Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MEHLK others(291): Show |
chr6 | 10975759 | 11049305 |
| a0002 | 0/0 | 296 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | MEHLK others(291): Show |
chr6 | 10975759 | 11049305 |
| a0003 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | MEHLK others(291): Show |
chr6 | 10975759 | 11049305 |
| a0004 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | MEHLK others(291): Show |
chr6 | 10975759 | 11049305 |
| a0005 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | MEHLK others(291): Show |
chr6 | 10975759 | 11049305 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 888 | 270 | 66 | 42 | 128 | 7 | 25 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
chr6 | 10975759 | 11049305 | ||
| a0001c0002 | 0/0 | 888 | 90 | 24 | 19 | 40 | 1 | 6 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
chr6 | 10975759 | 11049305 | ||
| a0001c0003 | 0/0 | 888 | 14 | 0 | 5 | 0 | 4 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
chr6 | 10975759 | 11049305 | ||
| a0001c0007 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
chr6 | 10975759 | 11049305 | ||
| a0002c0004 | 0/0 | 888 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
chr6 | 10975759 | 11049305 | ||
| a0003c0005 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
chr6 | 10975759 | 11049305 | ||
| a0004c0008 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
chr6 | 10975759 | 11049305 | ||
| a0005c0006 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | ATGGA others(883): Show |
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 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0003 | 0/0 | 3988 | 40 | 0 | 1 | 39 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0004 | 1/0 | 3988 | 37 | 0 | 12 | 18 | 3 | 3 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0005 | 0/0 | 3988 | 23 | 11 | 8 | 1 | 1 | 2 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0006 | 0/0 | 3988 | 18 | 16 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0007 | 0/0 | 3988 | 11 | 0 | 11 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0008 | 0/0 | 3988 | 10 | 10 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0010 | 0/0 | 3988 | 9 | 9 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0011 | 0/0 | 3988 | 7 | 0 | 0 | 7 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0012 | 0/0 | 3988 | 6 | 5 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0013 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0014 | 0/0 | 3988 | 5 | 0 | 0 | 2 | 0 | 3 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0015 | 0/0 | 3988 | 4 | 0 | 0 | 4 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0017 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0019 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0020 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0023 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0025 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0026 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0027 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0028 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0001t0029 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0002t0001 | 0/0 | 3988 | 21 | 19 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0002t0002 | 0/0 | 3988 | 53 | 1 | 18 | 29 | 0 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0002t0004 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0002t0009 | 0/0 | 3988 | 9 | 0 | 0 | 9 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0002t0013 | 0/0 | 3988 | 4 | 3 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0002t0021 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0002t0022 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0003t0005 | 0/0 | 3988 | 14 | 0 | 5 | 0 | 4 | 5 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0001c0007t0018 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0002c0004t0016 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0003c0005t0004 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0004c0008t0001 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| a0005c0006t0024 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | GGGCA others(3983): Show |
chr6 | 10975759 | 11049305 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0052 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0070 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0074 | 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 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 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 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0121 | 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 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0172 | 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 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0005g0208 | 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 |
| a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0008g0277 | 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 |
| a0001c0001t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0011g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0012g0301 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0014g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0015g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0015g0159 | 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 |
| a0001c0001t0017g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0020g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0023g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0025g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0026g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0027g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0028g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0001t0029g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0283 | 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 |
| a0001c0002t0001g0286 | 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 |
| 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 |
| a0001c0002t0001g0294 | 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 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0231 | 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 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0237 | 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 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0004g0240 | 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 |
| a0001c0002t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0013g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0021g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0002t0022g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0003t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0001c0007t0018g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0002c0004t0016g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0002c0004t0016g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0003c0005t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0004c0008t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| a0005c0006t0024g0304 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0141 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00280 | hp2 | a0001 | c0003 | t0005 | g0178 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0240 | EUR | FIN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | CHS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0257 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01070 | hp2 | a0001 | c0003 | t0005 | g0007 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01071 | hp1 | a0001 | c0003 | t0005 | g0007 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0093 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01074 | hp1 | a0001 | c0003 | t0005 | g0007 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01074 | hp2 | a0001 | c0003 | t0005 | g0181 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0213 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01099 | hp1 | a0001 | c0003 | t0005 | g0177 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0191 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0065 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0169 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0131 | 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 | g0144 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01358 | hp1 | a0001 | c0001 | t0007 | g0077 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0245 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01361 | hp2 | a0001 | c0001 | t0012 | g0301 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0146 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0186 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01515 | hp2 | a0001 | c0003 | t0005 | g0014 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01516 | hp2 | a0001 | c0003 | t0005 | g0167 | EUR | IBS | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01884 | hp2 | a0001 | c0002 | t0013 | g0289 | 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 | g0020 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0126 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0108 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01975 | hp2 | a0001 | c0001 | t0020 | g0174 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0097 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0114 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0254 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0089 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0255 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0303 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0313 | 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 | g0183 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0111 | 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 | g0067 | EAS | CDX | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02257 | hp2 | a0001 | c0007 | t0018 | g0204 | 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 | g0019 | 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 | g0010 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | PEL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0261 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | KHV | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0211 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0271 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0268 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0263 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02683 | hp1 | a0001 | c0003 | t0005 | g0165 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0193 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0151 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0209 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0210 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02738 | hp1 | a0001 | c0003 | t0005 | g0166 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0160 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02922 | hp1 | a0001 | c0002 | t0013 | g0295 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0200 | 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 | g0023 | 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 | g0293 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0299 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0203 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03017 | hp2 | a0001 | c0003 | t0005 | g0014 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0297 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0277 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0016 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0300 | 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 | g0208 | 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 | g0028 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03453 | hp2 | a0002 | c0004 | t0016 | g0199 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0187 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0298 | AFR | GWD | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0262 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03579 | hp2 | a0002 | c0004 | t0016 | g0198 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03654 | hp1 | a0001 | c0001 | t0014 | g0079 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03654 | hp2 | a0001 | c0001 | t0013 | g0094 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03669 | hp1 | a0001 | c0003 | t0005 | g0132 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03927 | hp2 | a0001 | c0001 | t0026 | g0149 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0192 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0251 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04184 | hp1 | a0001 | c0002 | t0013 | g0224 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04199 | hp1 | a0001 | c0003 | t0005 | g0179 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0142 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04204 | hp1 | a0001 | c0001 | t0014 | g0188 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0222 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0243 | SAS | STU | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18906 | hp1 | a0001 | c0001 | t0029 | g0341 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0063 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18947 | hp1 | a0001 | c0002 | t0009 | g0235 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18948 | hp1 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18948 | hp2 | a0001 | c0002 | t0009 | g0234 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18949 | hp1 | a0001 | c0001 | t0011 | g0122 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18953 | hp2 | a0003 | c0005 | t0004 | g0197 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18954 | hp2 | a0004 | c0008 | t0001 | g0041 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0055 | 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 | g0156 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18962 | hp2 | a0001 | c0001 | t0011 | g0113 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0118 | 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 | g0196 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0034 | 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 | g0162 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18974 | hp2 | a0001 | c0001 | t0011 | g0104 | 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 | g0273 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18983 | hp2 | a0001 | c0002 | t0009 | g0226 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18984 | hp1 | a0001 | c0001 | t0014 | g0190 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0071 | 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 | g0336 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0001 | 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 | g0119 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0115 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19000 | hp1 | a0001 | c0002 | t0009 | g0249 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0328 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0116 | 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 | g0158 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0044 | 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 | g0206 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19030 | hp2 | a0001 | c0001 | t0025 | g0272 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19043 | hp1 | a0005 | c0006 | t0024 | g0304 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0201 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19057 | hp2 | a0001 | c0001 | t0015 | g0159 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0064 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0340 | 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 | g0212 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19068 | hp1 | a0001 | c0001 | t0014 | g0189 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0231 | 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 | g0100 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19085 | hp2 | a0001 | c0001 | t0011 | g0120 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0305 | 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 | g0083 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20129 | hp2 | a0001 | c0001 | t0019 | g0207 | AFR | ASW | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0175 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20752 | hp2 | a0001 | c0003 | t0005 | g0133 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0176 | EUR | TSI | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG01123 | hp2 | a0001 | c0002 | t0022 | g0248 | AMR | CLM | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0302 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0264 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0276 | AFR | MSL | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | USA | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0021 | 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 | g0054 | EAS | JPT | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA21309 | hp1 | a0001 | c0002 | t0021 | g0217 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | LWK | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0033 | REF | REF | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0155 | REF | REF | ELOVL2_chr6_10975759_11049305 | ELOVL2 | chr6 | 10975759 | 11049305 |
| view | 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 | a0002 a0005 |
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 | a0004 | 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 | a0005 | 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 | a0003 | 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 |
| view | 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 |
| view | 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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(17): Show |
278 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(275): 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 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0023 |
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 | a0001c0002t0002 a0001c0002t0009 a0001c0002t0021 others(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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(23): Show |
292 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(289): 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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(28): Show |
339 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(336): 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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(11): Show |
240 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(237): 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 | a0005c0006t0024 | 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 | a0005c0006t0024 | 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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(19): Show |
271 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(268): 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 |
| view | 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 | 249 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
279 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(276): 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 | a0001c0001t0004g0147 | 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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0020g0174 | 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 | a0001c0001t0004g0143 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0068 |
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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0006g0003 others(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 | a0001c0001t0020g0174 | 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 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 others(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 | 200 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(197): Show |
221 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(218): 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.766-1348C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10985254 | |||||||
| chr6:10985319 | C | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): 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 |
261 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
292 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(289): 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 | a0001c0001t0020g0174 | 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | 33 | a0001c0001t0003g0001 a0001c0001t0003g0022 a0001c0001t0003g0305 others(30): 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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0002t0002g0236 |
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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0002t0001g0021 others(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 | a0005c0006t0024g0304 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0010g0004 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0002t0001g0021 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0002t0002g0050 | 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0020g0174 | 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 | 248 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(245): Show |
278 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(275): 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 | a0001c0002t0022g0248 | 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 | a0001c0001t0005g0208 | 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 | a0001c0001t0020g0174 a0001c0001t0025g0272 |
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 | 40 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0278 others(37): 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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): 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 | a0001c0001t0004g0148 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0070 | 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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0008g0200 a0001c0001t0027g0201 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0001t0008g0019 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0001t0006g0024 | 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 | 37 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(34): 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0020g0174 | 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0025g0272 | 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 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 |
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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0025g0272 | 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 | a0001c0003t0005g0177 a0001c0003t0005g0178 |
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 | a0001c0001t0001g0055 | 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 | a0001c0001t0005g0163 a0001c0001t0005g0168 a0001c0001t0005g0169 |
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 | a0001c0001t0025g0272 | 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0012g0298 | 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 | a0001c0002t0002g0229 a0001c0002t0002g0233 |
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 | a0001c0001t0004g0143 a0001c0001t0004g0175 |
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 | a0001c0001t0025g0272 | 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 | 1 | a0001c0001t0001g0013 | 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 | a0001c0001t0014g0079 | 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 | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.765+62dupT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 7/7 | chr6 | 10989640 | |||||||
| chr6:10989653 | A | G | 1 | a0005c0006t0024g0304 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0270 others(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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0006g0205 a0001c0007t0018g0204 |
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 | a0001c0001t0008g0019 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | a0003c0005t0004g0197 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0006g0003 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0020g0174 | 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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | a0001c0001t0004g0128 a0001c0001t0004g0130 a0001c0001t0004g0138 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0004g0144 | 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 | 233 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(230): Show |
260 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(257): 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0020g0174 | 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 | a0001c0002t0002g0273 | 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 | a0001c0002t0001g0265 a0001c0002t0001g0266 |
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 | 249 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
279 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(276): 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 | a0001c0001t0020g0174 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | 249 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
279 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(276): 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 | a0001c0001t0025g0272 | 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 | a0001c0002t0009g0002 a0001c0002t0009g0226 a0001c0002t0009g0234 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0008g0019 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0038 | 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 | a0001c0001t0003g0323 | 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0002t0001g0021 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0209 a0001c0001t0008g0210 others(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 | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0029g0341 | 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 | 303 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(300): Show |
340 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(337): Show |
intron_variant | MODIFIER | c.506-2262T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 5/7 | chr6 | 10992704 | |||||||
| chr6:10992747 | CACTGCAC others(16): Show |
C | 1 | a0001c0001t0005g0194 | 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 | a0001c0001t0005g0194 | 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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0046 others(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 | 98 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
111 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(108): 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 | a0001c0001t0004g0006 a0001c0001t0004g0144 a0001c0001t0015g0157 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0002t0001g0021 others(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 | a0001c0001t0011g0115 a0001c0001t0011g0122 |
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 | a0001c0001t0006g0202 a0001c0002t0001g0296 |
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 | a0001c0002t0001g0296 | 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 | a0001c0001t0006g0202 | 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 | 136 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): 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 | a0001c0001t0003g0317 | 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 | a0001c0001t0001g0123 a0001c0002t0002g0229 a0001c0002t0002g0233 |
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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0003g0317 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0005g0208 | 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 | a0001c0001t0012g0297 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0002t0001g0021 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0100 | 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 | a0001c0002t0002g0220 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0004g0129 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0046 others(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 | 74 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
79 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(76): 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 | a0001c0001t0012g0298 a0001c0001t0012g0299 a0001c0001t0012g0300 others(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 | a0001c0001t0004g0148 | 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 | a0001c0001t0003g0318 a0001c0001t0003g0325 a0001c0001t0008g0276 others(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 | 34 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0049 others(31): 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0006g0205 |
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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0008g0019 a0001c0001t0008g0262 a0001c0001t0008g0263 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0337 a0001c0001t0004g0150 others(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 | a0001c0001t0008g0019 a0001c0001t0008g0262 a0001c0001t0008g0264 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0119 |
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 | a0001c0001t0029g0341 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0085 a0001c0001t0001g0260 others(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 | 159 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(156): Show |
180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): 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 | a0001c0001t0001g0039 a0001c0001t0001g0337 a0001c0001t0001g0338 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0029g0341 | 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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(175): Show |
192 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(189): 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.334-217C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10995395 | |||||||
| chr6:10995519 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
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 | a0001c0001t0020g0174 | 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0002t0001g0021 others(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 | a0001c0002t0013g0224 | 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 | a0001c0002t0001g0290 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0025g0272 | 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 | a0001c0002t0001g0285 | 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 | a0001c0001t0025g0272 | 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 | 180 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(177): Show |
194 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(191): 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 | a0001c0001t0005g0008 a0001c0001t0005g0126 a0001c0001t0005g0136 others(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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0003g0330 | 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 | a0001c0001t0010g0268 | 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 | 32 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(29): 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 | a0001c0001t0005g0015 a0001c0001t0005g0208 |
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 | a0001c0001t0003g0312 | 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 | 2 | a0001c0001t0001g0011 a0001c0001t0001g0056 |
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 | 249 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
279 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(276): 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 | a0001c0002t0002g0244 | 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 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0286 others(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 | a0001c0002t0001g0286 a0001c0002t0001g0288 |
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 | a0001c0001t0025g0272 | 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 | a0001c0001t0001g0278 | 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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0002t0013g0224 | 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 | a0001c0001t0005g0171 a0001c0001t0005g0173 |
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 | a0001c0001t0025g0272 | 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 | a0001c0001t0008g0277 | 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 | 237 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(234): Show |
267 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.333+706dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999380 | |||||||
| chr6:10999409 | T | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.333+678A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 4/7 | chr6 | 10999409 | |||||||
| chr6:10999417 | T | C | 253 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): 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 | a0001c0003t0005g0177 a0001c0003t0005g0178 a0001c0003t0005g0179 |
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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0004g0176 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0008g0019 others(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 | a0001c0007t0018g0204 | 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 | a0001c0001t0003g0333 a0001c0001t0003g0334 a0001c0001t0003g0336 |
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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0006g0025 | 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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0007g0012 | 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 | a0001c0001t0005g0136 a0001c0001t0005g0161 a0001c0001t0005g0164 others(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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0004g0138 | 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 | a0001c0001t0029g0341 | 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 | a0001c0001t0005g0208 | 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 | a0001c0001t0001g0072 | 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 | 2 | a0001c0001t0001g0011 a0001c0001t0001g0056 |
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 | a0001c0001t0025g0272 | 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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.256-2386C>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 3/7 | chr6 | 11002550 | |||||||
| chr6:11002577 | T | C | 243 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
273 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(270): 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 | a0001c0001t0008g0200 | 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 | a0001c0002t0002g0241 | 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 | a0001c0002t0001g0021 a0001c0002t0001g0265 a0001c0002t0001g0266 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0029g0341 | 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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0029g0341 | 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 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | 302 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(299): Show |
339 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(336): 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 | a0001c0001t0006g0205 | 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 | a0001c0001t0006g0024 | 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 | a0001c0002t0009g0249 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0001t0006g0025 others(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 | a0001c0002t0001g0292 | 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 | a0001c0001t0005g0126 | 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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0001g0086 a0001c0001t0003g0330 a0001c0001t0004g0128 others(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 | a0001c0001t0008g0210 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0002t0002g0223 | 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 | 184 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(181): Show |
198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): 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 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0002t0001g0285 | 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0020g0174 | 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 | a0001c0001t0011g0115 a0001c0001t0011g0122 |
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 | a0001c0001t0007g0065 | 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 | 253 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.68-50A>G | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 2/7 | chr6 | 11005609 | |||||||
| chr6:11005793 | A | G | 184 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(181): Show |
198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0001t0008g0262 | 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 | a0001c0001t0001g0338 | 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 | a0001c0001t0019g0207 | 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 | a0001c0001t0029g0341 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0002t0001g0282 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0014g0188 | 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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0012g0298 | 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 | a0001c0001t0005g0015 | 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 | a0001c0001t0005g0015 | 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 | 33 | a0001c0001t0003g0001 a0001c0001t0003g0022 a0001c0001t0003g0305 others(30): 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 | a0001c0002t0001g0280 | 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 | a0001c0001t0029g0341 | 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 | a0001c0001t0008g0210 | 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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | a0005c0006t0024g0304 | 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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | 184 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(181): Show |
198 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(195): 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 | a0001c0003t0005g0007 a0001c0003t0005g0014 a0001c0003t0005g0132 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0002t0002g0231 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0078 a0001c0001t0001g0096 |
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 | a0001c0001t0006g0028 a0001c0001t0006g0029 a0001c0001t0006g0030 |
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 | 105 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0034 others(102): 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0008g0019 others(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 | a0001c0001t0001g0080 a0001c0002t0002g0231 |
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 | a0001c0001t0011g0120 | 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 | 253 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): 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 | a0001c0001t0019g0207 | 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 | 252 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(249): Show |
282 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(279): 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 | a0001c0001t0003g0334 | 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 | a0001c0002t0001g0021 a0001c0002t0001g0265 a0001c0002t0001g0266 others(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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0001g0087 | 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 | a0005c0006t0024g0304 | 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 | 33 | a0001c0001t0003g0001 a0001c0001t0003g0022 a0001c0001t0003g0305 others(30): 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 | 222 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(219): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): 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 | a0001c0001t0008g0262 a0001c0001t0010g0261 a0001c0001t0010g0268 |
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 | a0001c0001t0001g0338 | 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 | a0001c0001t0003g0315 | 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 | 253 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.4-489T>C | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11011298 | |||||||
| chr6:11011365 | C | CA | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0003g0327 a0001c0001t0006g0003 a0001c0001t0006g0020 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0005g0163 a0001c0001t0005g0168 a0001c0001t0005g0169 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | 2 | a0001c0001t0001g0013 a0001c0001t0001g0088 |
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 | a0001c0002t0002g0243 | 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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | a0001c0001t0004g0135 a0001c0001t0004g0154 a0001c0001t0004g0156 |
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 | a0001c0001t0006g0202 | 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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0001g0267 | 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 | 253 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0008g0019 a0001c0001t0008g0263 a0001c0001t0008g0264 |
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 | a0001c0001t0029g0341 | 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 | a0001c0002t0002g0275 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0029g0341 | 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 | a0001c0001t0014g0079 | 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 | 155 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(152): 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 | 20 | a0001c0001t0001g0072 a0001c0001t0001g0099 a0001c0001t0001g0105 others(17): Show |
20 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(17): 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 | 71 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0260 others(68): 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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | 250 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(247): Show |
280 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(277): 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 | a0001c0001t0020g0174 | 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 | 65 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0278 others(62): 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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0020g0174 | 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0008g0019 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0185 |
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 | a0001c0001t0008g0210 | 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0005c0006t0024g0304 | 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 |
222 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(219): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): 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 | a0001c0001t0001g0037 | 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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0003t0005g0007 a0001c0003t0005g0014 a0001c0003t0005g0132 others(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 | a0001c0002t0002g0018 | 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 | a0001c0001t0020g0174 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0270 others(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 | a0001c0002t0002g0257 a0001c0002t0002g0258 a0001c0002t0002g0259 |
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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0051 others(1): Show |
4 | HG01516.hp1 HG02698.hp2 HG03927.hp1 others(1): 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 | a0001c0001t0008g0262 | 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 | a0005c0006t0024g0304 | 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 | 250 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(247): Show |
280 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(277): 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0004g0156 | 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 | a0001c0002t0001g0287 | 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 | a0001c0001t0004g0180 | 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 | a0001c0001t0020g0174 | 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 | a0001c0002t0002g0223 | 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 | 253 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): 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 | a0001c0001t0003g0307 a0001c0001t0003g0311 a0001c0001t0003g0312 |
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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0020g0174 | 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 | a0001c0001t0005g0208 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0004g0143 | 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 | a0001c0002t0002g0218 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0012g0302 | 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 | a0001c0001t0003g0326 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0092 a0001c0001t0001g0110 others(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 | a0001c0001t0005g0163 a0001c0001t0005g0168 a0001c0001t0005g0169 others(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 | a0001c0001t0004g0151 a0001c0001t0004g0152 |
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 | 250 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(247): Show |
280 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.4-9375delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11020183 | |||||||
| chr6:11020202 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0002t0009g0226 | 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0020g0174 | 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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0008g0209 a0001c0001t0008g0210 |
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 | a0001c0001t0010g0032 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0005g0126 | 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 | a0001c0001t0014g0079 | 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0003g0309 a0001c0001t0003g0313 a0001c0001t0003g0314 others(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 | a0001c0001t0012g0300 | 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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0001g0337 others(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 | a0001c0001t0020g0174 | 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0005g0168 a0001c0001t0005g0169 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0002t0002g0216 | 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 | a0001c0002t0002g0215 | 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 | a0001c0002t0002g0225 | 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 | a0001c0002t0002g0214 | 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 | a0001c0001t0003g0319 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0270 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0002t0002g0230 | 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0005g0193 a0001c0001t0014g0189 a0001c0001t0014g0190 |
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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0006g0026 a0001c0001t0006g0027 |
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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0002t0004g0240 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | a0001c0001t0007g0012 a0001c0001t0007g0077 a0001c0001t0007g0089 |
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 | a0001c0001t0003g0307 a0001c0001t0003g0311 a0001c0001t0003g0312 |
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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0002t0002g0254 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): 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 | a0001c0001t0003g0319 | 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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): 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 | a0001c0001t0004g0142 | 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 | a0001c0001t0004g0142 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0020g0174 | 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 | a0001c0001t0005g0208 | 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 | a0001c0002t0002g0017 a0001c0002t0002g0239 a0001c0002t0002g0241 |
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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | 99 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(96): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): 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 | a0001c0001t0003g0333 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0029g0341 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0016 a0001c0001t0010g0032 others(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 | a0001c0002t0002g0247 | 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 | a0001c0001t0008g0200 a0001c0001t0027g0201 |
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 | a0001c0002t0001g0021 a0001c0002t0001g0232 a0001c0002t0001g0279 others(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 | a0001c0001t0006g0202 | 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 | a0001c0002t0002g0213 a0001c0002t0002g0221 a0001c0002t0002g0222 |
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 | 252 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(249): Show |
282 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(279): 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 | 252 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(249): Show |
282 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(279): 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 | a0001c0003t0005g0165 | 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 | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): 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 | a0001c0001t0029g0341 | 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0002t0001g0021 a0001c0002t0001g0232 a0001c0002t0001g0279 others(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 | a0001c0001t0004g0153 | 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 | a0001c0001t0014g0189 | 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 | a0001c0001t0020g0174 a0001c0001t0025g0272 |
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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0008g0019 others(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 | a0001c0001t0003g0310 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0048 others(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 | a0001c0001t0004g0141 | 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 | a0001c0002t0002g0231 | 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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0006g0028 | 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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3+15170delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11029057 | |||||||
| chr6:11029057 | CAA | C | 27 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0081 others(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 | 38 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0047 others(35): 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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0029g0341 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0008g0209 a0001c0001t0008g0210 |
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 | a0001c0001t0025g0272 | 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 | a0001c0001t0003g0321 a0001c0001t0014g0079 |
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 | a0001c0001t0025g0272 | 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 | a0001c0001t0008g0277 | 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 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0007t0018g0204 |
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 | a0001c0001t0025g0272 | 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | 32 | a0001c0001t0003g0001 a0001c0001t0003g0022 a0001c0001t0003g0305 others(29): 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 | a0001c0001t0003g0320 a0001c0001t0003g0321 a0001c0001t0003g0322 others(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 | a0001c0002t0001g0279 a0001c0002t0001g0282 a0001c0002t0001g0288 others(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 | a0001c0002t0001g0280 a0001c0002t0001g0283 a0001c0002t0001g0284 others(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 | a0001c0001t0008g0200 a0001c0001t0008g0210 a0001c0001t0025g0272 others(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 | a0001c0001t0012g0298 a0001c0001t0012g0299 |
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 | a0001c0001t0012g0297 a0001c0001t0012g0300 a0001c0001t0012g0301 |
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 | a0001c0001t0012g0302 | 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 | a0005c0006t0024g0304 | 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 | a0002c0004t0016g0198 | 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 | a0002c0004t0016g0199 | 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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0004g0130 a0001c0001t0004g0137 a0001c0001t0004g0176 others(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 | a0001c0001t0001g0278 a0001c0001t0010g0004 a0001c0001t0010g0016 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | 94 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(91): Show |
99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0001g0047 a0001c0001t0001g0092 a0001c0001t0001g0116 |
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 | a0001c0001t0008g0262 a0001c0001t0010g0261 a0001c0001t0010g0268 |
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 | a0001c0001t0006g0027 | 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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0004c0008t0001g0041 | 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 | a0001c0001t0003g0022 a0001c0001t0003g0305 a0001c0001t0003g0308 others(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 | a0001c0002t0002g0251 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
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 | a0001c0002t0013g0224 | 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 | a0005c0006t0024g0304 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0008g0277 | 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 | a0001c0003t0005g0007 a0001c0003t0005g0014 a0001c0003t0005g0132 others(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 | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): 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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0002t0001g0265 a0001c0002t0001g0266 |
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 | a0001c0002t0001g0292 a0001c0002t0001g0296 a0001c0002t0013g0293 others(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 | a0005c0006t0024g0304 | 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 | a0001c0001t0005g0015 | 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 | 137 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
151 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(148): 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0282 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0020g0174 | 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 | a0001c0001t0005g0173 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | a0001c0001t0008g0209 a0001c0001t0008g0210 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | 42 | a0001c0001t0003g0322 a0001c0001t0004g0006 a0001c0001t0004g0127 others(39): 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 | 143 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0073 others(140): 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 | 130 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(127): Show |
142 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(139): 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0007g0097 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0008g0019 a0001c0001t0008g0263 a0001c0001t0008g0264 others(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 | a0001c0001t0001g0052 a0004c0008t0001g0041 |
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 | a0001c0001t0025g0272 | 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 | a0001c0002t0001g0021 a0001c0002t0001g0232 a0001c0002t0001g0279 others(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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0023 others(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 | a0001c0001t0020g0174 | 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 | a0001c0001t0025g0272 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.3+11297C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11032931 | |||||||
| chr6:11033235 | T | C | 250 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(247): Show |
280 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(277): 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 | a0001c0001t0014g0079 | 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0003g0323 a0001c0001t0003g0324 |
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 | a0001c0001t0020g0174 | 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 | a0001c0001t0005g0194 | 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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): 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 | a0001c0001t0004g0143 a0001c0001t0004g0175 |
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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | 158 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
179 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(176): 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0010g0203 | 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 | a0001c0001t0001g0338 | 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 | 158 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
179 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.3+9036G>A | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035192 | |||||||
| chr6:11035193 | A | C | 158 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
179 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(176): 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 | a0001c0002t0002g0257 a0001c0002t0002g0258 a0001c0002t0002g0259 |
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 | a0001c0001t0023g0328 | 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 | a0001c0001t0014g0189 a0001c0001t0014g0190 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0003g0332 | 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 | a0001c0002t0001g0282 a0001c0002t0001g0303 |
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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.3+8608C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11035620 | |||||||
| chr6:11035739 | T | C | 104 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0267 others(101): 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 | a0001c0002t0002g0220 | 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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0001t0006g0025 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0260 a0001c0001t0001g0267 others(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 | 303 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(300): Show |
340 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(337): 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0078 a0001c0001t0001g0096 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0005g0208 others(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 | a0001c0001t0010g0032 | 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 | a0001c0001t0004g0175 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0005g0208 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0004g0182 | 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 | a0001c0001t0004g0182 | 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 | a0001c0001t0004g0182 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0031 |
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 |
32 | a0001c0001t0003g0001 a0001c0001t0003g0022 a0001c0001t0003g0305 others(29): 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 | a0001c0001t0023g0328 | 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 | a0001c0001t0004g0182 | 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 | a0001c0001t0004g0182 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0003g0336 | 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 | a0001c0001t0014g0187 a0001c0001t0014g0188 |
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 | a0001c0002t0009g0235 | 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 | 240 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(237): Show |
264 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.3+6688delT | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11037539 | |||||||
| chr6:11037809 | T | C | 2 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0005c0006t0024g0304 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0278 others(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 | a0001c0001t0010g0004 a0001c0001t0010g0032 |
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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0278 others(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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0025g0272 | 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 | 98 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(95): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): 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 | a0001c0001t0029g0341 | 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 | 1 | a0001c0001t0001g0013 | 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 | a0001c0001t0003g0326 | 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 | 1 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0004g0176 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
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 | a0001c0001t0006g0206 | 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 | a0001c0001t0029g0341 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0270 others(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 | a0001c0001t0029g0341 | 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 | a0001c0001t0029g0341 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(32): 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 | a0001c0001t0007g0077 | 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 | a0001c0001t0001g0095 | 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 | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): 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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0031 | 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 | 263 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(260): Show |
294 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(291): 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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0012g0302 | 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 | a0001c0001t0029g0341 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0337 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0023 others(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 | a0001c0001t0029g0341 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0278 others(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 | a0001c0003t0005g0014 a0001c0003t0005g0133 a0001c0003t0005g0177 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0023 others(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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0005g0208 a0001c0001t0008g0200 a0001c0001t0008g0209 others(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 | a0001c0001t0004g0180 a0001c0002t0002g0221 a0001c0002t0002g0222 |
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 | a0001c0002t0001g0021 a0001c0002t0001g0283 a0001c0002t0001g0284 others(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 | a0001c0002t0002g0269 | 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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0001t0001g0074 | 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 | a0001c0002t0001g0021 a0001c0002t0001g0283 a0001c0002t0001g0284 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0003t0005g0181 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0337 others(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 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0001t0006g0025 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0005c0006t0024g0304 | 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 | a0001c0001t0005g0208 a0001c0001t0008g0209 a0001c0001t0008g0210 |
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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): 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 | a0001c0001t0006g0027 | 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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.3+2296C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11041932 | |||||||
| chr6:11042001 | A | AT | 114 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(111): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.3+2226dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042001 | |||||||
| chr6:11042001 | A | ATT | 37 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0116 others(34): 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0337 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0337 others(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 | a0001c0001t0001g0123 | 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 | a0001c0003t0005g0133 | 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 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 |
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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0023 others(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 | a0001c0001t0025g0272 | 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 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
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 | 133 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.3+1827dupA | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11042400 | |||||||
| chr6:11042528 | T | A | 1 | a0001c0001t0003g0336 | 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 | a0001c0001t0005g0194 | 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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0048 others(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 | a0001c0002t0001g0232 a0001c0002t0001g0339 a0001c0002t0002g0009 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0006g0023 others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0008g0200 a0001c0001t0025g0272 a0001c0001t0027g0201 |
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 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0001t0006g0025 others(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 | 33 | a0001c0001t0003g0001 a0001c0001t0003g0022 a0001c0001t0003g0305 others(30): 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 | 34 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(31): 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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0278 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0008g0200 others(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 |
42 | a0001c0001t0001g0013 a0001c0001t0001g0123 a0001c0001t0005g0126 others(39): 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 |
19 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0006g0206 others(16): 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 |
20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0098 others(17): Show |
20 | HG01433.hp1 HG01952.hp2 HG01978.hp2 others(17): 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 |
25 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0080 others(22): 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 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
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 | a0001c0001t0001g0034 | 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 | a0001c0001t0003g0329 a0001c0001t0003g0330 a0001c0001t0003g0331 others(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 | a0001c0001t0003g0333 a0001c0001t0003g0334 a0001c0001t0003g0335 others(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 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0005g0015 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0001t0004g0006 a0001c0001t0004g0143 a0001c0001t0004g0144 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0001 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0314 a0001c0001t0003g0315 others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0106 |
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 |
16 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0047 others(13): Show |
16 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(13): 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 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0062 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0090 |
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 | a0001c0001t0001g0306 | 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 | a0001c0002t0002g0050 | 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 | a0001c0001t0008g0276 a0001c0001t0008g0277 a0001c0001t0029g0341 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0006g0003 others(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 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0005g0208 others(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 | a0001c0001t0006g0206 a0001c0001t0019g0207 |
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 | a0001c0001t0006g0030 a0001c0001t0006g0202 a0001c0001t0006g0205 others(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 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0001t0006g0025 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0002t0001g0279 others(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 | a0001c0002t0001g0021 a0001c0002t0001g0283 a0001c0002t0001g0284 others(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 | a0001c0001t0012g0297 a0001c0001t0012g0298 a0001c0001t0012g0299 others(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 | a0002c0004t0016g0198 a0002c0004t0016g0199 |
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 | a0001c0002t0001g0303 | 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 | a0001c0002t0001g0303 | 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 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0001t0006g0025 others(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 | a0001c0001t0008g0200 a0001c0001t0027g0201 |
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 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0278 others(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 | 135 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.3+381C>T | ELOVL2 | ENSG00000197977.4 | transcript | ENST00000354666.4 | protein_coding | 1/7 | chr6 | 11043847 | |||||||
| chr6:11043856 | C | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): 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 | a0001c0001t0010g0004 a0001c0001t0010g0032 |
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 | a0001c0002t0001g0339 a0001c0002t0002g0340 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0031 |
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 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0001t0006g0025 others(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 |