 others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGT | G | 103 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0089others(100): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.220+19418_220+1942 others(8): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGTGT | G | 29 | a0001c0001t0001g0196a0001c0001t0001g0268a0001c0001t0001g0270others(26): Show | 29 | HG01192.hp1 HG01243.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.220+19416_220+1942 others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGTGTG others(1): Show |
G | 8 | a0001c0001t0002g0017a0001c0001t0008g0288a0001c0001t0008g0289others(5): Show | 8 | HG02486.hp2 HG02698.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+19414_220+1942 others(12): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0002g0154a0001c0001t0015g0153 | 2 | NA19011.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.220+19412_220+1942 others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGTGTG others(5): Show |
G | 5 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+19410_220+1942 others(16): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0062g0254a0001c0001t0089g0255 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.220+19408_220+1942 others(18): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGTGTG others(9): Show |
G | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+19406_220+1942 others(20): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456221
|
GGTGTGTG others(11): Show |
G | 2 | a0001c0001t0006g0258a0001c0002t0079g0147 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.220+19404_220+1942 others(22): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456221 | ||||||
| chr12:102456445
|
A | G | 278 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(275): Show | 280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.220+19198T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456445 | ||||||
| chr12:102456524
|
A | G | 1 | a0001c0001t0016g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.220+19119T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456524 | ||||||
| chr12:102456565
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0015g0090 | 2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.220+19078C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456565 | ||||||
| chr12:102456684
|
T | G | 3 | a0001c0001t0005g0057a0001c0001t0060g0056a0001c0001t0061g0055 | 3 | HG00642.hp2 HG00733.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.220+18959A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456684 | ||||||
| chr12:102456755
|
C | T | 1 | a0001c0001t0080g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.220+18888G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456755 | ||||||
| chr12:102456801
|
T | C | 6 | a0001c0001t0009g0059a0001c0001t0009g0309a0001c0001t0009g0310others(3): Show | 6 | HG02080.hp2 NA18947.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+18842A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456801 | ||||||
| chr12:102456822
|
G | T | 1 | a0001c0001t0003g0248 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.220+18821C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456822 | ||||||
| chr12:102456940
|
G | C | 2 | a0001c0001t0038g0137a0001c0001t0038g0138 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.220+18703C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102456940 | ||||||
| chr12:102457023
|
A | T | 1 | a0001c0001t0093g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.220+18620T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457023 | ||||||
| chr12:102457026
|
G | A | 1 | a0001c0001t0030g0001 | 2 | HG00639.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.220+18617C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457026 | ||||||
| chr12:102457094
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.220+18549G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457094 | ||||||
| chr12:102457186
|
A | G | 17 | a0001c0001t0001g0196a0001c0001t0001g0268a0001c0001t0001g0270others(14): Show | 17 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.220+18457T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457186 | ||||||
| chr12:102457197
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.220+18446T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457197 | ||||||
| chr12:102457299
|
A | T | 1 | a0001c0001t0022g0020 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.220+18344T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457299 | ||||||
| chr12:102457454
|
AT | A | 4 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0012g0039others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+18188delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457454 | ||||||
| chr12:102457456
|
T | A | 4 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0012g0039others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+18187A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457456 | ||||||
| chr12:102457623
|
C | T | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0055g0244others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+18020G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457623 | ||||||
| chr12:102457881
|
T | A | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+17762A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457881 | ||||||
| chr12:102457916
|
C | T | 1 | a0001c0001t0051g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.220+17727G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102457916 | ||||||
| chr12:102458020
|
G | A | 2 | a0001c0001t0007g0187a0001c0001t0007g0238 | 2 | NA18953.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.220+17623C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458020 | ||||||
| chr12:102458243
|
C | T | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+17400G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458243 | ||||||
| chr12:102458282
|
C | T | 1 | a0001c0001t0007g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.220+17361G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458282 | ||||||
| chr12:102458612
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0130 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.220+17031G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458612 | ||||||
| chr12:102458730
|
C | CA | 16 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0197others(13): Show | 17 | HG02015.hp2 HG02056.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.220+16912dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458730 | ||||||
| chr12:102458730
|
C | CAAAAAAA others(2): Show |
89 | a0001c0001t0001g0052a0001c0001t0001g0086a0001c0001t0001g0120others(86): Show | 90 | HG00280.hp2 HG00597.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.220+16904_220+1691 others(13): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458730 | ||||||
| chr12:102458730
|
C | CAAAAAAA others(3): Show |
143 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.220+16903_220+1691 others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458730 | ||||||
| chr12:102458730
|
C | CAAAAAAA others(4): Show |
36 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0069others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.220+16902_220+1691 others(15): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458730 | ||||||
| chr12:102458730
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0020g0079a0001c0001t0020g0083a0001c0001t0056g0011others(1): Show | 4 | HG01167.hp2 HG02818.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+16900_220+1691 others(17): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458730 | ||||||
| chr12:102458730
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0010g0009a0001c0001t0010g0233a0001c0001t0020g0080others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+16899_220+1691 others(18): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458730 | ||||||
| chr12:102458730
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0010g0231a0001c0001t0010g0232a0002c0003t0063g0081 | 3 | HG02257.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.220+16898_220+1691 others(19): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458730 | ||||||
| chr12:102458742
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0002g0195 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.220+16900_220+1690 others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458742 | ||||||
| chr12:102458787
|
C | G | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+16856G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458787 | ||||||
| chr12:102458788
|
T | C | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+16855A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458788 | ||||||
| chr12:102458839
|
T | C | 7 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+16804A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458839 | ||||||
| chr12:102458850
|
A | G | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+16793T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458850 | ||||||
| chr12:102458906
|
C | T | 1 | a0001c0001t0012g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.220+16737G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102458906 | ||||||
| chr12:102459040
|
T | G | 1 | a0001c0001t0008g0234 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.220+16603A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102459040 | ||||||
| chr12:102459246
|
C | T | 1 | a0001c0001t0012g0100 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.220+16397G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102459246 | ||||||
| chr12:102459376
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.220+16267G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102459376 | ||||||
| chr12:102459394
|
T | C | 282 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(279): Show | 284 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.220+16249A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102459394 | ||||||
| chr12:102459465
|
C | T | 12 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0020g0079others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+16178G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102459465 | ||||||
| chr12:102460263
|
G | A | 3 | a0001c0001t0002g0017a0001c0001t0002g0026a0001c0001t0002g0027 | 3 | HG02572.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.220+15380C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460263 | ||||||
| chr12:102460329
|
A | C | 5 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0022g0281others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+15314T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460329 | ||||||
| chr12:102460465
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.220+15178G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460465 | ||||||
| chr12:102460489
|
C | A | 5 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200others(2): Show | 5 | HG03486.hp2 HG04115.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+15154G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460489 | ||||||
| chr12:102460571
|
T | C | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+15072A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460571 | ||||||
| chr12:102460696
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.220+14947G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460696 | ||||||
| chr12:102460698
|
G | T | 3 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190 | 3 | NA18945.hp2 NA18946.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.220+14945C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460698 | ||||||
| chr12:102460740
|
G | T | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+14903C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460740 | ||||||
| chr12:102460786
|
G | A | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0055g0244others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+14857C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460786 | ||||||
| chr12:102460874
|
T | C | 2 | a0001c0001t0034g0146a0001c0001t0034g0201 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.220+14769A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102460874 | ||||||
| chr12:102461051
|
A | G | 1 | a0001c0001t0076g0115 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.220+14592T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102461051 | ||||||
| chr12:102461192
|
C | T | 1 | a0001c0001t0007g0222 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.220+14451G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102461192 | ||||||
| chr12:102461467
|
T | TAAGAAAT others(324): Show |
1 | a0001c0001t0051g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.220+14175_220+1417 others(335): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102461467 | ||||||
| chr12:102461721
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.220+13922C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102461721 | ||||||
| chr12:102461733
|
A | G | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+13910T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102461733 | ||||||
| chr12:102462011
|
C | T | 1 | a0001c0001t0009g0309 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.220+13632G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462011 | ||||||
| chr12:102462074
|
A | C | 51 | a0001c0001t0001g0164a0001c0001t0001g0263a0001c0001t0002g0002others(48): Show | 52 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.220+13569T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462074 | ||||||
| chr12:102462132
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220+13511T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462132 | ||||||
| chr12:102462205
|
G | A | 4 | a0001c0001t0013g0014a0001c0001t0013g0037a0001c0001t0013g0045others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+13438C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462205 | ||||||
| chr12:102462636
|
T | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0074a0001c0001t0002g0075others(1): Show | 5 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+13007A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462636 | ||||||
| chr12:102462696
|
A | G | 134 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0003g0003others(131): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.220+12947T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462696 | ||||||
| chr12:102462866
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.220+12777A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462866 | ||||||
| chr12:102462869
|
A | G | 134 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0003g0003others(131): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.220+12774T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462869 | ||||||
| chr12:102462924
|
C | G | 140 | a0001c0001t0002g0280a0001c0001t0003g0003a0001c0001t0003g0072others(137): Show | 142 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.220+12719G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462924 | ||||||
| chr12:102462928
|
A | G | 1 | a0001c0001t0003g0018 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.220+12715T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102462928 | ||||||
| chr12:102463238
|
G | A | 2 | a0001c0001t0017g0235a0001c0001t0017g0236 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.220+12405C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102463238 | ||||||
| chr12:102463386
|
T | C | 2 | a0001c0001t0002g0280a0001c0001t0022g0281 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.220+12257A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102463386 | ||||||
| chr12:102463485
|
T | C | 145 | a0001c0001t0002g0280a0001c0001t0003g0003a0001c0001t0003g0072others(142): Show | 147 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.220+12158A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102463485 | ||||||
| chr12:102463601
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0091 | 2 | HG01516.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.220+12042G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102463601 | ||||||
| chr12:102464125
|
T | C | 1 | a0001c0001t0004g0308 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220+11518A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464125 | ||||||
| chr12:102464131
|
T | C | 9 | a0001c0001t0001g0052a0001c0001t0002g0036a0001c0001t0002g0044others(6): Show | 9 | HG01081.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+11512A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464131 | ||||||
| chr12:102464191
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | HG00642.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.220+11452C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464191 | ||||||
| chr12:102464310
|
CT | C | 67 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0142others(64): Show | 69 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.220+11332delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464310 | ||||||
| chr12:102464364
|
G | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG02145.hp1 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.220+11279C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464364 | ||||||
| chr12:102464814
|
A | T | 6 | a0001c0001t0010g0009a0001c0001t0010g0231a0001c0001t0010g0232others(3): Show | 6 | HG01167.hp2 HG02257.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+10829T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464814 | ||||||
| chr12:102464858
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.220+10785G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464858 | ||||||
| chr12:102464866
|
G | A | 1 | a0001c0001t0018g0334 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.220+10777C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102464866 | ||||||
| chr12:102465038
|
T | C | 73 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0142others(70): Show | 75 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.220+10605A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465038 | ||||||
| chr12:102465050
|
G | C | 61 | a0001c0001t0004g0287a0001c0001t0004g0294a0001c0001t0004g0295others(58): Show | 61 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.220+10593C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465050 | ||||||
| chr12:102465314
|
G | A | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+10329C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465314 | ||||||
| chr12:102465415
|
C | T | 6 | a0001c0001t0009g0059a0001c0001t0009g0309a0001c0001t0009g0310others(3): Show | 6 | HG02080.hp2 NA18947.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+10228G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465415 | ||||||
| chr12:102465527
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0074g0066 | 2 | HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.220+10116C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465527 | ||||||
| chr12:102465766
|
G | A | 1 | a0001c0001t0009g0328 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.220+9877C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465766 | ||||||
| chr12:102465809
|
T | C | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.220+9834A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465809 | ||||||
| chr12:102465842
|
C | T | 1 | a0001c0001t0025g0114 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.220+9801G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465842 | ||||||
| chr12:102465871
|
AGGTTGCA others(8): Show |
A | 46 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0142others(43): Show | 48 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.220+9757_220+9771d others(17): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465871 | ||||||
| chr12:102465897
|
A | G | 4 | a0001c0001t0004g0302a0001c0001t0004g0306a0001c0001t0004g0307others(1): Show | 4 | HG02129.hp2 NA18612.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+9746T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465897 | ||||||
| chr12:102465936
|
C | CAAAT | 8 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01167.hp2 HG01975.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.220+9703_220+9706d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465936 | ||||||
| chr12:102465936
|
CAAAT | C | 126 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0086others(123): Show | 127 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.220+9703_220+9706d others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465936 | ||||||
| chr12:102465936
|
CAAATAAA others(1): Show |
C | 181 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.220+9699_220+9706d others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465936 | ||||||
| chr12:102465936
|
CAAATAAA others(5): Show |
C | 7 | a0001c0001t0004g0335a0001c0001t0007g0238a0001c0001t0020g0079others(4): Show | 7 | HG01978.hp1 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+9695_220+9706d others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465936 | ||||||
| chr12:102465936
|
CAAATAAA others(9): Show |
C | 1 | a0001c0001t0042g0241 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220+9691_220+9706d others(18): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465936 | ||||||
| chr12:102465936
|
CAAATAAA others(17): Show |
C | 2 | a0001c0001t0062g0254a0001c0001t0089g0255 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.220+9683_220+9706d others(26): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102465936 | ||||||
| chr12:102466201
|
A | G | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0055g0244others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+9442T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102466201 | ||||||
| chr12:102466282
|
C | G | 62 | a0001c0001t0004g0287a0001c0001t0004g0294a0001c0001t0004g0295others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.220+9361G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102466282 | ||||||
| chr12:102466310
|
G | C | 61 | a0001c0001t0004g0287a0001c0001t0004g0294a0001c0001t0004g0295others(58): Show | 61 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.220+9333C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102466310 | ||||||
| chr12:102466311
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0014g0085a0001c0001t0025g0087 | 3 | NA18983.hp2 NA19068.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.220+9332G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102466311 | ||||||
| chr12:102467205
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220+8438A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102467205 | ||||||
| chr12:102467405
|
G | A | 5 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200others(2): Show | 5 | HG03486.hp2 HG04115.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+8238C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102467405 | ||||||
| chr12:102467492
|
C | A | 1 | a0001c0001t0006g0267 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.220+8151G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102467492 | ||||||
| chr12:102467760
|
A | C | 1 | a0001c0001t0004g0304 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.220+7883T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102467760 | ||||||
| chr12:102467770
|
A | G | 1 | a0001c0001t0032g0135 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.220+7873T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102467770 | ||||||
| chr12:102467951
|
G | A | 56 | a0001c0001t0004g0287a0001c0001t0004g0294a0001c0001t0004g0295others(53): Show | 56 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.220+7692C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102467951 | ||||||
| chr12:102467986
|
C | T | 62 | a0001c0001t0004g0287a0001c0001t0004g0294a0001c0001t0004g0295others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.220+7657G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102467986 | ||||||
| chr12:102468032
|
A | C | 62 | a0001c0001t0004g0287a0001c0001t0004g0294a0001c0001t0004g0295others(59): Show | 62 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.220+7611T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102468032 | ||||||
| chr12:102468326
|
G | C | 1 | a0001c0001t0003g0142 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.220+7317C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102468326 | ||||||
| chr12:102468494
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02027.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.220+7149C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102468494 | ||||||
| chr12:102468573
|
A | G | 3 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083 | 3 | HG02109.hp2 HG02818.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.220+7070T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102468573 | ||||||
| chr12:102468714
|
G | A | 1 | a0001c0001t0022g0281 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+6929C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102468714 | ||||||
| chr12:102468917
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0180 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.220+6726C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102468917 | ||||||
| chr12:102469032
|
T | C | 1 | a0001c0001t0004g0337 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.220+6611A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469032 | ||||||
| chr12:102469074
|
A | G | 1 | a0001c0001t0075g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220+6569T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469074 | ||||||
| chr12:102469201
|
C | T | 146 | a0001c0001t0002g0280a0001c0001t0003g0003a0001c0001t0003g0072others(143): Show | 148 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.220+6442G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469201 | ||||||
| chr12:102469252
|
C | T | 9 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0297others(6): Show | 9 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+6391G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469252 | ||||||
| chr12:102469345
|
T | C | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+6298A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469345 | ||||||
| chr12:102469700
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.220+5943G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469700 | ||||||
| chr12:102469776
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.220+5867T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469776 | ||||||
| chr12:102469818
|
T | C | 1 | a0001c0001t0075g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220+5825A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102469818 | ||||||
| chr12:102470201
|
A | T | 61 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0142others(58): Show | 63 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.220+5442T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102470201 | ||||||
| chr12:102470296
|
A | C | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+5347T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102470296 | ||||||
| chr12:102470492
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.220+5151C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102470492 | ||||||
| chr12:102470647
|
C | A | 17 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(14): Show | 17 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.220+4996G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102470647 | ||||||
| chr12:102470857
|
A | G | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+4786T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102470857 | ||||||
| chr12:102471046
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.220+4597G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102471046 | ||||||
| chr12:102471274
|
A | T | 141 | a0001c0001t0002g0280a0001c0001t0003g0003a0001c0001t0003g0072others(138): Show | 143 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.220+4369T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102471274 | ||||||
| chr12:102471391
|
C | T | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+4252G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102471391 | ||||||
| chr12:102471526
|
G | C | 1 | a0001c0001t0056g0011 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.220+4117C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102471526 | ||||||
| chr12:102471876
|
A | G | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.220+3767T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102471876 | ||||||
| chr12:102472308
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG02135.hp1 HG02155.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+3335C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102472308 | ||||||
| chr12:102472388
|
A | C | 1 | a0001c0001t0019g0015 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.220+3255T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102472388 | ||||||
| chr12:102472797
|
T | G | 1 | a0001c0001t0004g0338 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.220+2846A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102472797 | ||||||
| chr12:102472860
|
T | C | 73 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0142others(70): Show | 75 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.220+2783A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102472860 | ||||||
| chr12:102472884
|
C | A | 3 | a0001c0001t0001g0111a0001c0001t0029g0112a0001c0001t0029g0113 | 3 | HG00733.hp1 HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.220+2759G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102472884 | ||||||
| chr12:102472884
|
CA | C | 140 | a0001c0001t0002g0280a0001c0001t0003g0003a0001c0001t0003g0072others(137): Show | 142 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.220+2758delT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102472884 | ||||||
| chr12:102473181
|
T | G | 2 | a0001c0001t0002g0280a0001c0001t0022g0281 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.220+2462A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102473181 | ||||||
| chr12:102473330
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.220+2313T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102473330 | ||||||
| chr12:102473420
|
A | G | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+2223T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102473420 | ||||||
| chr12:102473532
|
G | A | 4 | a0001c0001t0002g0280a0001c0001t0022g0281a0001c0001t0034g0146others(1): Show | 4 | HG02280.hp2 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+2111C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102473532 | ||||||
| chr12:102473557
|
A | G | 2 | a0001c0001t0046g0149a0001c0001t0046g0204 | 2 | NA18992.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.220+2086T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102473557 | ||||||
| chr12:102473858
|
A | C | 349 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(346): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.220+1785T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102473858 | ||||||
| chr12:102473889
|
G | A | 33 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(30): Show | 33 | HG00280.hp1 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.220+1754C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102473889 | ||||||
| chr12:102474122
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.220+1521G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474122 | ||||||
| chr12:102474236
|
A | G | 8 | a0001c0001t0011g0005a0001c0001t0011g0346a0001c0001t0011g0348others(5): Show | 8 | HG02132.hp1 NA18941.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+1407T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474236 | ||||||
| chr12:102474477
|
T | G | 1 | a0001c0001t0046g0204 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.220+1166A>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474477 | ||||||
| chr12:102474487
|
C | G | 1 | a0001c0001t0010g0009 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220+1156G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474487 | ||||||
| chr12:102474621
|
A | G | 1 | a0001c0001t0003g0198 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.220+1022T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474621 | ||||||
| chr12:102474786
|
T | C | 1 | a0001c0001t0032g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.220+857A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474786 | ||||||
| chr12:102474875
|
T | C | 1 | a0001c0001t0032g0135 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.220+768A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474875 | ||||||
| chr12:102474895
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | HG01070.hp2 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+748A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474895 | ||||||
| chr12:102474984
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220+659C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102474984 | ||||||
| chr12:102475079
|
T | C | 1 | a0001c0001t0033g0355 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.220+564A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102475079 | ||||||
| chr12:102475193
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.220+450A>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102475193 | ||||||
| chr12:102475321
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220+322T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102475321 | ||||||
| chr12:102475543
|
C | T | 1 | a0001c0001t0015g0148 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.220+100G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102475543 | ||||||
| chr12:102475615
|
C | G | 2 | a0001c0001t0062g0254a0001c0001t0089g0255 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.220+28G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 2/3 | chr12 | 102475615 | ||||||
| chr12:102475822
|
G | T | 6 | a0001c0001t0020g0079a0001c0001t0020g0080a0001c0001t0020g0083others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-23C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102475822 | ||||||
| chr12:102475953
|
G | T | 1 | a0001c0001t0004g0301 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.64-154C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102475953 | ||||||
| chr12:102475971
|
G | A | 1 | a0001c0001t0018g0339 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.64-172C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102475971 | ||||||
| chr12:102476093
|
A | C | 1 | a0001c0001t0003g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.64-294T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476093 | ||||||
| chr12:102476095
|
G | A | 3 | a0001c0001t0016g0183a0001c0001t0016g0184a0001c0001t0082g0185 | 3 | HG02976.hp1 HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-296C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476095 | ||||||
| chr12:102476120
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.64-321T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476120 | ||||||
| chr12:102476127
|
C | T | 2 | a0001c0001t0034g0146a0001c0001t0034g0201 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-328G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476127 | ||||||
| chr12:102476303
|
C | T | 1 | a0001c0001t0003g0213 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.64-504G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476303 | ||||||
| chr12:102476410
|
T | TGA | 33 | a0001c0001t0001g0052a0001c0001t0001g0139a0001c0001t0001g0268others(30): Show | 33 | HG00642.hp2 HG00733.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-613_64-612dupTC | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGA | 53 | a0001c0001t0001g0140a0001c0001t0004g0287a0001c0001t0004g0301others(50): Show | 53 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.64-615_64-612dupTC others(2): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGAGA | 17 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0003g0198others(14): Show | 18 | HG00323.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-617_64-612dupTC others(4): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGAGAG others(1): Show |
3 | a0001c0001t0007g0187a0001c0001t0075g0143a0001c0001t0093g0243 | 3 | HG01192.hp2 HG03579.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.64-619_64-612dupTC others(6): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGAGAG others(3): Show |
7 | a0001c0001t0003g0209a0001c0001t0007g0208a0001c0001t0007g0238others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-621_64-612dupTC others(8): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGAGAG others(5): Show |
14 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190others(11): Show | 14 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-623_64-612dupTC others(10): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGAGAG others(7): Show |
14 | a0001c0001t0003g0003a0001c0001t0003g0072a0001c0001t0003g0191others(11): Show | 15 | HG00597.hp1 HG02056.hp2 HG03831.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-625_64-612dupTC others(12): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGAGAG others(9): Show |
6 | a0001c0001t0003g0223a0001c0001t0003g0224a0001c0001t0003g0225others(3): Show | 6 | HG02523.hp2 NA18940.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-627_64-612dupTC others(14): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476410
|
T | TGAGAGAG others(11): Show |
6 | a0001c0001t0003g0142a0001c0001t0003g0227a0001c0001t0003g0228others(3): Show | 6 | HG00423.hp2 HG02145.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-629_64-612dupTC others(16): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476410 | ||||||
| chr12:102476442
|
A | AGAGAGAG others(13): Show |
1 | a0001c0001t0053g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.64-644_64-643insCC others(18): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476442 | ||||||
| chr12:102476464
|
A | C | 3 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200 | 3 | NA18964.hp2 NA19003.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.64-665T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476464 | ||||||
| chr12:102476551
|
A | G | 1 | a0001c0001t0004g0353 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.64-752T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476551 | ||||||
| chr12:102476796
|
C | T | 6 | a0001c0001t0010g0009a0001c0001t0010g0231a0001c0001t0010g0232others(3): Show | 6 | HG01167.hp2 HG02257.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-997G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102476796 | ||||||
| chr12:102477023
|
G | A | 1 | a0001c0001t0075g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.64-1224C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477023 | ||||||
| chr12:102477023
|
G | T | 63 | a0001c0001t0003g0197a0001c0001t0004g0287a0001c0001t0004g0294others(60): Show | 63 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.64-1224C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477023 | ||||||
| chr12:102477274
|
G | GA | 14 | a0001c0001t0001g0196a0001c0001t0001g0230a0001c0001t0001g0279others(11): Show | 14 | HG00323.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-1476dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477274 | ||||||
| chr12:102477425
|
A | C | 6 | a0001c0001t0010g0009a0001c0001t0010g0231a0001c0001t0010g0232others(3): Show | 6 | HG01167.hp2 HG02257.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-1626T>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477425 | ||||||
| chr12:102477437
|
C | G | 1 | a0001c0001t0013g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-1638G>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477437 | ||||||
| chr12:102477481
|
C | T | 219 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0067others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.64-1682G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477481 | ||||||
| chr12:102477535
|
A | AT | 166 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0033others(163): Show | 168 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.64-1737dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477535 | ||||||
| chr12:102477535
|
A | ATT | 87 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0182others(84): Show | 88 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-1738_64-1737dup others(2): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477535 | ||||||
| chr12:102477535
|
A | ATTT | 80 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0067others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.64-1739_64-1737dup others(3): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477535 | ||||||
| chr12:102477566
|
G | A | 6 | a0001c0001t0042g0241a0001c0001t0042g0242a0001c0001t0055g0244others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1767C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477566 | ||||||
| chr12:102477578
|
T | C | 8 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0247others(5): Show | 9 | HG00099.hp2 HG00323.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-1779A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477578 | ||||||
| chr12:102477630
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.64-1831C>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477630 | ||||||
| chr12:102477687
|
G | A | 1 | a0001c0001t0096g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-1888C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477687 | ||||||
| chr12:102477915
|
A | G | 3 | a0001c0001t0020g0079a0001c0001t0020g0080a0002c0003t0063g0081 | 3 | HG02109.hp2 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.64-2116T>C | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477915 | ||||||
| chr12:102477989
|
C | T | 1 | a0001c0001t0019g0012 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-2190G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477989 | ||||||
| chr12:102477997
|
CT | C | 223 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0067others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.64-2199delA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477997 | ||||||
| chr12:102477997
|
CTT | C | 77 | a0001c0001t0001g0253a0001c0001t0001g0284a0001c0001t0001g0292others(74): Show | 77 | HG00408.hp1 HG00423.hp1 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.64-2200_64-2199del others(2): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102477997 | ||||||
| chr12:102478093
|
T | C | 1 | a0001c0001t0001g0356 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.63+2226A>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102478093 | ||||||
| chr12:102478199
|
C | A | 1 | a0001c0001t0036g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.63+2120G>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102478199 | ||||||
| chr12:102478325
|
A | T | 1 | a0001c0001t0035g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.63+1994T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102478325 | ||||||
| chr12:102478377
|
C | CT | 292 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0088others(289): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.63+1941dupA | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102478377 | ||||||
| chr12:102478377
|
C | CTT | 14 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0067others(11): Show | 14 | HG01123.hp2 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+1940_63+1941dup others(2): Show |
IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102478377 | ||||||
| chr12:102478648
|
A | T | 1 | a0001c0001t0014g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63+1671T>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102478648 | ||||||
| chr12:102478786
|
G | A | 9 | a0001c0001t0001g0263a0001c0001t0006g0260a0001c0001t0006g0261others(6): Show | 9 | HG00408.hp2 HG02027.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+1533C>T | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102478786 | ||||||
| chr12:102479459
|
G | C | 19 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0001g0271others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+860C>G | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102479459 | ||||||
| chr12:102479894
|
C | T | 1 | a0001c0001t0004g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.63+425G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102479894 | ||||||
| chr12:102479976
|
G | GA | 233 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0067others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.63+342dupT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102479976 | ||||||
| chr12:102479976
|
G | GAA | 71 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0356others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+341_63+342dupTT | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102479976 | ||||||
| chr12:102480017
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.63+302G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102480017 | ||||||
| chr12:102480062
|
C | T | 1 | a0001c0001t0011g0005 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.63+257G>A | IGF1 | ENSG00000017427.17 | transcript | ENST00000337514.11 | protein_coding | 1/3 | chr12 | 102480062 |