Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54898 |
|---|---|
| ensemblid | ENSG00000197977.4 |
| hgncid | 14416 |
| symbol | ELOVL2 |
| name | ELOVL fatty acid elongase 2 |
| refseq_nuc | NM_017770.4 |
| refseq_prot | NP_060240.3 |
| ensembl_nuc | ENST00000354666.4 |
| ensembl_prot | ENSP00000346693.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 10980759 |
| end | 11044305 |
| strand | - |
| ver | v1.2 |
| region | chr6:10980759-11044305 |
| region5000 | chr6:10975759-11049305 |
| regionname0 | ELOVL2_chr6_10980759_11044305 |
| regionname5000 | ELOVL2_chr6_10975759_11049305 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 296 | 375 | 91 | 66 | 168 | 12 | 36 | 136 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0002 | 0/0 | 296 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0003 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0004 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0005 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 891 | 270 | 66 | 42 | 128 | 7 | 25 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| c0002 | 0/0 | 891 | 90 | 24 | 19 | 40 | 1 | 6 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| c0003 | 0/0 | 891 | 14 | 0 | 5 | 0 | 4 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| c0004 | 0/0 | 891 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| c0005 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| c0006 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| c0007 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| c0008 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3098 | 112 | 28 | 6 | 59 | 3 | 15 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0002 | 0/0 | 3098 | 53 | 1 | 18 | 29 | 0 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0003 | 0/0 | 3098 | 40 | 0 | 1 | 39 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0004 | 1/0 | 3098 | 39 | 0 | 12 | 19 | 4 | 3 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0005 | 0/0 | 3098 | 37 | 11 | 13 | 1 | 5 | 7 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0006 | 0/0 | 3098 | 18 | 16 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0007 | 0/0 | 3098 | 11 | 0 | 11 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0008 | 0/0 | 3098 | 10 | 10 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0009 | 0/0 | 3098 | 9 | 0 | 0 | 9 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0010 | 0/0 | 3098 | 9 | 9 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0011 | 0/0 | 3098 | 7 | 0 | 0 | 7 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0012 | 0/0 | 3098 | 6 | 5 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0013 | 0/0 | 3098 | 5 | 3 | 0 | 0 | 0 | 2 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0014 | 0/0 | 3098 | 5 | 0 | 0 | 2 | 0 | 3 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0015 | 0/0 | 3098 | 4 | 0 | 0 | 4 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0016 | 0/0 | 3098 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0017 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0018 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0019 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0020 | 0/0 | 3098 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0021 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0022 | 0/0 | 3098 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0023 | 0/0 | 3098 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0024 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0025 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0026 | 0/0 | 3098 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0027 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0028 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| t0029 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 891 | 270 | 66 | 42 | 128 | 7 | 25 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002 | 0/0 | 891 | 90 | 24 | 19 | 40 | 1 | 6 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0003 | 0/0 | 891 | 14 | 0 | 5 | 0 | 4 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0007 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0002c0004 | 0/0 | 891 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0003c0008 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0004c0006 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0005c0005 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3988 | 90 | 9 | 6 | 56 | 3 | 15 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0003 | 0/0 | 3988 | 40 | 0 | 1 | 39 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0004 | 1/0 | 3988 | 37 | 0 | 12 | 18 | 3 | 3 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0005 | 0/0 | 3988 | 23 | 11 | 8 | 1 | 1 | 2 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0006 | 0/0 | 3988 | 18 | 16 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0007 | 0/0 | 3988 | 11 | 0 | 11 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0008 | 0/0 | 3988 | 10 | 10 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0010 | 0/0 | 3988 | 9 | 9 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0011 | 0/0 | 3988 | 7 | 0 | 0 | 7 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0012 | 0/0 | 3988 | 6 | 5 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0013 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0014 | 0/0 | 3988 | 5 | 0 | 0 | 2 | 0 | 3 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0015 | 0/0 | 3988 | 4 | 0 | 0 | 4 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0017 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0019 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0020 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0023 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0025 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0026 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0027 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0028 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0001t0029 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002t0001 | 0/0 | 3988 | 21 | 19 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002t0002 | 0/0 | 3988 | 53 | 1 | 18 | 29 | 0 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002t0004 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002t0009 | 0/0 | 3988 | 9 | 0 | 0 | 9 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002t0013 | 0/0 | 3988 | 4 | 3 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002t0021 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0002t0022 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0003t0005 | 0/0 | 3988 | 14 | 0 | 5 | 0 | 4 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0001c0007t0018 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0002c0004t0016 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0003c0008t0001 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0004c0006t0024 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| a0005c0005t0004 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | copy fasta | chr6 | 10975759 | 11049305 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0015g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0015g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0015g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0017g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0020g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0023g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0025g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0026g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0027g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0028g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0029g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0021g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0022g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0007t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0002c0004t0016g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0002c0004t0016g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0003c0008t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0004c0006t0024g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0005c0005t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0148 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00280 | hp2 | a0001 | c0003 | t0005 | g0183 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0245 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0189 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0262 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01070 | hp2 | a0001 | c0003 | t0005 | g0005 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01071 | hp1 | a0001 | c0003 | t0005 | g0005 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0079 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01074 | hp1 | a0001 | c0003 | t0005 | g0005 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01074 | hp2 | a0001 | c0003 | t0005 | g0186 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01099 | hp1 | a0001 | c0003 | t0005 | g0182 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0196 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0052 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0225 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0263 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0190 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01358 | hp1 | a0001 | c0001 | t0007 | g0061 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0258 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0250 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01361 | hp2 | a0001 | c0001 | t0012 | g0306 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0151 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0166 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0191 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01515 | hp2 | a0001 | c0003 | t0005 | g0011 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01516 | hp2 | a0001 | c0003 | t0005 | g0172 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01884 | hp2 | a0001 | c0002 | t0013 | g0294 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0133 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0069 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01975 | hp2 | a0001 | c0001 | t0020 | g0179 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0081 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0083 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0261 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0067 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0082 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0260 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0246 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0070 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02257 | hp2 | a0001 | c0007 | t0018 | g0209 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0330 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0266 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0185 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0216 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0276 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0273 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0268 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02683 | hp1 | a0001 | c0003 | t0005 | g0170 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0198 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0214 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0215 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02738 | hp1 | a0001 | c0003 | t0005 | g0171 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0165 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02922 | hp1 | a0001 | c0002 | t0013 | g0300 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0205 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02970 | hp2 | a0001 | c0002 | t0013 | g0298 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0304 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0208 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03017 | hp2 | a0001 | c0003 | t0005 | g0011 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0302 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0282 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0305 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03453 | hp2 | a0002 | c0004 | t0016 | g0204 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0192 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0303 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0267 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03579 | hp2 | a0002 | c0004 | t0016 | g0203 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03654 | hp1 | a0001 | c0001 | t0014 | g0063 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03654 | hp2 | a0001 | c0001 | t0013 | g0068 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03669 | hp1 | a0001 | c0003 | t0005 | g0139 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03927 | hp2 | a0001 | c0001 | t0026 | g0154 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0197 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0256 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04184 | hp1 | a0001 | c0002 | t0013 | g0229 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04199 | hp1 | a0001 | c0003 | t0005 | g0184 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0149 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04204 | hp1 | a0001 | c0001 | t0014 | g0193 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0227 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0248 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0275 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18906 | hp1 | a0001 | c0001 | t0029 | g0347 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18947 | hp1 | a0001 | c0002 | t0009 | g0240 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18948 | hp1 | a0001 | c0001 | t0015 | g0162 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18948 | hp2 | a0001 | c0002 | t0009 | g0239 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18949 | hp1 | a0001 | c0001 | t0011 | g0096 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18953 | hp2 | a0005 | c0005 | t0004 | g0202 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18954 | hp2 | a0003 | c0008 | t0001 | g0086 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18960 | hp2 | a0001 | c0002 | t0009 | g0002 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18962 | hp2 | a0001 | c0001 | t0011 | g0109 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18969 | hp1 | a0001 | c0002 | t0009 | g0002 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18970 | hp2 | a0001 | c0002 | t0009 | g0002 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18972 | hp1 | a0001 | c0001 | t0015 | g0167 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18974 | hp2 | a0001 | c0001 | t0011 | g0094 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18983 | hp2 | a0001 | c0002 | t0009 | g0231 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18984 | hp1 | a0001 | c0001 | t0014 | g0195 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0110 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19000 | hp1 | a0001 | c0002 | t0009 | g0254 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0336 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19010 | hp1 | a0001 | c0001 | t0015 | g0163 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19012 | hp2 | a0001 | c0002 | t0009 | g0002 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0211 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19030 | hp2 | a0001 | c0001 | t0025 | g0277 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19043 | hp1 | a0004 | c0006 | t0024 | g0310 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0206 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19057 | hp2 | a0001 | c0001 | t0015 | g0164 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0099 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0346 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19068 | hp1 | a0001 | c0001 | t0014 | g0194 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19085 | hp2 | a0001 | c0001 | t0011 | g0112 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19088 | hp2 | a0001 | c0002 | t0009 | g0002 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0013 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20129 | hp2 | a0001 | c0001 | t0019 | g0212 | AFR | ASW | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0180 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20752 | hp2 | a0001 | c0003 | t0005 | g0140 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0181 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01123 | hp2 | a0001 | c0002 | t0022 | g0253 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0307 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0269 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0281 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | USA | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | USA | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA21309 | hp1 | a0001 | c0002 | t0021 | g0222 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0106 | REF | REF | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0160 | REF | REF | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10989795
|
C | T | 2 | a0002a0004 | 3 | HG03453.hp2 HG03579.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.673G>A | p.Val225Met | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/8 | 748/3988 | 673/891 | 225/296 | chr6 | 10989795 | ||
| chr6:10990367
|
G | C | 1 | a0003 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.581C>G | p.Ser194Cys | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/8 | 656/3988 | 581/891 | 194/296 | chr6 | 10990367 | ||
| chr6:11005389
|
C | T | 1 | a0004 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.238G>A | p.Ala80Thr | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/8 | 313/3988 | 238/891 | 80/296 | chr6 | 11005389 | ||
| chr6:11005547
|
C | G | 1 | a0005 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.80G>C | p.Arg27Thr | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/8 | 155/3988 | 80/891 | 27/296 | chr6 | 11005547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10989709
|
G | A | 1 | a0001c0003 | 14 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
synonymous_variant | LOW | c.759C>T | p.Tyr253Tyr | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/8 | 834/3988 | 759/891 | 253/296 | chr6 | 10989709 | ||
| chr6:11005387
|
C | T | 1 | a0001c0007 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.240G>A | p.Ala80Ala | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/8 | 315/3988 | 240/891 | 80/296 | chr6 | 11005387 | ||
| chr6:11005453
|
G | A | 1 | a0001c0002 | 90 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(87): Show |
synonymous_variant | LOW | c.174C>T | p.Asn58Asn | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/8 | 249/3988 | 174/891 | 58/296 | chr6 | 11005453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10980820
|
G | A | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(17): Show | 279 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*2961C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2961 | chr6 | 10980820 | |||||
| chr6:10980832
|
G | C | 1 | a0001c0001t0026 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2949C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2949 | chr6 | 10980832 | |||||
| chr6:10980904
|
G | A | 1 | a0001c0001t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2877C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2877 | chr6 | 10980904 | |||||
| chr6:10981208
|
A | G | 1 | a0001c0007t0018 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2573T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2573 | chr6 | 10981208 | |||||
| chr6:10981226
|
G | A | 1 | a0001c0001t0020 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2555C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2555 | chr6 | 10981226 | |||||
| chr6:10981251
|
G | A | 1 | a0001c0001t0029 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2530C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2530 | chr6 | 10981251 | |||||
| chr6:10981265
|
A | G | 3 | a0001c0001t0003a0001c0001t0017a0001c0001t0023 | 42 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2516T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2516 | chr6 | 10981265 | |||||
| chr6:10981442
|
C | T | 1 | a0001c0001t0028 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2339G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2339 | chr6 | 10981442 | |||||
| chr6:10981610
|
T | C | 1 | a0001c0001t0011 | 7 | NA18939.hp2 NA18949.hp1 NA18962.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2171A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2171 | chr6 | 10981610 | |||||
| chr6:10981779
|
C | A | 1 | a0001c0001t0007 | 11 | HG01071.hp2 HG01106.hp1 HG01257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2002G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 2002 | chr6 | 10981779 | |||||
| chr6:10982126
|
G | A | 4 | a0001c0002t0002a0001c0002t0009a0001c0002t0021others(1): Show | 64 | HG00621.hp2 HG00642.hp2 HG00733.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1655C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1655 | chr6 | 10982126 | |||||
| chr6:10982405
|
T | G | 1 | a0001c0001t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1376A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1376 | chr6 | 10982405 | |||||
| chr6:10982419
|
C | T | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(23): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*1362G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1362 | chr6 | 10982419 | |||||
| chr6:10982428
|
A | G | 1 | a0001c0001t0012 | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1353T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1353 | chr6 | 10982428 | |||||
| chr6:10982457
|
G | A | 1 | a0001c0002t0022 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1324 | chr6 | 10982457 | |||||
| chr6:10982615
|
G | A | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(28): Show | 340 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*1166C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1166 | chr6 | 10982615 | |||||
| chr6:10982706
|
C | T | 1 | a0002c0004t0016 | 2 | HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1075G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1075 | chr6 | 10982706 | |||||
| chr6:10982740
|
T | C | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(11): Show | 241 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*1041A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 1041 | chr6 | 10982740 | |||||
| chr6:10982833
|
C | G | 1 | a0001c0001t0015 | 4 | NA18948.hp1 NA18972.hp1 NA19010.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*948G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 948 | chr6 | 10982833 | |||||
| chr6:10983109
|
C | G | 1 | a0001c0001t0025 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*672G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 672 | chr6 | 10983109 | |||||
| chr6:10983306
|
T | C | 1 | a0001c0001t0023 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*475A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 475 | chr6 | 10983306 | |||||
| chr6:10983335
|
C | T | 1 | a0001c0002t0009 | 9 | NA18947.hp1 NA18948.hp2 NA18960.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*446G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 446 | chr6 | 10983335 | |||||
| chr6:10983443
|
C | G | 1 | a0004c0006t0024 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 338 | chr6 | 10983443 | |||||
| chr6:10983444
|
T | A | 1 | a0004c0006t0024 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 337 | chr6 | 10983444 | |||||
| chr6:10983631
|
T | G | 1 | a0001c0001t0025 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 150 | chr6 | 10983631 | |||||
| chr6:10983738
|
C | G | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(19): Show | 272 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 43 | chr6 | 10983738 | |||||
| chr6:10983755
|
A | G | 1 | a0001c0001t0029 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 8/8 | 26 | chr6 | 10983755 | |||||
| chr6:11044246
|
T | C | 1 | a0001c0001t0029 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/8 | 16 | chr6 | 11044246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10984097
|
G | A | 255 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(252): Show | 280 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.766-191C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984097 | ||||||
| chr6:10984103
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.766-197G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984103 | ||||||
| chr6:10984163
|
G | A | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.766-257C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984163 | ||||||
| chr6:10984173
|
A | G | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-267T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984173 | ||||||
| chr6:10984279
|
A | T | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-373T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984279 | ||||||
| chr6:10984281
|
G | A | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.766-375C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984281 | ||||||
| chr6:10984305
|
A | T | 1 | a0001c0001t0004g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.766-399T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984305 | ||||||
| chr6:10984358
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0059 | 3 | NA18943.hp1 NA18946.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.766-452T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984358 | ||||||
| chr6:10984731
|
G | A | 103 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0006g0003others(100): Show | 119 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.766-825C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984731 | ||||||
| chr6:10984764
|
T | C | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.766-858A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984764 | ||||||
| chr6:10984930
|
C | A | 4 | a0001c0002t0002g0259a0001c0002t0002g0260a0001c0002t0002g0261others(1): Show | 4 | HG01981.hp2 HG01993.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-1024G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10984930 | ||||||
| chr6:10985097
|
T | C | 205 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(202): Show | 222 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.766-1191A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985097 | ||||||
| chr6:10985185
|
G | A | 8 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(5): Show | 8 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-1279C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985185 | ||||||
| chr6:10985254
|
G | A | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.766-1348C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985254 | ||||||
| chr6:10985319
|
C | T | 141 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(138): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.766-1413G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985319 | ||||||
| chr6:10985466
|
G | GTTTTCTT others(6): Show |
267 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(264): Show | 293 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.766-1561_766-1560i others(15): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985466 | ||||||
| chr6:10985488
|
C | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.766-1582G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985488 | ||||||
| chr6:10985663
|
C | T | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-1757G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985663 | ||||||
| chr6:10985687
|
G | T | 8 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(5): Show | 8 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-1781C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985687 | ||||||
| chr6:10985722
|
A | C | 34 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0311others(31): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.766-1816T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985722 | ||||||
| chr6:10985761
|
T | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.766-1855A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985761 | ||||||
| chr6:10985779
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0002t0002g0241 | 4 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-1873G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985779 | ||||||
| chr6:10985829
|
A | G | 19 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0002t0001g0018others(16): Show | 20 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.766-1923T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985829 | ||||||
| chr6:10985861
|
G | A | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.766-1955C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985861 | ||||||
| chr6:10985895
|
G | T | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-1989C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985895 | ||||||
| chr6:10985995
|
C | T | 86 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0010g0004others(83): Show | 98 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.766-2089G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985995 | ||||||
| chr6:10986033
|
T | G | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766-2127A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986033 | ||||||
| chr6:10986064
|
A | G | 19 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0002t0001g0018others(16): Show | 20 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.766-2158T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986064 | ||||||
| chr6:10986111
|
T | C | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.766-2205A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986111 | ||||||
| chr6:10986234
|
T | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.766-2328A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986234 | ||||||
| chr6:10986313
|
C | G | 1 | a0001c0002t0002g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.766-2407G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986313 | ||||||
| chr6:10986364
|
G | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766-2458C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986364 | ||||||
| chr6:10986474
|
TG | T | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2569delC | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986474 | ||||||
| chr6:10986482
|
G | C | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-2576C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986482 | ||||||
| chr6:10986518
|
G | A | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.766-2612C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986518 | ||||||
| chr6:10986579
|
A | G | 254 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(251): Show | 279 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.766-2673T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986579 | ||||||
| chr6:10986743
|
C | T | 1 | a0001c0002t0022g0253 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.766-2837G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986743 | ||||||
| chr6:10986751
|
C | A | 1 | a0001c0001t0005g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.766-2845G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986751 | ||||||
| chr6:10986896
|
G | A | 2 | a0001c0001t0020g0179a0001c0001t0025g0277 | 2 | HG01975.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.765+2807C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986896 | ||||||
| chr6:10986957
|
C | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0283others(38): Show | 49 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.765+2746G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10986957 | ||||||
| chr6:10987123
|
C | T | 141 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(138): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.765+2580G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987123 | ||||||
| chr6:10987185
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.765+2518G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987185 | ||||||
| chr6:10987285
|
C | T | 103 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0006g0003others(100): Show | 119 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.765+2418G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987285 | ||||||
| chr6:10987350
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.765+2353G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987350 | ||||||
| chr6:10987412
|
G | C | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.765+2291C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987412 | ||||||
| chr6:10987535
|
T | C | 2 | a0001c0001t0008g0205a0001c0001t0027g0206 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.765+2168A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987535 | ||||||
| chr6:10987549
|
T | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.765+2154A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987549 | ||||||
| chr6:10987676
|
A | G | 6 | a0001c0001t0008g0016a0001c0001t0008g0267a0001c0001t0008g0268others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+2027T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987676 | ||||||
| chr6:10987872
|
C | T | 1 | a0001c0001t0006g0021 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+1831G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987872 | ||||||
| chr6:10987887
|
C | CT | 38 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(35): Show | 46 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.765+1815dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987887 | ||||||
| chr6:10987988
|
A | C | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765+1715T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10987988 | ||||||
| chr6:10988020
|
G | A | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.765+1683C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988020 | ||||||
| chr6:10988041
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765+1662G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988041 | ||||||
| chr6:10988098
|
T | G | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765+1605A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988098 | ||||||
| chr6:10988108
|
G | A | 3 | a0001c0002t0002g0259a0001c0002t0002g0260a0001c0002t0002g0261 | 3 | HG01981.hp2 HG01993.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.765+1595C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988108 | ||||||
| chr6:10988129
|
G | A | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+1574C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988129 | ||||||
| chr6:10988221
|
A | T | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.765+1482T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988221 | ||||||
| chr6:10988424
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765+1279G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988424 | ||||||
| chr6:10988455
|
T | G | 2 | a0001c0003t0005g0182a0001c0003t0005g0183 | 2 | HG00280.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.765+1248A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988455 | ||||||
| chr6:10988753
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.765+950T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988753 | ||||||
| chr6:10988768
|
C | A | 3 | a0001c0001t0005g0168a0001c0001t0005g0173a0001c0001t0005g0174 | 3 | HG01109.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.765+935G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988768 | ||||||
| chr6:10988804
|
G | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765+899C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988804 | ||||||
| chr6:10988922
|
T | C | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765+781A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988922 | ||||||
| chr6:10988930
|
A | G | 1 | a0001c0001t0012g0303 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.765+773T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988930 | ||||||
| chr6:10988991
|
A | T | 2 | a0001c0002t0002g0234a0001c0002t0002g0238 | 2 | NA18940.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.765+712T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10988991 | ||||||
| chr6:10989089
|
T | C | 2 | a0001c0001t0004g0130a0001c0001t0004g0180 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.765+614A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989089 | ||||||
| chr6:10989254
|
T | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765+449A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989254 | ||||||
| chr6:10989412
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0116 | 2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.765+291C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989412 | ||||||
| chr6:10989607
|
C | T | 1 | a0001c0001t0014g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.765+96G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989607 | ||||||
| chr6:10989640
|
C | CA | 101 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.765+62dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989640 | ||||||
| chr6:10989653
|
A | G | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.765+50T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989653 | ||||||
| chr6:10989699
|
G | A | 4 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0275others(1): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.765+4C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989699 | ||||||
| chr6:10989920
|
A | T | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.631-83T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10989920 | ||||||
| chr6:10989944
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.631-107A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10989944 | ||||||
| chr6:10989980
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.631-143G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10989980 | ||||||
| chr6:10990002
|
A | C | 2 | a0001c0001t0006g0210a0001c0007t0018g0209 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.631-165T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10990002 | ||||||
| chr6:10990029
|
T | A | 8 | a0001c0001t0008g0016a0001c0001t0008g0267a0001c0001t0008g0268others(5): Show | 9 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.631-192A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10990029 | ||||||
| chr6:10990076
|
T | C | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-239A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10990076 | ||||||
| chr6:10990146
|
A | G | 1 | a0005c0005t0004g0202 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.630+172T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10990146 | ||||||
| chr6:10990151
|
GCA | G | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+165_630+166del others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10990151 | ||||||
| chr6:10990260
|
A | G | 103 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0006g0003others(100): Show | 119 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.630+58T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 6/7 | chr6 | 10990260 | ||||||
| chr6:10990488
|
G | C | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-46C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990488 | ||||||
| chr6:10990492
|
A | C | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-50T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990492 | ||||||
| chr6:10990509
|
G | A | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.506-67C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990509 | ||||||
| chr6:10990518
|
T | G | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.506-76A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990518 | ||||||
| chr6:10990576
|
A | G | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.506-134T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990576 | ||||||
| chr6:10990617
|
CACCAAAA | C | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-182_506-176del others(7): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990617 | ||||||
| chr6:10990667
|
G | GC | 25 | a0001c0001t0004g0135a0001c0001t0004g0137a0001c0001t0004g0145others(22): Show | 27 | HG00741.hp2 HG01070.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.506-226dupG | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990667 | ||||||
| chr6:10990667
|
G | GCCCCCCC others(5): Show |
1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-226_506-225ins others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990667 | ||||||
| chr6:10990671
|
C | G | 1 | a0001c0001t0004g0131 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.506-229G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990671 | ||||||
| chr6:10990673
|
C | CCG | 239 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(236): Show | 261 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.506-232_506-231ins others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990673 | ||||||
| chr6:10990727
|
G | A | 22 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(19): Show | 29 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.506-285C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990727 | ||||||
| chr6:10990800
|
G | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.506-358C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990800 | ||||||
| chr6:10990947
|
G | A | 1 | a0001c0002t0002g0278 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.506-505C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990947 | ||||||
| chr6:10990966
|
A | C | 2 | a0001c0002t0001g0270a0001c0002t0001g0271 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.506-524T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10990966 | ||||||
| chr6:10991434
|
C | CT | 255 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(252): Show | 280 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.506-993_506-992ins others(1): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991434 | ||||||
| chr6:10991501
|
G | A | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.506-1059C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991501 | ||||||
| chr6:10991607
|
G | A | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.506-1165C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991607 | ||||||
| chr6:10991702
|
C | T | 255 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(252): Show | 280 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.506-1260G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991702 | ||||||
| chr6:10991792
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-1350G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991792 | ||||||
| chr6:10991837
|
G | C | 5 | a0001c0002t0009g0002a0001c0002t0009g0231a0001c0002t0009g0239others(2): Show | 9 | NA18947.hp1 NA18948.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.506-1395C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991837 | ||||||
| chr6:10991882
|
T | C | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-1440A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991882 | ||||||
| chr6:10991979
|
T | C | 6 | a0001c0001t0008g0016a0001c0001t0008g0267a0001c0001t0008g0268others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-1537A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10991979 | ||||||
| chr6:10992053
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0043 | 2 | NA18955.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.506-1611T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992053 | ||||||
| chr6:10992068
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.506-1626G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992068 | ||||||
| chr6:10992249
|
A | G | 1 | a0001c0001t0003g0331 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.506-1807T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992249 | ||||||
| chr6:10992326
|
G | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-1884C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992326 | ||||||
| chr6:10992417
|
G | GCAT | 80 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0002t0001g0018others(77): Show | 89 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.506-1978_506-1976d others(5): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992417 | ||||||
| chr6:10992522
|
G | A | 19 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(16): Show | 23 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.506-2080C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992522 | ||||||
| chr6:10992545
|
C | T | 4 | a0001c0001t0008g0205a0001c0001t0008g0214a0001c0001t0008g0215others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.506-2103G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992545 | ||||||
| chr6:10992556
|
C | T | 101 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.506-2114G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992556 | ||||||
| chr6:10992566
|
G | A | 8 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(5): Show | 8 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.506-2124C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992566 | ||||||
| chr6:10992605
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.506-2163T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992605 | ||||||
| chr6:10992681
|
C | T | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.506-2239G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992681 | ||||||
| chr6:10992704
|
A | G | 309 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(306): Show | 341 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.506-2262T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992704 | ||||||
| chr6:10992713
|
C | CG | 345 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(342): Show | 378 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(375): Show |
intron_variant | MODIFIER | c.506-2272dupC | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992713 | ||||||
| chr6:10992747
|
CACTGCAC others(16): Show |
C | 1 | a0001c0001t0005g0199 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.505+2237_505+2259d others(25): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992747 | ||||||
| chr6:10992774
|
G | T | 1 | a0001c0001t0005g0199 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.505+2233C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992774 | ||||||
| chr6:10992778
|
C | T | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.505+2229G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992778 | ||||||
| chr6:10992786
|
C | CA | 5 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0056others(2): Show | 5 | HG00423.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.505+2220dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992786 | ||||||
| chr6:10992790
|
AAAAACAA others(3): Show |
A | 37 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(34): Show | 38 | HG00597.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.505+2207_505+2216d others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992790 | ||||||
| chr6:10992795
|
C | A | 104 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(101): Show | 112 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.505+2212G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992795 | ||||||
| chr6:10992795
|
CAAAACAA others(3): Show |
C | 6 | a0001c0001t0004g0131a0001c0001t0004g0132a0001c0001t0015g0162others(3): Show | 6 | HG00639.hp1 HG01175.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+2202_505+2211d others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992795 | ||||||
| chr6:10992799
|
A | ACAAAAC | 22 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(19): Show | 29 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.505+2207_505+2208i others(8): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992799 | ||||||
| chr6:10992800
|
C | CAAAACA | 78 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0002t0001g0018others(75): Show | 87 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.505+2206_505+2207i others(8): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992800 | ||||||
| chr6:10992800
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0011g0096a0001c0001t0011g0110 | 2 | NA18949.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.505+2193_505+2206d others(16): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992800 | ||||||
| chr6:10992810
|
C | A | 2 | a0001c0001t0006g0207a0001c0002t0001g0301 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.505+2197G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992810 | ||||||
| chr6:10992811
|
A | C | 1 | a0001c0002t0001g0301 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.505+2196T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992811 | ||||||
| chr6:10992812
|
A | C | 1 | a0001c0001t0006g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.505+2195T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992812 | ||||||
| chr6:10992846
|
T | A | 142 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(139): Show | 151 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.505+2161A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992846 | ||||||
| chr6:10992971
|
T | C | 1 | a0001c0001t0003g0326 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.505+2036A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992971 | ||||||
| chr6:10993010
|
CAGAG | C | 3 | a0001c0001t0001g0084a0001c0002t0002g0234a0001c0002t0002g0238 | 3 | HG02523.hp1 NA18940.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.505+1993_505+1996d others(6): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993010 | ||||||
| chr6:10993098
|
TAATGTA | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.505+1903_505+1908d others(8): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993098 | ||||||
| chr6:10993226
|
C | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.505+1781G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993226 | ||||||
| chr6:10993271
|
C | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.505+1736G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993271 | ||||||
| chr6:10993321
|
T | C | 1 | a0001c0001t0003g0326 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.505+1686A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993321 | ||||||
| chr6:10993436
|
TTAACA | T | 8 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(5): Show | 8 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.505+1566_505+1570d others(7): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993436 | ||||||
| chr6:10993613
|
G | A | 1 | a0001c0001t0005g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.505+1394C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993613 | ||||||
| chr6:10993614
|
G | C | 1 | a0001c0001t0012g0302 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.505+1393C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993614 | ||||||
| chr6:10993646
|
T | C | 21 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0002t0001g0018others(18): Show | 22 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.505+1361A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993646 | ||||||
| chr6:10993748
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.505+1259G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993748 | ||||||
| chr6:10993780
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.505+1227G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993780 | ||||||
| chr6:10993847
|
C | T | 1 | a0001c0002t0002g0225 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.505+1160G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993847 | ||||||
| chr6:10993857
|
A | AT | 36 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0004g0131others(33): Show | 36 | HG00280.hp2 HG00597.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.505+1149dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
AT | A | 55 | a0001c0001t0001g0032a0001c0001t0001g0076a0001c0001t0001g0090others(52): Show | 64 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.505+1149delA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATT | A | 27 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0042others(24): Show | 30 | HG00558.hp1 HG01071.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.505+1148_505+1149d others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATTT | A | 79 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0036others(76): Show | 80 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.505+1147_505+1149d others(5): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATTTTTTT others(2): Show |
A | 7 | a0001c0001t0012g0303a0001c0001t0012g0304a0001c0001t0012g0305others(4): Show | 7 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.505+1141_505+1149d others(11): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0004g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.505+1140_505+1149d others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATTTTTTT others(4): Show |
A | 5 | a0001c0001t0003g0327a0001c0001t0003g0333a0001c0001t0008g0281others(2): Show | 5 | HG03139.hp2 HG03471.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.505+1139_505+1149d others(13): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATTTTTTT others(5): Show |
A | 35 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0098others(32): Show | 43 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.505+1138_505+1149d others(14): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0006g0210 | 3 | HG02451.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.505+1137_505+1149d others(15): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10993857
|
ATTTTTTT others(7): Show |
A | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.505+1136_505+1149d others(16): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10993857 | ||||||
| chr6:10994009
|
T | C | 6 | a0001c0001t0008g0016a0001c0001t0008g0267a0001c0001t0008g0268others(3): Show | 7 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.505+998A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994009 | ||||||
| chr6:10994012
|
C | CA | 60 | a0001c0001t0001g0056a0001c0001t0001g0343a0001c0001t0004g0155others(57): Show | 68 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.505+994dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994012 | ||||||
| chr6:10994012
|
C | CAA | 10 | a0001c0001t0008g0016a0001c0001t0008g0267a0001c0001t0008g0269others(7): Show | 11 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.505+993_505+994dup others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994012 | ||||||
| chr6:10994012
|
CA | C | 33 | a0001c0001t0001g0038a0001c0001t0001g0057a0001c0001t0001g0117others(30): Show | 40 | HG00558.hp2 HG00735.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.505+994delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994012 | ||||||
| chr6:10994103
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | NA18944.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.505+904G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994103 | ||||||
| chr6:10994109
|
G | A | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.505+898C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994109 | ||||||
| chr6:10994296
|
G | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0272 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.505+711C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994296 | ||||||
| chr6:10994328
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.505+679G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994328 | ||||||
| chr6:10994341
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.505+666C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994341 | ||||||
| chr6:10994483
|
A | AAGAAAAG | 83 | a0001c0001t0001g0033a0001c0001t0001g0065a0001c0001t0001g0265others(80): Show | 92 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.505+523_505+524ins others(7): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994483 | ||||||
| chr6:10994483
|
A | AGAAAAG | 165 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(162): Show | 181 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.505+523_505+524ins others(6): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994483 | ||||||
| chr6:10994483
|
A | G | 6 | a0001c0001t0001g0118a0001c0001t0001g0343a0001c0001t0001g0344others(3): Show | 6 | HG01516.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.505+524T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994483 | ||||||
| chr6:10994574
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+433G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994574 | ||||||
| chr6:10994746
|
G | A | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.505+261C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994746 | ||||||
| chr6:10994782
|
G | C | 183 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(180): Show | 193 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.505+225C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994782 | ||||||
| chr6:10994806
|
C | T | 19 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(16): Show | 23 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.505+201G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994806 | ||||||
| chr6:10994849
|
A | G | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+158T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994849 | ||||||
| chr6:10994947
|
C | T | 19 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(16): Show | 23 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.505+60G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10994947 | ||||||
| chr6:10995362
|
T | TAGTG | 59 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(56): Show | 67 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.334-188_334-185dup others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995362 | ||||||
| chr6:10995395
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.334-217C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995395 | ||||||
| chr6:10995427
|
AC | A | 346 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(343): Show | 379 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(376): Show |
intron_variant | MODIFIER | c.334-250delG | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995427 | ||||||
| chr6:10995519
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0098 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.334-341C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995519 | ||||||
| chr6:10995637
|
T | C | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.334-459A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995637 | ||||||
| chr6:10995752
|
T | C | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-574A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995752 | ||||||
| chr6:10995890
|
T | G | 2 | a0001c0001t0004g0187a0001c0001t0004g0188 | 2 | HG02015.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.334-712A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995890 | ||||||
| chr6:10996119
|
T | TAACA | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.334-945_334-942dup others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996119 | ||||||
| chr6:10996223
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.334-1045G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996223 | ||||||
| chr6:10996407
|
G | A | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-1229C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996407 | ||||||
| chr6:10996435
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334-1257G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996435 | ||||||
| chr6:10996451
|
C | T | 19 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0002t0001g0018others(16): Show | 20 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.334-1273G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996451 | ||||||
| chr6:10996640
|
G | A | 1 | a0001c0002t0013g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.334-1462C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996640 | ||||||
| chr6:10996703
|
C | T | 1 | a0001c0002t0001g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.334-1525G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996703 | ||||||
| chr6:10996724
|
T | C | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-1546A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996724 | ||||||
| chr6:10996743
|
T | TGAGGCAG others(25): Show |
1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334-1597_334-1566d others(34): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996743 | ||||||
| chr6:10996779
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.334-1601C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996779 | ||||||
| chr6:10996786
|
G | C | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334-1608C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996786 | ||||||
| chr6:10996933
|
C | T | 185 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(182): Show | 195 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.334-1755G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10996933 | ||||||
| chr6:10997042
|
TTTAG | T | 19 | a0001c0001t0005g0006a0001c0001t0005g0133a0001c0001t0005g0143others(16): Show | 21 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.334-1868_334-1865d others(6): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997042 | ||||||
| chr6:10997070
|
TTAA | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.334-1895_334-1893d others(5): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997070 | ||||||
| chr6:10997159
|
C | T | 1 | a0001c0001t0003g0338 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.334-1981G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997159 | ||||||
| chr6:10997234
|
G | A | 1 | a0001c0001t0010g0273 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334-2056C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997234 | ||||||
| chr6:10997275
|
A | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(30): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.334-2097T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997275 | ||||||
| chr6:10997328
|
CA | C | 2 | a0001c0001t0005g0012a0001c0001t0005g0213 | 3 | HG02896.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.334-2151delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997328 | ||||||
| chr6:10997342
|
T | C | 1 | a0001c0001t0003g0323 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.334-2164A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997342 | ||||||
| chr6:10997479
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0064 | 3 | HG00323.hp1 HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.334-2301T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997479 | ||||||
| chr6:10997590
|
G | A | 255 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(252): Show | 280 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.334-2412C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997590 | ||||||
| chr6:10997753
|
C | T | 1 | a0001c0002t0002g0249 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.333+2334G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997753 | ||||||
| chr6:10997779
|
G | A | 4 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0291others(1): Show | 4 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+2308C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10997779 | ||||||
| chr6:10998029
|
C | T | 2 | a0001c0002t0001g0291a0001c0002t0001g0293 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.333+2058G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10998029 | ||||||
| chr6:10998039
|
G | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.333+2048C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10998039 | ||||||
| chr6:10998412
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.333+1675G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10998412 | ||||||
| chr6:10998735
|
C | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.333+1352G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10998735 | ||||||
| chr6:10998787
|
C | A | 1 | a0001c0002t0013g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.333+1300G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10998787 | ||||||
| chr6:10998974
|
G | A | 2 | a0001c0001t0005g0176a0001c0001t0005g0178 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.333+1113C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10998974 | ||||||
| chr6:10999020
|
T | C | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.333+1067A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999020 | ||||||
| chr6:10999366
|
C | T | 1 | a0001c0001t0008g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333+721G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999366 | ||||||
| chr6:10999380
|
C | CT | 243 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(240): Show | 268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.333+706dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999380 | ||||||
| chr6:10999409
|
T | C | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.333+678A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999409 | ||||||
| chr6:10999417
|
T | C | 259 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(256): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.333+670A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999417 | ||||||
| chr6:10999511
|
G | A | 3 | a0001c0003t0005g0182a0001c0003t0005g0183a0001c0003t0005g0184 | 3 | HG00280.hp2 HG01099.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.333+576C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999511 | ||||||
| chr6:10999602
|
C | G | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+485G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999602 | ||||||
| chr6:10999708
|
C | T | 8 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(5): Show | 8 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+379G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999708 | ||||||
| chr6:10999777
|
C | T | 1 | a0001c0001t0004g0181 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.333+310G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999777 | ||||||
| chr6:11000284
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0008g0016others(5): Show | 9 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-120A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11000284 | ||||||
| chr6:11000315
|
C | T | 1 | a0001c0007t0018g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.256-151G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11000315 | ||||||
| chr6:11000399
|
T | C | 3 | a0001c0001t0003g0315a0001c0001t0003g0316a0001c0001t0003g0342 | 3 | NA18974.hp1 NA18986.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.256-235A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11000399 | ||||||
| chr6:11000433
|
T | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.256-269A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11000433 | ||||||
| chr6:11000571
|
A | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.256-407T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11000571 | ||||||
| chr6:11000607
|
ATTAAAAA others(5): Show |
A | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-455_256-444del others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11000607 | ||||||
| chr6:11000722
|
C | G | 1 | a0001c0001t0006g0022 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.256-558G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11000722 | ||||||
| chr6:11001043
|
A | G | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.256-879T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001043 | ||||||
| chr6:11001175
|
G | T | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-1011C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001175 | ||||||
| chr6:11001176
|
A | T | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-1012T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001176 | ||||||
| chr6:11001464
|
A | T | 1 | a0001c0001t0007g0009 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.256-1300T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001464 | ||||||
| chr6:11001465
|
T | C | 6 | a0001c0001t0005g0143a0001c0001t0005g0166a0001c0001t0005g0169others(3): Show | 6 | HG01496.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-1301A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001465 | ||||||
| chr6:11001621
|
A | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.256-1457T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001621 | ||||||
| chr6:11001767
|
C | T | 1 | a0001c0001t0004g0145 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.256-1603G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001767 | ||||||
| chr6:11001902
|
C | T | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.256-1738G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11001902 | ||||||
| chr6:11002066
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.256-1902T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002066 | ||||||
| chr6:11002240
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.256-2076C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002240 | ||||||
| chr6:11002253
|
CA | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0064 | 3 | HG00323.hp1 HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.256-2090delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002253 | ||||||
| chr6:11002527
|
T | C | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.256-2363A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002527 | ||||||
| chr6:11002550
|
G | C | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.256-2386C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002550 | ||||||
| chr6:11002577
|
T | C | 249 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(246): Show | 274 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.256-2413A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002577 | ||||||
| chr6:11002608
|
G | T | 1 | a0001c0001t0008g0205 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.256-2444C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002608 | ||||||
| chr6:11002651
|
T | C | 1 | a0001c0002t0002g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.256-2487A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002651 | ||||||
| chr6:11002697
|
G | C | 17 | a0001c0002t0001g0018a0001c0002t0001g0270a0001c0002t0001g0271others(14): Show | 18 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.256-2533C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002697 | ||||||
| chr6:11002782
|
C | A | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+2590G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002782 | ||||||
| chr6:11002874
|
T | C | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.255+2498A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002874 | ||||||
| chr6:11002911
|
A | C | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.255+2461T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002911 | ||||||
| chr6:11003038
|
C | G | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.255+2334G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003038 | ||||||
| chr6:11003175
|
T | G | 4 | a0001c0002t0002g0259a0001c0002t0002g0260a0001c0002t0002g0261others(1): Show | 4 | HG01981.hp2 HG01993.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+2197A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003175 | ||||||
| chr6:11003316
|
C | G | 7 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(4): Show | 7 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.255+2056G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003316 | ||||||
| chr6:11003498
|
T | C | 60 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(57): Show | 68 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.255+1874A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003498 | ||||||
| chr6:11003533
|
A | G | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+1839T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003533 | ||||||
| chr6:11003642
|
G | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(305): Show | 340 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(337): Show |
intron_variant | MODIFIER | c.255+1730C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003642 | ||||||
| chr6:11003764
|
C | T | 1 | a0001c0001t0006g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.255+1608G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003764 | ||||||
| chr6:11003847
|
C | T | 1 | a0001c0001t0006g0021 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.255+1525G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003847 | ||||||
| chr6:11003879
|
C | T | 1 | a0001c0002t0009g0254 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.255+1493G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003879 | ||||||
| chr6:11003942
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.255+1430C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11003942 | ||||||
| chr6:11004017
|
A | C | 8 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0022others(5): Show | 8 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+1355T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004017 | ||||||
| chr6:11004036
|
T | C | 1 | a0001c0002t0001g0297 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.255+1336A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004036 | ||||||
| chr6:11004044
|
T | C | 1 | a0001c0001t0005g0133 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.255+1328A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004044 | ||||||
| chr6:11004055
|
C | G | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+1317G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004055 | ||||||
| chr6:11004082
|
C | CA | 23 | a0001c0001t0001g0103a0001c0001t0003g0338a0001c0001t0004g0135others(20): Show | 27 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.255+1289dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004082 | ||||||
| chr6:11004098
|
T | G | 1 | a0001c0001t0008g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.255+1274A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004098 | ||||||
| chr6:11004161
|
CATT | C | 21 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(18): Show | 28 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.255+1208_255+1210d others(5): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004161 | ||||||
| chr6:11004310
|
A | C | 1 | a0001c0002t0002g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.255+1062T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004310 | ||||||
| chr6:11004328
|
C | G | 189 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(186): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.255+1044G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004328 | ||||||
| chr6:11004416
|
CTTT | C | 13 | a0001c0001t0001g0041a0001c0001t0001g0097a0001c0001t0001g0105others(10): Show | 13 | HG00597.hp1 NA18939.hp2 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.255+953_255+955del others(3): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004416 | ||||||
| chr6:11004416
|
CTTTTTTT | C | 21 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(18): Show | 28 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.255+949_255+955del others(7): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004416 | ||||||
| chr6:11004495
|
T | C | 1 | a0001c0002t0001g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.255+877A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004495 | ||||||
| chr6:11004779
|
G | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.255+593C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004779 | ||||||
| chr6:11004828
|
A | C | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.255+544T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11004828 | ||||||
| chr6:11005011
|
T | C | 2 | a0001c0001t0011g0096a0001c0001t0011g0110 | 2 | NA18949.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.255+361A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11005011 | ||||||
| chr6:11005580
|
T | C | 1 | a0001c0001t0007g0052 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.68-21A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11005580 | ||||||
| chr6:11005609
|
T | C | 259 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(256): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.68-50A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11005609 | ||||||
| chr6:11005793
|
A | G | 189 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(186): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.68-234T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11005793 | ||||||
| chr6:11005830
|
A | C | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68-271T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11005830 | ||||||
| chr6:11005904
|
GA | G | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-346delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11005904 | ||||||
| chr6:11005967
|
A | C | 1 | a0001c0001t0008g0267 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-408T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11005967 | ||||||
| chr6:11006118
|
G | C | 1 | a0001c0001t0001g0344 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.68-559C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006118 | ||||||
| chr6:11006119
|
T | A | 1 | a0001c0001t0019g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-560A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006119 | ||||||
| chr6:11006216
|
C | A | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-657G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006216 | ||||||
| chr6:11006269
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.68-710C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006269 | ||||||
| chr6:11006399
|
T | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.68-840A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006399 | ||||||
| chr6:11006402
|
A | C | 1 | a0001c0002t0001g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68-843T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006402 | ||||||
| chr6:11006561
|
T | A | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1002A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006561 | ||||||
| chr6:11006570
|
T | C | 1 | a0001c0001t0014g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.68-1011A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006570 | ||||||
| chr6:11006628
|
C | T | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.68-1069G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11006628 | ||||||
| chr6:11007179
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.68-1620G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007179 | ||||||
| chr6:11007205
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.68-1646A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007205 | ||||||
| chr6:11007219
|
A | C | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1660T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007219 | ||||||
| chr6:11007251
|
T | A | 1 | a0001c0001t0012g0303 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.68-1692A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007251 | ||||||
| chr6:11007841
|
T | C | 1 | a0001c0001t0005g0012 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.68-2282A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007841 | ||||||
| chr6:11007849
|
A | G | 1 | a0001c0001t0005g0012 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.68-2290T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007849 | ||||||
| chr6:11007869
|
A | G | 34 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0311others(31): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.68-2310T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007869 | ||||||
| chr6:11007935
|
T | C | 1 | a0001c0002t0001g0285 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.68-2376A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11007935 | ||||||
| chr6:11008010
|
T | G | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-2451A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008010 | ||||||
| chr6:11008049
|
T | C | 1 | a0001c0001t0008g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.68-2490A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008049 | ||||||
| chr6:11008118
|
C | T | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-2559G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008118 | ||||||
| chr6:11008130
|
A | C | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-2571T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008130 | ||||||
| chr6:11008233
|
C | A | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2513G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008233 | ||||||
| chr6:11008235
|
G | A | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2511C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008235 | ||||||
| chr6:11008389
|
G | C | 189 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(186): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.67+2357C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008389 | ||||||
| chr6:11008416
|
G | A | 11 | a0001c0003t0005g0005a0001c0003t0005g0011a0001c0003t0005g0139others(8): Show | 14 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+2330C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008416 | ||||||
| chr6:11008495
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.67+2251G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008495 | ||||||
| chr6:11008673
|
G | C | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2073C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008673 | ||||||
| chr6:11008700
|
A | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67+2046T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11008700 | ||||||
| chr6:11009007
|
G | A | 17 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(14): Show | 21 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+1739C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11009007 | ||||||
| chr6:11009072
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.67+1674A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11009072 | ||||||
| chr6:11009592
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.67+1154C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11009592 | ||||||
| chr6:11009753
|
C | T | 1 | a0001c0002t0002g0236 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.67+993G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11009753 | ||||||
| chr6:11009949
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0001g0092 | 3 | HG01123.hp1 HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.67+797C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11009949 | ||||||
| chr6:11009976
|
C | CTAA | 3 | a0001c0001t0006g0025a0001c0001t0006g0026a0001c0001t0006g0027 | 3 | HG01884.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.67+767_67+769dupTT others(1): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11009976 | ||||||
| chr6:11010023
|
C | CT | 106 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0040others(103): Show | 122 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.67+722dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11010023 | ||||||
| chr6:11010280
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0008g0016others(5): Show | 9 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+466G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11010280 | ||||||
| chr6:11010324
|
C | T | 2 | a0001c0001t0001g0077a0001c0002t0002g0236 | 2 | HG03491.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.67+422G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11010324 | ||||||
| chr6:11010378
|
T | C | 1 | a0001c0001t0011g0112 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.67+368A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11010378 | ||||||
| chr6:11010567
|
T | G | 259 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(256): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.67+179A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11010567 | ||||||
| chr6:11010685
|
A | G | 1 | a0001c0001t0019g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+61T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11010685 | ||||||
| chr6:11010841
|
T | G | 258 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(255): Show | 283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.4-32A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11010841 | ||||||
| chr6:11010842
|
T | G | 1 | a0001c0001t0003g0316 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4-33A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11010842 | ||||||
| chr6:11010996
|
A | C | 21 | a0001c0002t0001g0018a0001c0002t0001g0270a0001c0002t0001g0271others(18): Show | 22 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.4-187T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11010996 | ||||||
| chr6:11011045
|
T | C | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-236A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011045 | ||||||
| chr6:11011128
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4-319C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011128 | ||||||
| chr6:11011139
|
C | T | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4-330G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011139 | ||||||
| chr6:11011160
|
C | T | 34 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0311others(31): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.4-351G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011160 | ||||||
| chr6:11011172
|
G | A | 228 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(225): Show | 246 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.4-363C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011172 | ||||||
| chr6:11011210
|
A | G | 3 | a0001c0001t0008g0267a0001c0001t0010g0266a0001c0001t0010g0273 | 3 | HG02451.hp2 HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4-401T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011210 | ||||||
| chr6:11011262
|
A | T | 1 | a0001c0001t0001g0344 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4-453T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011262 | ||||||
| chr6:11011283
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4-474C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011283 | ||||||
| chr6:11011298
|
A | G | 259 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(256): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.4-489T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011298 | ||||||
| chr6:11011365
|
C | CA | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.4-557dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011365 | ||||||
| chr6:11011365
|
C | CAA | 19 | a0001c0001t0003g0335a0001c0001t0006g0003a0001c0001t0006g0017others(16): Show | 23 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.4-558_4-557dupTT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011365 | ||||||
| chr6:11011365
|
C | CAAAA | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-560_4-557dupTTTT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011365 | ||||||
| chr6:11011416
|
T | C | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-607A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011416 | ||||||
| chr6:11011452
|
T | G | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-643A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011452 | ||||||
| chr6:11011506
|
G | T | 5 | a0001c0001t0005g0168a0001c0001t0005g0173a0001c0001t0005g0174others(2): Show | 5 | HG01109.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-697C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011506 | ||||||
| chr6:11011524
|
C | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4-715G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011524 | ||||||
| chr6:11011562
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0113a0001c0001t0001g0116 | 3 | HG00408.hp1 NA18951.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.4-753C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011562 | ||||||
| chr6:11011618
|
C | T | 1 | a0001c0002t0002g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4-809G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011618 | ||||||
| chr6:11011723
|
GATTA | G | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-918_4-915delTAAT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011723 | ||||||
| chr6:11011762
|
C | T | 3 | a0001c0001t0004g0142a0001c0001t0004g0159a0001c0001t0004g0161 | 3 | NA18941.hp2 NA18962.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.4-953G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011762 | ||||||
| chr6:11011829
|
G | A | 1 | a0001c0001t0006g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4-1020C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011829 | ||||||
| chr6:11011894
|
C | T | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-1085G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011894 | ||||||
| chr6:11011912
|
G | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-1103C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011912 | ||||||
| chr6:11011973
|
T | C | 22 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(19): Show | 29 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.4-1164A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011973 | ||||||
| chr6:11012200
|
G | GT | 17 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(14): Show | 21 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.4-1392_4-1391insA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11012200 | ||||||
| chr6:11012566
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4-1757C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11012566 | ||||||
| chr6:11012626
|
G | A | 259 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(256): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.4-1817C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11012626 | ||||||
| chr6:11012661
|
G | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-1852C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11012661 | ||||||
| chr6:11012669
|
G | A | 3 | a0001c0001t0008g0016a0001c0001t0008g0268a0001c0001t0008g0269 | 4 | HG02258.hp2 HG02630.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-1860C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11012669 | ||||||
| chr6:11013079
|
G | C | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-2270C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013079 | ||||||
| chr6:11013241
|
T | C | 1 | a0001c0002t0002g0280 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4-2432A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013241 | ||||||
| chr6:11013590
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4-2781C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013590 | ||||||
| chr6:11013667
|
G | A | 21 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(18): Show | 28 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.4-2858C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013667 | ||||||
| chr6:11013695
|
C | T | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-2886G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013695 | ||||||
| chr6:11013831
|
C | G | 1 | a0001c0001t0014g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4-3022G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013831 | ||||||
| chr6:11013868
|
C | CA | 159 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(156): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.4-3060dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013868 | ||||||
| chr6:11013868
|
C | CAA | 21 | a0001c0001t0001g0076a0001c0001t0001g0106a0001c0001t0001g0115others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.4-3061_4-3060dupTT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013868 | ||||||
| chr6:11013868
|
CA | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0265others(69): Show | 88 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.4-3060delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013868 | ||||||
| chr6:11013984
|
C | G | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-3175G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013984 | ||||||
| chr6:11013987
|
A | G | 256 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(253): Show | 281 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.4-3178T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013987 | ||||||
| chr6:11013994
|
C | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-3185G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11013994 | ||||||
| chr6:11014323
|
A | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0283others(63): Show | 81 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.4-3514T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11014323 | ||||||
| chr6:11014382
|
G | A | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4-3573C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11014382 | ||||||
| chr6:11014401
|
T | C | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-3592A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11014401 | ||||||
| chr6:11014550
|
G | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-3741C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11014550 | ||||||
| chr6:11014555
|
T | G | 10 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0008g0016others(7): Show | 11 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.4-3746A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11014555 | ||||||
| chr6:11014695
|
T | C | 22 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(19): Show | 29 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.4-3886A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11014695 | ||||||
| chr6:11014954
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4-4145G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11014954 | ||||||
| chr6:11015041
|
A | T | 22 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(19): Show | 29 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.4-4232T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11015041 | ||||||
| chr6:11015082
|
T | A | 2 | a0001c0001t0005g0006a0001c0001t0005g0190 | 4 | HG00741.hp2 HG01081.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-4273A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11015082 | ||||||
| chr6:11015348
|
T | A | 1 | a0001c0001t0008g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4-4539A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11015348 | ||||||
| chr6:11015504
|
T | A | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-4695A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11015504 | ||||||
| chr6:11015614
|
G | A | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4-4805C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11015614 | ||||||
| chr6:11015741
|
G | T | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4-4932C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11015741 | ||||||
| chr6:11016173
|
C | CCCTTCCT others(24): Show |
228 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(225): Show | 246 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.4-5365_4-5364insTA others(29): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016173 | ||||||
| chr6:11016232
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4-5423A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016232 | ||||||
| chr6:11016291
|
T | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.4-5482A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016291 | ||||||
| chr6:11016539
|
G | A | 11 | a0001c0003t0005g0005a0001c0003t0005g0011a0001c0003t0005g0139others(8): Show | 14 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.4-5730C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016539 | ||||||
| chr6:11016553
|
C | T | 1 | a0001c0002t0002g0015 | 2 | NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4-5744G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016553 | ||||||
| chr6:11016570
|
C | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-5761G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016570 | ||||||
| chr6:11016598
|
T | C | 4 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0275others(1): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-5789A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016598 | ||||||
| chr6:11016613
|
AGAG | A | 3 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264 | 3 | HG00642.hp2 HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.4-5807_4-5805delCT others(1): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016613 | ||||||
| chr6:11016792
|
CT | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.4-5984delA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016792 | ||||||
| chr6:11016835
|
A | G | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4-6026T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016835 | ||||||
| chr6:11016944
|
ACT | A | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(20): Show | 30 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.4-6137_4-6136delAG | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11016944 | ||||||
| chr6:11017078
|
T | G | 4 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0275others(1): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-6269A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017078 | ||||||
| chr6:11017248
|
C | T | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(20): Show | 30 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.4-6439G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017248 | ||||||
| chr6:11017251
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0001t0001g0106others(2): Show | 5 | HG01516.hp1 HG02698.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-6442A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017251 | ||||||
| chr6:11017392
|
G | A | 1 | a0001c0001t0008g0267 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4-6583C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017392 | ||||||
| chr6:11017586
|
C | T | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4-6777G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017586 | ||||||
| chr6:11017592
|
A | G | 256 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(253): Show | 281 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.4-6783T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017592 | ||||||
| chr6:11017603
|
T | C | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-6794A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017603 | ||||||
| chr6:11017672
|
T | C | 1 | a0001c0001t0004g0161 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4-6863A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017672 | ||||||
| chr6:11017748
|
C | G | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4-6939G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017748 | ||||||
| chr6:11017941
|
A | G | 1 | a0001c0001t0004g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4-7132T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11017941 | ||||||
| chr6:11018228
|
G | C | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-7419C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11018228 | ||||||
| chr6:11018476
|
C | T | 1 | a0001c0002t0002g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4-7667G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11018476 | ||||||
| chr6:11018579
|
T | G | 259 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(256): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.4-7770A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11018579 | ||||||
| chr6:11019337
|
A | T | 3 | a0001c0001t0003g0318a0001c0001t0003g0322a0001c0001t0003g0323 | 3 | HG02015.hp2 HG02129.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.4-8528T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019337 | ||||||
| chr6:11019410
|
G | A | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4-8601C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019410 | ||||||
| chr6:11019472
|
A | G | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-8663T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019472 | ||||||
| chr6:11019561
|
A | C | 1 | a0001c0001t0005g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4-8752T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019561 | ||||||
| chr6:11019660
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4-8851C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019660 | ||||||
| chr6:11019717
|
A | C | 1 | a0001c0001t0004g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4-8908T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019717 | ||||||
| chr6:11019805
|
G | A | 1 | a0001c0002t0002g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4-8996C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019805 | ||||||
| chr6:11019839
|
A | G | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-9030T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019839 | ||||||
| chr6:11019905
|
G | A | 1 | a0001c0001t0012g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4-9096C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019905 | ||||||
| chr6:11019917
|
T | G | 1 | a0001c0001t0003g0334 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4-9108A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019917 | ||||||
| chr6:11019950
|
G | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0107others(1): Show | 4 | HG00597.hp1 NA18993.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-9141C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11019950 | ||||||
| chr6:11020143
|
G | A | 5 | a0001c0001t0005g0168a0001c0001t0005g0173a0001c0001t0005g0174others(2): Show | 5 | HG01109.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-9334C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020143 | ||||||
| chr6:11020179
|
G | A | 2 | a0001c0001t0004g0156a0001c0001t0004g0157 | 2 | HG01070.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.4-9370C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020179 | ||||||
| chr6:11020183
|
TA | T | 256 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(253): Show | 281 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.4-9375delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020183 | ||||||
| chr6:11020202
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4-9393G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020202 | ||||||
| chr6:11020590
|
C | T | 1 | a0001c0002t0009g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4-9781G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020590 | ||||||
| chr6:11020622
|
A | G | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-9813T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020622 | ||||||
| chr6:11020839
|
A | G | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-10030T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020839 | ||||||
| chr6:11020915
|
G | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-10106C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020915 | ||||||
| chr6:11021071
|
C | T | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-10262G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021071 | ||||||
| chr6:11021222
|
G | A | 2 | a0001c0001t0008g0214a0001c0001t0008g0215 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4-10413C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021222 | ||||||
| chr6:11021233
|
T | C | 1 | a0001c0001t0010g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4-10424A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021233 | ||||||
| chr6:11021289
|
C | G | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(20): Show | 30 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.4-10480G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021289 | ||||||
| chr6:11021332
|
A | G | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-10523T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021332 | ||||||
| chr6:11021366
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4-10557C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021366 | ||||||
| chr6:11021492
|
T | C | 1 | a0001c0001t0014g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4-10683A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021492 | ||||||
| chr6:11021804
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4-10995G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021804 | ||||||
| chr6:11021877
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4-11068G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021877 | ||||||
| chr6:11021892
|
C | T | 5 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0003g0314others(2): Show | 5 | HG02027.hp1 HG02074.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-11083G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021892 | ||||||
| chr6:11021893
|
G | A | 1 | a0001c0001t0012g0305 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4-11084C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021893 | ||||||
| chr6:11021921
|
T | C | 87 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(84): Show | 96 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.4-11112A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021921 | ||||||
| chr6:11021955
|
C | T | 34 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0343others(31): Show | 41 | HG00735.hp2 HG01243.hp2 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.4-11146G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11021955 | ||||||
| chr6:11022297
|
C | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-11488G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022297 | ||||||
| chr6:11022298
|
G | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4-11489C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022298 | ||||||
| chr6:11022558
|
G | A | 2 | a0001c0001t0005g0173a0001c0001t0005g0174 | 2 | HG01109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4-11749C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022558 | ||||||
| chr6:11022813
|
C | A | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-12004G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022813 | ||||||
| chr6:11022817
|
AAT | A | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-12010_4-12009del others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022817 | ||||||
| chr6:11022838
|
A | ACTATAAT others(321): Show |
1 | a0001c0002t0002g0221 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.4-12030_4-12029ins others(328): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022838 | ||||||
| chr6:11022838
|
A | ACTATAAT others(322): Show |
1 | a0001c0002t0002g0220 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4-12030_4-12029ins others(329): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022838 | ||||||
| chr6:11022838
|
A | ACTATAAT others(335): Show |
1 | a0001c0002t0002g0230 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4-12030_4-12029ins others(342): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022838 | ||||||
| chr6:11022838
|
A | ACTATAAT others(347): Show |
1 | a0001c0002t0002g0219 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4-12030_4-12029ins others(354): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022838 | ||||||
| chr6:11022958
|
G | A | 1 | a0001c0001t0003g0328 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4-12149C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022958 | ||||||
| chr6:11022972
|
T | G | 4 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0275others(1): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-12163A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11022972 | ||||||
| chr6:11023114
|
A | G | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-12305T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023114 | ||||||
| chr6:11023118
|
A | T | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-12309T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023118 | ||||||
| chr6:11023372
|
T | C | 1 | a0001c0002t0002g0235 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4-12563A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023372 | ||||||
| chr6:11023455
|
T | A | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-12646A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023455 | ||||||
| chr6:11023712
|
T | A | 3 | a0001c0001t0005g0198a0001c0001t0014g0194a0001c0001t0014g0195 | 3 | HG02683.hp2 NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4-12903A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023712 | ||||||
| chr6:11023732
|
G | A | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4-12923C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023732 | ||||||
| chr6:11023905
|
T | C | 2 | a0001c0001t0006g0023a0001c0001t0006g0024 | 2 | HG00735.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.4-13096A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023905 | ||||||
| chr6:11023989
|
T | A | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-13180A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11023989 | ||||||
| chr6:11024155
|
A | G | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-13346T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11024155 | ||||||
| chr6:11024270
|
C | T | 1 | a0001c0002t0004g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.4-13461G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11024270 | ||||||
| chr6:11024399
|
T | C | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-13590A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11024399 | ||||||
| chr6:11024557
|
G | T | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-13748C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11024557 | ||||||
| chr6:11024582
|
G | A | 3 | a0001c0001t0007g0009a0001c0001t0007g0061a0001c0001t0007g0067 | 4 | HG01257.hp1 HG01258.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-13773C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11024582 | ||||||
| chr6:11025088
|
A | ACGG | 3 | a0001c0001t0003g0318a0001c0001t0003g0322a0001c0001t0003g0323 | 3 | HG02015.hp2 HG02129.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.4-14282_4-14280dup others(3): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025088 | ||||||
| chr6:11025187
|
T | C | 60 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(57): Show | 68 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.4-14378A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025187 | ||||||
| chr6:11025189
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4-14380C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025189 | ||||||
| chr6:11025375
|
T | G | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-14566A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025375 | ||||||
| chr6:11025711
|
C | G | 1 | a0001c0002t0002g0259 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4-14902G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025711 | ||||||
| chr6:11025715
|
TCTA | T | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-14909_4-14907del others(3): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025715 | ||||||
| chr6:11025719
|
T | A | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-14910A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025719 | ||||||
| chr6:11025750
|
C | T | 141 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(138): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.4-14941G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025750 | ||||||
| chr6:11025757
|
T | C | 1 | a0001c0001t0003g0328 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4-14948A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025757 | ||||||
| chr6:11025928
|
T | C | 141 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(138): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.4-15119A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025928 | ||||||
| chr6:11025954
|
T | C | 1 | a0001c0001t0004g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4-15145A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11025954 | ||||||
| chr6:11026087
|
C | T | 1 | a0001c0001t0004g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4-15278G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026087 | ||||||
| chr6:11026088
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4-15279C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026088 | ||||||
| chr6:11026112
|
C | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4-15303G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026112 | ||||||
| chr6:11026118
|
T | C | 1 | a0001c0001t0005g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4-15309A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026118 | ||||||
| chr6:11026199
|
A | G | 3 | a0001c0002t0002g0014a0001c0002t0002g0244a0001c0002t0002g0246 | 4 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-15390T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026199 | ||||||
| chr6:11026238
|
G | A | 141 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(138): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.4-15429C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026238 | ||||||
| chr6:11026505
|
C | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4-15696G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026505 | ||||||
| chr6:11026541
|
T | C | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4-15732A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026541 | ||||||
| chr6:11026543
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.4-15734C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026543 | ||||||
| chr6:11026569
|
C | T | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-15760G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026569 | ||||||
| chr6:11026684
|
C | A | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-15875G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026684 | ||||||
| chr6:11026766
|
G | A | 104 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(101): Show | 105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.4-15957C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026766 | ||||||
| chr6:11026852
|
A | G | 1 | a0001c0001t0003g0315 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4-16043T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026852 | ||||||
| chr6:11026862
|
T | TTCTA | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-16054_4-16053ins others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026862 | ||||||
| chr6:11026960
|
A | G | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-16151T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11026960 | ||||||
| chr6:11027016
|
A | C | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4-16207T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027016 | ||||||
| chr6:11027313
|
G | A | 4 | a0001c0001t0010g0004a0001c0001t0010g0013a0001c0001t0010g0029others(1): Show | 7 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-16504C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027313 | ||||||
| chr6:11027343
|
G | A | 1 | a0001c0002t0002g0252 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4-16534C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027343 | ||||||
| chr6:11027368
|
G | A | 2 | a0001c0001t0008g0205a0001c0001t0027g0206 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4-16559C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027368 | ||||||
| chr6:11027509
|
A | G | 79 | a0001c0002t0001g0018a0001c0002t0001g0237a0001c0002t0001g0284others(76): Show | 88 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.4-16700T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027509 | ||||||
| chr6:11027671
|
A | T | 1 | a0001c0001t0006g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3+16557T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027671 | ||||||
| chr6:11027679
|
C | T | 3 | a0001c0002t0002g0218a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG01081.hp2 HG02735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3+16549G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027679 | ||||||
| chr6:11027709
|
CTAAGA | C | 258 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(255): Show | 283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.3+16514_3+16518del others(5): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027709 | ||||||
| chr6:11027716
|
A | C | 258 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(255): Show | 283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.3+16512T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027716 | ||||||
| chr6:11027719
|
G | A | 1 | a0001c0003t0005g0170 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3+16509C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11027719 | ||||||
| chr6:11028060
|
C | T | 101 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3+16168G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028060 | ||||||
| chr6:11028185
|
T | A | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+16043A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028185 | ||||||
| chr6:11028328
|
G | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3+15900C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028328 | ||||||
| chr6:11028421
|
G | A | 79 | a0001c0002t0001g0018a0001c0002t0001g0237a0001c0002t0001g0284others(76): Show | 88 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.3+15807C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028421 | ||||||
| chr6:11028510
|
T | C | 1 | a0001c0001t0004g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3+15718A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028510 | ||||||
| chr6:11028519
|
G | C | 1 | a0001c0001t0014g0194 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3+15709C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028519 | ||||||
| chr6:11028525
|
A | G | 2 | a0001c0001t0020g0179a0001c0001t0025g0277 | 2 | HG01975.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3+15703T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028525 | ||||||
| chr6:11028593
|
A | AT | 14 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0008g0016others(11): Show | 15 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3+15634dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028593 | ||||||
| chr6:11028625
|
G | T | 1 | a0001c0001t0003g0321 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3+15603C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028625 | ||||||
| chr6:11028658
|
C | CT | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3+15569_3+15570ins others(1): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028658 | ||||||
| chr6:11028721
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0117others(1): Show | 4 | HG01516.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+15507T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028721 | ||||||
| chr6:11028817
|
C | T | 1 | a0001c0001t0004g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3+15411G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028817 | ||||||
| chr6:11028886
|
T | G | 1 | a0001c0002t0002g0236 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3+15342A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028886 | ||||||
| chr6:11028934
|
C | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3+15294G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11028934 | ||||||
| chr6:11029018
|
T | C | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+15210A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029018 | ||||||
| chr6:11029019
|
A | G | 1 | a0001c0001t0006g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3+15209T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029019 | ||||||
| chr6:11029057
|
CA | C | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3+15170delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029057 | ||||||
| chr6:11029057
|
CAA | C | 27 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0001t0001g0101others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+15169_3+15170del others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029057 | ||||||
| chr6:11029057
|
CAAA | C | 39 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0097others(36): Show | 47 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3+15168_3+15170del others(3): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029057 | ||||||
| chr6:11029057
|
CAAAAAAA others(3): Show |
C | 88 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(85): Show | 97 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.3+15161_3+15170del others(10): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029057 | ||||||
| chr6:11029057
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+15160_3+15170del others(11): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029057 | ||||||
| chr6:11029058
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3+15170T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029058 | ||||||
| chr6:11029134
|
G | A | 2 | a0001c0001t0008g0214a0001c0001t0008g0215 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3+15094C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029134 | ||||||
| chr6:11029159
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+15069G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029159 | ||||||
| chr6:11029160
|
G | A | 2 | a0001c0001t0003g0330a0001c0001t0014g0063 | 2 | HG02300.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3+15068C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029160 | ||||||
| chr6:11029171
|
G | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+15057C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029171 | ||||||
| chr6:11029185
|
G | A | 1 | a0001c0001t0008g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3+15043C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029185 | ||||||
| chr6:11029203
|
G | A | 3 | a0001c0001t0006g0207a0001c0001t0006g0210a0001c0007t0018g0209 | 3 | HG02257.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3+15025C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029203 | ||||||
| chr6:11029207
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+15021G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029207 | ||||||
| chr6:11029214
|
G | A | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+15014C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029214 | ||||||
| chr6:11029223
|
C | CA | 33 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0311others(30): Show | 40 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.3+15004dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAA | 13 | a0001c0001t0003g0314a0001c0001t0003g0315a0001c0001t0003g0316others(10): Show | 14 | HG02145.hp2 HG02258.hp2 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.3+15003_3+15004dup others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAA | 7 | a0001c0002t0001g0284a0001c0002t0001g0287a0001c0002t0001g0293others(4): Show | 7 | HG00323.hp2 HG01496.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+15001_3+15004dup others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAA | 54 | a0001c0002t0001g0285a0001c0002t0001g0288a0001c0002t0001g0289others(51): Show | 62 | HG00621.hp2 HG00642.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.3+15000_3+15004dup others(5): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAA | 22 | a0001c0001t0008g0205a0001c0001t0008g0215a0001c0001t0025g0277others(19): Show | 23 | HG00423.hp2 HG00741.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.3+14999_3+15004dup others(6): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0012g0303a0001c0001t0012g0304 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3+14994_3+15004dup others(11): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0012g0302a0001c0001t0012g0305a0001c0001t0012g0306 | 3 | HG01361.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3+14993_3+15004dup others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0012g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3+14992_3+15004dup others(13): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAAA others(8): Show |
1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3+14990_3+15004dup others(15): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAAA others(10): Show |
1 | a0002c0004t0016g0203 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3+14988_3+15004dup others(17): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAAA others(11): Show |
1 | a0002c0004t0016g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3+14987_3+15004dup others(18): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3+14985_3+15004dup others(20): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
CA | C | 8 | a0001c0001t0004g0137a0001c0001t0004g0144a0001c0001t0004g0181others(5): Show | 8 | HG01099.hp1 HG01099.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+15004delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
CAAAAAA | C | 6 | a0001c0001t0001g0283a0001c0001t0010g0004a0001c0001t0010g0013others(3): Show | 9 | HG01891.hp1 HG02976.hp2 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+14999_3+15004del others(6): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
CAAAAAAA | C | 17 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(14): Show | 21 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3+14998_3+15004del others(7): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
CAAAAAAA others(2): Show |
C | 99 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(96): Show | 100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.3+14996_3+15004del others(9): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029223
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3+14995_3+15004del others(10): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029223 | ||||||
| chr6:11029254
|
G | C | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3+14974C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029254 | ||||||
| chr6:11029258
|
G | GCATT | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3+14966_3+14969dup others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029258 | ||||||
| chr6:11029277
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0111 | 3 | HG00597.hp1 NA19001.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.3+14951C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029277 | ||||||
| chr6:11029333
|
C | G | 3 | a0001c0001t0008g0267a0001c0001t0010g0266a0001c0001t0010g0273 | 3 | HG02451.hp2 HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3+14895G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029333 | ||||||
| chr6:11029444
|
T | G | 1 | a0001c0001t0006g0024 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3+14784A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029444 | ||||||
| chr6:11029652
|
C | CT | 5 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(2): Show | 5 | HG02717.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+14575dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029652 | ||||||
| chr6:11029655
|
T | C | 1 | a0003c0008t0001g0086 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3+14573A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029655 | ||||||
| chr6:11029812
|
T | C | 4 | a0001c0001t0003g0019a0001c0001t0003g0317a0001c0001t0003g0319others(1): Show | 5 | HG02056.hp2 NA18997.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+14416A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029812 | ||||||
| chr6:11029824
|
G | A | 1 | a0001c0002t0002g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3+14404C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029824 | ||||||
| chr6:11030033
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.3+14195C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030033 | ||||||
| chr6:11030253
|
C | T | 1 | a0001c0002t0013g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3+13975G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030253 | ||||||
| chr6:11030277
|
G | C | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3+13951C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030277 | ||||||
| chr6:11030368
|
C | A | 21 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(18): Show | 28 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.3+13860G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030368 | ||||||
| chr6:11030462
|
G | A | 1 | a0001c0001t0008g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3+13766C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030462 | ||||||
| chr6:11030547
|
A | C | 11 | a0001c0003t0005g0005a0001c0003t0005g0011a0001c0003t0005g0139others(8): Show | 14 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+13681T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030547 | ||||||
| chr6:11030561
|
G | A | 101 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3+13667C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030561 | ||||||
| chr6:11030563
|
C | T | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3+13665G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030563 | ||||||
| chr6:11030597
|
T | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3+13631A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030597 | ||||||
| chr6:11030597
|
T | G | 2 | a0001c0002t0001g0270a0001c0002t0001g0271 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3+13631A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030597 | ||||||
| chr6:11030620
|
T | C | 4 | a0001c0002t0001g0297a0001c0002t0001g0301a0001c0002t0013g0298others(1): Show | 4 | HG02055.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+13608A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030620 | ||||||
| chr6:11030648
|
C | T | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3+13580G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030648 | ||||||
| chr6:11030677
|
A | G | 1 | a0001c0001t0005g0012 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3+13551T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030677 | ||||||
| chr6:11030682
|
T | C | 143 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(140): Show | 152 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3+13546A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030682 | ||||||
| chr6:11030692
|
CT | C | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+13535delA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030692 | ||||||
| chr6:11030891
|
TCCTGTGT others(2): Show |
T | 4 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0287others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+13328_3+13336del others(9): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030891 | ||||||
| chr6:11030941
|
T | G | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3+13287A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11030941 | ||||||
| chr6:11031011
|
G | A | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3+13217C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11031011 | ||||||
| chr6:11031039
|
T | C | 1 | a0001c0001t0005g0178 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3+13189A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11031039 | ||||||
| chr6:11031120
|
G | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG02056.hp1 NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.3+13108C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11031120 | ||||||
| chr6:11031720
|
T | C | 2 | a0001c0001t0008g0214a0001c0001t0008g0215 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3+12508A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11031720 | ||||||
| chr6:11031797
|
T | A | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3+12431A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11031797 | ||||||
| chr6:11031938
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3+12290G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11031938 | ||||||
| chr6:11032151
|
T | C | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3+12077A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032151 | ||||||
| chr6:11032342
|
CA | C | 43 | a0001c0001t0003g0314a0001c0001t0004g0010a0001c0001t0004g0130others(40): Show | 44 | HG00280.hp1 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.3+11885delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032342 | ||||||
| chr6:11032342
|
CAA | C | 144 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0080others(141): Show | 165 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.3+11884_3+11885del others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032342 | ||||||
| chr6:11032342
|
CAAA | C | 135 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(132): Show | 143 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.3+11883_3+11885del others(3): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032342 | ||||||
| chr6:11032342
|
CAAAA | C | 9 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0007g0081others(6): Show | 12 | HG01891.hp1 HG01978.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+11882_3+11885del others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032342 | ||||||
| chr6:11032342
|
CAAAAAAA | C | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+11879_3+11885del others(7): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032342 | ||||||
| chr6:11032359
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3+11869T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032359 | ||||||
| chr6:11032578
|
A | G | 5 | a0001c0001t0008g0016a0001c0001t0008g0268a0001c0001t0008g0269others(2): Show | 6 | HG02145.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+11650T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032578 | ||||||
| chr6:11032699
|
C | G | 2 | a0001c0001t0001g0073a0003c0008t0001g0086 | 2 | HG02027.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.3+11529G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032699 | ||||||
| chr6:11032784
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+11444G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032784 | ||||||
| chr6:11032795
|
C | G | 79 | a0001c0002t0001g0018a0001c0002t0001g0237a0001c0002t0001g0284others(76): Show | 88 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.3+11433G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032795 | ||||||
| chr6:11032798
|
G | A | 21 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0020others(18): Show | 28 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.3+11430C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032798 | ||||||
| chr6:11032840
|
C | T | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3+11388G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032840 | ||||||
| chr6:11032849
|
G | A | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+11379C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032849 | ||||||
| chr6:11032885
|
G | C | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(20): Show | 30 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3+11343C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032885 | ||||||
| chr6:11032931
|
G | A | 100 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3+11297C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032931 | ||||||
| chr6:11033235
|
T | C | 256 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(253): Show | 281 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.3+10993A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11033235 | ||||||
| chr6:11033254
|
G | A | 1 | a0001c0001t0014g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3+10974C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11033254 | ||||||
| chr6:11033259
|
A | G | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+10969T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11033259 | ||||||
| chr6:11033392
|
G | T | 90 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(87): Show | 99 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.3+10836C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11033392 | ||||||
| chr6:11033756
|
T | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3+10472A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11033756 | ||||||
| chr6:11033787
|
G | A | 2 | a0001c0001t0003g0331a0001c0001t0003g0332 | 2 | NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3+10441C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11033787 | ||||||
| chr6:11034088
|
A | G | 1 | a0001c0001t0020g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3+10140T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034088 | ||||||
| chr6:11034147
|
C | T | 1 | a0001c0001t0005g0199 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3+10081G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034147 | ||||||
| chr6:11034401
|
TGCCGGGC others(128): Show |
T | 139 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(136): Show | 148 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.3+9692_3+9826del | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034401 | ||||||
| chr6:11034402
|
G | T | 2 | a0001c0001t0004g0130a0001c0001t0004g0180 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3+9826C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034402 | ||||||
| chr6:11034539
|
C | T | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+9689G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034539 | ||||||
| chr6:11034602
|
A | G | 164 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(161): Show | 180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.3+9626T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034602 | ||||||
| chr6:11034769
|
G | A | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3+9459C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034769 | ||||||
| chr6:11034784
|
C | T | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+9444G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034784 | ||||||
| chr6:11034875
|
C | A | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3+9353G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034875 | ||||||
| chr6:11034928
|
A | G | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+9300T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034928 | ||||||
| chr6:11034951
|
C | T | 1 | a0001c0001t0010g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3+9277G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11034951 | ||||||
| chr6:11035084
|
G | C | 1 | a0001c0001t0001g0344 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+9144C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035084 | ||||||
| chr6:11035192
|
C | T | 164 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(161): Show | 180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.3+9036G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035192 | ||||||
| chr6:11035193
|
A | C | 164 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(161): Show | 180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.3+9035T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035193 | ||||||
| chr6:11035211
|
C | T | 3 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0264 | 3 | HG00642.hp2 HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.3+9017G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035211 | ||||||
| chr6:11035254
|
G | A | 1 | a0001c0001t0023g0336 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3+8974C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035254 | ||||||
| chr6:11035379
|
C | T | 2 | a0001c0001t0014g0194a0001c0001t0014g0195 | 2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3+8849G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035379 | ||||||
| chr6:11035383
|
C | T | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(20): Show | 30 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3+8845G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035383 | ||||||
| chr6:11035437
|
T | C | 24 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(21): Show | 31 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3+8791A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035437 | ||||||
| chr6:11035495
|
T | C | 1 | a0001c0001t0003g0340 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3+8733A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035495 | ||||||
| chr6:11035502
|
C | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0308 | 2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.3+8726G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035502 | ||||||
| chr6:11035620
|
G | A | 139 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(136): Show | 148 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.3+8608C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035620 | ||||||
| chr6:11035739
|
T | C | 105 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0272others(102): Show | 129 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.3+8489A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035739 | ||||||
| chr6:11035883
|
T | C | 1 | a0001c0002t0002g0225 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3+8345A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035883 | ||||||
| chr6:11036083
|
T | TA | 60 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(57): Show | 68 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.3+8144dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036083 | ||||||
| chr6:11036137
|
G | A | 8 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0022others(5): Show | 8 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+8091C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036137 | ||||||
| chr6:11036214
|
A | G | 102 | a0001c0001t0001g0072a0001c0001t0001g0265a0001c0001t0001g0272others(99): Show | 112 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.3+8014T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036214 | ||||||
| chr6:11036351
|
T | A | 309 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(306): Show | 341 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(338): Show |
intron_variant | MODIFIER | c.3+7877A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036351 | ||||||
| chr6:11036489
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3+7739C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036489 | ||||||
| chr6:11036564
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0001g0092 | 3 | HG01123.hp1 HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3+7664G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036564 | ||||||
| chr6:11036569
|
T | C | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+7659A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036569 | ||||||
| chr6:11036592
|
C | T | 60 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(57): Show | 68 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.3+7636G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036592 | ||||||
| chr6:11036593
|
G | C | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+7635C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036593 | ||||||
| chr6:11036725
|
G | GA | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+7502dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036725 | ||||||
| chr6:11036911
|
AT | A | 114 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0005g0213others(111): Show | 131 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.3+7316delA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036911 | ||||||
| chr6:11036993
|
G | A | 1 | a0001c0001t0010g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3+7235C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11036993 | ||||||
| chr6:11037044
|
G | A | 1 | a0001c0001t0004g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3+7184C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037044 | ||||||
| chr6:11037064
|
T | C | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+7164A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037064 | ||||||
| chr6:11037064
|
TAGAG | T | 101 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0005g0213others(98): Show | 111 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.3+7160_3+7163delCT others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037064 | ||||||
| chr6:11037078
|
G | C | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+7150C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037078 | ||||||
| chr6:11037135
|
G | A | 1 | a0001c0001t0004g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+7093C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037135 | ||||||
| chr6:11037136
|
G | C | 1 | a0001c0001t0004g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+7092C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037136 | ||||||
| chr6:11037154
|
C | A | 1 | a0001c0001t0004g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+7074G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037154 | ||||||
| chr6:11037171
|
A | AAGAGAGG others(13): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0028 | 3 | HG02145.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3+7037_3+7056dupCT others(18): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037171 | ||||||
| chr6:11037171
|
A | AAGAGAGG others(33): Show |
33 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0311others(30): Show | 40 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.3+7017_3+7056dupCT others(38): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037171 | ||||||
| chr6:11037171
|
A | AAGAGAGG others(53): Show |
1 | a0001c0001t0023g0336 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3+7056_3+7057insCT others(58): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037171 | ||||||
| chr6:11037172
|
A | G | 1 | a0001c0001t0004g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+7056T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037172 | ||||||
| chr6:11037178
|
G | T | 1 | a0001c0001t0004g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+7050C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037178 | ||||||
| chr6:11037295
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3+6933A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037295 | ||||||
| chr6:11037306
|
G | A | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+6922C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037306 | ||||||
| chr6:11037329
|
A | G | 1 | a0001c0001t0003g0342 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3+6899T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037329 | ||||||
| chr6:11037335
|
A | T | 2 | a0001c0001t0014g0192a0001c0001t0014g0193 | 2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3+6893T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037335 | ||||||
| chr6:11037421
|
T | G | 1 | a0001c0002t0009g0240 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3+6807A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037421 | ||||||
| chr6:11037539
|
TA | T | 246 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(243): Show | 265 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.3+6688delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037539 | ||||||
| chr6:11037809
|
T | C | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3+6419A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037809 | ||||||
| chr6:11037875
|
G | A | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3+6353C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037875 | ||||||
| chr6:11038059
|
T | A | 128 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0283others(125): Show | 145 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(142): Show |
intron_variant | MODIFIER | c.3+6169A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038059 | ||||||
| chr6:11038111
|
AT | A | 2 | a0001c0001t0010g0004a0001c0001t0010g0029 | 4 | HG01891.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+6116delA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038111 | ||||||
| chr6:11038278
|
T | G | 128 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0283others(125): Show | 145 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(142): Show |
intron_variant | MODIFIER | c.3+5950A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038278 | ||||||
| chr6:11038344
|
C | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3+5884G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038344 | ||||||
| chr6:11038373
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+5855G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038373 | ||||||
| chr6:11038395
|
C | T | 103 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(100): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.3+5833G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038395 | ||||||
| chr6:11038434
|
T | C | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+5794A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038434 | ||||||
| chr6:11038437
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0116 | 2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3+5791G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038437 | ||||||
| chr6:11038698
|
T | C | 1 | a0001c0001t0003g0334 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3+5530A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038698 | ||||||
| chr6:11038728
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0116 | 2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3+5500C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038728 | ||||||
| chr6:11038752
|
T | A | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+5476A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038752 | ||||||
| chr6:11038759
|
T | A | 1 | a0001c0001t0004g0181 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3+5469A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038759 | ||||||
| chr6:11038781
|
A | G | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+5447T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038781 | ||||||
| chr6:11038878
|
T | G | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3+5350A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038878 | ||||||
| chr6:11038923
|
C | T | 1 | a0001c0001t0006g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3+5305G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038923 | ||||||
| chr6:11038976
|
C | G | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+5252G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038976 | ||||||
| chr6:11038984
|
G | GT | 4 | a0001c0001t0006g0003a0001c0001t0006g0017a0001c0001t0006g0275others(1): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+5243dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038984 | ||||||
| chr6:11038984
|
G | T | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+5244C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038984 | ||||||
| chr6:11038992
|
G | A | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+5236C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11038992 | ||||||
| chr6:11039003
|
T | C | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+5225A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039003 | ||||||
| chr6:11039146
|
T | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3+5082A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039146 | ||||||
| chr6:11039168
|
T | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(33): Show | 44 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.3+5060A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039168 | ||||||
| chr6:11039544
|
C | T | 1 | a0001c0001t0007g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3+4684G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039544 | ||||||
| chr6:11039558
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3+4670T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039558 | ||||||
| chr6:11039566
|
T | C | 101 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3+4662A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039566 | ||||||
| chr6:11039621
|
AAT | A | 27 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0003others(24): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+4605_3+4606delAT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039621 | ||||||
| chr6:11039696
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3+4532T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039696 | ||||||
| chr6:11039769
|
G | A | 269 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(266): Show | 295 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.3+4459C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039769 | ||||||
| chr6:11039802
|
G | A | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+4426C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039802 | ||||||
| chr6:11039842
|
T | G | 1 | a0001c0001t0012g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3+4386A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039842 | ||||||
| chr6:11039938
|
C | T | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+4290G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039938 | ||||||
| chr6:11039950
|
A | C | 107 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0343others(104): Show | 121 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.3+4278T>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11039950 | ||||||
| chr6:11040156
|
A | G | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0020others(20): Show | 26 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3+4072T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040156 | ||||||
| chr6:11040181
|
C | G | 1 | a0001c0001t0029g0347 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+4047G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040181 | ||||||
| chr6:11040190
|
A | G | 129 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0283others(126): Show | 146 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.3+4038T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040190 | ||||||
| chr6:11040227
|
T | C | 5 | a0001c0003t0005g0011a0001c0003t0005g0140a0001c0003t0005g0182others(2): Show | 6 | HG00280.hp2 HG01099.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+4001A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040227 | ||||||
| chr6:11040405
|
A | G | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0020others(20): Show | 26 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3+3823T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040405 | ||||||
| chr6:11040430
|
AT | A | 86 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(83): Show | 95 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.3+3797delA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040430 | ||||||
| chr6:11040435
|
G | C | 86 | a0001c0001t0005g0213a0001c0001t0008g0205a0001c0001t0008g0214others(83): Show | 95 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.3+3793C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040435 | ||||||
| chr6:11040456
|
AC | A | 3 | a0001c0001t0004g0185a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02602.hp1 HG02735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3+3771delG | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040456 | ||||||
| chr6:11040474
|
T | C | 15 | a0001c0002t0001g0018a0001c0002t0001g0288a0001c0002t0001g0289others(12): Show | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+3754A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040474 | ||||||
| chr6:11040480
|
T | C | 1 | a0001c0002t0002g0274 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3+3748A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040480 | ||||||
| chr6:11040534
|
T | G | 59 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(56): Show | 67 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3+3694A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040534 | ||||||
| chr6:11040761
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3+3467A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11040761 | ||||||
| chr6:11041256
|
G | A | 15 | a0001c0002t0001g0018a0001c0002t0001g0288a0001c0002t0001g0289others(12): Show | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+2972C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041256 | ||||||
| chr6:11041277
|
A | G | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+2951T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041277 | ||||||
| chr6:11041431
|
G | A | 1 | a0001c0003t0005g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3+2797C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041431 | ||||||
| chr6:11041487
|
G | A | 102 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0343others(99): Show | 116 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.3+2741C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041487 | ||||||
| chr6:11041491
|
G | T | 15 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0022others(12): Show | 16 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+2737C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041491 | ||||||
| chr6:11041663
|
C | G | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+2565G>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041663 | ||||||
| chr6:11041672
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0125 | 2 | NA18945.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.3+2556C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041672 | ||||||
| chr6:11041691
|
C | T | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+2537G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041691 | ||||||
| chr6:11041702
|
T | C | 1 | a0004c0006t0024g0310 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3+2526A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041702 | ||||||
| chr6:11041751
|
TAAAC | T | 3 | a0001c0001t0005g0213a0001c0001t0008g0214a0001c0001t0008g0215 | 3 | HG02717.hp2 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3+2473_3+2476delGT others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041751 | ||||||
| chr6:11041796
|
A | T | 139 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(136): Show | 148 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.3+2432T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041796 | ||||||
| chr6:11041821
|
T | C | 1 | a0001c0001t0006g0024 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3+2407A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041821 | ||||||
| chr6:11041932
|
G | A | 139 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(136): Show | 148 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.3+2296C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041932 | ||||||
| chr6:11042001
|
A | AT | 119 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(116): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.3+2226dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042001 | ||||||
| chr6:11042001
|
A | ATT | 38 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0111others(35): Show | 46 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.3+2225_3+2226dupAA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042001 | ||||||
| chr6:11042005
|
T | TC | 104 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0343others(101): Show | 118 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.3+2222_3+2223insG | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042005 | ||||||
| chr6:11042045
|
C | CA | 18 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0343others(15): Show | 23 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.3+2182dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042045 | ||||||
| chr6:11042060
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3+2168G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042060 | ||||||
| chr6:11042076
|
C | T | 1 | a0001c0003t0005g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3+2152G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042076 | ||||||
| chr6:11042147
|
T | C | 3 | a0001c0002t0002g0259a0001c0002t0002g0260a0001c0002t0002g0261 | 3 | HG01981.hp2 HG01993.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.3+2081A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042147 | ||||||
| chr6:11042185
|
C | T | 59 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(56): Show | 67 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3+2043G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042185 | ||||||
| chr6:11042205
|
C | A | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0020others(20): Show | 26 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3+2023G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042205 | ||||||
| chr6:11042309
|
C | T | 1 | a0001c0001t0025g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+1919G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042309 | ||||||
| chr6:11042340
|
C | A | 2 | a0001c0001t0004g0187a0001c0001t0004g0188 | 2 | HG02015.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.3+1888G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042340 | ||||||
| chr6:11042400
|
C | CT | 139 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(136): Show | 148 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.3+1827dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042400 | ||||||
| chr6:11042528
|
T | A | 1 | a0001c0001t0003g0342 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3+1700A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042528 | ||||||
| chr6:11042528
|
T | C | 1 | a0001c0001t0005g0199 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3+1700A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042528 | ||||||
| chr6:11042542
|
A | G | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+1686T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042542 | ||||||
| chr6:11042617
|
C | T | 2 | a0001c0001t0008g0281a0001c0001t0008g0282 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3+1611G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042617 | ||||||
| chr6:11042618
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0117others(1): Show | 4 | HG01516.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+1610G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042618 | ||||||
| chr6:11042676
|
G | A | 59 | a0001c0002t0001g0237a0001c0002t0001g0345a0001c0002t0002g0007others(56): Show | 67 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3+1552C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042676 | ||||||
| chr6:11042806
|
C | T | 23 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0006g0020others(20): Show | 26 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3+1422G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042806 | ||||||
| chr6:11042832
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3+1396G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042832 | ||||||
| chr6:11042849
|
A | T | 3 | a0001c0001t0008g0205a0001c0001t0025g0277a0001c0001t0027g0206 | 3 | HG02922.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3+1379T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042849 | ||||||
| chr6:11042940
|
CT | C | 15 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0022others(12): Show | 16 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+1287delA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042940 | ||||||
| chr6:11043241
|
G | A | 34 | a0001c0001t0003g0001a0001c0001t0003g0019a0001c0001t0003g0311others(31): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.3+987C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043241 | ||||||
| chr6:11043404
|
A | AAC | 35 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(32): Show | 47 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3+822_3+823dupGT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACAC | 24 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0283others(21): Show | 26 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3+820_3+823dupGTGT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACAC | 12 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0008g0205others(9): Show | 12 | HG00642.hp2 HG00741.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.3+818_3+823dupGTGT others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(1): Show |
43 | a0001c0001t0001g0084a0001c0001t0001g0113a0001c0001t0001g0116others(40): Show | 46 | HG00323.hp2 HG00408.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.3+816_3+823dupGTGT others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(3): Show |
30 | a0001c0001t0001g0057a0001c0001t0001g0095a0001c0001t0001g0111others(27): Show | 34 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.3+814_3+823dupGTGT others(6): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(5): Show |
21 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0107others(18): Show | 23 | HG00544.hp2 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.3+812_3+823dupGTGT others(8): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(7): Show |
21 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0047others(18): Show | 21 | HG01433.hp1 HG01952.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.3+810_3+823dupGTGT others(10): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(9): Show |
26 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0045others(23): Show | 27 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.3+808_3+823dupGTGT others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(11): Show |
30 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0038others(27): Show | 30 | HG00408.hp2 HG01106.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.3+806_3+823dupGTGT others(14): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(13): Show |
10 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0058others(7): Show | 10 | HG00597.hp1 HG01123.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+804_3+823dupGTGT others(16): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(15): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0071 | 3 | HG02074.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3+802_3+823dupGTGT others(18): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
A | AACACACA others(19): Show |
1 | a0001c0001t0001g0041 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3+798_3+823dupGTGT others(22): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
AAC | A | 8 | a0001c0001t0003g0337a0001c0001t0003g0338a0001c0001t0003g0339others(5): Show | 8 | HG00621.hp1 HG00642.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+822_3+823delGT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
AACAC | A | 17 | a0001c0001t0003g0315a0001c0001t0003g0316a0001c0001t0003g0341others(14): Show | 21 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.3+820_3+823delGTGT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043404
|
AACACAC | A | 4 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0005g0012others(1): Show | 5 | HG00597.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+818_3+823delGTGT others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043404 | ||||||
| chr6:11043430
|
CACAGCTT others(30): Show |
C | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+761_3+797delTCAC others(33): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043430 | ||||||
| chr6:11043467
|
A | AAC | 3 | a0001c0001t0004g0130a0001c0001t0004g0131a0001c0001t0004g0132 | 3 | HG00639.hp1 HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.3+759_3+760dupGT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACAC | 30 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0003g0001others(27): Show | 38 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.3+755_3+760dupGTGT others(2): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(1): Show |
8 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0003g0313others(5): Show | 8 | HG02027.hp1 HG02922.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+753_3+760dupGTGT others(4): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(5): Show |
1 | a0001c0001t0001g0125 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3+749_3+760dupGTGT others(8): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(9): Show |
1 | a0001c0001t0001g0124 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3+745_3+760dupGTGT others(12): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(11): Show |
3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG02056.hp1 NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.3+743_3+760dupGTGT others(14): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(13): Show |
5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG01516.hp1 NA18944.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+741_3+760dupGTGT others(16): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(15): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG03942.hp2 NA18989.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(18): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(17): Show |
17 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0100others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(20): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(19): Show |
12 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00408.hp2 HG01123.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(22): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(21): Show |
14 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01071.hp2 HG01975.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(24): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(23): Show |
13 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(10): Show | 13 | HG00323.hp1 HG01358.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(26): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(25): Show |
8 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(5): Show | 8 | HG01106.hp1 HG01256.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(28): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(27): Show |
9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG00544.hp2 HG03669.hp2 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(30): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(29): Show |
7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 8 | HG01257.hp1 HG01258.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(32): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(31): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA18979.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(34): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(33): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01928.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.3+760_3+761insGTGT others(36): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | AACACACA others(37): Show |
1 | a0001c0001t0001g0309 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3+760_3+761insGTGT others(40): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043467
|
A | ACACACAC others(20): Show |
1 | a0001c0002t0002g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3+760_3+761insGTGT others(23): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043467 | ||||||
| chr6:11043471
|
C | CACACACA others(10): Show |
6 | a0001c0001t0008g0281a0001c0001t0008g0282a0001c0001t0029g0347others(3): Show | 6 | HG03139.hp2 HG03471.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+740_3+756dupTGTG others(13): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043471 | ||||||
| chr6:11043471
|
C | CACACACA others(12): Show |
86 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0006g0003others(83): Show | 100 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.3+756_3+757insTGTG others(15): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043471 | ||||||
| chr6:11043471
|
C | CACACACA others(14): Show |
13 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0005g0213others(10): Show | 15 | HG01361.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.3+756_3+757insTGTG others(17): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043471 | ||||||
| chr6:11043471
|
C | CACACACA others(16): Show |
2 | a0001c0001t0006g0211a0001c0001t0019g0212 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3+756_3+757insTGTG others(19): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043471 | ||||||
| chr6:11043471
|
C | CACACACA others(18): Show |
6 | a0001c0001t0006g0027a0001c0001t0006g0207a0001c0001t0006g0210others(3): Show | 7 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+756_3+757insTGTG others(21): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043471 | ||||||
| chr6:11043471
|
C | CACACACA others(20): Show |
7 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0022others(4): Show | 7 | HG00735.hp2 HG01243.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+756_3+757insTGTG others(23): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043471 | ||||||
| chr6:11043475
|
C | CACACACA others(10): Show |
6 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0002t0001g0284others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+752_3+753insTGTG others(13): Show |
ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043475 | ||||||
| chr6:11043541
|
T | C | 15 | a0001c0002t0001g0018a0001c0002t0001g0288a0001c0002t0001g0289others(12): Show | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+687A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043541 | ||||||
| chr6:11043609
|
G | A | 6 | a0001c0001t0012g0302a0001c0001t0012g0303a0001c0001t0012g0304others(3): Show | 6 | HG01361.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+619C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043609 | ||||||
| chr6:11043686
|
T | A | 2 | a0002c0004t0016g0203a0002c0004t0016g0204 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3+542A>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043686 | ||||||
| chr6:11043687
|
G | A | 1 | a0001c0002t0001g0308 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3+541C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043687 | ||||||
| chr6:11043688
|
C | A | 1 | a0001c0002t0001g0308 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3+540G>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043688 | ||||||
| chr6:11043715
|
A | T | 15 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0022others(12): Show | 16 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+513T>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043715 | ||||||
| chr6:11043760
|
G | C | 2 | a0001c0001t0008g0205a0001c0001t0027g0206 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3+468C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043760 | ||||||
| chr6:11043835
|
T | G | 124 | a0001c0001t0001g0265a0001c0001t0001g0272a0001c0001t0001g0283others(121): Show | 141 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.3+393A>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043835 | ||||||
| chr6:11043847
|
G | A | 141 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(138): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.3+381C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043847 | ||||||
| chr6:11043856
|
C | T | 101 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3+372G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043856 | ||||||
| chr6:11043884
|
A | G | 2 | a0001c0001t0010g0004a0001c0001t0010g0029 | 4 | HG01891.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+344T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043884 | ||||||
| chr6:11043890
|
G | A | 2 | a0001c0002t0001g0345a0001c0002t0002g0346 | 2 | NA18988.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.3+338C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043890 | ||||||
| chr6:11043974
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0028 | 3 | HG02145.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3+254C>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043974 | ||||||
| chr6:11044038
|
C | T | 8 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0022others(5): Show | 8 | HG00735.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+190G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11044038 |