Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9415 |
|---|---|
| ensemblid | ENSG00000134824.14 |
| hgncid | 3575 |
| symbol | FADS2 |
| name | fatty acid desaturase 2 |
| refseq_nuc | NM_004265.4 |
| refseq_prot | NP_004256.1 |
| ensembl_nuc | ENST00000278840.9 |
| ensembl_prot | ENSP00000278840.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 61828300 |
| end | 61867354 |
| strand | + |
| ver | v1.2 |
| region | chr11:61828300-61867354 |
| region5000 | chr11:61823300-61872354 |
| regionname0 | FADS2_chr11_61828300_61867354 |
| regionname5000 | FADS2_chr11_61823300_61872354 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 444 | 280 | 84 | 54 | 106 | 12 | 22 | 72 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1335 | 276 | 81 | 54 | 105 | 12 | 22 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| c0002 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| c0003 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| c0004 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| c0005 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1757 | 226 | 52 | 42 | 102 | 8 | 21 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0002 | 0/0 | 1757 | 17 | 8 | 7 | 0 | 2 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0003 | 0/0 | 1757 | 8 | 7 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0004 | 0/0 | 1757 | 6 | 4 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0005 | 0/1 | 1757 | 5 | 1 | 1 | 0 | 2 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0006 | 0/0 | 1757 | 4 | 3 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0007 | 0/0 | 1757 | 4 | 0 | 0 | 3 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0008 | 0/0 | 1757 | 3 | 3 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0009 | 0/0 | 1757 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0010 | 0/0 | 1757 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0011 | 0/0 | 1757 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0012 | 0/0 | 1757 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0013 | 0/0 | 1757 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| t0014 | 0/0 | 1757 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1335 | 276 | 81 | 54 | 105 | 12 | 22 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0002 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0003 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0004 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0005 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3091 | 224 | 51 | 42 | 101 | 8 | 21 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0002 | 0/0 | 3091 | 17 | 8 | 7 | 0 | 2 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0003 | 0/0 | 3091 | 7 | 6 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0004 | 0/0 | 3091 | 6 | 4 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0005 | 0/1 | 3091 | 5 | 1 | 1 | 0 | 2 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0006 | 0/0 | 3091 | 4 | 3 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0007 | 0/0 | 3091 | 4 | 0 | 0 | 3 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0008 | 0/0 | 3091 | 3 | 3 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0009 | 0/0 | 3091 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0010 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0012 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0013 | 0/0 | 3091 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0001t0014 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0002t0001 | 0/0 | 3091 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0003t0003 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0004t0011 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| a0001c0005t0001 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | copy fasta | chr11 | 61823300 | 61872354 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0005g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0013g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0001t0014g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0004t0011g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| a0001c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0053 | EUR | GBR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0259 | EAS | CHS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0132 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02083 | hp2 | a0001 | c0001 | t0013 | g0228 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0107 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02630 | hp1 | a0001 | c0004 | t0011 | g0028 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0151 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0142 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0127 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0129 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0074 | SAS | BEB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18989 | hp1 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19056 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0157 | AFR | YRI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0041 | EUR | TSI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | TSI | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0155 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | USA | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | USA | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0008 | REF | REF | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0026 | REF | REF | FADS2_chr11_61823300_61872354 | FADS2 | chr11 | 61823300 | 61872354 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61837813
|
C | T | 1 | a0001c0005 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.243C>T | p.Phe81Phe | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/12 | 334/3091 | 243/1335 | 81/444 | chr11 | 61837813 | ||
| chr11:61837858
|
G | A | 1 | a0001c0002 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.288G>A | p.Pro96Pro | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/12 | 379/3091 | 288/1335 | 96/444 | chr11 | 61837858 | ||
| chr11:61848203
|
C | T | 1 | a0001c0004 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.663C>T | p.His221His | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/12 | 754/3091 | 663/1335 | 221/444 | chr11 | 61848203 | ||
| chr11:61865224
|
T | C | 1 | a0001c0003 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1230T>C | p.His410His | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 11/12 | 1321/3091 | 1230/1335 | 410/444 | chr11 | 61865224 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61828314
|
G | A | 1 | a0001c0001t0010 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/12 | 77 | chr11 | 61828314 | |||||
| chr11:61865702
|
C | T | 1 | a0001c0001t0007 | 4 | HG00621.hp2 HG04184.hp1 NA18989.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*13C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 13 | chr11 | 61865702 | |||||
| chr11:61865710
|
C | T | 1 | a0001c0001t0005 | 5 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*21C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 21 | chr11 | 61865710 | |||||
| chr11:61866086
|
G | A | 3 | a0001c0001t0003a0001c0003t0003a0001c0004t0011 | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*397G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 397 | chr11 | 61866086 | |||||
| chr11:61866116
|
A | G | 3 | a0001c0001t0007a0001c0001t0008a0001c0001t0010 | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*427A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 427 | chr11 | 61866116 | |||||
| chr11:61866180
|
G | A | 2 | a0001c0001t0004a0001c0001t0009 | 8 | HG01109.hp1 HG01261.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*491G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 491 | chr11 | 61866180 | |||||
| chr11:61866232
|
G | A | 3 | a0001c0001t0007a0001c0001t0008a0001c0001t0010 | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*543G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 543 | chr11 | 61866232 | |||||
| chr11:61866248
|
G | A | 2 | a0001c0001t0003a0001c0003t0003 | 8 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*559G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 559 | chr11 | 61866248 | |||||
| chr11:61866298
|
C | T | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(3): Show | 31 | HG00738.hp2 HG01081.hp1 HG01109.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 609 | chr11 | 61866298 | |||||
| chr11:61866349
|
T | C | 6 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(3): Show | 15 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*660T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 660 | chr11 | 61866349 | |||||
| chr11:61866475
|
C | T | 1 | a0001c0001t0002 | 17 | HG00738.hp2 HG01081.hp1 HG01192.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*786C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 786 | chr11 | 61866475 | |||||
| chr11:61866491
|
G | A | 1 | a0001c0001t0009 | 2 | HG02970.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*802G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 802 | chr11 | 61866491 | |||||
| chr11:61866683
|
G | A | 6 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(3): Show | 15 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*994G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 994 | chr11 | 61866683 | |||||
| chr11:61866805
|
C | T | 1 | a0001c0001t0013 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1116C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 1116 | chr11 | 61866805 | |||||
| chr11:61866876
|
G | A | 1 | a0001c0001t0009 | 2 | HG02970.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1187G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 1187 | chr11 | 61866876 | |||||
| chr11:61866957
|
C | A | 1 | a0001c0001t0014 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 1268 | chr11 | 61866957 | |||||
| chr11:61867080
|
C | G | 3 | a0001c0001t0006a0001c0001t0012a0001c0001t0014 | 6 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1391C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 12/12 | 1391 | chr11 | 61867080 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61828732
|
A | G | 1 | a0001c0001t0007g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.207+135A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61828732 | ||||||
| chr11:61828850
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.207+253C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61828850 | ||||||
| chr11:61828850
|
CA | C | 112 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.207+255delA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61828850 | |||||
| chr11:61828851
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.207+254A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61828851 | ||||||
| chr11:61829161
|
C | T | 139 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.207+564C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61829161 | ||||||
| chr11:61829740
|
C | T | 88 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(85): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.207+1143C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61829740 | ||||||
| chr11:61829956
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0175others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+1359C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61829956 | ||||||
| chr11:61829989
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.207+1392T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61829989 | ||||||
| chr11:61830102
|
C | T | 1 | a0001c0001t0008g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207+1505C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61830102 | ||||||
| chr11:61830342
|
A | G | 7 | a0001c0001t0001g0150a0001c0001t0002g0148a0001c0001t0002g0149others(4): Show | 7 | HG00735.hp1 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+1745A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61830342 | ||||||
| chr11:61830500
|
A | G | 113 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(110): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.207+1903A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61830500 | ||||||
| chr11:61830816
|
C | T | 56 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(53): Show | 61 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.207+2219C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61830816 | ||||||
| chr11:61830858
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.207+2261C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61830858 | ||||||
| chr11:61830891
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0004g0121a0001c0001t0006g0123 | 3 | HG01261.hp2 HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.207+2294A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61830891 | ||||||
| chr11:61830919
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG00140.hp1 HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.207+2322A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61830919 | ||||||
| chr11:61831107
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.207+2510T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831107 | ||||||
| chr11:61831146
|
A | T | 1 | a0001c0003t0003g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.207+2549A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831146 | ||||||
| chr11:61831195
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.207+2598G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831195 | ||||||
| chr11:61831320
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.207+2723G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831320 | ||||||
| chr11:61831689
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0002g0156a0001c0001t0012g0154others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+3092G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831689 | ||||||
| chr11:61831733
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207+3136C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831733 | ||||||
| chr11:61831857
|
G | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0173others(1): Show | 4 | HG00140.hp1 HG01891.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3260G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831857 | ||||||
| chr11:61831875
|
G | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0161a0001c0001t0001g0162others(10): Show | 14 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.207+3278G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831875 | ||||||
| chr11:61831894
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.207+3297G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831894 | ||||||
| chr11:61831907
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.207+3310G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61831907 | ||||||
| chr11:61832695
|
C | G | 27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0234others(24): Show | 29 | HG00423.hp2 HG00735.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.207+4098C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61832695 | ||||||
| chr11:61832855
|
G | A | 57 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(54): Show | 62 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.207+4258G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61832855 | ||||||
| chr11:61832870
|
A | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(100): Show | 113 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.207+4273A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61832870 | ||||||
| chr11:61832983
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.207+4386C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61832983 | ||||||
| chr11:61833109
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.207+4512C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833109 | ||||||
| chr11:61833222
|
G | C | 1 | a0001c0001t0001g0178 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.208-4556G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833222 | ||||||
| chr11:61833377
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 5 | HG01243.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-4401G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833377 | ||||||
| chr11:61833403
|
T | G | 1 | a0001c0001t0006g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.208-4375T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833403 | ||||||
| chr11:61833680
|
G | A | 1 | a0001c0001t0009g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.208-4098G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833680 | ||||||
| chr11:61833687
|
G | A | 1 | a0001c0001t0008g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208-4091G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833687 | ||||||
| chr11:61833730
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0173others(1): Show | 4 | HG00140.hp1 HG01891.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-4048G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833730 | ||||||
| chr11:61833737
|
T | A | 8 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | NA18946.hp2 NA18953.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-4041T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833737 | ||||||
| chr11:61833788
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208-3990C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833788 | ||||||
| chr11:61833906
|
C | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0176others(47): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.208-3872C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833906 | ||||||
| chr11:61833969
|
A | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.208-3809A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833969 | ||||||
| chr11:61833990
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0175others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-3788G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61833990 | ||||||
| chr11:61834013
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0030 | 3 | HG01168.hp2 HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.208-3765C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834013 | ||||||
| chr11:61834026
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.208-3752C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834026 | ||||||
| chr11:61834219
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.208-3559C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834219 | ||||||
| chr11:61834400
|
C | T | 51 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0143others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.208-3378C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834400 | ||||||
| chr11:61834436
|
A | G | 51 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0143others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.208-3342A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834436 | ||||||
| chr11:61834465
|
C | T | 1 | a0001c0003t0003g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.208-3313C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834465 | ||||||
| chr11:61834531
|
C | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(68): Show | 80 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.208-3247C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834531 | ||||||
| chr11:61834696
|
A | G | 1 | a0001c0001t0010g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.208-3082A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834696 | ||||||
| chr11:61834746
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 5 | HG02074.hp2 HG02129.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-3032C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834746 | ||||||
| chr11:61834784
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.208-2994A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834784 | ||||||
| chr11:61834986
|
CCCA | C | 52 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0176others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.208-2789_208-2787d others(5): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61834986 | |||||
| chr11:61834988
|
CA | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(51): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.208-2789delA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834988 | ||||||
| chr11:61834989
|
A | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 17 | HG00642.hp1 HG01168.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.208-2789A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61834989 | ||||||
| chr11:61835024
|
CCTCCCTG others(15): Show |
C | 136 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.208-2713_208-2692d others(24): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61835024 | |||||
| chr11:61835154
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 13 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-2624C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835154 | ||||||
| chr11:61835193
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.208-2585G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835193 | ||||||
| chr11:61835286
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.208-2492A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835286 | ||||||
| chr11:61835397
|
C | CT | 44 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0093others(41): Show | 45 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.208-2366dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61835397 | |||||
| chr11:61835539
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.208-2239G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835539 | ||||||
| chr11:61835560
|
A | AT | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0029others(56): Show | 62 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.208-2201dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61835560 | |||||
| chr11:61835560
|
AT | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0097a0001c0001t0001g0143others(3): Show | 6 | HG02451.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-2201delT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61835560 | |||||
| chr11:61835756
|
C | G | 16 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0002g0130others(13): Show | 16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.208-2022C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835756 | ||||||
| chr11:61835765
|
C | T | 57 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0152others(54): Show | 58 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.208-2013C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835765 | ||||||
| chr11:61835886
|
A | T | 57 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0152others(54): Show | 58 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.208-1892A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835886 | ||||||
| chr11:61835943
|
A | G | 1 | a0001c0001t0009g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-1835A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61835943 | ||||||
| chr11:61836038
|
C | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(120): Show | 133 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.208-1740C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836038 | ||||||
| chr11:61836089
|
T | TTTTG | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 8 | HG01168.hp2 HG02258.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-1669_208-1666d others(6): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61836089 | |||||
| chr11:61836093
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.208-1685G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836093 | ||||||
| chr11:61836119
|
T | A | 2 | a0001c0001t0009g0127a0001c0001t0009g0140 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.208-1659T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836119 | ||||||
| chr11:61836151
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.208-1627G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836151 | ||||||
| chr11:61836253
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 7 | HG01168.hp2 HG02258.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-1525A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836253 | ||||||
| chr11:61836311
|
C | T | 2 | a0001c0001t0009g0127a0001c0001t0009g0140 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.208-1467C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836311 | ||||||
| chr11:61836312
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(4): Show | 9 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-1466G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836312 | ||||||
| chr11:61836350
|
G | A | 2 | a0001c0001t0009g0127a0001c0001t0009g0140 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.208-1428G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836350 | ||||||
| chr11:61836472
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.208-1306T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836472 | ||||||
| chr11:61836816
|
A | G | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0193others(8): Show | 11 | HG00597.hp1 HG02027.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-962A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836816 | ||||||
| chr11:61836845
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.208-933A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836845 | ||||||
| chr11:61836852
|
T | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG00140.hp1 HG00438.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-926T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61836852 | ||||||
| chr11:61837112
|
G | GA | 5 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0145others(2): Show | 5 | HG00735.hp1 HG02572.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-659dupA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 61837112 | |||||
| chr11:61837146
|
T | A | 1 | a0001c0001t0002g0227 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.208-632T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837146 | ||||||
| chr11:61837310
|
A | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0031others(64): Show | 70 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.208-468A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837310 | ||||||
| chr11:61837342
|
C | A | 139 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(136): Show | 149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.208-436C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837342 | ||||||
| chr11:61837430
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.208-348G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837430 | ||||||
| chr11:61837495
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0031others(62): Show | 68 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.208-283C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837495 | ||||||
| chr11:61837520
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18944.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.208-258A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837520 | ||||||
| chr11:61837576
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208-202G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837576 | ||||||
| chr11:61837743
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0031others(62): Show | 68 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.208-35A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 1/11 | chr11 | 61837743 | ||||||
| chr11:61838027
|
T | A | 139 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(136): Show | 149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.318+139T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61838027 | ||||||
| chr11:61838069
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+181C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61838069 | ||||||
| chr11:61838106
|
T | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(10): Show | 15 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.318+218T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61838106 | ||||||
| chr11:61838141
|
C | T | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(47): Show | 55 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+253C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61838141 | ||||||
| chr11:61838656
|
A | G | 1 | a0001c0001t0006g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.318+768A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61838656 | ||||||
| chr11:61838803
|
C | T | 16 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0002g0130others(13): Show | 16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.318+915C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61838803 | ||||||
| chr11:61839028
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.318+1140C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839028 | ||||||
| chr11:61839170
|
A | G | 139 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(136): Show | 149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.319-1164A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839170 | ||||||
| chr11:61839211
|
G | A | 139 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(136): Show | 149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.319-1123G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839211 | ||||||
| chr11:61839259
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.319-1075C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839259 | ||||||
| chr11:61839265
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.319-1069G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839265 | ||||||
| chr11:61839329
|
C | CT | 14 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(11): Show | 16 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.319-994dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 61839329 | |||||
| chr11:61839461
|
T | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0003g0144others(3): Show | 6 | HG00735.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-873T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839461 | ||||||
| chr11:61839575
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0203a0001c0001t0001g0204others(5): Show | 9 | HG01175.hp2 HG01433.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.319-759G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839575 | ||||||
| chr11:61839591
|
G | A | 3 | a0001c0001t0009g0127a0001c0001t0009g0140a0001c0001t0010g0157 | 3 | HG02970.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.319-743G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839591 | ||||||
| chr11:61839635
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(10): Show | 15 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.319-699G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839635 | ||||||
| chr11:61839696
|
A | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(52): Show | 62 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.319-638A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839696 | ||||||
| chr11:61839821
|
C | T | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.319-513C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839821 | ||||||
| chr11:61839985
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0171 | 2 | HG01081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.319-349G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61839985 | ||||||
| chr11:61840199
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.319-135G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61840199 | ||||||
| chr11:61840248
|
T | C | 9 | a0001c0001t0002g0130a0001c0001t0002g0149a0001c0001t0003g0128others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.319-86T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61840248 | ||||||
| chr11:61840265
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319-69A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 2/11 | chr11 | 61840265 | ||||||
| chr11:61840821
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618+96G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840821 | ||||||
| chr11:61840941
|
G | C | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+216G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840941 | ||||||
| chr11:61840943
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+218C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840943 | ||||||
| chr11:61840946
|
G | T | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+221G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840946 | ||||||
| chr11:61840947
|
C | G | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+222C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840947 | ||||||
| chr11:61840950
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+225A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840950 | ||||||
| chr11:61840951
|
C | G | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+226C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840951 | ||||||
| chr11:61840952
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+227A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840952 | ||||||
| chr11:61840953
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+228C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61840953 | ||||||
| chr11:61841055
|
A | AT | 61 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0090others(58): Show | 63 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.618+345dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61841055 | |||||
| chr11:61841145
|
G | A | 3 | a0001c0001t0009g0127a0001c0001t0009g0140a0001c0001t0010g0157 | 3 | HG02970.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.618+420G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841145 | ||||||
| chr11:61841183
|
C | T | 1 | a0001c0004t0011g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.618+458C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841183 | ||||||
| chr11:61841267
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.618+542G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841267 | ||||||
| chr11:61841525
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.618+800C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841525 | ||||||
| chr11:61841527
|
C | G | 2 | a0001c0001t0001g0097a0001c0001t0004g0105 | 2 | HG01109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.618+802C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841527 | ||||||
| chr11:61841530
|
C | T | 16 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0002g0130others(13): Show | 16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.618+805C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841530 | ||||||
| chr11:61841532
|
C | A | 52 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0176others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.618+807C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841532 | ||||||
| chr11:61841539
|
C | CA | 14 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0134others(11): Show | 16 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.618+826dupA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61841539 | |||||
| chr11:61841661
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.618+936T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841661 | ||||||
| chr11:61841815
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.618+1090C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841815 | ||||||
| chr11:61841818
|
C | T | 2 | a0001c0001t0012g0154a0001c0001t0014g0155 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.618+1093C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841818 | ||||||
| chr11:61841851
|
A | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(10): Show | 15 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.618+1126A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61841851 | ||||||
| chr11:61842166
|
A | C | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+1441A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842166 | ||||||
| chr11:61842170
|
C | T | 1 | a0001c0001t0010g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.618+1445C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842170 | ||||||
| chr11:61842236
|
C | G | 1 | a0001c0001t0002g0015 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.618+1511C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842236 | ||||||
| chr11:61842278
|
C | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(120): Show | 133 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.618+1553C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842278 | ||||||
| chr11:61842279
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 10 | NA18946.hp1 NA18951.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+1554G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842279 | ||||||
| chr11:61842371
|
G | A | 3 | a0001c0001t0009g0127a0001c0001t0009g0140a0001c0001t0010g0157 | 3 | HG02970.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.618+1646G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842371 | ||||||
| chr11:61842495
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618+1770G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842495 | ||||||
| chr11:61842571
|
G | A | 1 | a0001c0001t0006g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.618+1846G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842571 | ||||||
| chr11:61842736
|
G | A | 1 | a0001c0004t0011g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.618+2011G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61842736 | ||||||
| chr11:61843122
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.618+2397T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843122 | ||||||
| chr11:61843168
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.618+2443G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843168 | ||||||
| chr11:61843178
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.618+2453T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843178 | ||||||
| chr11:61843278
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(137): Show | 150 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.618+2553G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843278 | ||||||
| chr11:61843286
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.618+2561C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843286 | ||||||
| chr11:61843559
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.618+2834A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843559 | ||||||
| chr11:61843561
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG00140.hp1 HG00438.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+2836T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843561 | ||||||
| chr11:61843608
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.618+2883G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843608 | ||||||
| chr11:61843744
|
C | T | 52 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0176others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.618+3019C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843744 | ||||||
| chr11:61843942
|
T | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 7 | HG01168.hp2 HG02258.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+3217T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61843942 | ||||||
| chr11:61844222
|
G | A | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(47): Show | 55 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.618+3497G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844222 | ||||||
| chr11:61844238
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.618+3513T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844238 | ||||||
| chr11:61844274
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0158 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.618+3549C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844274 | ||||||
| chr11:61844441
|
C | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG00140.hp1 HG00438.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+3716C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844441 | ||||||
| chr11:61844461
|
A | G | 5 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0145others(2): Show | 5 | HG00735.hp1 HG02572.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-3698A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844461 | ||||||
| chr11:61844564
|
A | G | 7 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0002g0148others(4): Show | 7 | HG00735.hp1 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-3595A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844564 | ||||||
| chr11:61844652
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.619-3507G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844652 | ||||||
| chr11:61844663
|
C | T | 2 | a0001c0001t0012g0154a0001c0001t0014g0155 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.619-3496C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844663 | ||||||
| chr11:61844798
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.619-3361G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844798 | ||||||
| chr11:61844996
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(8): Show | 13 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-3163C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61844996 | ||||||
| chr11:61845030
|
C | CT | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0002g0149others(2): Show | 5 | HG01433.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-3098dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845030 | |||||
| chr11:61845030
|
CT | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(121): Show | 134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.619-3098delT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845030 | |||||
| chr11:61845030
|
CTT | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 71 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.619-3099_619-3098d others(4): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845030 | |||||
| chr11:61845030
|
CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(8): Show | 13 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-3107_619-3098d others(12): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845030 | |||||
| chr11:61845030
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.619-3109_619-3098d others(14): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845030 | |||||
| chr11:61845030
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0001g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.619-3110_619-3098d others(15): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845030 | |||||
| chr11:61845082
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.619-3077G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845082 | ||||||
| chr11:61845088
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0002g0015 | 3 | HG01515.hp1 HG01517.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.619-3071C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845088 | ||||||
| chr11:61845236
|
C | A | 1 | a0001c0001t0005g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.619-2923C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845236 | ||||||
| chr11:61845358
|
C | T | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(47): Show | 55 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.619-2801C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845358 | ||||||
| chr11:61845450
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.619-2709C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845450 | ||||||
| chr11:61845557
|
C | T | 14 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0190others(11): Show | 14 | HG00558.hp2 HG00597.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.619-2602C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845557 | ||||||
| chr11:61845665
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(8): Show | 13 | HG00140.hp1 HG00438.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-2494C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845665 | ||||||
| chr11:61845673
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.619-2486A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845673 | ||||||
| chr11:61845784
|
C | CA | 10 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0072others(7): Show | 10 | HG01109.hp1 HG02135.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-2355dupA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845784 | |||||
| chr11:61845784
|
CA | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0143a0001c0001t0001g0158others(7): Show | 11 | HG01433.hp2 HG02027.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.619-2355delA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845784 | |||||
| chr11:61845784
|
CAA | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(74): Show | 81 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.619-2356_619-2355d others(4): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61845784 | |||||
| chr11:61845805
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.619-2354T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845805 | ||||||
| chr11:61845984
|
C | T | 1 | a0001c0001t0008g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.619-2175C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61845984 | ||||||
| chr11:61846019
|
T | C | 5 | a0001c0001t0009g0127a0001c0001t0009g0140a0001c0001t0010g0157others(2): Show | 5 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-2140T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846019 | ||||||
| chr11:61846036
|
C | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(4): Show | 9 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.619-2123C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846036 | ||||||
| chr11:61846103
|
G | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0254a0001c0001t0001g0257 | 3 | HG00423.hp2 HG02523.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.619-2056G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846103 | ||||||
| chr11:61846131
|
C | CTT | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 37 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.619-2011_619-2010d others(4): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61846131 | |||||
| chr11:61846131
|
CT | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(63): Show | 75 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.619-2010delT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61846131 | |||||
| chr11:61846136
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0004g0121 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.619-2023T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846136 | ||||||
| chr11:61846273
|
C | T | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(47): Show | 55 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.619-1886C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846273 | ||||||
| chr11:61846369
|
A | G | 24 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0097others(21): Show | 27 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.619-1790A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846369 | ||||||
| chr11:61846408
|
CT | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0033others(23): Show | 27 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.619-1736delT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61846408 | |||||
| chr11:61846417
|
T | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0097others(19): Show | 25 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.619-1742T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846417 | ||||||
| chr11:61846422
|
TTC | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0097others(20): Show | 26 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.619-1718_619-1717d others(4): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61846422 | |||||
| chr11:61846423
|
TC | T | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 54 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.619-1735delC | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846423 | ||||||
| chr11:61846424
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.619-1735C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846424 | ||||||
| chr11:61846426
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0097others(19): Show | 25 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.619-1733C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846426 | ||||||
| chr11:61846477
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00741.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.619-1682G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846477 | ||||||
| chr11:61846551
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0097others(19): Show | 25 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.619-1608C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846551 | ||||||
| chr11:61846804
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.619-1355T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61846804 | ||||||
| chr11:61846954
|
CT | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(133): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.619-1191delT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 61846954 | |||||
| chr11:61847123
|
G | A | 52 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0174others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.619-1036G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61847123 | ||||||
| chr11:61847303
|
T | C | 1 | a0001c0001t0012g0154 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.619-856T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61847303 | ||||||
| chr11:61847414
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.619-745T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61847414 | ||||||
| chr11:61847533
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.619-626G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61847533 | ||||||
| chr11:61847577
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.619-582C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61847577 | ||||||
| chr11:61847842
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.619-317C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61847842 | ||||||
| chr11:61848037
|
G | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 8 | HG01168.hp2 HG02258.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-122G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61848037 | ||||||
| chr11:61848066
|
G | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0219 | 2 | HG02015.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.619-93G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61848066 | ||||||
| chr11:61848070
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0097others(19): Show | 25 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.619-89C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 4/11 | chr11 | 61848070 | ||||||
| chr11:61848331
|
C | G | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(47): Show | 55 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.744+47C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848331 | ||||||
| chr11:61848406
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.744+122C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848406 | ||||||
| chr11:61848431
|
G | A | 16 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0002g0130others(13): Show | 16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+147G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848431 | ||||||
| chr11:61848433
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.744+149G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848433 | ||||||
| chr11:61848540
|
A | G | 52 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0174others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.744+256A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848540 | ||||||
| chr11:61848597
|
A | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0097others(19): Show | 25 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.744+313A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848597 | ||||||
| chr11:61848827
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.744+543T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848827 | ||||||
| chr11:61848850
|
A | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(13): Show | 17 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.744+566A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848850 | ||||||
| chr11:61848867
|
C | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(3): Show | 8 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.744+583C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848867 | ||||||
| chr11:61848867
|
C | T | 1 | a0001c0001t0010g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.744+583C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61848867 | ||||||
| chr11:61849120
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.744+836C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849120 | ||||||
| chr11:61849184
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.744+900C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849184 | ||||||
| chr11:61849505
|
G | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(64): Show | 76 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.744+1221G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849505 | ||||||
| chr11:61849543
|
C | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 16 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+1259C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849543 | ||||||
| chr11:61849674
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.744+1390C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849674 | ||||||
| chr11:61849867
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(13): Show | 17 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.744+1583G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849867 | ||||||
| chr11:61849880
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.744+1596G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849880 | ||||||
| chr11:61849938
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.744+1654G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61849938 | ||||||
| chr11:61850044
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.744+1760A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850044 | ||||||
| chr11:61850066
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.744+1782C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850066 | ||||||
| chr11:61850115
|
C | A | 1 | a0001c0001t0001g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.744+1831C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850115 | ||||||
| chr11:61850204
|
T | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(80): Show | 93 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.744+1920T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850204 | ||||||
| chr11:61850281
|
T | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(13): Show | 17 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.744+1997T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850281 | ||||||
| chr11:61850338
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.744+2054C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850338 | ||||||
| chr11:61850540
|
C | T | 47 | a0001c0001t0001g0031a0001c0001t0001g0072a0001c0001t0001g0174others(44): Show | 47 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.744+2256C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850540 | ||||||
| chr11:61850544
|
T | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 16 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+2260T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850544 | ||||||
| chr11:61850616
|
C | CT | 15 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 16 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+2341dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61850616 | |||||
| chr11:61850697
|
A | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0161a0001c0001t0001g0162others(10): Show | 14 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+2413A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61850697 | ||||||
| chr11:61851000
|
G | T | 4 | a0001c0001t0001g0139a0001c0001t0010g0157a0001c0001t0012g0154others(1): Show | 4 | HG02486.hp1 HG02717.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+2716G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851000 | ||||||
| chr11:61851013
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.744+2729C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851013 | ||||||
| chr11:61851058
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.744+2774A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851058 | ||||||
| chr11:61851108
|
C | G | 1 | a0001c0001t0002g0148 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.744+2824C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851108 | ||||||
| chr11:61851136
|
A | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(150): Show | 164 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.744+2852A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851136 | ||||||
| chr11:61851187
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.744+2903T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851187 | ||||||
| chr11:61851215
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.744+2931G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851215 | ||||||
| chr11:61851292
|
G | A | 1 | a0001c0001t0008g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.744+3008G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851292 | ||||||
| chr11:61851359
|
T | C | 64 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(61): Show | 70 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.744+3075T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851359 | ||||||
| chr11:61851454
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.744+3170C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851454 | ||||||
| chr11:61851556
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.744+3272C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851556 | ||||||
| chr11:61851627
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.744+3343A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851627 | ||||||
| chr11:61851709
|
T | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(14): Show | 18 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.744+3425T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851709 | ||||||
| chr11:61851822
|
G | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 16 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.744+3538G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61851822 | ||||||
| chr11:61852166
|
C | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 5 | HG01243.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+3882C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852166 | ||||||
| chr11:61852280
|
A | AGACAAGG others(31): Show |
1 | a0001c0001t0001g0220 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.744+3998_744+4035d others(40): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61852280 | |||||
| chr11:61852357
|
C | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(66): Show | 77 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.744+4073C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852357 | ||||||
| chr11:61852421
|
C | T | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 54 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.744+4137C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852421 | ||||||
| chr11:61852489
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.744+4205G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852489 | ||||||
| chr11:61852530
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.744+4246G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852530 | ||||||
| chr11:61852556
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(5): Show | 10 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.744+4272C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852556 | ||||||
| chr11:61852607
|
G | A | 1 | a0001c0001t0002g0015 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.744+4323G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852607 | ||||||
| chr11:61852657
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.745-4354T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852657 | ||||||
| chr11:61852664
|
G | A | 1 | a0001c0001t0007g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.745-4347G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852664 | ||||||
| chr11:61852802
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(28): Show | 37 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.745-4209T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852802 | ||||||
| chr11:61852833
|
G | GGGAGGGA others(286): Show |
1 | a0001c0001t0002g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.745-4178_745-4177i others(295): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852833 | ||||||
| chr11:61852834
|
A | T | 1 | a0001c0001t0002g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.745-4177A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852834 | ||||||
| chr11:61852835
|
T | A | 1 | a0001c0001t0002g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.745-4176T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852835 | ||||||
| chr11:61852950
|
C | T | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.745-4061C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61852950 | ||||||
| chr11:61853016
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0204 | 3 | HG01175.hp2 HG01934.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.745-3995A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853016 | ||||||
| chr11:61853116
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.745-3895C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853116 | ||||||
| chr11:61853150
|
G | A | 2 | a0001c0001t0009g0127a0001c0001t0009g0140 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.745-3861G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853150 | ||||||
| chr11:61853156
|
AAACAAC | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.745-3834_745-3829d others(8): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853156 | |||||
| chr11:61853176
|
AC | A | 16 | a0001c0001t0001g0150a0001c0001t0002g0130a0001c0001t0002g0148others(13): Show | 16 | HG00735.hp1 HG01109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.745-3834delC | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853176 | ||||||
| chr11:61853231
|
CTCTT | C | 114 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(111): Show | 120 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.745-3768_745-3765d others(6): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853231 | |||||
| chr11:61853241
|
CTT | C | 2 | a0001c0001t0001g0137a0001c0001t0002g0005 | 3 | HG03041.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.745-3768_745-3767d others(4): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853241 | |||||
| chr11:61853241
|
CTTTCTCT others(7): Show |
C | 3 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030 | 4 | HG01168.hp2 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3768_745-3755d others(16): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853241 | |||||
| chr11:61853243
|
T | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(102): Show | 110 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.745-3768T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853243 | ||||||
| chr11:61853247
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0135 | 3 | HG02451.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.745-3764C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853247 | ||||||
| chr11:61853250
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.745-3761T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853250 | ||||||
| chr11:61853251
|
C | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0019others(43): Show | 50 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.745-3760C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853251 | ||||||
| chr11:61853254
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0135 | 3 | HG02451.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.745-3757T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853254 | ||||||
| chr11:61853255
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0135 | 3 | HG02451.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.745-3756T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853255 | ||||||
| chr11:61853258
|
T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0019others(30): Show | 37 | HG00140.hp1 HG00438.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.745-3753T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853258 | ||||||
| chr11:61853259
|
T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0019others(44): Show | 51 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.745-3752T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853259 | ||||||
| chr11:61853262
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(98): Show | 109 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.745-3749T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853262 | ||||||
| chr11:61853263
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030 | 4 | HG01168.hp2 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3748C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853263 | ||||||
| chr11:61853263
|
CTCCCTCC others(6): Show |
C | 1 | a0001c0001t0003g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.745-3734_745-3722d others(15): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853263 | |||||
| chr11:61853271
|
CTCCCT | C | 3 | a0001c0001t0001g0139a0001c0001t0012g0154a0001c0001t0014g0155 | 3 | HG02486.hp1 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.745-3734_745-3730d others(7): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853271 | |||||
| chr11:61853275
|
CT | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0029others(16): Show | 23 | HG00735.hp1 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.745-3734delT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853275 | |||||
| chr11:61853276
|
T | TCCC | 13 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0113others(10): Show | 13 | HG00438.hp2 HG01167.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-3735_745-3734i others(5): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853276 | ||||||
| chr11:61853276
|
T | TCCCTCCC | 15 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0048others(12): Show | 16 | HG00140.hp1 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.745-3735_745-3734i others(9): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853276 | ||||||
| chr11:61853276
|
T | TCCCTCCC others(4): Show |
4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0086others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3735_745-3734i others(13): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853276 | ||||||
| chr11:61853276
|
T | TCCCTCCC others(8): Show |
3 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0004g0042 | 3 | HG02922.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.745-3735_745-3734i others(17): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853276 | ||||||
| chr11:61853282
|
C | CCCTT | 7 | a0001c0001t0001g0176a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG00408.hp1 HG02027.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.745-3726_745-3725i others(6): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853282 | |||||
| chr11:61853282
|
C | CCCTTCCT others(1): Show |
25 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0177others(22): Show | 27 | HG00558.hp2 HG00597.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.745-3726_745-3725i others(10): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853282 | |||||
| chr11:61853282
|
C | CCCTTCCT others(5): Show |
13 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 13 | HG00408.hp2 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.745-3726_745-3725i others(14): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853282 | |||||
| chr11:61853282
|
C | CCCTTCCT others(9): Show |
5 | a0001c0001t0001g0183a0001c0001t0001g0201a0001c0001t0001g0207others(2): Show | 5 | HG00609.hp1 HG02132.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-3726_745-3725i others(18): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853282 | |||||
| chr11:61853282
|
C | CCCTTCCT others(13): Show |
2 | a0001c0001t0001g0219a0001c0002t0001g0208 | 2 | HG00423.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.745-3726_745-3725i others(22): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853282 | |||||
| chr11:61853282
|
C | CCCTTCCT others(17): Show |
1 | a0001c0001t0001g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.745-3726_745-3725i others(26): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853282 | |||||
| chr11:61853282
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0048others(12): Show | 16 | HG00140.hp1 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.745-3729C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853282 | ||||||
| chr11:61853286
|
C | CCCTTCCT others(5): Show |
1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.745-3722_745-3721i others(14): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853286 | |||||
| chr11:61853286
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0031others(67): Show | 74 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.745-3725C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853286 | ||||||
| chr11:61853290
|
C | CCCTCCCT others(5): Show |
1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.745-3718_745-3717i others(14): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTCCCT others(13): Show |
1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.745-3718_745-3717i others(22): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTT | 6 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0122others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-3680_745-3677d others(6): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.745-3714_745-3713i others(18): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTTCCT others(1): Show |
23 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(20): Show | 27 | HG00642.hp2 HG01243.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.745-3684_745-3677d others(10): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTTCCT others(5): Show |
44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0021others(41): Show | 49 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.745-3688_745-3677d others(14): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTTCCT others(9): Show |
16 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0033others(13): Show | 17 | HG01070.hp2 HG01361.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.745-3692_745-3677d others(18): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTTCCT others(13): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0054 | 2 | HG03209.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.745-3696_745-3677d others(22): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | CCCTTCCT others(17): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0088 | 2 | HG02683.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.745-3700_745-3677d others(26): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
C | T | 83 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(80): Show | 88 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.745-3721C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853290 | ||||||
| chr11:61853290
|
CCCTT | C | 39 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(36): Show | 43 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.745-3680_745-3677d others(6): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
CCCTTCCT others(1): Show |
C | 5 | a0001c0001t0001g0236a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01496.hp2 NA18982.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-3684_745-3677d others(10): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853290
|
CCCTTCCT others(5): Show |
C | 2 | a0001c0001t0001g0143a0001c0001t0001g0158 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.745-3688_745-3677d others(14): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 61853290 | |||||
| chr11:61853294
|
T | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 18 | HG00735.hp1 HG01168.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.745-3717T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853294 | ||||||
| chr11:61853298
|
T | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 11 | HG01168.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.745-3713T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853298 | ||||||
| chr11:61853302
|
T | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0010g0157others(2): Show | 5 | HG02486.hp1 HG02717.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-3709T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853302 | ||||||
| chr11:61853306
|
T | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0158others(2): Show | 5 | HG02486.hp1 HG02717.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-3705T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853306 | ||||||
| chr11:61853310
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.745-3701T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853310 | ||||||
| chr11:61853425
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.745-3586C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853425 | ||||||
| chr11:61853534
|
C | T | 2 | a0001c0001t0012g0154a0001c0001t0014g0155 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.745-3477C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853534 | ||||||
| chr11:61853564
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.745-3447G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853564 | ||||||
| chr11:61853568
|
G | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(72): Show | 83 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.745-3443G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853568 | ||||||
| chr11:61853722
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(129): Show | 142 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.745-3289G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853722 | ||||||
| chr11:61853797
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0158 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.745-3214G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61853797 | ||||||
| chr11:61854003
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.745-3008G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854003 | ||||||
| chr11:61854070
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.745-2941G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854070 | ||||||
| chr11:61854084
|
G | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(159): Show | 173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.745-2927G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854084 | ||||||
| chr11:61854139
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(53): Show | 60 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.745-2872A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854139 | ||||||
| chr11:61854333
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.745-2678C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854333 | ||||||
| chr11:61854361
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.745-2650G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854361 | ||||||
| chr11:61854719
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.745-2292A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854719 | ||||||
| chr11:61854755
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(121): Show | 132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.745-2256T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854755 | ||||||
| chr11:61854965
|
C | T | 6 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0145others(3): Show | 6 | HG00735.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.745-2046C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61854965 | ||||||
| chr11:61855011
|
A | G | 4 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0012g0154others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-2000A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855011 | ||||||
| chr11:61855029
|
C | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.745-1982C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855029 | ||||||
| chr11:61855245
|
G | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(4): Show | 9 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.745-1766G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855245 | ||||||
| chr11:61855258
|
G | A | 2 | a0001c0001t0009g0127a0001c0001t0009g0140 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.745-1753G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855258 | ||||||
| chr11:61855433
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.745-1578A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855433 | ||||||
| chr11:61855433
|
A | T | 2 | a0001c0001t0009g0127a0001c0001t0009g0140 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.745-1578A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855433 | ||||||
| chr11:61855496
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.745-1515G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855496 | ||||||
| chr11:61855565
|
A | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 15 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.745-1446A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855565 | ||||||
| chr11:61855569
|
T | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0077others(1): Show | 4 | HG03669.hp2 HG04204.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1442T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855569 | ||||||
| chr11:61855668
|
C | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(159): Show | 173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.745-1343C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855668 | ||||||
| chr11:61855931
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.745-1080T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61855931 | ||||||
| chr11:61856321
|
G | A | 54 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0037others(51): Show | 54 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.745-690G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856321 | ||||||
| chr11:61856335
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 7 | HG01168.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-676C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856335 | ||||||
| chr11:61856341
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.745-670C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856341 | ||||||
| chr11:61856449
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.745-562A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856449 | ||||||
| chr11:61856511
|
C | T | 1 | a0001c0001t0006g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.745-500C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856511 | ||||||
| chr11:61856539
|
G | A | 1 | a0001c0001t0006g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.745-472G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856539 | ||||||
| chr11:61856550
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0136others(2): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-461G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856550 | ||||||
| chr11:61856709
|
T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(66): Show | 77 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.745-302T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856709 | ||||||
| chr11:61856725
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.745-286C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856725 | ||||||
| chr11:61856775
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0134 | 4 | HG01884.hp1 HG02109.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-236C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856775 | ||||||
| chr11:61856812
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0073others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-199C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856812 | ||||||
| chr11:61856942
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(125): Show | 139 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.745-69T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856942 | ||||||
| chr11:61856978
|
A | C | 4 | a0001c0001t0008g0129a0001c0001t0009g0127a0001c0001t0009g0140others(1): Show | 4 | HG02970.hp2 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-33A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 5/11 | chr11 | 61856978 | ||||||
| chr11:61857233
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.805+162T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 6/11 | chr11 | 61857233 | ||||||
| chr11:61857373
|
G | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0050others(4): Show | 7 | HG01261.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.806-81G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 6/11 | chr11 | 61857373 | ||||||
| chr11:61857413
|
G | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(168): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.806-41G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 6/11 | chr11 | 61857413 | ||||||
| chr11:61857601
|
C | T | 1 | a0001c0001t0006g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+71C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857601 | ||||||
| chr11:61857637
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.882+107G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857637 | ||||||
| chr11:61857643
|
G | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(33): Show | 41 | HG00558.hp1 HG01109.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.882+113G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857643 | ||||||
| chr11:61857693
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.882+163G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857693 | ||||||
| chr11:61857793
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+263A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857793 | ||||||
| chr11:61857872
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.882+342C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857872 | ||||||
| chr11:61857995
|
C | T | 2 | a0001c0001t0009g0127a0001c0001t0009g0140 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.882+465C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857995 | ||||||
| chr11:61857999
|
C | T | 2 | a0001c0001t0008g0129a0001c0001t0008g0151 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.882+469C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61857999 | ||||||
| chr11:61858251
|
CA | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(107): Show | 120 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.882+723delA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61858251 | |||||
| chr11:61858499
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.882+969T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61858499 | ||||||
| chr11:61858536
|
T | C | 2 | a0001c0001t0008g0131a0001c0001t0010g0157 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.882+1006T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61858536 | ||||||
| chr11:61858593
|
C | CT | 6 | a0001c0001t0005g0008a0001c0001t0005g0041a0001c0001t0005g0053others(3): Show | 7 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+1073dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61858593 | |||||
| chr11:61858689
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0150 | 2 | HG00735.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.882+1159G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61858689 | ||||||
| chr11:61858695
|
C | T | 6 | a0001c0001t0005g0008a0001c0001t0005g0041a0001c0001t0005g0053others(3): Show | 7 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+1165C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61858695 | ||||||
| chr11:61858734
|
G | A | 100 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(97): Show | 109 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.882+1204G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61858734 | ||||||
| chr11:61858773
|
A | G | 1 | a0001c0001t0008g0131 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.882+1243A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61858773 | ||||||
| chr11:61858798
|
C | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(125): Show | 138 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.882+1268C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61858798 | ||||||
| chr11:61859119
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.882+1589G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859119 | ||||||
| chr11:61859127
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.882+1597G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859127 | ||||||
| chr11:61859346
|
C | T | 12 | a0001c0001t0002g0005a0001c0001t0002g0148a0001c0001t0002g0149others(9): Show | 13 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+1816C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859346 | ||||||
| chr11:61859384
|
A | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+1854A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859384 | ||||||
| chr11:61859449
|
G | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0076others(25): Show | 30 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+1919G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859449 | ||||||
| chr11:61859496
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.882+1966C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859496 | ||||||
| chr11:61859501
|
G | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(130): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.882+1971G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859501 | ||||||
| chr11:61859533
|
C | G | 1 | a0001c0001t0001g0241 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.882+2003C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859533 | ||||||
| chr11:61859553
|
C | G | 1 | a0001c0004t0011g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+2023C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859553 | ||||||
| chr11:61859556
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.882+2026G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859556 | ||||||
| chr11:61859712
|
C | T | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+2182C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859712 | ||||||
| chr11:61859723
|
A | AGTCACTC others(2): Show |
25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG00140.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+2193_882+2194i others(11): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859723 | ||||||
| chr11:61859728
|
T | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG00140.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+2198T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859728 | ||||||
| chr11:61859729
|
G | GGCGCA | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG00140.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+2199_882+2200i others(7): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859729 | ||||||
| chr11:61859730
|
T | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG00140.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+2200T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859730 | ||||||
| chr11:61859732
|
A | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG00140.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+2202A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859732 | ||||||
| chr11:61859733
|
T | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG00140.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+2203T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859733 | ||||||
| chr11:61859814
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0138others(12): Show | 17 | HG01109.hp1 HG01109.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.882+2284G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859814 | ||||||
| chr11:61859849
|
G | C | 27 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0076others(24): Show | 29 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.882+2319G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859849 | ||||||
| chr11:61859883
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+2353G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859883 | ||||||
| chr11:61859918
|
G | A | 3 | a0001c0001t0007g0085a0001c0001t0007g0206a0001c0001t0007g0259 | 3 | HG00621.hp2 NA18989.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.882+2388G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61859918 | ||||||
| chr11:61859939
|
C | CT | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(101): Show | 113 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.882+2417dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61859939 | |||||
| chr11:61860012
|
A | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0076others(27): Show | 32 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+2482A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860012 | ||||||
| chr11:61860023
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+2493A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860023 | ||||||
| chr11:61860043
|
C | A | 5 | a0001c0001t0006g0023a0001c0001t0006g0102a0001c0001t0006g0123others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+2513C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860043 | ||||||
| chr11:61860081
|
G | A | 2 | a0001c0001t0006g0102a0001c0001t0006g0123 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.882+2551G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860081 | ||||||
| chr11:61860147
|
CTT | C | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+2620_882+2621d others(4): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61860147 | |||||
| chr11:61860246
|
G | A | 1 | a0001c0001t0013g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.882+2716G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860246 | ||||||
| chr11:61860282
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.883-2690A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860282 | ||||||
| chr11:61860339
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.883-2633T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860339 | ||||||
| chr11:61860361
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(132): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.883-2611A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860361 | ||||||
| chr11:61860409
|
T | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0076others(27): Show | 32 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-2563T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860409 | ||||||
| chr11:61860480
|
C | G | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.883-2492C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860480 | ||||||
| chr11:61860488
|
C | T | 52 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(49): Show | 56 | HG00423.hp2 HG00438.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.883-2484C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860488 | ||||||
| chr11:61860511
|
C | G | 1 | a0001c0001t0001g0249 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.883-2461C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860511 | ||||||
| chr11:61860723
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.883-2249C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860723 | ||||||
| chr11:61860793
|
A | G | 4 | a0001c0001t0002g0005a0001c0001t0002g0126a0001c0001t0002g0148others(1): Show | 5 | HG02717.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-2179A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860793 | ||||||
| chr11:61860794
|
C | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(132): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.883-2178C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860794 | ||||||
| chr11:61860818
|
G | C | 4 | a0001c0001t0005g0008a0001c0001t0005g0041a0001c0001t0005g0053others(1): Show | 5 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-2154G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61860818 | ||||||
| chr11:61861020
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.883-1952G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861020 | ||||||
| chr11:61861031
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.883-1941C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861031 | ||||||
| chr11:61861129
|
C | T | 5 | a0001c0001t0006g0023a0001c0001t0006g0102a0001c0001t0006g0123others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-1843C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861129 | ||||||
| chr11:61861130
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0030others(2): Show | 6 | HG01168.hp2 HG01361.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1842G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861130 | ||||||
| chr11:61861143
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0137others(7): Show | 12 | HG00735.hp1 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.883-1829A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861143 | ||||||
| chr11:61861211
|
G | A | 3 | a0001c0001t0006g0023a0001c0001t0012g0154a0001c0001t0014g0155 | 3 | HG02486.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.883-1761G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861211 | ||||||
| chr11:61861235
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-1737A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861235 | ||||||
| chr11:61861341
|
G | A | 3 | a0001c0001t0007g0085a0001c0001t0007g0206a0001c0001t0007g0259 | 3 | HG00621.hp2 NA18989.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.883-1631G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861341 | ||||||
| chr11:61861353
|
C | CAAAAA | 6 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-1605_883-1601d others(7): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(1): Show |
23 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0020others(20): Show | 24 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.883-1608_883-1601d others(10): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0049others(10): Show | 14 | HG00140.hp1 HG00741.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-1609_883-1601d others(11): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0188a0001c0001t0001g0214a0001c0001t0006g0132 | 3 | HG00558.hp1 HG01243.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.883-1610_883-1601d others(12): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG03239.hp2 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.883-1611_883-1601d others(13): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.883-1612_883-1601d others(14): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0030others(5): Show | 9 | HG01168.hp2 HG01361.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-1613_883-1601d others(15): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0233 | 2 | HG02135.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.883-1614_883-1601d others(16): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.883-1615_883-1601d others(17): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0007g0085a0001c0001t0007g0206 | 2 | NA18989.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.883-1617_883-1601d others(19): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0007g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.883-1618_883-1601d others(20): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.883-1601_883-1600i others(22): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0197 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.883-1601_883-1600i others(25): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(17): Show |
6 | a0001c0001t0001g0052a0001c0001t0001g0119a0001c0001t0001g0193others(3): Show | 6 | HG00408.hp2 HG02015.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(26): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(18): Show |
20 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0032others(17): Show | 23 | HG00597.hp1 HG00609.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(27): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(19): Show |
15 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(12): Show | 18 | HG00597.hp2 HG00609.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(28): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(20): Show |
11 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0071others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(29): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(21): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0080others(1): Show | 4 | HG02451.hp1 NA18953.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(30): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0064 | 3 | HG03139.hp2 HG03195.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.883-1601_883-1600i others(31): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(23): Show |
3 | a0001c0001t0001g0050a0001c0001t0001g0231a0001c0001t0001g0234 | 3 | HG02129.hp1 NA18906.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.883-1601_883-1600i others(32): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(24): Show |
5 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0066others(2): Show | 5 | HG00140.hp2 HG00621.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(33): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(25): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0065others(1): Show | 4 | HG01106.hp2 NA18950.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(34): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(26): Show |
1 | a0001c0002t0001g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.883-1601_883-1600i others(35): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(27): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0120 | 3 | HG01433.hp1 HG01516.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.883-1601_883-1600i others(36): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883-1601_883-1600i others(37): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0007g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.883-1601_883-1600i others(39): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.883-1601_883-1600i others(27): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(17): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(26): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861353
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.883-1604_883-1603i others(31): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861353 | |||||
| chr11:61861358
|
A | AAAAAAAC | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 54 | HG00423.hp2 HG00438.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-1608_883-1607i others(9): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861358 | |||||
| chr11:61861358
|
A | AAAAAAC | 20 | a0001c0001t0001g0029a0001c0001t0001g0150a0001c0001t0001g0245others(17): Show | 21 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.883-1609_883-1608i others(8): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861358 | |||||
| chr11:61861365
|
A | AAAAAAAA others(1): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(10): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861365 | |||||
| chr11:61861365
|
A | AAAAAAC | 13 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(10): Show | 14 | HG00099.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-1602_883-1601i others(8): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61861365 | |||||
| chr11:61861365
|
A | C | 69 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(66): Show | 75 | HG00423.hp2 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.883-1607A>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861365 | ||||||
| chr11:61861371
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0114 | 2 | HG00642.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.883-1601_883-1600i others(17): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861371 | ||||||
| chr11:61861371
|
A | AAAAAAAA others(7): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 7 | HG00741.hp2 HG01167.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-1601_883-1600i others(16): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861371 | ||||||
| chr11:61861443
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.883-1529T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861443 | ||||||
| chr11:61861477
|
A | G | 3 | a0001c0001t0007g0085a0001c0001t0007g0206a0001c0001t0007g0259 | 3 | HG00621.hp2 NA18989.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.883-1495A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861477 | ||||||
| chr11:61861492
|
T | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.883-1480T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861492 | ||||||
| chr11:61861524
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.883-1448T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861524 | ||||||
| chr11:61861649
|
C | T | 3 | a0001c0001t0007g0085a0001c0001t0007g0206a0001c0001t0007g0259 | 3 | HG00621.hp2 NA18989.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.883-1323C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861649 | ||||||
| chr11:61861650
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.883-1322G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861650 | ||||||
| chr11:61861663
|
C | G | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-1309C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861663 | ||||||
| chr11:61861664
|
T | A | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-1308T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861664 | ||||||
| chr11:61861694
|
A | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(134): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.883-1278A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861694 | ||||||
| chr11:61861695
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.883-1277G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861695 | ||||||
| chr11:61861850
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(83): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.883-1122T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861850 | ||||||
| chr11:61861905
|
C | T | 11 | a0001c0001t0002g0015a0001c0001t0002g0059a0001c0001t0002g0112others(8): Show | 12 | HG00738.hp2 HG01081.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.883-1067C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61861905 | ||||||
| chr11:61862036
|
G | C | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-936G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862036 | ||||||
| chr11:61862046
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.883-926T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862046 | ||||||
| chr11:61862104
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0112 | 3 | HG01258.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.883-868C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862104 | ||||||
| chr11:61862121
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.883-851G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862121 | ||||||
| chr11:61862184
|
A | ACT | 133 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(130): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.883-787_883-786dup others(2): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 61862184 | |||||
| chr11:61862194
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(100): Show | 112 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.883-778A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862194 | ||||||
| chr11:61862275
|
A | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(83): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.883-697A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862275 | ||||||
| chr11:61862350
|
C | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0194a0001c0001t0001g0212others(1): Show | 4 | NA18998.hp1 NA19003.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-622C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862350 | ||||||
| chr11:61862351
|
C | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0194a0001c0001t0001g0212others(1): Show | 4 | NA18998.hp1 NA19003.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-621C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862351 | ||||||
| chr11:61862376
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | NA18951.hp1 NA18960.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.883-596A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862376 | ||||||
| chr11:61862384
|
C | T | 1 | a0001c0004t0011g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.883-588C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862384 | ||||||
| chr11:61862385
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.883-587G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862385 | ||||||
| chr11:61862386
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.883-586T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862386 | ||||||
| chr11:61862412
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.883-560C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862412 | ||||||
| chr11:61862482
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.883-490C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862482 | ||||||
| chr11:61862570
|
G | T | 6 | a0001c0001t0006g0023a0001c0001t0006g0102a0001c0001t0006g0123others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-402G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862570 | ||||||
| chr11:61862620
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.883-352G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862620 | ||||||
| chr11:61862631
|
C | A | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-341C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862631 | ||||||
| chr11:61862632
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(42): Show | 48 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.883-340G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862632 | ||||||
| chr11:61862643
|
G | A | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-329G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862643 | ||||||
| chr11:61862661
|
T | C | 56 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(53): Show | 60 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.883-311T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862661 | ||||||
| chr11:61862691
|
C | T | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-281C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862691 | ||||||
| chr11:61862721
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.883-251G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862721 | ||||||
| chr11:61862814
|
C | T | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-158C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862814 | ||||||
| chr11:61862861
|
C | T | 3 | a0001c0001t0002g0126a0001c0001t0002g0148a0001c0001t0002g0149 | 3 | HG02717.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.883-111C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862861 | ||||||
| chr11:61862862
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.883-110G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862862 | ||||||
| chr11:61862911
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.883-61C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862911 | ||||||
| chr11:61862911
|
C | G | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-61C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862911 | ||||||
| chr11:61862912
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-60G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 7/11 | chr11 | 61862912 | ||||||
| chr11:61863162
|
T | C | 6 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(3): Show | 6 | HG00621.hp2 HG02886.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+93T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 8/11 | chr11 | 61863162 | ||||||
| chr11:61863176
|
C | T | 1 | a0001c0001t0008g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.981-106C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 8/11 | chr11 | 61863176 | ||||||
| chr11:61863497
|
T | C | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077+119T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 9/11 | chr11 | 61863497 | ||||||
| chr11:61863592
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0249 | 2 | NA18945.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1078-115C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 9/11 | chr11 | 61863592 | ||||||
| chr11:61863597
|
T | A | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-110T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 9/11 | chr11 | 61863597 | ||||||
| chr11:61863655
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1078-52C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 9/11 | chr11 | 61863655 | ||||||
| chr11:61863792
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp2 | splice_region_variant&intron_variant | LOW | c.1157+6C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61863792 | ||||||
| chr11:61863810
|
C | T | 4 | a0001c0001t0005g0008a0001c0001t0005g0041a0001c0001t0005g0053others(1): Show | 5 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157+24C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61863810 | ||||||
| chr11:61863838
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1157+52G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61863838 | ||||||
| chr11:61863859
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0005g0008a0001c0001t0005g0041others(10): Show | 14 | HG00099.hp1 HG00621.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1157+73A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61863859 | ||||||
| chr11:61863905
|
G | A | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+119G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61863905 | ||||||
| chr11:61863915
|
G | A | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+129G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61863915 | ||||||
| chr11:61863982
|
T | G | 13 | a0001c0001t0001g0029a0001c0001t0005g0008a0001c0001t0005g0041others(10): Show | 14 | HG00099.hp1 HG00621.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1157+196T>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61863982 | ||||||
| chr11:61864005
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1157+219G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864005 | ||||||
| chr11:61864029
|
C | T | 4 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(1): Show | 4 | HG01261.hp2 HG02559.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1157+243C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864029 | ||||||
| chr11:61864038
|
A | T | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 53 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1157+252A>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864038 | ||||||
| chr11:61864139
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0150 | 2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1157+353G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864139 | ||||||
| chr11:61864142
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0005g0008a0001c0001t0005g0041others(2): Show | 6 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1157+356G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864142 | ||||||
| chr11:61864170
|
T | C | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+384T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864170 | ||||||
| chr11:61864186
|
G | GT | 47 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(44): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1157+415dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 61864186 | |||||
| chr11:61864186
|
GT | G | 17 | a0001c0001t0001g0029a0001c0001t0001g0100a0001c0001t0001g0119others(14): Show | 18 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1157+415delT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 61864186 | |||||
| chr11:61864186
|
GTT | G | 6 | a0001c0001t0006g0023a0001c0001t0006g0102a0001c0001t0006g0123others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1157+414_1157+415d others(4): Show |
FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 61864186 | |||||
| chr11:61864199
|
T | A | 9 | a0001c0001t0003g0027a0001c0001t0003g0128a0001c0001t0003g0133others(6): Show | 9 | HG01109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1157+413T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864199 | ||||||
| chr11:61864201
|
T | TA | 4 | a0001c0001t0002g0005a0001c0001t0002g0126a0001c0001t0002g0148others(1): Show | 5 | HG02717.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+416dupA | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 61864201 | |||||
| chr11:61864218
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(25): Show | 34 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1157+432T>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864218 | ||||||
| chr11:61864295
|
C | T | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+509C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864295 | ||||||
| chr11:61864305
|
G | T | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+519G>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864305 | ||||||
| chr11:61864377
|
C | CT | 5 | a0001c0001t0001g0029a0001c0001t0005g0008a0001c0001t0005g0041others(2): Show | 6 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1157+602dupT | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 61864377 | |||||
| chr11:61864455
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(36): Show | 42 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1157+669G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864455 | ||||||
| chr11:61864491
|
T | A | 8 | a0001c0001t0007g0074a0001c0001t0007g0085a0001c0001t0007g0206others(5): Show | 8 | HG00621.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1158-661T>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864491 | ||||||
| chr11:61864626
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1158-526C>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864626 | ||||||
| chr11:61864643
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1158-509C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864643 | ||||||
| chr11:61864795
|
C | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0190a0001c0001t0001g0201 | 3 | HG02132.hp1 NA18950.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1158-357C>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864795 | ||||||
| chr11:61864826
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-326G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864826 | ||||||
| chr11:61864826
|
G | C | 4 | a0001c0001t0005g0008a0001c0001t0005g0041a0001c0001t0005g0053others(1): Show | 5 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158-326G>C | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864826 | ||||||
| chr11:61864838
|
A | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(60): Show | 69 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1158-314A>G | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864838 | ||||||
| chr11:61864958
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02027.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1158-194G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61864958 | ||||||
| chr11:61865096
|
G | A | 1 | a0001c0001t0004g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1158-56G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 10/11 | chr11 | 61865096 | ||||||
| chr11:61865294
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1283+17C>T | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 11/11 | chr11 | 61865294 | ||||||
| chr11:61865441
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0137others(10): Show | 15 | HG00621.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1283+164G>A | FADS2 | ENSG00000134824.14 | transcript | ENST00000278840.9 | protein_coding | 11/11 | chr11 | 61865441 |